5149 NP_002531 R282H not found in SNVbox database
1291 NP_705833 S177F not found in SNVbox database
2284 NP_705833 S508A not found in SNVbox database
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr19:58862775 G>A maps to NM_130786.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:58863826 A>G maps to NM_130786.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr10:52588037 C>A maps to NM_138932.2 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:52596038 C>T maps to NM_138932.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr10:52573625 G>T maps to NM_138932.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:7383040 C>T maps to NM_145891.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:7759063 A>G maps to NM_145891.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:7703853 C>T maps to NM_145891.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr16:7383010 G>A maps to NM_145891.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr16:7383010 G>A maps to NM_145891.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr16:7703859 C>T maps to NM_145891.2 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr16:7568354 G>A maps to NM_145891.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:7680638 A>G maps to NM_145891.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr16:7383067 T>A maps to NM_145891.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr16:7645561 C>T maps to NM_145891.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:9246137 C>T maps to NM_000014.4 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:9231877 G>T maps to NM_000014.4 T1027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:9251307 G>A maps to NM_000014.4 H582H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:9251271 G>T maps to NM_000014.4 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:9229986 G>A maps to NM_000014.4 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:9264787 G>T maps to NM_000014.4 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:9265015 G>A maps to NM_000014.4 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:9251307 G>A maps to NM_000014.4 H582H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr12:9254147 G>A maps to NM_000014.4 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr12:9264995 G>T maps to NM_000014.4 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:9251352 C>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:9260176 G>A maps to NM_000014.4 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr12:9251208 C>T maps to NM_000014.4 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:9230314 C>T maps to NM_000014.4 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:9231867 G>A maps to NM_000014.4 R1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:9004514 C>T maps to NM_144670.3 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:9001488 G>A maps to NM_144670.3 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr12:8975276 G>A maps to NM_144670.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr12:8988260 T>C maps to NM_144670.3 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:9004598 T>C maps to NM_144670.3 D818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:8995752 A>G maps to NM_144670.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr12:8975819 C>T maps to NM_144670.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:9004403 C>T maps to NM_144670.3 H753H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:137843318 G>A maps to NM_016161.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:125613956 C>T maps to NM_023928.3 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:125621343 C>T maps to NM_023928.3 D605D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:151531953 G>T maps to NM_001086.2 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:151458607 C>T maps to NM_207365.3 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:12779577 G>A maps to NM_001103170.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:12779562 C>T maps to NM_001103170.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:12726187 T>A maps to NM_001013630.1 Y222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:12725974 C>T maps to NM_001013630.1 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:69732776 T>C maps to NM_014911.3 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:69748101 G>A maps to NM_014911.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr2:69709918 A>G maps to NM_014911.3 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr2:69757801 G>C maps to NM_014911.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:219130405 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:219131232 C>T maps to ENST00000444053 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:74465821 C>T maps to NM_001166579.1 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr17:74464953 G>T maps to NM_001166579.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:74465952 C>T maps to NM_001166579.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:70286779 G>A maps to ENST00000418685 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:70294944 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:70304203 G>A maps to ENST00000418685 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:70295026 G>A maps to ENST00000418685 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:70305733 G>A maps to ENST00000418685 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr16:70302203 A>T maps to ENST00000418685 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:44275065 C>T maps to NM_020745.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr6:44274229 C>G did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:44271115 C>A maps to NM_020745.2 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:44278801 G>A maps to NM_020745.2 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:41108274 G>A maps to NM_001136042.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr17:41122334 T>A maps to NM_001136042.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:57204654 A>G maps to NM_181806.2 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:57221418 A>G maps to NM_181806.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr4:57204861 G>T maps to NM_181806.2 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:57220333 T>C maps to NM_181806.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:57220868 A>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:57221487 C>T maps to NM_181806.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:105967613 C>T maps to NM_015423.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:121773675 G>T maps to NM_005763.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr7:121717961 G>A maps to NM_005763.3 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:121753237 C>T maps to NM_005763.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr7:121773648 G>C maps to NM_005763.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:35306442 C>A maps to NM_012138.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:35346003 T>A maps to NM_012138.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:79094123 C>T maps to NM_001080395.2 A1204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:79108236 G>A maps to NM_001080395.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr17:79095614 G>A maps to NM_001080395.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:79095488 G>A maps to NM_001080395.2 C749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:79095728 C>T maps to NM_001080395.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:79094231 G>A maps to NM_001080395.2 S1168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:79108176 G>A maps to NM_001080395.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:79095755 G>A maps to NM_001080395.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:79093369 G>A maps to NM_001080395.2 F1298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:79108230 G>T maps to NM_001080395.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:8862105 G>A maps to NM_001127448.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr16:8870334 G>A maps to NM_001127448.1 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:107554237 G>A maps to NM_005502.3 C1933C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:107546688 T>C maps to NM_005502.3 K2231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr9:107571748 G>A maps to NM_005502.3 I1424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr9:107568521 T>C maps to NM_005502.3 Q1488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:107591375 G>A maps to NM_005502.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:107564405 G>A maps to NM_005502.3 Q1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:107588033 C>T maps to NM_005502.3 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:67170782 C>A maps to NM_080282.3 G1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:67210856 G>A maps to NM_080282.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr17:67212058 C>T maps to NM_080282.3 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr17:67170745 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:67186553 T>C maps to NM_080282.3 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr2:215884379 C>T maps to NM_173076.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:215838762 C>T maps to NM_173076.2 Q1824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:215809819 C>T maps to NM_173076.2 P2416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:215843716 T>C maps to NM_173076.2 T1596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:215833441 A>G did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr2:215802239 G>A maps to NM_173076.2 Y2512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:215896543 C>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:215835097 T>C maps to NM_173076.2 P1863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr2:215843626 T>C maps to NM_173076.2 K1626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:215866294 G>A maps to NM_173076.2 N950N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr2:215884364 G>A maps to NM_173076.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr2:215812211 A>G maps to NM_173076.2 S2391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr2:215891622 A>G maps to NM_173076.2 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:215821415 G>A maps to NM_173076.2 G2068G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:215839500 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:215813765 G>A maps to NM_173076.2 T2320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr2:215797378 T>C maps to NM_173076.2 Q2589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:215851417 A>G maps to NM_173076.2 P1337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:215914481 G>A maps to NM_173076.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:215843554 G>A maps to NM_173076.2 Y1650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr2:215843536 G>A maps to NM_173076.2 T1656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:215872504 C>T maps to NM_173076.2 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr2:215823129 G>T maps to NM_173076.2 G1996G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr2:215831607 G>A maps to NM_173076.2 R1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr2:215876322 G>T maps to NM_173076.2 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:215838672 C>T maps to NM_173076.2 Q1854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:48312523 C>T maps to NM_152701.3 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:48682919 T>C maps to NM_152701.3 C4958C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:48315256 T>C maps to NM_152701.3 I1998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:48318230 T>C maps to NM_152701.3 G2480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:48318638 T>C maps to NM_152701.3 S2616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr7:48314869 A>G maps to NM_152701.3 E1869E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr7:48391961 C>A maps to NM_152701.3 Y3522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:48313561 T>C maps to NM_152701.3 S1433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:48269511 G>A maps to NM_152701.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:48318152 G>A maps to NM_152701.3 T2454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr7:48452059 C>T maps to NM_152701.3 T4113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:48654928 C>T maps to NM_152701.3 N4931N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr7:48313581 G>A maps to NM_152701.3 W1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:48313720 T>C maps to NM_152701.3 F1486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:48319361 C>T maps to NM_152701.3 T2857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:48319445 T>C maps to NM_152701.3 C2885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:48318389 G>A maps to NM_152701.3 S2533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr7:48314797 G>T maps to NM_152701.3 G1845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:48280633 C>T maps to NM_152701.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:48335319 G>A maps to NM_152701.3 S2993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr7:48654928 C>T maps to NM_152701.3 N4931N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr7:48375056 T>G maps to NM_152701.3 T3346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr7:48312082 A>G maps to NM_152701.3 E940E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:139905557 C>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:139903447 G>A maps to ENST00000355090 D2325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr9:139903859 G>T maps to ENST00000355090 R2293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:139904434 C>A maps to ENST00000355090 R2195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:139915841 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr16:2354101 G>A maps to NM_001089.2 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:2333348 G>C maps to NM_001089.2 Y1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr16:2331441 G>A maps to NM_001089.2 I1368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:2334406 C>A maps to NM_001089.2 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:2349485 G>A maps to NM_001089.2 N553N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:2367684 G>A maps to NM_001089.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:2349440 G>A maps to NM_001089.2 N568N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:2329103 G>A maps to NM_001089.2 Q1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr16:2331216 G>A maps to NM_001089.2 Y1390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:2326761 G>A maps to NM_001089.2 D1676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:2376254 C>T maps to NM_001089.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:94512629 C>T maps to NM_000350.2 E921E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:94502715 G>A maps to NM_000350.2 D1266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:94476477 C>T maps to NM_000350.2 E1864E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:94463452 G>A maps to NM_000350.2 I2231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:94568686 G>A maps to NM_000350.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:94495141 C>T maps to NM_000350.2 V1466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:94528699 G>A maps to NM_000350.2 D576D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:94485136 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:94528780 G>A maps to NM_000350.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:67293434 T>G maps to ENST00000392677 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:67303001 G>A maps to ENST00000392677 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:67298972 A>C maps to ENST00000392677 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:67246652 C>A maps to ENST00000392677 E1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr17:67273962 G>A maps to ENST00000392677 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr17:67280172 G>T maps to ENST00000392677 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:67110968 G>A maps to NM_080284.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:67125774 G>A maps to NM_080284.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:67099023 A>C maps to NM_080284.2 T942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:67101675 G>A maps to NM_080284.2 N889N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:67119482 T>G maps to NM_080284.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:67130777 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:1047259 C>T maps to NM_019112.3 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr19:1042791 C>T maps to NM_019112.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:1049319 G>A maps to NM_019112.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr19:1052100 C>T maps to NM_019112.3 R1041R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr19:1047343 G>A maps to NM_019112.3 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:66937010 G>A maps to NM_007168.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:66925728 G>A maps to NM_007168.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:66880476 G>A maps to NM_007168.2 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:66873709 G>A maps to NM_007168.2 Y1343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:66925369 A>G maps to NM_007168.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr17:66929369 G>C maps to NM_007168.2 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:67016614 G>A maps to NM_080283.3 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:67039676 G>A maps to NM_080283.3 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:67024766 A>G maps to NM_080283.3 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:66982371 G>A maps to NM_080283.3 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr17:66980282 C>T maps to NM_080283.3 E1471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:66980294 A>G maps to NM_080283.3 F1467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:66981198 G>T maps to NM_080283.3 R1427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:66981226 G>C maps to NM_080283.3 P1417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:67047246 G>A maps to NM_080283.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:87160728 G>A maps to NM_000927.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:87179870 C>T maps to NM_000927.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr7:87179354 G>A maps to NM_000927.3 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr7:87160629 C>A maps to NM_000927.3 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr7:87179781 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:87150159 G>A maps to NM_000927.3 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:87183249 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:87144567 G>A maps to NM_000927.3 Y1087Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:87179211 A>C maps to NM_000927.3 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr7:87175265 A>C maps to NM_000927.3 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr2:169792823 G>A maps to NM_003742.2 F910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:169836426 G>A maps to NM_003742.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:169828383 G>T maps to NM_003742.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr7:87035759 A>G maps to NM_018849.2 A1117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr7:87031413 A>G maps to NM_018849.2 *1287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:87032524 G>A maps to NM_018849.2 R1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:87035768 C>T maps to NM_018849.2 W1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:87092220 G>A maps to NM_018849.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:87073077 A>G maps to NM_018849.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr7:87035741 A>G maps to NM_018849.2 S1123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:20793130 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:20738130 T>G maps to NM_001163941.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:20782591 T>C maps to NM_001163941.1 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr7:20698709 T>C maps to NM_001163942.1 *132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:20767943 C>T maps to NM_001163941.1 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:20778695 G>A maps to NM_001163941.1 A986A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:20689715 G>T maps to NM_001163941.1 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:20793014 A>G maps to NM_001163941.1 A1154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:220075830 C>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:74318829 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:74289247 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:74376092 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:74288919 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:74296376 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:74289231 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr23:74318840 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:150742327 C>T maps to ENST00000297504 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr7:150733040 C>T maps to ENST00000297504 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:150739067 G>A maps to ENST00000297504 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:150730958 G>A maps to ENST00000297504 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:123419950 G>A maps to NM_203444.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:123444644 C>T maps to NM_203444.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:123428955 G>A maps to NM_203444.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr6:43415495 G>A maps to NM_033450.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:43411999 C>T maps to NM_033450.2 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:43400359 T>C maps to NM_033450.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:43410856 C>T maps to NM_033450.2 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:43415558 C>T maps to NM_033450.2 R1253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr6:43399999 C>T maps to NM_033450.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr6:43400110 G>C maps to NM_033450.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr6:43415570 C>G maps to NM_033450.2 G1257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:48227792 C>T maps to NM_032583.3 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:48244966 G>A maps to NM_032583.3 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:48249222 C>T maps to NM_032583.3 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr16:48212522 T>A maps to NM_032583.3 I1111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:48232051 C>T maps to NM_032583.3 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:48226615 G>A maps to NM_032583.3 R841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr16:48226538 G>A maps to NM_032583.3 Y866Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:48210853 G>A maps to NM_032583.3 I1173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr16:48234311 G>A maps to NM_032583.3 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:48210973 C>T maps to NM_032583.3 Q1133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:48173145 C>T maps to NM_033226.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:48139202 G>A maps to NM_033226.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:48149418 G>A maps to NM_033226.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr16:48121986 G>T maps to NM_033226.2 S1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:48149394 G>A maps to NM_033226.2 H640H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GH-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:101590490 G>A maps to NM_000392.3 R922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr10:101590608 G>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr10:101565152 G>A maps to NM_000392.3 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:101591388 G>T maps to NM_000392.3 E969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:48744970 C>T maps to NM_003786.3 N496N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr17:48761440 G>T maps to NM_003786.3 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:48757226 G>A maps to NM_003786.3 E1258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:48753396 C>T maps to NM_003786.3 Q1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:48742572 C>T maps to NM_003786.3 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:95813533 G>A maps to NM_005845.3 Y788Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr13:95723914 C>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr13:95822844 A>G maps to NM_005845.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:183682975 C>T maps to NM_005688.2 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:183699620 G>A maps to NM_005688.2 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:183667869 G>A maps to NM_005688.2 N996N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:183669328 A>G maps to NM_005688.2 H948H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:183667836 G>A maps to NM_005688.2 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr3:183660617 G>A maps to NM_005688.2 N1197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:183660653 A>G maps to NM_005688.2 P1185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:183703132 A>G maps to NM_001023587.1 *209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:16248762 G>A maps to NM_001171.5 H1336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:16302687 G>A maps to NM_001171.5 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:16256992 C>T maps to NM_001171.5 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:16259623 C>T maps to NM_001171.5 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:16267260 C>T maps to NM_001171.5 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:16263539 C>T maps to NM_001171.5 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:16244061 G>A maps to NM_001171.5 S1480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr16:16281041 G>A maps to NM_001171.5 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:17428578 G>A maps to ENST00000302539 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:17452413 T>C maps to ENST00000302539 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:17434262 G>A maps to ENST00000302539 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:17428575 G>A maps to ENST00000302539 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:17491699 G>A maps to ENST00000302539 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:17449859 G>A maps to ENST00000302539 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr11:17450206 G>A maps to ENST00000302539 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:17482093 G>A maps to ENST00000302539 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:22015948 A>G maps to NM_005691.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:21971083 C>T maps to NM_005691.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:22025569 A>G maps to NM_005691.2 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:22005060 A>G maps to NM_005691.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:21958203 G>A maps to NM_005691.2 V1518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:22035765 G>A maps to NM_005691.2 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr12:21981945 G>A maps to NM_005691.2 N1205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:22005346 G>A maps to NM_005691.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:22012554 G>A maps to NM_005691.2 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr12:22040795 C>T maps to NM_005691.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:153001645 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:152991451 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:152991360 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:153006122 A>G did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr23:153001825 C>A did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr23:152991317 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153001667 C>T did not map to a codon.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr23:153008475 T>C did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr23:153008475 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:152994805 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:153008475 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153005684 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:39998621 G>A maps to NM_005164.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:94955519 T>C maps to ENST00000454898 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr1:94956790 C>T maps to ENST00000454898 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:94953477 C>T maps to ENST00000454898 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:146025623 A>G maps to NM_002940.2 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:30554266 C>A maps to NM_001025091.1 Y634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:150913090 G>A maps to NM_005692.3 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:183911335 G>A maps to NM_018358.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:183911389 G>A maps to NM_018358.2 W678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:183908908 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:183908988 C>T maps to NM_018358.2 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:43716282 C>T maps to NM_004915.3 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:89036196 C>T maps to NM_004827.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:89034589 G>A maps to NM_004827.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:119029554 G>A maps to NM_001142505.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:44051073 G>A maps to NM_022436.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr2:44065003 G>A maps to NM_022436.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr2:44059007 T>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:44053637 T>C maps to NM_022436.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:44049988 G>A maps to NM_022436.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:44079963 C>T maps to NM_022437.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr2:44100979 G>A maps to NM_022437.2 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:111700730 C>T maps to NM_018394.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:25300923 G>A maps to NM_015600.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:25287522 C>T maps to NM_015600.3 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:51347271 T>C maps to ENST00000337334 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:51352375 A>G maps to ENST00000337334 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:51368575 T>C maps to ENST00000337334 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr14:51347205 G>A maps to ENST00000337334 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:108882336 A>G maps to NM_032859.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:52011900 C>A maps to ENST00000463937 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:52004060 G>T maps to NM_032750.2 S117S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8369-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:89698697 C>T maps to NM_152924.4 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:89719193 C>T maps to NM_152924.4 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr15:89736500 C>T maps to NM_152924.4 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr15:89719109 C>T maps to NM_152924.4 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr18:19283681 C>T maps to NM_138340.4 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr18:19282374 G>A maps to NM_138340.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:23072500 C>T maps to NM_022060.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:23072463 C>T maps to NM_022060.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:17412368 G>A maps to NM_024527.4 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:17411738 C>T maps to NM_024527.4 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:17411759 G>A maps to NM_024527.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:27066139 G>A maps to NM_005470.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr10:27057878 T>C maps to NM_005470.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr10:27149759 C>T maps to NM_005470.3 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:27048065 G>A maps to NM_005470.3 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:204291993 T>G maps to ENST00000295851 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr17:47295216 G>A maps to NM_016428.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:100469454 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:133738376 C>T maps to NM_007313.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:133759405 C>T maps to NM_007313.2 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:133730284 G>A maps to NM_007313.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:133759578 C>T maps to NM_007313.2 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:133760421 G>A maps to NM_007313.2 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:133759854 C>T maps to NM_007313.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:133738295 C>T maps to NM_007313.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:133738376 C>T maps to NM_007313.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr9:133748331 C>T maps to NM_007313.2 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:179090926 G>A maps to NM_007314.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr1:179077709 G>A maps to NM_007314.3 R898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:179086566 T>C maps to NM_007314.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:179077354 G>C maps to NM_007314.3 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:179077317 G>A maps to NM_007314.3 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:179077481 G>A maps to NM_007314.3 R974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr10:116361625 G>C maps to ENST00000277895 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:116247767 G>A maps to ENST00000277895 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:8010820 G>A maps to NM_001130083.1 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:7985011 G>A maps to NM_001130083.1 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:8037890 C>T maps to NM_001130083.1 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:7985020 C>T maps to NM_001130083.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:8079393 A>G maps to NM_001130083.1 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:148619446 C>T maps to NM_014945.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:148619395 C>T maps to NM_014945.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:148630059 C>T maps to NM_014945.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:136131619 G>T maps to NM_020469.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:150554733 G>A maps to ENST00000416793 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:150554718 C>T maps to ENST00000416793 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:150555015 C>T maps to ENST00000416793 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:1028589 C>T maps to NM_021962.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:973306 G>A maps to NM_021962.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:107782295 G>A maps to NM_139166.4 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr8:107773615 G>A maps to NM_139166.4 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr6:26598839 C>T maps to NM_013375.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:127396373 C>T maps to NM_172027.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:127395249 T>C maps to NM_172027.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:127399131 C>T maps to NM_172027.2 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:34184327 C>T maps to NM_145804.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr11:34218972 G>A maps to NM_145804.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:34226097 C>T maps to NM_145804.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr11:34192491 C>T maps to NM_145804.2 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:38173486 C>T maps to NM_001607.3 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:38170827 C>T maps to NM_001607.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:47329199 G>A maps to NM_006111.2 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:47320716 T>C maps to NM_006111.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:35470032 G>A maps to NM_198834.1 R2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:35601596 G>A maps to NM_198834.1 G883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr17:35567387 G>A maps to NM_198834.1 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr17:35545333 G>A maps to NM_198834.1 N1553N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:35615208 A>G maps to NM_198834.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:35486327 G>A maps to NM_198834.1 Y1969Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:35687287 G>A maps to NM_198834.1 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr12:109605780 C>T maps to NM_001093.3 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:109604664 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:109625967 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:109644516 T>C maps to NM_001093.3 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:109637205 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:109702083 C>T maps to NM_001093.3 L2279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr12:109637356 G>A maps to NM_001093.3 E926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:109704118 G>A maps to NM_001093.3 A2443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:109702079 C>T maps to NM_001093.3 G2277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:109703291 G>A maps to NM_001093.3 T2404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:112140084 C>T maps to NM_001136538.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:112182512 G>A maps to NM_001136538.1 W625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:112184962 C>T maps to NM_001136538.1 R820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:112184869 G>A maps to NM_001136538.1 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:112185166 C>T maps to NM_001136538.1 N852N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr3:132350305 C>T maps to NM_032169.4 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:132345662 T>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:134131675 C>T maps to NM_014384.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:128618206 A>C maps to NM_014049.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:211069400 G>A maps to NM_001608.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:211081207 A>C maps to NM_001608.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:76200473 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:121177115 C>T maps to NM_000017.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr12:121176171 G>A maps to NM_000017.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:7125994 T>C maps to ENST00000356839 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr15:89398569 A>G maps to NM_013227.3 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr15:89384997 C>A maps to NM_013227.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr15:89384997 C>T maps to NM_013227.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:89391192 C>T maps to NM_013227.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr15:89398470 G>A maps to NM_013227.3 Q885Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:7252341 G>A maps to NM_014716.3 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:1233228 G>A maps to NM_030649.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:1229850 G>A maps to NM_030649.2 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr6:160188040 T>A maps to NM_005891.2 C65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:226349292 G>A maps to NM_022735.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr1:226352630 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:226352566 G>T maps to NM_022735.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:43220881 C>A maps to NM_001135706.1 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:27497330 C>T maps to ENST00000375888 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:27499856 C>A maps to ENST00000375888 G373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:27512288 G>A maps to ENST00000375888 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr10:27494140 G>A maps to ENST00000375888 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:180471272 G>A maps to NM_032360.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:180366722 G>A maps to NM_032360.3 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:15121002 G>A maps to NM_001039844.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:31618467 G>A maps to NM_183377.1 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr17:31618767 G>A maps to NM_183377.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:31416000 C>T maps to NM_183377.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:31618835 G>A maps to NM_183377.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:31343003 G>A maps to NM_183377.1 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:31618529 C>A maps to NM_183377.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr17:31415931 G>T maps to NM_183377.1 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:50452563 C>T maps to NM_020039.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:50452563 C>T maps to NM_020039.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr7:150746115 C>T maps to NM_020321.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:150746478 A>G maps to NM_020321.2 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr7:150747658 G>T maps to NM_020321.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:150749149 G>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:220401862 C>T maps to NM_018674.4 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:220379397 G>A maps to NM_018674.4 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr2:220379472 C>T maps to NM_018674.4 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:156751148 C>T maps to NM_017419.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr4:156763419 C>T maps to NM_017419.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:44105260 G>A maps to NM_032592.3 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr11:44101117 C>T maps to NM_032592.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:44102616 T>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:44069843 C>T maps to NM_001031854.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:44080010 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:44077742 C>T maps to NM_001031854.2 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:61559949 C>T maps to NM_000789.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:61571352 C>T maps to NM_000789.3 V1069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:61561281 A>G maps to NM_000789.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:61570795 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:61557710 G>A maps to NM_000789.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:61573877 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:61568703 C>T maps to NM_000789.3 H958H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr17:61557755 C>T maps to NM_000789.3 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:61559015 G>A maps to NM_000789.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:15585914 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:15607506 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:15596274 C>T did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:15593857 T>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:15599425 T>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:15580093 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:15589814 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr23:15607558 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:15599401 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:6309742 C>T maps to NM_133492.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:6306757 G>A maps to NM_133492.2 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:19424785 T>G maps to NM_001010887.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:19450474 C>T maps to NM_001010887.2 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:100488913 C>T maps to NM_000665.3 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:100491559 A>G maps to NM_000665.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr7:100489998 G>A maps to NM_000665.3 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:100491547 T>C maps to NM_000665.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:100488955 A>G maps to NM_000665.3 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:100489953 C>T did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr14:23559302 T>G maps to NM_014977.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr14:23532170 G>T maps to NM_014977.3 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:23528386 T>C maps to NM_014977.3 T1332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr14:23531678 G>T maps to NM_014977.3 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:23530626 G>A maps to NM_014977.3 R1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:23531714 T>C maps to NM_014977.3 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:23528448 G>A maps to NM_014977.3 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr14:23530732 C>T maps to NM_014977.3 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr17:40049325 G>A maps to ENST00000401700 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:40070066 A>G maps to ENST00000401700 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:135625177 C>T maps to NM_138326.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:135628619 C>T maps to NM_138326.2 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:32427422 G>T maps to NM_002197.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:41919893 G>A maps to ENST00000396512 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr22:41911463 C>T maps to ENST00000396512 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr22:41923305 G>A maps to ENST00000396512 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr14:74009848 C>T maps to NM_001037161.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr14:74009788 C>G maps to NM_001037161.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr14:74009926 C>T maps to NM_001037161.1 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:55067073 G>A maps to NM_015547.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:55073632 G>A maps to NM_015547.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:55059687 C>T maps to NM_015547.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:55065020 C>T maps to NM_015547.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:80626716 C>T maps to NM_130767.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:80639677 C>A maps to NM_130767.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:80689867 C>T maps to NM_130767.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:80689867 C>T maps to NM_130767.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr5:80640733 A>G maps to NM_130767.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:74040290 C>T maps to NM_006821.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr14:74036519 C>T maps to NM_006821.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr14:74060457 C>T maps to NM_152331.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:6399490 A>G did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:6393548 C>T maps to NM_007274.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:6409811 G>A maps to NM_007274.3 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:44472919 G>A maps to NM_005469.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:23748966 G>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:23740850 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:23722910 C>T did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:23752470 T>G did not map to a codon.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr23:23724826 A>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:73946859 C>T maps to NM_004035.6 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:73951987 G>A maps to NM_004035.6 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:73947534 G>A maps to NM_004035.6 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:58519211 G>A maps to NM_003500.3 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:8368786 G>A maps to NM_003501.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr4:8372709 A>G maps to NM_003501.2 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:8394072 G>A maps to NM_003501.2 H429H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr4:8398822 C>T maps to NM_003501.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:8390918 G>A maps to NM_003501.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:8398741 A>G maps to NM_003501.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:111556606 C>T maps to NM_001142807.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:271875 T>C maps to NM_004300.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr11:47264442 G>A maps to NM_001610.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr19:11685995 C>T maps to NM_001111036.1 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:11687883 G>A maps to NM_001111036.1 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:11687261 G>A maps to NM_001111036.1 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:11686046 G>A maps to NM_001111036.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:141011878 C>T maps to NM_001037172.1 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr3:141011728 C>T maps to NM_001037172.1 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:141011881 C>T maps to NM_001037172.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:132068824 A>G maps to NM_001134194.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:132071667 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:51297839 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:51298303 A>G maps to NM_033068.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr19:51294974 G>A maps to NM_033068.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:6752704 C>T maps to NM_032489.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:6749363 G>A maps to NM_032489.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:6749556 G>T maps to NM_032489.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:70823684 G>A did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:70824236 T>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:70824104 T>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:70824110 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:70823665 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:70832301 T>A did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr23:70823606 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:70823941 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:70824125 A>C did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:70823564 A>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:70823573 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:70823606 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:70823750 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr23:70823669 C>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:70814182 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:78466055 G>A maps to NM_015162.4 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:78473157 G>A maps to NM_015162.4 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:78526804 G>A maps to NM_015162.4 H13H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr15:78466819 G>A maps to NM_015162.4 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:6187701 C>T maps to NM_030924.3 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:6165950 G>A maps to NM_030924.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:6187701 C>T maps to NM_030924.3 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:48539864 C>T maps to ENST00000427954 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:48551588 C>T maps to ENST00000427954 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:48551124 C>T maps to ENST00000427954 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:89167400 C>T maps to NM_174917.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:89169085 C>T maps to NM_174917.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:89211762 C>T maps to NM_174917.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:89167697 T>C maps to NM_174917.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr4:185691576 G>A maps to NM_001995.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:185687128 G>A maps to NM_001995.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:185687871 G>A maps to NM_001995.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:223791753 C>T maps to NM_203372.1 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:223791734 C>T maps to NM_203372.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:223783786 A>C maps to NM_203372.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr2:223773615 T>G maps to NM_203372.1 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:108887402 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:108924227 G>A did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:108887373 T>C did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:108911350 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:108904808 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:108926678 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:108902692 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:114173038 C>T maps to NM_016234.3 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:114176692 G>A maps to NM_016234.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:131298257 C>T maps to NM_001009185.1 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:131321103 C>T maps to NM_001009185.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr5:131324531 C>G maps to NM_001009185.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:131310504 C>T maps to NM_015256.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:20693648 G>A maps to NM_052956.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:20681259 C>T maps to NM_052956.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr16:20480969 T>G maps to NM_001010845.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr16:20497993 G>A maps to NM_001010845.2 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:20471448 C>T maps to NM_001010845.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:20482475 T>C maps to NM_001010845.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr16:20497943 C>T maps to NM_001010845.2 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:20471448 C>T maps to NM_001010845.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr16:20492160 C>A maps to NM_001010845.2 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr16:20487004 T>C maps to NM_001010845.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr16:20559472 C>A maps to NM_182617.3 G337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr16:20566688 T>C maps to NM_182617.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:7480935 C>T maps to NM_001080454.1 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:7477157 G>A maps to NM_001080454.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:20439147 C>T maps to NM_017888.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:25004170 C>T maps to NM_032501.2 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:25038591 T>A maps to NM_032501.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr20:25004161 C>T maps to NM_032501.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr20:24993555 G>A maps to NM_032501.2 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:25004176 G>A maps to NM_032501.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr20:25000724 C>T maps to NM_032501.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:33509130 A>G did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr20:33509632 C>T maps to NM_001076552.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:81503374 C>T maps to NM_024560.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr12:81647272 G>C did not map to a codon.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr12:81624874 G>A maps to NM_024560.2 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:229567810 G>A maps to NM_001100.3 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:229568140 G>A maps to NM_001100.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr1:229568155 G>A maps to NM_001100.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:229567786 G>A maps to NM_001100.3 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:229568321 G>A maps to NM_001100.3 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:90701548 G>A maps to NM_001141945.1 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr10:90699288 C>T maps to NM_001141945.1 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:5567754 G>A maps to NM_001101.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr7:5568044 G>A maps to NM_001101.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:5567981 G>A maps to NM_001101.3 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:56778342 G>A maps to NM_001017992.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr5:56777877 G>A maps to NM_001017992.2 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr5:56777907 A>G maps to NM_001017992.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr5:56777861 C>A maps to NM_001017992.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:79477814 G>A maps to NM_001614.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:74135804 G>A maps to NM_001615.3 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:179292256 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:111625160 C>T maps to NM_006687.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:111625267 C>T maps to NM_006687.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:111624758 G>T maps to NM_006687.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:111625267 C>T maps to NM_006687.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr9:111625636 G>A maps to NM_006687.2 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:111617895 C>T maps to NM_006686.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:111617646 G>A maps to NM_006686.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:111617073 G>A maps to NM_006686.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:111618105 C>T maps to NM_006686.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr9:111618015 G>A maps to NM_006686.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:111617136 C>T maps to NM_006686.3 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:111617760 G>A maps to NM_006686.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:111617946 G>A maps to NM_006686.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:111617574 G>A maps to NM_006686.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:18149782 G>T maps to NM_030812.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:18149613 G>A maps to NM_030812.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:8808717 G>A maps to NM_178525.3 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:8808898 C>T maps to NM_178525.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:8807971 G>A maps to NM_178525.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr19:8808508 C>T maps to NM_178525.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:8808574 G>A maps to NM_178525.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:8808991 G>A maps to NM_178525.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr14:69369232 G>A maps to NM_001130004.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr14:69358880 C>T maps to NM_001130004.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:69371426 C>T maps to NM_001130004.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:69392308 G>A maps to NM_001130004.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:69358970 C>T maps to NM_001130004.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:69358907 G>A maps to NM_001130004.1 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:69387780 G>A maps to NM_001130004.1 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:236902753 C>A maps to NM_001103.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:236925909 C>T maps to NM_001103.2 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:236908052 C>T maps to NM_001103.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr1:236910981 C>T maps to NM_001103.2 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr1:236881195 C>T maps to NM_001103.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:236925801 G>A maps to NM_001103.2 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:236925858 G>A maps to NM_001103.2 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:236908016 C>T maps to NM_001103.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:39207919 G>A maps to NM_004924.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:39214942 C>T maps to NM_004924.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:39207940 G>A maps to NM_004924.3 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:39200066 C>T maps to NM_004924.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:39215079 C>T maps to NM_004924.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:39220044 G>A maps to NM_004924.3 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:39214319 C>T maps to NM_004924.3 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:58678051 C>T maps to NM_018477.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:65473671 T>C maps to NM_001005386.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:65473845 A>C maps to NM_001005386.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:65482776 G>A maps to NM_001005386.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr2:114699798 G>T maps to NM_005721.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr7:149990466 C>A maps to NM_001164458.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:37384639 G>A maps to NM_024855.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:37400239 C>T maps to NM_024855.3 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:37380929 G>A maps to NM_024855.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:53902861 T>A maps to NM_022899.4 K587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:53911736 A>G maps to NM_022899.4 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:127185297 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:127185199 T>C did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:127185858 G>A did not map to a codon.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr23:127185977 A>C did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:127185304 A>C did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr23:127185686 G>T did not map to a codon.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr23:127185060 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:127186141 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:127185701 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:127185758 C>T did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:127185407 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr23:127185408 G>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:2938780 C>T maps to NM_080431.4 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:2938363 C>T maps to NM_080431.4 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:158636921 G>A maps to NM_001111067.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:158594105 C>A maps to NM_001111067.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr12:52378995 C>T maps to NM_020328.3 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:52385714 C>T maps to NM_020328.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:52385714 C>T maps to NM_020328.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:52377792 C>A maps to NM_020328.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:52385714 C>T maps to NM_020328.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:52385714 C>T maps to NM_020328.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr12:52387833 G>A maps to NM_020328.3 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:158485126 G>A maps to NM_145259.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:158412845 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:158390495 G>A maps to NM_145259.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:158399321 T>C maps to NM_145259.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr2:148657056 T>C maps to NM_001616.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr2:148602740 T>A maps to NM_001616.3 L7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:148684692 C>T maps to NM_001616.3 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:148654068 C>A maps to NM_001616.3 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:38518871 C>T maps to NM_001106.3 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:38519933 T>C maps to NM_001106.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:38523798 G>A maps to NM_001106.3 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:38518856 C>T maps to NM_001106.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:38524693 C>T maps to NM_001106.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:38524696 G>A maps to NM_001106.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:52308232 C>T maps to NM_001077401.1 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:52307538 C>T maps to NM_001077401.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:67412624 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:54365781 G>T maps to NM_138448.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:43249691 G>A maps to NM_000022.2 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:43257797 G>A maps to NM_000022.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:43249742 C>T maps to NM_000022.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:123350869 C>A maps to NM_139243.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:123336585 T>C maps to NM_139243.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:123342457 T>C maps to NM_139243.3 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:123332512 T>C maps to NM_139243.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:84224940 A>G maps to NM_139174.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr16:84229579 C>T maps to NM_139174.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:43627976 C>T maps to ENST00000422466 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:58925421 G>A maps to NM_001110.2 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:42855086 C>T maps to NM_002390.4 D642D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:42849122 G>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:128076636 G>A maps to NM_003474.4 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:155032816 C>T maps to NM_207197.1 Y735Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:155032781 C>T maps to NM_207197.1 R724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:155028288 C>G maps to NM_207197.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr1:155026660 T>C maps to NM_207197.1 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:155030117 C>T maps to NM_207197.1 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:155029472 T>C maps to NM_207197.1 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:9634873 C>G maps to NM_003183.4 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr2:9630306 T>A maps to NM_003183.4 *825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:9630329 A>G maps to NM_003183.4 V817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr2:9676833 G>A maps to NM_003183.4 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:9630356 G>T maps to NM_003183.4 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr2:9663398 G>C maps to NM_003183.4 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr8:39587446 C>T maps to NM_014237.2 D736D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr8:39550159 A>T maps to NM_014237.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr8:39466562 C>A maps to NM_014237.2 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:156964959 A>C maps to ENST00000430702 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:156917388 G>T maps to ENST00000430702 C725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:39624770 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:39644522 A>G maps to NM_001464.3 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:39613416 C>A maps to NM_001464.3 G543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:70989593 A>G maps to NM_003814.4 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr14:70990274 A>G maps to NM_003814.4 Y450Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr14:70990514 A>G maps to NM_003814.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:70989839 A>G maps to NM_003814.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr14:70990571 T>C maps to NM_003814.4 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:70925991 T>C maps to NM_003813.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:70925508 C>T maps to NM_003813.2 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr14:70925358 T>A maps to NM_003813.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr14:70925355 C>T maps to NM_003813.2 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:87780324 A>T maps to NM_021723.3 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:87759746 G>A maps to NM_021723.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr7:87564470 G>A maps to NM_021723.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:87762256 C>T maps to NM_021723.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:87778315 C>T maps to NM_021723.3 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:87762256 C>T maps to NM_021723.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:207406813 C>T maps to NM_003812.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr2:207431959 C>T maps to NM_003812.2 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr2:207413053 G>A maps to NM_003812.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:207459517 G>A maps to NM_003812.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr2:207424842 G>A did not map to a codon.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr8:24207413 G>A maps to NM_014265.4 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:24171017 C>T maps to NM_014265.4 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr4:175897989 T>G maps to NM_014269.4 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:175898754 T>C maps to NM_014269.4 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr4:175896942 C>T maps to NM_014269.4 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:175896699 T>C maps to NM_014269.4 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr4:175897785 T>C maps to NM_014269.4 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:120438782 G>A maps to NM_021794.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:120436587 T>C maps to NM_021794.2 *791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:120436657 G>A maps to NM_021794.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:120438725 C>T maps to NM_021794.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr1:120437528 G>T maps to NM_021794.2 C477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:120437438 G>A maps to NM_021794.2 C507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:39068794 C>T maps to NM_145004.5 G395G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-6852-01A-11D-1882-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:39022628 T>C maps to NM_145004.5 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:39089550 A>C maps to NM_145004.5 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:39131866 C>T maps to NM_145004.5 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr8:39091555 A>G maps to NM_145004.5 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:39068680 G>A maps to NM_145004.5 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:3653475 G>A maps to NM_025220.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr20:3653523 G>A maps to NM_025220.2 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:24321457 G>A maps to ENST00000380789 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr8:24358342 C>T maps to ENST00000380789 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:24358376 C>T maps to ENST00000380789 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr8:24350014 A>T maps to ENST00000380789 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr10:135087517 G>A maps to NM_001109.4 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:135083929 C>T maps to NM_001109.4 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:38913109 T>C maps to NM_003816.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr8:38874806 C>T maps to NM_003816.2 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:38934827 G>A maps to NM_003816.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr8:38854596 G>A maps to NM_003816.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:38934827 G>A maps to NM_003816.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:24254939 C>T maps to NM_014479.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:24256905 C>T maps to NM_014479.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr21:28212245 G>C maps to NM_006988.3 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr21:28216850 G>A maps to NM_006988.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:28216895 G>A maps to NM_006988.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:8656951 C>T maps to NM_030957.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:8657676 C>T maps to NM_030957.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:8661958 G>A maps to NM_030957.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:8670085 C>T maps to NM_030957.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:8654233 G>A maps to NM_030957.2 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:8656933 G>A maps to NM_030957.2 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr19:8669959 G>A maps to NM_030957.2 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:8670160 C>T maps to NM_030957.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr19:8668684 T>C maps to NM_030957.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:8656903 G>A maps to NM_030957.2 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr5:33577247 A>G maps to NM_030955.2 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr5:33588883 C>T maps to NM_030955.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:33751614 A>G maps to NM_030955.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:33624405 G>A maps to NM_030955.2 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:33576947 G>A maps to NM_030955.2 D1061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr5:33891847 C>T maps to NM_030955.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:136321689 G>A maps to NM_139025.3 R1247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:136304556 C>T maps to NM_139025.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr9:136310893 C>T maps to NM_139025.3 H895H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:136321248 G>A maps to NM_139025.3 G1209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr10:72511301 G>A maps to NM_139155.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:72495032 C>T maps to NM_139155.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:72511869 C>T maps to NM_139155.2 Y875Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:72493784 G>A did not map to a codon.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr10:72517773 C>T maps to NM_139155.2 N1001N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr10:72489860 C>T maps to NM_139155.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr10:72468395 G>A maps to NM_139155.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:130341116 G>A maps to NM_139055.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:130331433 T>C maps to NM_139055.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr11:130332449 C>T maps to NM_139055.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:130319788 C>T maps to NM_139055.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:130341186 C>T maps to NM_139055.2 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:130319162 C>T maps to NM_139055.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:5209337 C>T maps to NM_139056.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:5232557 T>G maps to NM_139056.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr5:5235250 C>T maps to NM_139056.2 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:5186364 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:5303683 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:5303788 C>T maps to NM_139056.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:5146475 C>T maps to NM_139056.2 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr5:5239959 T>G maps to NM_139056.2 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:5186297 C>T maps to NM_139056.2 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:5146480 T>G maps to NM_139056.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr5:5239959 T>G maps to NM_139056.2 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:100695506 G>A maps to NM_139057.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr15:100692873 G>A maps to NM_139057.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:100801715 C>T maps to NM_139057.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:100692867 C>T maps to NM_139057.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr15:100537679 G>C maps to NM_139057.2 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:100802555 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:100692870 G>A maps to NM_139057.2 N473N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr16:77328918 T>G maps to NM_199355.2 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:77334208 G>T maps to NM_199355.2 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr16:77387680 A>G maps to NM_199355.2 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:77369732 G>A maps to NM_199355.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr16:77334268 A>T maps to NM_199355.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:77356244 G>A maps to NM_199355.2 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:129015538 C>T maps to NM_133638.3 T857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:128862007 A>C maps to NM_133638.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:128977571 A>G maps to NM_133638.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:129070743 C>T maps to NM_133638.3 C1138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr5:128984622 C>A maps to NM_133638.3 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:128983568 C>T maps to NM_133638.3 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:128797350 G>A maps to NM_133638.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:128956400 T>C maps to NM_133638.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:129015461 C>T maps to NM_133638.3 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:178555035 G>A maps to NM_014244.4 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:178555065 A>G maps to NM_014244.4 H837H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:178540987 A>G maps to NM_014244.4 D1172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:178771082 G>A maps to NM_014244.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr5:178548683 C>T maps to NM_014244.4 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:178563002 G>A maps to NM_014244.4 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:178552048 G>A maps to NM_014244.4 D961D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:178699957 C>T maps to NM_014244.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:178770845 G>A maps to NM_014244.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:178581819 G>A maps to NM_014244.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:178585790 G>A maps to NM_014244.4 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr5:178700026 G>A maps to NM_014244.4 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:43826208 G>A maps to ENST00000389420 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:43944882 G>A maps to ENST00000389420 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:43846181 A>G maps to ENST00000389420 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:43770327 G>A maps to ENST00000389420 D1708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr12:43925974 G>A maps to ENST00000389420 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:43821194 G>A maps to ENST00000389420 Y1341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr12:43750285 C>T did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr12:43777756 T>C maps to ENST00000389420 G1492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr12:43826502 A>G maps to ENST00000389420 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:43837645 G>A maps to ENST00000389420 N746N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:73176815 C>T maps to NM_014243.1 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:73280580 T>C maps to NM_014243.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:73149281 T>C maps to NM_014243.1 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:73205405 C>T maps to NM_014243.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:73205378 A>G maps to NM_014243.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr4:73169657 A>T maps to NM_014243.1 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr4:73414335 G>A maps to NM_014243.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:73148870 T>C maps to NM_014243.1 S1200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr4:73148876 T>G maps to NM_014243.1 T1198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr4:73175180 G>C maps to NM_014243.1 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:161165405 G>A maps to NM_005099.4 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:161163913 G>A maps to NM_005099.4 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr1:161166027 C>T maps to NM_005099.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:161167853 G>A maps to NM_005099.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:161163531 G>T maps to NM_005099.4 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:161161323 G>A maps to NM_005099.4 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:161163481 G>A maps to NM_005099.4 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:161163531 G>A maps to NM_005099.4 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:28302341 G>A maps to NM_007038.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr21:28296839 T>C maps to NM_007038.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr21:28315747 C>T maps to NM_007038.3 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr21:28337870 C>T maps to NM_007038.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:28338428 G>A maps to NM_007038.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:28296686 C>T maps to NM_007038.3 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:28338269 G>A maps to NM_007038.3 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:28305339 T>C maps to NM_007038.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr21:28296533 C>T maps to NM_007038.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr21:28327175 A>G maps to NM_007038.3 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr21:28338412 A>G maps to NM_007038.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr21:28306883 C>A maps to NM_007038.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr21:28306853 C>T maps to NM_007038.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr21:28296836 G>A maps to NM_007038.3 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr5:64511237 A>G maps to NM_197941.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:64556429 T>C maps to NM_197941.2 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:64756032 G>A maps to NM_197941.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:64595831 G>A maps to NM_197941.2 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:64520822 G>A maps to NM_197941.2 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:64466573 C>T maps to NM_197941.2 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:79083118 C>T maps to ENST00000258883 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr15:79089072 C>T maps to ENST00000258883 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr15:79090416 A>G maps to ENST00000258883 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:79092632 C>T maps to ENST00000258883 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:79063956 C>T maps to ENST00000258883 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr15:79082074 C>A maps to ENST00000258883 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:79059228 G>A maps to ENST00000258883 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:79051864 G>A maps to ENST00000258883 G1656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:79083559 A>G maps to ENST00000258883 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:79092718 G>A maps to ENST00000258883 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:79092647 G>A maps to ENST00000258883 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr15:79066975 C>T maps to ENST00000258883 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:130278393 G>A maps to NM_007037.4 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr11:130297578 C>T maps to NM_007037.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:64589922 G>A maps to NM_182920.1 R1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:64627597 C>T maps to NM_182920.1 W594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:64672444 G>A maps to NM_182920.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:64644465 T>C maps to NM_182920.1 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:64619437 G>A maps to NM_182920.1 D658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr3:64635378 G>A maps to NM_182920.1 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:18681925 C>T maps to NM_001040272.4 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:18706802 C>T maps to NM_001040272.4 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr9:18657713 G>A maps to NM_001040272.4 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:18574212 T>C maps to NM_001040272.4 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:18721612 C>T maps to NM_001040272.4 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:18777505 C>T maps to NM_001040272.4 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr9:18777841 C>T maps to NM_001040272.4 I1205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:18504846 C>T maps to NM_001040272.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:18770610 G>A maps to NM_001040272.4 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr9:18776992 G>A maps to NM_001040272.4 T922T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:18777308 C>T maps to NM_001040272.4 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:18657699 C>T maps to NM_001040272.4 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:18777172 G>A maps to NM_001040272.4 A982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr9:18662026 C>A maps to NM_001040272.4 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr9:136409626 C>T maps to ENST00000393061 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:136406013 C>T maps to ENST00000393061 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:136406067 C>T maps to ENST00000393061 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:136406085 C>T maps to ENST00000393061 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr15:84566717 G>T maps to NM_207517.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:84651706 C>T maps to NM_207517.2 T1109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:84442354 C>A maps to NM_207517.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:84651223 G>A maps to NM_207517.2 K948K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:84442273 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:84527578 A>G maps to NM_207517.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr15:84611716 G>A maps to NM_207517.2 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:84611420 C>T maps to NM_207517.2 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr15:84324518 T>G maps to NM_207517.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr15:84690186 G>A maps to NM_207517.2 W1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr15:84651799 C>A maps to NM_207517.2 G1140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr15:84582077 T>G maps to NM_207517.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr15:84651193 A>C maps to NM_207517.2 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:84373226 G>A maps to NM_207517.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr15:84539668 T>G maps to NM_207517.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr15:84527584 C>T maps to NM_207517.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr1:150529979 C>A maps to ENST00000369039 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:150530528 C>A maps to ENST00000369039 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:150531942 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:150529725 G>A maps to ENST00000369039 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr1:150532569 C>T maps to ENST00000369039 P1064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:150526543 C>T maps to ENST00000369039 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:150531070 C>A maps to ENST00000369039 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:1510218 C>T maps to NM_213604.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:29283257 G>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:29281494 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:29261278 A>G maps to ENST00000394782 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:154557386 G>A maps to ENST00000292205 Y1235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr1:154574724 C>T maps to ENST00000292205 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr21:46596224 C>T maps to NM_015833.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:46591576 T>C maps to NM_015833.3 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr21:46603399 C>T maps to NM_015833.3 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:46596125 C>T maps to NM_015833.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:1405276 G>A maps to NM_018702.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:1405798 G>A maps to NM_018702.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:1279634 C>T did not map to a codon.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr10:1405936 C>T maps to NM_018702.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:1279635 G>A maps to NM_018702.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:1262904 C>T maps to NM_018702.2 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:1405264 G>A maps to NM_018702.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:75654553 G>A maps to NM_012091.3 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr16:75642761 G>A maps to NM_012091.3 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:1912975 C>T maps to NM_138422.1 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:1912906 C>T maps to NM_138422.1 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr19:1912906 C>T maps to NM_138422.1 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:1912912 C>T maps to NM_138422.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:33560205 C>T maps to ENST00000373441 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:33547939 C>A maps to ENST00000373441 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:78285416 T>C maps to NM_020421.3 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr14:78392219 C>A maps to NM_020421.3 Y374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr14:78397958 C>T maps to NM_020421.3 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:140389470 C>A maps to NM_052853.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:41198067 G>A maps to NM_024876.3 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:41220299 T>A maps to NM_024876.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:145608326 G>A maps to NM_174922.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:145616431 G>T maps to NM_174922.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:145616150 G>A maps to NM_174922.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr8:145617193 C>T maps to NM_174922.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:45753311 G>A maps to NM_021116.2 R1026R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr7:45753345 C>T maps to NM_021116.2 R1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:45743051 C>T maps to NM_021116.2 H844H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr7:45614570 C>T maps to NM_021116.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:45699706 C>T maps to NM_021116.2 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr7:45701776 C>A maps to NM_021116.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:45742986 C>T maps to NM_021116.2 R823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr7:45753497 C>T maps to NM_021116.2 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:45614582 G>T maps to NM_021116.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:45662317 C>T maps to NM_021116.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:45743054 C>T maps to NM_021116.2 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr7:45688315 C>T maps to NM_021116.2 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:45753551 A>G maps to NM_021116.2 P1106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr7:45743281 C>T maps to NM_021116.2 D885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:45614402 G>A maps to NM_021116.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:167844424 C>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:167823636 T>C maps to NM_018417.4 Q754Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:167863156 C>T maps to NM_018417.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:167792354 C>T maps to NM_018417.4 P1353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:167830191 G>A maps to NM_018417.4 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr1:167793760 A>G maps to NM_018417.4 H1335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:7709436 G>A maps to NM_020546.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:7626359 G>A maps to NM_020546.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr5:7707833 T>C maps to NM_020546.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:7709481 C>T maps to NM_020546.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr5:7396564 C>G maps to NM_020546.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:7396480 C>T maps to NM_020546.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr5:7789858 C>T maps to NM_020546.2 N858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:7626395 G>A maps to NM_020546.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:7706928 C>T maps to NM_020546.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:7789774 A>G maps to NM_020546.2 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:7789843 C>T maps to NM_020546.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:7414768 C>T maps to NM_020546.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:7707860 C>T maps to NM_020546.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:7817073 C>T maps to NM_020546.2 N993N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:25042947 G>A maps to NM_004036.3 Y1096Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr2:25141529 G>A maps to NM_004036.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:25141232 G>A maps to NM_004036.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:25043703 G>A maps to NM_004036.3 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:25047329 G>A maps to NM_004036.3 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:25141778 G>A maps to NM_004036.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:25044434 C>T maps to NM_004036.3 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:24792216 C>T maps to NM_139247.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:24791427 A>G maps to NM_139247.3 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:24789067 G>A maps to NM_139247.3 C871C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr14:24798737 G>A maps to NM_139247.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:24801131 G>A maps to NM_139247.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:24799124 G>A maps to NM_139247.3 Y386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:123166318 G>A maps to NM_183357.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr3:123166564 G>A maps to NM_183357.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:123021991 C>T maps to NM_183357.2 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr3:123019007 C>T maps to NM_183357.2 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:123046524 G>A maps to NM_183357.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr3:123038601 G>A maps to NM_183357.2 D725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:123010073 C>T maps to NM_183357.2 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:123021991 C>T maps to NM_183357.2 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:123066663 G>A maps to NM_183357.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr3:123166564 G>A maps to NM_183357.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:49170888 G>A maps to NM_015270.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:49177013 G>A maps to NM_015270.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:49176914 G>A maps to NM_015270.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:50342600 G>A maps to NM_001114.3 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:50338341 G>A maps to NM_001114.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:50342321 G>A maps to NM_001114.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:50346847 C>T maps to NM_001114.3 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr16:50338446 C>T maps to NM_001114.3 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:50332891 C>A maps to NM_001114.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:131797705 G>A maps to NM_001115.2 R1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:131848566 G>A maps to NM_001115.2 Y877Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:131916288 C>A did not map to a codon.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr8:131916176 A>C maps to NM_001115.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr8:131793085 G>A maps to NM_001115.2 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr8:132051787 G>A maps to NM_001115.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr8:131859735 C>T maps to NM_001115.2 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:132051763 G>A maps to NM_001115.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:132002704 T>C maps to NM_001115.2 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:131812713 T>C maps to NM_001115.2 E1006E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:131916176 A>G maps to NM_001115.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:131916176 A>C maps to NM_001115.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr8:131916176 A>C maps to NM_001115.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:131797709 T>C maps to NM_001115.2 E1024E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr8:131793085 G>A maps to NM_001115.2 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr8:132052324 G>A maps to NM_001115.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:131916224 G>A maps to NM_001115.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr8:132052234 G>A maps to NM_001115.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr8:131792851 G>T maps to NM_001115.2 I1180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr8:131955665 C>T maps to NM_001115.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:131833590 C>T maps to NM_001115.2 Q917Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:131922047 G>A maps to NM_001115.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr16:4164837 G>A maps to NM_001116.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:4016486 C>T maps to NM_001116.3 A1117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:4164369 G>A maps to NM_001116.3 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:4164492 A>G maps to NM_001116.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:4164996 C>T maps to NM_001116.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr16:4016159 T>C maps to NM_001116.3 R1226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:4164855 C>T maps to NM_001116.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:4015870 G>T maps to NM_001116.3 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:4016450 G>A maps to NM_001116.3 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:4016603 G>A maps to NM_001116.3 G1078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:4164579 G>A maps to NM_001116.3 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:4016444 C>T maps to NM_001116.3 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:31102903 C>T maps to ENST00000409489 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr7:31102891 C>T maps to ENST00000409489 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr4:2896322 A>G maps to NM_014189.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:2899981 T>C maps to NM_014189.2 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:2877674 C>A maps to NM_014189.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:70933381 G>A maps to NM_001185054.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:70933546 G>A maps to NM_001185055.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:70890742 G>A maps to NM_001185054.1 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:70890787 G>A maps to NM_001185054.1 N650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:70922921 G>A maps to NM_001185054.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:70900459 T>C maps to ENST00000356565 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr2:70910803 G>A maps to NM_001185054.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:70933423 C>T maps to NM_001185054.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr10:111860579 C>T maps to NM_016824.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr10:111860437 G>A maps to NM_016824.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:111877149 A>G maps to NM_016824.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:111893087 C>T maps to NM_016824.3 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:100205627 C>T maps to NM_000667.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:100201342 G>A maps to NM_000667.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr4:100237382 G>A maps to NM_000668.4 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:100052675 A>G maps to ENST00000505590 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr4:99997595 G>A maps to NM_000671.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:67361170 C>T maps to NM_144650.2 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:67364292 C>T maps to NM_144650.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:186571970 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:202911317 G>A maps to NM_015999.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:1882030 T>C maps to NM_024551.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:1882024 A>G maps to NM_024551.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr12:1890114 T>C maps to NM_024551.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:10327579 C>T maps to NM_001124.1 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:49510460 G>T maps to NM_181442.1 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:49520467 T>A maps to NM_181442.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:49508349 G>A maps to NM_181442.1 D967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:77894582 C>T maps to NM_014913.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:77894087 G>A maps to NM_014913.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:77894777 G>A maps to NM_014913.3 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:77895695 T>C maps to NM_014913.3 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:77894426 A>G maps to NM_014913.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:77894934 C>T maps to NM_014913.3 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr10:64565193 C>T maps to NM_032804.5 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:203097974 G>A maps to NM_001048230.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr1:203134526 C>T maps to NM_001048230.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:203134421 G>A maps to NM_001048230.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr1:203134712 G>A maps to NM_001048230.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr1:203098169 C>A maps to NM_001048230.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr22:24837198 T>C maps to NM_000675.4 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:24836595 C>T maps to NM_000675.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr1:112045631 G>A maps to NM_020683.6 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:112042828 G>A maps to NM_000677.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:73048720 G>A maps to NM_031284.4 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:73052856 G>A maps to NM_031284.4 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:73048786 C>A maps to NM_031284.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr13:114077205 G>A maps to NM_138430.3 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr13:114107632 G>T maps to NM_138430.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:114077154 C>T maps to NM_138430.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr8:26628133 T>G maps to ENST00000356368 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:26722435 C>T maps to ENST00000356368 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr5:159344847 C>A maps to NM_000679.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:159344088 C>T maps to NM_000679.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:4202256 T>C maps to NM_000678.3 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:4202220 G>A maps to NM_000678.3 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:4229310 G>A maps to NM_000678.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr20:4228497 C>T maps to NM_000678.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:112838326 C>T maps to NM_000681.3 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:112838875 G>A maps to NM_000681.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:96781450 C>T maps to NM_000682.5 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:96781138 C>T maps to NM_000682.5 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:96781639 C>T maps to NM_000682.5 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr2:96781708 C>A maps to NM_000682.5 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:3768920 C>T maps to NM_000683.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr4:3768800 C>T maps to NM_000683.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr10:115804229 G>A maps to NM_000684.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:148207338 C>T maps to NM_000024.5 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:148206747 G>A maps to NM_000024.5 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr5:148207464 C>T maps to NM_000024.5 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:37823753 C>T maps to NM_000025.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:67052655 C>T maps to NM_001619.3 C634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:67048583 C>T maps to NM_001619.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr11:67046684 C>T maps to NM_001619.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:67049407 C>A maps to NM_001619.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:26110385 C>T maps to NM_005160.3 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:26091136 C>T maps to NM_005160.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:26086187 C>T maps to NM_005160.3 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:26070496 T>C did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr22:26100173 C>T maps to NM_005160.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr20:60883473 C>T maps to NM_175573.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:60881311 C>T maps to NM_175573.1 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr22:40754924 C>T maps to ENST00000428371 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:244615082 G>A maps to NM_001126.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:105208224 C>T maps to NM_199165.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:105208218 C>A maps to NM_199165.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:105207518 C>T maps to NM_199165.1 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr14:105201395 A>T maps to NM_199165.1 K121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:44151799 T>C maps to NM_001129.3 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:44153499 C>T maps to NM_001129.3 N1039N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:44151519 G>A maps to NM_001129.3 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:44150347 C>T maps to NM_001129.3 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:44149840 G>A maps to NM_001129.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr7:44147231 G>A maps to NM_001129.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:44144462 C>T maps to NM_001129.3 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:44150786 G>A maps to NM_001129.3 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr12:19615473 C>T maps to NM_001114176.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:19593268 T>C maps to NM_001114176.1 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:89172497 G>A maps to NM_022767.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:89169601 C>T maps to NM_022767.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr15:89172602 G>A maps to NM_022767.3 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:3053822 C>T maps to NM_198969.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:7788019 A>G maps to NM_001134647.1 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:7840355 C>T maps to NM_001134647.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:7774588 C>T maps to NM_001134647.1 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:7857229 C>T maps to NM_001134647.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:7802369 G>A maps to NM_001134647.1 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:7780582 G>T maps to NM_001134647.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:148685929 C>T maps to NM_152406.2 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:148679891 C>T maps to NM_152406.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:148687127 C>T maps to NM_152406.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr5:148686977 C>T maps to NM_152406.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr10:116064681 C>T maps to NM_001001936.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:116073683 G>A maps to NM_001001936.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:116060073 G>A maps to NM_001001936.1 T612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:116060388 G>A maps to NM_001001936.1 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:88011179 G>A maps to NM_001166693.1 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:88036258 G>A maps to NM_001166693.1 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:88055676 A>G maps to NM_001166693.1 V1122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:88035904 C>T maps to NM_001166693.1 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr4:88055781 A>G maps to NM_001166693.1 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:87968254 G>T maps to NM_001166693.1 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr4:87968289 A>G maps to NM_001166693.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:88036090 C>T maps to NM_001166693.1 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:88056808 C>T maps to NM_001166693.1 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:148037707 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:148037981 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:148068942 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:148072814 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:148038100 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:148049193 A>C did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:147891441 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:147743679 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:147733535 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:147744086 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:147967421 G>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:148037395 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:147743733 T>C did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:148044286 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:147744111 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:148044333 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:148037359 A>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:147967479 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:148037623 A>G did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:148037714 G>C did not map to a codon.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr23:148048537 C>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:147743467 A>T did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:148037908 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:147744021 A>T did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:148039900 A>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:148037755 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:148037279 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:148048439 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:148059470 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr23:148055008 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:148055040 C>T did not map to a codon.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr23:147743963 C>T did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:147743835 C>A did not map to a codon.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr23:148044422 A>C did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:147744268 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:147743656 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:148037275 A>C did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr23:148037499 A>G did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr2:100170899 C>T maps to NM_001025108.1 P1169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:100203725 G>A maps to NM_001025108.1 D852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:100368729 G>A maps to NM_001025108.1 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr2:100210397 C>T maps to NM_001025108.1 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:100167950 G>A maps to NM_001025108.1 S1247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:100170815 G>A maps to NM_001025108.1 Y1197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr2:100199323 G>C maps to NM_001025108.1 S935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:132232455 T>C maps to NM_014423.3 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:132238132 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:132223800 A>G maps to NM_014423.3 N928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:132227942 C>T maps to NM_014423.3 E850E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:12367304 A>G maps to NM_006796.2 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:12356743 G>A maps to NM_006796.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr18:12367346 T>C maps to NM_006796.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:74357800 G>A maps to NM_001133.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr4:74351730 C>A maps to NM_001133.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr4:74367521 G>A maps to NM_001133.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:74367502 G>T did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr4:74364920 T>C maps to NM_001133.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:74354475 G>A maps to NM_001133.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:74318230 C>T maps to NM_001134.1 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr2:64779732 T>A maps to ENST00000422803 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:64778748 C>T maps to ENST00000422803 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:64778947 G>T maps to ENST00000422803 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:64794727 C>T maps to ENST00000422803 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:178354502 T>C did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr4:178358634 G>T maps to NM_000027.3 Y182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:236706490 C>T maps to NM_001037131.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:236706463 G>A maps to NM_001037131.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:236957794 C>T maps to NM_001037131.1 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:88768860 G>A maps to NM_133447.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:88769343 C>A maps to NM_133447.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:88769419 C>T maps to NM_133447.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:88768350 C>T maps to NM_133447.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr12:58135697 G>A maps to NM_014770.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:58127811 G>A maps to NM_001122772.1 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:75435610 C>T maps to NM_001144000.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:75434449 G>A maps to NM_001144000.1 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr10:51472610 C>G maps to ENST00000416142 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:51465444 G>A maps to ENST00000416142 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:51225181 G>A maps to ENST00000425119 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:86813173 C>T maps to NM_152336.2 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:87531238 G>T maps to NM_152336.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:86838490 T>C maps to NM_152336.2 H696H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:86800190 C>A maps to NM_152336.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr15:86807658 G>T maps to NM_152336.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr15:86838559 G>A maps to NM_152336.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr11:47711959 G>A maps to ENST00000357610 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr11:47698916 G>A maps to ENST00000357610 R685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:27278612 G>A maps to NM_021831.5 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:27282078 C>T maps to NM_021831.5 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:27278918 C>T maps to NM_021831.5 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:27278630 A>G maps to NM_021831.5 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:27276774 G>A maps to NM_021831.5 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:27278600 C>T maps to NM_021831.5 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:27280179 T>C maps to NM_021831.5 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr2:27278795 C>T maps to NM_021831.5 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:100162614 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:100153231 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:76344001 G>A maps to NM_018046.4 W406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:76331393 C>T maps to NM_018046.4 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:100340250 C>T maps to ENST00000311030 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:100336319 C>T maps to ENST00000311030 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:100382218 G>A maps to ENST00000311030 P1472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:100345507 A>G maps to ENST00000311030 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:100342154 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:100380955 C>T maps to ENST00000311030 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:100378008 C>T maps to ENST00000311030 R1296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:100340250 C>T maps to ENST00000311030 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:15909691 G>T maps to NM_024758.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:15900199 C>T maps to NM_024758.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:15905524 G>A maps to NM_024758.3 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:32137061 G>A maps to NM_032741.4 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:139571493 G>A maps to NM_006412.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:139571988 G>A maps to NM_006412.3 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:139571442 G>A maps to NM_006412.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:45401009 C>T maps to NM_001037553.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr21:45391317 G>A maps to NM_001037553.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:161560484 C>T maps to NM_020133.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:161574396 C>T maps to NM_020133.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr8:41467366 G>A maps to NM_178819.3 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:41467267 C>T maps to NM_178819.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:78807370 C>A maps to NM_001013619.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:78825819 C>T maps to NM_001013619.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:178388534 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:178386062 T>C maps to NM_003659.3 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr2:178386011 C>T maps to NM_003659.3 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:178386002 G>A maps to NM_003659.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr7:16841345 G>A maps to ENST00000223274 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr7:16841333 G>A maps to ENST00000223274 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:978990 C>T maps to NM_198576.2 C559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:985289 C>T maps to NM_198576.2 T1584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:980634 C>T maps to NM_198576.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr1:980790 C>T maps to NM_198576.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:981386 C>T maps to NM_198576.2 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:980539 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:979558 C>T maps to NM_198576.2 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:979718 C>T maps to NM_198576.2 C718C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:978820 G>A maps to NM_198576.2 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:67516942 A>C maps to NM_001138.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:67516935 A>G maps to NM_001138.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr1:230839015 G>T maps to NM_000029.3 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:230846218 G>A maps to NM_000029.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr9:88193990 G>A maps to ENST00000395847 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:88193896 C>A maps to ENST00000395847 G1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:88190327 T>C maps to ENST00000395847 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:88287482 G>A maps to ENST00000395847 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:88200432 C>T maps to ENST00000395847 W1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:88200386 C>T maps to ENST00000395847 T1052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:88204536 A>G maps to ENST00000395847 D876D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr3:148459061 T>G maps to NM_032049.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:115303555 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:115304593 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:115304469 G>A did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr1:11808640 G>A maps to NM_001040196.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:241818168 C>T maps to NM_000030.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:241808356 G>T maps to NM_000030.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:35047908 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:35025912 G>T maps to NM_031900.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr5:35010215 T>C maps to NM_031900.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr5:35047946 G>A maps to NM_031900.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:35026571 A>G maps to NM_031900.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr5:35039556 C>T maps to NM_031900.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr4:109674149 A>C maps to NM_031279.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:177638919 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr5:177657056 C>T maps to NM_153373.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:247048892 G>A maps to ENST00000428671 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr1:247054342 A>G maps to ENST00000428671 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:247014120 G>A maps to ENST00000428671 S1767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:247071022 T>C maps to ENST00000428671 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr1:247006018 C>T maps to ENST00000428671 T2233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:247024357 C>T maps to ENST00000428671 P1363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:247039432 G>A maps to ENST00000428671 D1036D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:247013667 T>C maps to ENST00000428671 E1918E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:247024357 C>T maps to ENST00000428671 P1363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:247076641 G>A maps to ENST00000428671 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:247051508 G>A maps to ENST00000428671 D803D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:32878576 G>A maps to NM_000687.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:32878615 G>A maps to NM_000687.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr20:32883311 C>T maps to NM_000687.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:32880242 G>A maps to NM_000687.2 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:32868965 A>G maps to NM_000687.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:32880296 G>A maps to NM_000687.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:110559019 T>C maps to NM_006621.4 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:110563413 T>C maps to NM_006621.4 D509D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:110561199 G>A maps to NM_006621.4 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:129062713 C>T maps to NM_015328.3 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:27875575 G>A maps to NM_001029882.2 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr1:27876481 C>A maps to NM_001029882.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:27875215 G>A maps to NM_001029882.2 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:27875590 G>A maps to NM_001029882.2 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr1:27876607 G>A maps to NM_001029882.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:27875065 G>A maps to NM_001029882.2 S1187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:27873886 G>C maps to NM_001029882.2 G1580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:27874132 C>T maps to NM_001029882.2 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:27876814 G>A maps to NM_001029882.2 D604D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr1:27874147 G>A maps to NM_001029882.2 G1493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:27874999 G>A maps to NM_001029882.2 N1209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr6:135784437 C>T maps to NM_017651.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:62298465 G>A maps to NM_001620.1 G1141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:62292450 C>T maps to NM_001620.1 W3146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:62297303 C>A maps to NM_001620.1 E1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:62285595 G>A maps to NM_001620.1 G5431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr11:62299902 G>A maps to NM_001620.1 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr11:62286162 G>A maps to NM_001620.1 G5242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr11:62294046 G>A maps to NM_001620.1 D2614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:62290260 A>G maps to NM_001620.1 P3876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr11:62297319 A>G maps to NM_001620.1 F1523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr11:62298591 T>A maps to NM_001620.1 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:62287620 G>A maps to NM_001620.1 D4756D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:62285757 A>G maps to NM_001620.1 S5377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr11:62299851 T>C maps to NM_001620.1 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:62289450 G>A maps to NM_001620.1 D4146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:62289567 A>G maps to NM_001620.1 G4107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr11:62297322 G>A maps to NM_001620.1 G1522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr11:62290002 G>A maps to NM_001620.1 D3962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr11:62300831 G>A maps to NM_001620.1 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr11:62292267 G>A maps to NM_001620.1 F3207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:62298375 G>A maps to NM_001620.1 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr11:62291190 G>A maps to NM_001620.1 P3566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:62291859 G>A maps to NM_001620.1 I3343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:105411839 C>T maps to NM_138420.2 P3316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:105409289 G>A maps to NM_138420.2 D4166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:105412735 G>A maps to NM_138420.2 Q3018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:105418817 G>A maps to NM_138420.2 D990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:105419600 G>A maps to NM_138420.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:105409901 C>A maps to NM_138420.2 T3962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:105409907 G>A maps to NM_138420.2 D3960D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:105409964 T>C maps to NM_138420.2 P3941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:105413159 C>T maps to NM_138420.2 Q2876Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:105416426 G>A maps to NM_138420.2 P1787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:105411773 C>T maps to NM_138420.2 A3338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr14:105413099 C>G maps to NM_138420.2 L2896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:105413903 C>T maps to NM_138420.2 A2628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:105416462 C>T maps to NM_138420.2 A1775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr14:105417278 G>A maps to NM_138420.2 F1503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:105407180 C>T maps to NM_138420.2 K4869K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:105418202 G>A maps to NM_138420.2 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr14:105418916 G>A maps to NM_138420.2 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr14:105415658 G>A maps to NM_138420.2 A2043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr14:105412334 C>T maps to NM_138420.2 P3151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:105406796 C>T maps to NM_138420.2 P4997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:105416435 C>T maps to NM_138420.2 V1784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr14:105411497 A>G maps to NM_138420.2 P3430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:105419600 G>A maps to NM_138420.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:105414482 C>T maps to NM_138420.2 T2435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:105409289 G>A maps to NM_138420.2 D4166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:105409661 G>C maps to NM_138420.2 P4042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:105413723 T>C maps to NM_138420.2 Q2688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr14:105415601 G>A maps to NM_138420.2 P2062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr14:105416441 C>G maps to NM_138420.2 V1782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:105414281 G>A maps to NM_138420.2 I2502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr14:105419696 C>T maps to NM_138420.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr14:105415658 G>A maps to NM_138420.2 A2043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:105410846 T>C maps to NM_138420.2 S3647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:105410861 T>C maps to NM_138420.2 K3642K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:105418826 G>A maps to NM_138420.2 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:105407933 G>A maps to NM_138420.2 H4618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr14:105409787 G>A maps to NM_138420.2 A4000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr14:105411992 G>A maps to NM_138420.2 P3265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:105410342 C>T maps to NM_138420.2 V3815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:105416189 G>C maps to NM_138420.2 L1866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:105414443 G>A maps to NM_138420.2 S2448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr14:105414752 C>T maps to NM_138420.2 A2345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr14:105417086 G>A maps to NM_138420.2 S1567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:105406586 G>A maps to NM_138420.2 D5067D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:105419165 C>T maps to NM_138420.2 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:17379186 G>T maps to NM_001621.4 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr7:17373616 T>C maps to NM_001621.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:17378634 C>T maps to NM_001621.4 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:434066 G>A maps to NM_020731.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:433982 G>A maps to NM_020731.3 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:424010 G>A maps to NM_020731.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:353843 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:434621 C>T maps to NM_020731.3 H611H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr5:353859 G>A maps to NM_020731.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:432969 C>T maps to NM_020731.3 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:434093 G>A maps to NM_020731.3 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:61411874 G>A maps to ENST00000389584 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:61413632 G>A did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr3:186335006 A>G maps to ENST00000273784 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:186330968 C>G maps to ENST00000273784 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:186334973 A>G maps to ENST00000273784 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:186333562 C>T maps to ENST00000273784 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:8759608 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:8757504 G>T maps to NM_020661.2 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr1:222843512 C>T maps to NM_022831.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr1:222849459 G>C maps to NM_022831.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:31583457 C>T maps to NM_001623.3 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:129267363 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:129272623 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:129270060 G>A did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr10:71876516 G>A maps to NM_032797.5 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:71880940 C>T maps to NM_032797.5 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:71883804 C>T maps to NM_032797.5 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:71874700 C>T maps to NM_032797.5 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:71883163 G>A maps to NM_032797.5 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:143382142 C>A maps to NM_016108.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:106968175 G>A maps to NM_001624.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:106989471 A>G maps to NM_001624.2 K1211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:106973141 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:106968175 G>A maps to NM_001624.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:26655304 G>A maps to NM_001039775.3 I1458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr1:26655304 G>A maps to NM_001039775.3 I1458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:159035717 A>C maps to NM_004833.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr1:159043115 C>T maps to NM_004833.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:6063240 A>G maps to NM_006303.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:6057563 G>A maps to NM_006303.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:6063066 G>A maps to NM_006303.3 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr11:67254508 C>T maps to NM_003977.2 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:6328974 C>T maps to NM_014336.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:6329091 G>A maps to NM_014336.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:6331700 G>A maps to NM_014336.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr21:45708226 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:4772103 C>T maps to NM_018836.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:4832465 G>A maps to NM_018836.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:4832465 G>T maps to NM_018836.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr1:4832492 T>C maps to NM_018836.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:4834504 G>A maps to NM_018836.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:4832432 G>A maps to NM_018836.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr1:4772109 G>A maps to NM_018836.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr9:4741003 A>T maps to NM_016282.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:4718477 C>T maps to NM_016282.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr9:4712976 C>G maps to NM_016282.3 *228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr9:4741006 G>A maps to NM_016282.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:4719172 G>A maps to NM_016282.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr9:4740940 G>A maps to NM_016282.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:65691784 G>A maps to NM_013410.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:77987582 C>T maps to NM_174858.1 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:77752750 G>A maps to NM_174858.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr14:96904252 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:96924478 G>A maps to NM_152327.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:55183826 T>C maps to ENST00000427138 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:55189187 G>A maps to ENST00000427138 Q668Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:19823396 G>A maps to NM_007202.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:19827779 C>G maps to NM_007202.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr17:19844303 G>T maps to NM_007202.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:42876607 G>A maps to NM_016248.2 S1242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr13:42874174 G>A maps to NM_016248.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:42877675 C>T maps to NM_016248.2 C1598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:42871201 T>C maps to NM_016248.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:42876040 A>G maps to NM_016248.2 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:42873556 T>C maps to NM_016248.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:42874606 A>G maps to NM_016248.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr13:42875434 A>G maps to NM_016248.2 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:42876652 C>T maps to NM_016248.2 C1257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:151671214 C>T maps to NM_005100.3 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:151670578 C>T maps to NM_005100.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr6:151671965 C>T maps to NM_005100.3 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:151674331 G>A maps to NM_005100.3 Q1602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:151672363 A>G maps to NM_005100.3 E946E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr6:151672609 C>T maps to NM_005100.3 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr6:151670623 C>T maps to NM_005100.3 H366H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:151669963 C>T maps to NM_005100.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:151671352 C>A maps to NM_005100.3 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:151673446 A>G maps to NM_005100.3 E1307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:86278286 C>T maps to NM_006738.4 S2453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:86198865 C>T maps to NM_006738.4 G1531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr15:86124025 T>C maps to NM_006738.4 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:86205627 G>A maps to NM_006738.4 W1585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:86124319 G>A maps to NM_006738.4 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:86284608 C>T maps to NM_006738.4 Y2651Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:86124394 C>A maps to NM_006738.4 A1032A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:86270412 C>T maps to NM_006738.4 V2317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr15:86273855 A>C maps to NM_006738.4 T2404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:119053877 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:119037279 T>G did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:119037548 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:112900595 A>G maps to NM_007203.4 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr9:112899718 C>A maps to NM_007203.4 S632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:112900544 C>T maps to NM_007203.4 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr9:112918659 T>G maps to NM_007203.4 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:4735742 G>A maps to NM_006422.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:4737922 G>A maps to NM_006422.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:49958234 C>T did not map to a codon.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr23:49957931 C>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:49957255 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:49958091 C>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:49958504 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:49958147 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:49958223 G>A did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:49958928 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:49958567 G>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:49958700 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:49962240 C>T did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:49957535 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:49957563 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:49957451 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:49957584 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:49958915 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:64936005 G>A maps to NM_004857.3 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr14:64935786 G>C maps to NM_004857.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:33290605 A>G did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr14:33290804 C>T maps to NM_004274.4 D1262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:33293171 C>T maps to NM_004274.4 A2051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr14:33290765 G>A maps to NM_004274.4 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr14:33046438 G>A maps to NM_004274.4 E820E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr14:33291821 T>G maps to NM_004274.4 T1601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:33291715 C>A maps to NM_004274.4 S1566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr14:33205030 T>A maps to NM_004274.4 C1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:33291545 C>T maps to NM_004274.4 C1509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:33293351 G>A maps to NM_004274.4 S2111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr14:33293354 C>T maps to NM_004274.4 Y2112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr14:33291959 G>A maps to NM_004274.4 E1647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr14:33015654 C>G maps to NM_004274.4 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:33292871 A>G maps to NM_004274.4 E1951E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:131540893 C>T maps to ENST00000431975 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:15483889 C>T maps to NM_005858.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:15466094 A>G maps to NM_005858.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:15511827 G>A maps to NM_014371.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15510110 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:91652317 G>A maps to NM_005751.4 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:91737870 C>T maps to NM_005751.4 Y3870Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr7:91682265 C>T maps to NM_005751.4 S1865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:91670109 G>A maps to NM_005751.4 T1605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:91641855 C>T maps to NM_005751.4 C1144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:91668043 A>G maps to NM_005751.4 E1550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:91630523 A>G maps to NM_005751.4 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:91632320 T>C maps to NM_005751.4 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:91645528 C>T maps to NM_005751.4 Y1233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:91691588 C>T maps to NM_005751.4 G1922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:109867150 G>A maps to NM_001145128.2 N1048N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:88385593 T>C maps to NM_018064.3 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:88387677 T>C maps to NM_018064.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:88387649 C>A maps to NM_018064.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:88391419 T>C maps to NM_018064.3 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:117124103 C>T maps to NM_030767.4 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:117124786 G>A maps to NM_030767.4 H605H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr9:117099369 G>A maps to NM_030767.4 R1428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:117139519 G>A maps to NM_030767.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr9:117139519 G>A maps to NM_030767.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:109358852 A>G maps to NM_152763.3 I817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:109377641 G>A maps to NM_152763.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:109369860 A>G maps to NM_152763.3 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:109377678 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:109392198 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:46034901 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:134133173 G>A maps to NM_001628.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:134135549 C>T maps to NM_001628.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:134221502 A>G maps to NM_020299.4 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:134225822 C>A maps to NM_020299.4 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:134222346 C>T maps to NM_020299.4 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:134254169 G>A maps to ENST00000418096 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:5008191 T>C maps to NM_001353.5 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr10:5008191 T>C maps to NM_001353.5 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:5144397 C>T maps to NM_003739.4 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr10:5144379 G>T maps to NM_003739.4 G220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:137776527 T>C maps to NM_005989.3 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr10:4884668 C>T maps to NM_001040177.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr10:4879676 G>A maps to NM_001040177.1 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:19632509 A>G did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:19611226 G>A maps to NM_012067.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:19610543 G>A maps to NM_012067.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:19612804 C>T maps to NM_012067.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr1:19612420 G>C maps to NM_012067.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr1:19610504 G>A maps to NM_012067.2 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:19612768 A>G maps to NM_012067.2 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:105241991 G>A maps to NM_001014432.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:105238716 G>A maps to NM_001014432.1 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:105239378 G>A maps to NM_001014432.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:50373221 C>T maps to ENST00000391835 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:243727144 C>T maps to NM_005465.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:243778457 T>C maps to NM_005465.3 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:243777026 G>T maps to NM_005465.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:243809286 C>A maps to NM_005465.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:53528484 C>T maps to ENST00000425875 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:116152750 C>T maps to ENST00000277315 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:116152093 G>A maps to ENST00000277315 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr9:116151290 G>C maps to ENST00000277315 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr9:116151365 G>A maps to ENST00000277315 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:52240612 G>A maps to ENST00000441729 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr3:52236730 A>G maps to ENST00000441729 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:52233280 C>T maps to ENST00000441729 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:52237966 C>T maps to ENST00000441729 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:55051230 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:55047482 A>G did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:55052270 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:55042054 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:55052393 G>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:55040073 T>G did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:55050236 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:55039969 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:55041234 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:55035638 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr23:55052356 A>C did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:55042054 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:55042165 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:49971688 C>T maps to NM_153329.3 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:49962307 G>A maps to NM_153329.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr19:49967995 G>A maps to NM_153329.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:49973651 C>T maps to NM_153329.3 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:97402811 G>A maps to NM_002860.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:97371129 G>A maps to NM_002860.3 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:97387226 A>G maps to NM_002860.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:75533735 A>G maps to NM_000689.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:75545878 C>T maps to NM_000689.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:75567907 G>T maps to NM_000689.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:75539030 T>G maps to NM_000689.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:75555147 C>T maps to NM_000689.3 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:58357818 G>A maps to NM_003888.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:58285255 G>A maps to NM_003888.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:58357785 C>T maps to NM_003888.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:58253408 G>A maps to NM_003888.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr15:58306437 T>C maps to NM_003888.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr15:101445801 C>T maps to NM_000693.2 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:101434256 C>T maps to NM_000693.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:101433159 C>T maps to NM_000693.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:38396149 C>T maps to NM_000692.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:38397268 C>T maps to NM_000692.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:38397184 G>A maps to NM_000692.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr3:125850283 G>A maps to ENST00000273450 H532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:125824740 G>T maps to ENST00000273450 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:125844512 C>T maps to ENST00000273450 W592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:112229917 C>A maps to NM_000690.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr17:19643781 G>A maps to NM_000691.4 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:19641725 G>A maps to NM_000691.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:19643781 G>A maps to NM_000691.4 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:19568353 G>T maps to NM_001031806.1 G401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:19555012 G>T maps to NM_001031806.1 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:67789014 C>T maps to NM_001161473.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:67432885 G>A maps to NM_001031615.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:19199401 C>T maps to NM_003748.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:19208375 G>A maps to NM_003748.3 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:19209680 C>T maps to NM_003748.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:24533871 C>T maps to NM_170740.1 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:24528247 C>T maps to NM_170740.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:24528265 C>T maps to NM_170740.1 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:24520717 C>T maps to NM_170740.1 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:74551091 C>T maps to NM_005589.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:125903996 G>A maps to NM_001182.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:125912805 G>A maps to NM_001182.3 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:135239849 C>T maps to NM_022568.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:135239564 G>A maps to NM_022568.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:165638533 G>A maps to NM_000696.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:165664629 T>G maps to NM_000696.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr9:104187733 C>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:26902511 C>T maps to NM_005165.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:26901544 G>A maps to NM_005165.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:26900950 T>C maps to NM_005165.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:5130945 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:34179675 T>C maps to NM_032834.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr12:38714573 G>A maps to NM_001013620.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:52598399 C>T maps to NM_001004127.2 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:52598189 C>T maps to NM_001004127.2 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr13:52602509 C>T maps to NM_001004127.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr13:52598570 C>A maps to NM_001004127.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:52598174 C>T maps to NM_001004127.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr13:52598171 C>T maps to NM_001004127.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:110954935 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:110925501 A>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:111002995 T>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:110928332 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:110951410 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:110928251 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:110988112 C>T did not map to a codon.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr23:110988125 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:110951263 T>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:110951471 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:110925364 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:111000876 A>G did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr1:95530568 C>T maps to NM_144988.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:125648341 C>T maps to NM_001195223.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:63876939 C>T maps to ENST00000263440 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:63876979 A>T maps to ENST00000263440 K222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:29462671 G>A maps to NM_004304.3 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr2:29416758 C>T maps to NM_004304.3 P1398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr2:29551214 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:29446356 C>T maps to NM_004304.3 Q1070Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr2:29462632 G>A maps to NM_004304.3 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr2:29416140 G>A maps to NM_004304.3 Y1604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr2:29473981 G>A maps to NM_004304.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr2:29450509 G>A maps to NM_004304.3 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:29416152 T>C maps to NM_004304.3 G1600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:29917827 C>T maps to NM_004304.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr2:30143012 G>A maps to NM_004304.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:43908176 C>T maps to NM_139178.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:43913678 C>T maps to NM_139178.3 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:102100206 G>A maps to NM_017621.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr17:18088228 T>A maps to ENST00000261650 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:36503973 G>T maps to ENST00000455847 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:107381714 C>T maps to ENST00000417449 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:107403093 C>T maps to ENST00000417449 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:107427669 C>T maps to ENST00000417449 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr11:107403036 A>G maps to ENST00000417449 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:3744990 A>T maps to ENST00000403787 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:3743889 G>A maps to ENST00000403787 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:73680415 T>C maps to NM_015120.4 N2253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:73717260 C>T maps to NM_015120.4 C2724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:73678504 C>T maps to NM_015120.4 S1616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:73747132 C>T maps to NM_015120.4 R3256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:73800367 C>T maps to NM_015120.4 A3787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:73677595 A>G maps to NM_015120.4 S1313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:73679413 T>G maps to NM_015120.4 V1919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:73717090 C>T maps to NM_015120.4 R2668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:73826649 T>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:73800416 C>T maps to NM_015120.4 R3804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:73677404 C>T maps to NM_015120.4 Q1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:73826619 A>G maps to NM_015120.4 V3879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:73717194 G>A maps to NM_015120.4 P2702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:73784419 A>C maps to NM_015120.4 T3383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr2:73829376 G>A maps to NM_015120.4 K4059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:73799650 C>T maps to NM_015120.4 S3548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:73799575 A>G maps to NM_015120.4 E3523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr2:73800202 T>G maps to NM_015120.4 T3732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:73678744 A>G maps to NM_015120.4 P1696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:6913274 C>T maps to NM_000697.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:7978910 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:7976516 C>T maps to NM_001139.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7976207 C>A maps to NM_001139.2 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:4539051 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7942595 C>T maps to NM_001141.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr10:45891346 C>T maps to NM_000698.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:45939254 C>T maps to NM_000698.2 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr10:45938959 C>T maps to NM_000698.2 Y516Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr10:45938619 C>T maps to NM_000698.2 Y469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:45938634 C>T maps to NM_000698.2 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:8013439 G>T maps to ENST00000380149 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr17:8012631 G>A maps to ENST00000380149 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:8020175 G>A maps to ENST00000380149 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:233323609 G>A maps to NM_001631.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:233322831 C>A maps to NM_001631.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr2:233323083 T>C maps to NM_001631.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:233321170 C>T maps to NM_001631.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:233322327 T>G maps to NM_001631.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:113353417 C>T maps to NM_025144.3 C905C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:113353666 G>A maps to NM_025144.3 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:113346861 C>T maps to NM_025144.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:113352013 C>T maps to NM_025144.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:113352967 C>T maps to NM_025144.3 C755C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:113352169 C>T maps to NM_025144.3 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:113353408 C>T maps to NM_025144.3 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:113351601 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr4:113353714 C>T maps to NM_025144.3 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:56203449 T>C maps to NM_052947.3 V1323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:56204820 T>C maps to NM_052947.3 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:56204715 T>G maps to NM_052947.3 T901T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:85400380 G>A maps to NM_020778.4 P1006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:85383679 C>A maps to NM_020778.4 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:85399885 G>A maps to NM_020778.4 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:85405989 T>C maps to NM_020778.4 C1620C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:85383098 G>T maps to NM_020778.4 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:85407850 C>T maps to NM_020778.4 L1762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:85411578 T>C maps to NM_020778.4 S1872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:85383248 C>T maps to NM_020778.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:85400476 C>T maps to NM_020778.4 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:21887701 C>T maps to NM_000478.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:21890654 C>T maps to NM_000478.4 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:21903106 C>T maps to NM_000478.4 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr1:21890600 C>T maps to NM_000478.4 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:233245417 C>T maps to NM_001632.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:233244006 A>G maps to NM_001632.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:233244009 T>C maps to NM_001632.3 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:233244486 A>C maps to NM_001632.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr2:233246018 C>T maps to NM_001632.3 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:233243792 C>T maps to NM_001632.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:233246264 C>T maps to NM_001632.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:233246069 C>T maps to NM_001632.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:233244552 C>T maps to NM_001632.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:233246213 C>T maps to NM_001632.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr2:233274323 C>T maps to NM_031313.2 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:202606541 G>A maps to NM_020919.3 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:202575806 C>T maps to NM_020919.3 Q1343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:202574689 G>A maps to NM_020919.3 Y1398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:202626158 G>T maps to NM_020919.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:202571651 G>A maps to NM_020919.3 R1499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:46722845 G>A maps to NM_147129.3 H442H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:46722764 G>A maps to NM_147129.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:202483622 G>A maps to NM_001168221.1 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:202438987 G>A maps to NM_001168221.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr2:202483772 G>C maps to NM_001168221.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:202466488 G>A maps to NM_001168221.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:202494477 C>T maps to ENST00000409099 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:202488986 G>A maps to ENST00000409099 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:202507330 C>T did not map to a codon.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr2:203846291 G>T maps to NM_024744.14 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr12:85677377 A>G maps to NM_006982.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:44286457 C>T maps to NM_021926.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:44331483 G>A maps to NM_021926.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:44286580 A>C maps to NM_021926.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:44296998 G>A maps to NM_021926.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:33520939 G>A maps to NM_152462.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:11189445 C>A maps to NM_054028.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr8:11189025 T>C maps to NM_054028.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:7385572 T>C maps to NM_001102614.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:7386028 G>A maps to NM_001102614.1 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:7386190 G>A maps to NM_001102614.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:34004801 C>T maps to NM_001167595.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr4:71468516 C>A maps to NM_016519.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr4:71467310 A>G maps to NM_016519.4 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr4:71472056 C>T maps to NM_016519.4 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:71472341 C>T maps to NM_016519.4 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:71471999 C>T maps to NM_016519.4 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:116835295 C>T maps to NM_001633.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:116840387 G>A maps to NM_001633.3 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:46419226 G>A maps to ENST00000458649 R1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:46419226 G>A maps to ENST00000458649 R1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:46419419 G>A maps to ENST00000458649 G1159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:46455112 G>A maps to ENST00000458649 R963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:46567254 C>T maps to ENST00000458649 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr11:46430168 C>T maps to ENST00000458649 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:46419434 C>A maps to ENST00000458649 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:46568661 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr11:46563751 G>A maps to ENST00000458649 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr11:46569855 A>C maps to ENST00000458649 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:46439469 G>A maps to ENST00000458649 R1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:46430153 G>T maps to ENST00000458649 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:46431836 G>A maps to ENST00000458649 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:96361563 C>T maps to NM_152435.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:96350719 C>T maps to NM_152435.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:2577819 G>A maps to NM_001145815.1 A154A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D7-A6EY-01A-21D-A31L-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FP-A4BE-01A-12D-A24D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-VQ-A8DZ-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:2578331 G>A maps to NM_001145815.1 T271T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:2580432 C>T maps to NM_001145815.1 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:11316821 T>G did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:11316865 C>T did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr24:6736348 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr24:6736490 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:56419829 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:53818997 C>G maps to NM_020547.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:53818977 C>T maps to NM_020547.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:53818997 C>G maps to NM_020547.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:53819000 G>C maps to NM_020547.2 L159L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D7-6528-01A-11D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr11:118083274 A>G maps to NM_153206.2 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:110050334 G>T maps to NM_020703.2 C400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr1:110051072 G>A maps to NM_020703.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:110051153 C>T maps to NM_020703.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr12:47471345 G>A maps to NM_001143668.1 N480N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr12:47471423 G>A maps to NM_001143668.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:49756811 A>G maps to NM_198722.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:49756751 G>C maps to NM_198722.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr3:49755764 G>A maps to NM_198722.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:49755431 G>T maps to NM_198722.2 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:109441847 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:109507780 C>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:109444243 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:109561046 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:109444219 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr2:128622688 G>T maps to NM_031445.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:103390156 G>A maps to NM_030943.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:103390132 C>T maps to NM_030943.3 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:112035097 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:112035059 C>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:112054509 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:112033827 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:112058801 T>G did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:112054601 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:112035137 T>C did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:112035176 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:112025830 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:112054515 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:112054535 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:112024223 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:112033858 T>G did not map to a codon.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr23:112048265 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:94602447 C>A maps to NM_130847.2 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr11:94602561 C>T maps to NM_130847.2 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:94564660 C>T maps to NM_130847.2 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr11:94532865 G>A maps to NM_130847.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:94554824 T>C maps to NM_130847.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:134090185 C>T maps to ENST00000514516 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:134089573 G>A maps to ENST00000514516 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr3:134090184 G>A maps to ENST00000514516 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:134080613 G>A maps to ENST00000514516 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:115221073 T>C maps to NM_000036.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:10517232 G>A maps to NM_000480.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:10523118 C>T maps to NM_000480.2 H617H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:10508901 C>T maps to NM_000480.2 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:10503704 G>A maps to NM_000480.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:10521673 C>T maps to NM_000480.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr7:38462018 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr7:38574554 A>T maps to NM_001635.3 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:104297193 C>T maps to NM_001008218.1 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:104297216 C>A maps to NM_001008218.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:104117946 T>A maps to NM_020978.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:104117935 G>T maps to NM_020978.3 G324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:2740093 G>A maps to NM_133463.1 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:2752319 C>T maps to NM_133463.1 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:2752349 C>T maps to NM_133463.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:2752319 C>T maps to NM_133463.1 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:2752034 G>A maps to NM_133463.1 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:2740114 C>T maps to NM_133463.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:66251927 G>T maps to NM_016627.4 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:66246995 T>C maps to NM_016627.4 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:66250542 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:112578909 G>A maps to NM_022662.2 R1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:112621310 T>C maps to NM_022662.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:145916686 A>G maps to NM_014885.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:79857370 T>C maps to NM_001002244.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:134201676 G>A maps to NM_015391.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:140079367 G>A maps to NM_013366.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr9:140079431 G>A maps to NM_013366.3 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr14:21162100 C>T maps to NM_001097577.2 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr1:213181647 A>G maps to NM_144567.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:213170496 C>A maps to NM_144567.3 G495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:213178620 A>G maps to NM_144567.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr8:108306232 A>T maps to NM_001146.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:108334271 T>C maps to NM_001146.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr8:108334267 A>G maps to NM_001146.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr8:108334271 T>C maps to NM_001146.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:108334259 A>G maps to NM_001146.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr8:108359226 G>T maps to NM_001146.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr8:108334208 G>A maps to NM_001146.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:108348405 C>A maps to NM_001146.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:6372236 G>A maps to NM_001147.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:6371314 C>T maps to NM_001147.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:6372233 G>A maps to NM_001147.2 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:6366531 G>A maps to NM_001147.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:6389933 C>T maps to NM_001147.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr20:853671 C>T maps to NM_015985.2 W481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr20:860425 G>A maps to NM_015985.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:129870707 C>T maps to NM_012098.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:129870415 G>A maps to NM_012098.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:129856047 G>T maps to NM_012098.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr9:129856053 C>T maps to NM_012098.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:129870557 G>A maps to NM_012098.2 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:129870995 G>A maps to NM_012098.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:63068013 G>A maps to NM_014495.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:63070425 T>C maps to NM_014495.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:8436326 C>T maps to NM_139314.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:10203375 G>A maps to NM_031917.2 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:11253812 G>A maps to NM_021146.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:11249873 C>T maps to NM_021146.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:41530008 A>G maps to ENST00000415018 S1653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr8:41577289 G>A maps to ENST00000415018 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:41572499 G>A maps to ENST00000415018 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr8:41530410 G>A maps to ENST00000415018 D1519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:41583410 G>A maps to ENST00000415018 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:41577304 G>A maps to ENST00000415018 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:41522388 G>A maps to NM_020478.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:41753956 G>A maps to NM_001142446.1 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr8:41550269 G>A maps to ENST00000415018 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:41583341 G>A maps to ENST00000415018 N183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:41571751 G>A maps to ENST00000415018 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:41577331 G>A maps to ENST00000415018 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:114277793 A>T maps to NM_001148.4 K2674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr4:114278656 T>C maps to NM_001148.4 S2961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr4:114161711 G>A maps to NM_001148.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr4:114274835 C>T maps to NM_001148.4 Q1688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr4:114223991 G>T maps to NM_001148.4 E849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:114275551 G>A maps to NM_001148.4 P1926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:114276904 C>T maps to NM_001148.4 D2377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:114278302 C>T maps to NM_001148.4 S2843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:114284540 C>T maps to NM_001148.4 R3602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr4:114195726 C>T maps to NM_001148.4 H535H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr4:114277912 C>T maps to NM_001148.4 V2713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:114275425 G>A maps to NM_001148.4 S1884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:114158318 A>G maps to NM_001148.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:114213627 C>T maps to NM_001148.4 N778N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr4:114158237 G>T maps to NM_001148.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr4:114275317 A>C maps to NM_001148.4 S1848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:114278086 C>T maps to NM_001148.4 I2771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:61835973 C>T maps to NM_020987.2 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:61815517 A>G maps to NM_020987.2 C4321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:62021640 C>T maps to NM_020987.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:62021645 G>A maps to NM_020987.2 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:61828701 G>A maps to NM_020987.2 S3979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:61834284 G>A maps to NM_020987.2 H2118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:61843306 C>T maps to NM_020987.2 Q1381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:61835940 G>A maps to NM_020987.2 D1566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:61955985 G>A maps to NM_020987.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:61844545 C>T maps to NM_020987.2 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:61827768 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:61941098 G>A maps to NM_020987.2 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:61831290 T>C maps to NM_020987.2 K3116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:61958142 G>A maps to NM_020987.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:61831670 G>A maps to NM_020987.2 L2990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:61831896 T>G maps to NM_020987.2 S2914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr10:61946580 T>G maps to NM_020987.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr10:61832825 C>A maps to NM_020987.2 E2605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:61815514 C>T maps to NM_020987.2 V4322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:61847918 G>A maps to NM_020987.2 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:190593147 T>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:190606164 G>A maps to NM_144708.3 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:190611169 T>G maps to NM_144708.3 P1374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:190554310 T>C maps to NM_144708.3 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:190541689 G>A maps to NM_144708.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr15:65209595 G>T maps to NM_182703.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:54526504 C>T maps to NM_153228.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:54535228 T>A maps to NM_153228.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:4139184 G>A maps to NM_016376.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4076677 G>A maps to NM_016376.3 C996C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:14713762 C>T maps to NM_054027.4 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr5:14713672 G>A maps to NM_054027.4 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:14751264 G>A maps to NM_054027.4 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:139876354 G>A maps to ENST00000253810 K832K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr5:139917029 C>T maps to ENST00000253810 R2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:92020589 G>A maps to NM_019004.1 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr11:113270373 C>T maps to NM_178510.1 Y561Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:113268036 C>T maps to NM_178510.1 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:113270343 G>C maps to NM_178510.1 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:17396287 G>A maps to NM_152363.4 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:17397361 G>A maps to ENST00000438921 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:133303971 G>A maps to NM_015114.1 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:133313523 C>T maps to NM_015114.1 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:133304694 G>A maps to NM_015114.1 D846D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:133331276 G>A maps to NM_015114.1 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:133310977 G>T maps to NM_015114.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:133304628 C>T maps to NM_015114.1 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr12:133324588 G>A maps to NM_015114.1 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:133319772 G>A maps to NM_015114.1 N440N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:241496620 A>G maps to ENST00000401804 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:241492465 A>G maps to ENST00000401804 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:241463639 G>A maps to ENST00000401804 H498H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr2:241439955 G>A maps to ENST00000401804 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:241492465 A>G maps to ENST00000401804 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:241463558 C>T maps to ENST00000401804 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr2:241494401 C>A maps to ENST00000401804 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:16650273 C>A maps to NM_020319.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:72857048 A>G maps to NM_023039.4 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:111532319 A>G maps to NM_017664.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:89348800 G>A maps to NM_013275.4 G1383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:89351371 G>A maps to NM_013275.4 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:89349000 G>A maps to NM_013275.4 L1317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:89345695 G>A maps to NM_013275.4 I2418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr16:89351932 G>C maps to NM_013275.4 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:89347375 C>T maps to NM_013275.4 P1858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:89345551 G>A maps to NM_013275.4 Y2466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:89350036 C>T maps to NM_013275.4 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:89348368 A>G maps to NM_013275.4 D1527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:89345632 G>A maps to NM_013275.4 F2439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:89351278 C>T maps to NM_013275.4 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:89348965 T>C maps to NM_013275.4 P1328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr16:89357493 G>A maps to NM_013275.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr16:89349169 C>T maps to NM_013275.4 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:89351148 G>A maps to NM_013275.4 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:89347144 G>A maps to NM_013275.4 D1935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:89347723 C>T maps to NM_013275.4 S1742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:89347771 G>T maps to NM_013275.4 S1726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:9211675 T>C maps to NM_015208.3 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:9255538 C>T maps to NM_015208.3 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:9254420 C>T maps to NM_015208.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr18:9255013 T>C maps to NM_015208.3 Y583Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr18:9204525 T>G maps to NM_015208.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr12:110466442 C>T maps to NM_033121.1 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:27934851 G>A maps to NM_152345.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr17:27939280 A>G maps to NM_152345.4 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:27935103 C>T maps to NM_152345.4 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:70766509 C>T maps to NM_030816.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:70766479 A>G maps to NM_030816.4 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr1:70790596 C>T maps to NM_030816.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:70766509 C>T maps to NM_030816.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:67068550 C>T maps to NM_207354.2 N388N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:67069007 C>T maps to NM_207354.2 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr11:67068795 C>T maps to NM_207354.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:67069219 C>A maps to NM_207354.2 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:5925937 T>C maps to NM_001009941.2 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:5920140 T>C maps to NM_001009941.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:5931080 G>T maps to NM_001009941.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:5926003 G>A maps to NM_001009941.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:74124064 G>A maps to NM_032217.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:73981535 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:99341171 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:69423515 T>G maps to NM_001098805.1 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:90591678 C>T maps to NM_144590.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:4216956 A>G maps to ENST00000262970 K690K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:4217181 G>A maps to ENST00000262970 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:27335400 T>C maps to NM_014915.2 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:27324396 A>G maps to NM_014915.2 N994N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr10:27381348 T>C maps to NM_014915.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr19:33090903 G>A maps to NM_032139.2 Y940Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:33140669 G>T maps to NM_032139.2 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:15736299 T>G maps to NM_015199.3 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:15765942 T>G maps to NM_015199.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:15755083 G>A maps to NM_015199.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr10:37505289 A>G maps to ENST00000374660 K1080K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr10:37508308 C>T maps to ENST00000374660 F1286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:37430910 G>A maps to ENST00000374660 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr10:37486382 G>A maps to ENST00000374660 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr10:37508707 T>C maps to ENST00000374660 F1419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr18:14752956 G>A maps to NM_001145029.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:14848926 A>T maps to NM_001145029.1 R1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr18:14791464 C>T maps to NM_001145029.1 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr18:14787071 C>T maps to NM_001145029.1 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:94024236 G>A maps to NM_032290.3 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:94027788 C>T maps to NM_032290.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:52284395 T>C maps to NM_182608.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:52285023 C>T maps to NM_182608.3 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:145474329 C>T maps to NM_001039888.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:79854680 G>A maps to NM_001004441.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:145558842 T>C maps to NM_144698.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:145562805 C>T maps to NM_144698.3 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:145555744 G>T maps to NM_144698.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:145561337 G>A maps to NM_144698.3 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:97858782 T>C maps to NM_001164315.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:97866206 G>A maps to NM_001164315.1 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:97784148 G>A maps to NM_001164315.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:186318401 C>T maps to NM_181726.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:48773431 G>A maps to NM_052855.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:48777177 A>T maps to NM_052855.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr11:82938900 T>A maps to ENST00000260047 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr11:82935913 G>T maps to ENST00000260047 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:82909564 C>T maps to ENST00000260047 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:197987424 G>T maps to NM_001195144.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr2:197878391 C>T maps to NM_001195144.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:197986169 G>A maps to NM_001195144.1 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:197986193 G>A maps to NM_001195144.1 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:197986244 T>C maps to NM_001195144.1 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:173616050 C>A maps to ENST00000367712 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:101540170 G>T maps to NM_198401.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:94231634 A>G maps to NM_017704.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr11:94231298 T>C maps to NM_017704.2 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:10019011 G>A maps to NM_198798.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr20:10023848 C>T maps to NM_198798.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:10026337 T>G maps to NM_198798.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:10036203 C>T maps to NM_198798.1 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:10025098 C>T maps to NM_198798.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:10025142 C>T maps to NM_198798.1 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr20:10025098 C>T maps to NM_198798.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr20:10030350 C>T maps to NM_198798.1 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:10026253 C>T maps to NM_198798.1 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:125591398 T>C maps to NM_020337.2 E1011E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:125590621 C>T maps to NM_020337.2 G1270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:125591593 A>G maps to NM_020337.2 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:125592250 G>A maps to NM_020337.2 H727H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:56648051 G>T maps to NM_173595.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:56639296 C>T maps to NM_173595.3 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:56638204 G>A maps to NM_173595.3 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:56648703 G>A maps to NM_173595.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:56647934 C>T maps to NM_173595.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:56647934 C>T maps to NM_173595.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr2:71211787 C>T maps to NM_001115116.1 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr2:71206307 C>T maps to NM_001115116.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:55407542 G>A maps to NM_024669.2 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:55407145 G>A maps to NM_024669.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr5:55412548 C>T maps to NM_024669.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:55455710 C>T maps to NM_024669.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:55471984 G>A maps to NM_024669.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:55407272 C>T maps to NM_024669.2 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr4:77817361 T>C maps to NM_001029870.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:77817772 A>G maps to NM_001029870.1 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:110373094 C>T maps to NM_023016.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:110373583 A>G maps to NM_023016.3 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:118893081 T>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:118893546 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:118893434 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr23:118893486 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:90312800 C>T maps to ENST00000339746 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:90312800 C>T maps to ENST00000339746 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr6:90333682 C>T maps to ENST00000339746 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:117876921 T>C maps to ENST00000357099 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr7:117876120 C>T maps to ENST00000357099 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:117876852 T>C maps to ENST00000357099 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:35053697 C>T maps to NM_015245.2 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:34953018 T>C maps to NM_015245.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:34953006 G>A maps to NM_015245.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:34937795 C>T maps to NM_015245.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:34957008 T>C maps to NM_015245.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr6:34949610 C>T maps to NM_015245.2 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:35053550 C>A maps to NM_015245.2 T1047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:100200244 C>T maps to NM_152788.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr12:99640322 G>C maps to NM_152788.3 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr12:100206066 G>A maps to NM_152788.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:99837449 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:4780144 G>A maps to NM_133450.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:21261871 C>T maps to NM_145865.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:21245075 C>T maps to NM_145865.2 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr16:21262072 C>T maps to NM_145865.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:21261924 G>A maps to NM_145865.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr16:21261885 C>T maps to NM_145865.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:101552785 G>A maps to ENST00000375018 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:101552584 G>T maps to ENST00000375018 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:220098594 C>T maps to NM_001042410.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:220098559 C>T maps to NM_001042410.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:220100485 G>A maps to NM_001042410.1 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr7:36492148 T>C maps to NM_018685.2 V1105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:36438709 G>A maps to NM_018685.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:36459785 G>T maps to NM_018685.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:70031743 C>A maps to NM_018043.5 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:70031791 C>T maps to NM_018043.5 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:70009434 C>T maps to NM_018043.5 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr11:69999182 C>T maps to NM_018043.5 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr3:43618238 C>G maps to NM_018075.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:43618451 A>G maps to NM_018075.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:6031893 A>G maps to ENST00000356134 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr12:5908716 C>T maps to ENST00000356134 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:5687529 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr12:5708659 G>T maps to ENST00000356134 Y742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr12:5724440 A>G maps to ENST00000356134 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr12:5915235 G>A maps to ENST00000356134 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr11:26619975 C>T maps to NM_031418.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:26655758 C>T maps to NM_031418.2 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:26663443 T>C maps to NM_031418.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:26556077 C>T maps to NM_031418.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:26529808 G>A maps to NM_031418.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr11:26538453 G>A maps to NM_031418.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr11:26581276 G>A maps to NM_031418.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:101381325 A>G maps to ENST00000392977 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr12:101520835 C>T maps to ENST00000392977 N952N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr12:101437373 T>C maps to ENST00000392977 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:101504233 A>T maps to ENST00000392977 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr12:101436228 G>A maps to ENST00000392977 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:101477464 C>T maps to ENST00000392977 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:22284590 T>C did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:22232832 C>G maps to NM_213599.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:22291981 G>T maps to NM_213599.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:22296134 G>A maps to NM_213599.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr12:45795714 G>A maps to NM_001142679.1 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:45741845 C>T maps to NM_001142679.1 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:45771876 A>G maps to NM_001142679.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:45814888 C>T maps to NM_001142679.1 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr12:45822904 G>A maps to NM_001025356.2 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:242163333 G>A maps to NM_001001891.3 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr2:242142896 C>G maps to NM_001001891.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr2:242141700 C>T maps to NM_001001891.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:242154252 C>T maps to NM_001001891.3 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:17444228 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:17444268 C>T maps to NM_020959.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:17439207 C>T maps to NM_020959.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:17438602 G>A maps to NM_020959.2 C771C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:17438569 G>A maps to NM_020959.2 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:418465 G>A maps to NM_001012302.2 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:432029 G>A maps to NM_001012302.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:418559 G>A maps to NM_001012302.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr11:421036 G>A maps to NM_001012302.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr15:69080153 G>A maps to NM_006305.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:48866815 C>T maps to NM_012404.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr12:48866791 C>A maps to NM_012404.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:48866560 A>G maps to NM_012404.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:150204191 C>A maps to NM_030920.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:150203028 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:90344793 G>A maps to NM_001150.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:90346958 G>T maps to NM_001150.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr15:90347521 G>T maps to NM_001150.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:69420481 T>C maps to NM_032208.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:69379377 G>A maps to NM_032208.2 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:80906002 A>T maps to NM_001145794.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:75774282 C>T maps to NM_000700.1 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:169083677 G>A did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr4:169083756 C>T maps to NM_007193.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr4:169108526 C>A maps to NM_007193.3 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:124707926 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:124714887 G>A maps to NM_001003954.1 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:124714941 C>T maps to NM_001003954.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:60641384 C>T maps to NM_001002858.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:60639873 G>A maps to NM_001002858.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:70039822 C>T maps to NM_001153.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:70033527 C>T maps to NM_001153.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr2:70015259 C>T maps to NM_001153.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:122599046 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:122592750 G>A maps to NM_001154.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:150489326 C>T maps to NM_001155.4 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr5:150515864 G>A maps to NM_001155.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:150505974 C>A maps to NM_001155.4 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:75143061 G>A maps to NM_004034.2 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:75143003 G>A maps to NM_004034.2 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:150958864 C>T maps to NM_003568.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:150957152 G>C did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:36580048 G>A maps to NM_001177506.1 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:36677462 C>T maps to NM_001177506.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr7:36588290 A>G maps to NM_001177506.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:36671673 C>T maps to NM_001177506.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:36763672 G>A maps to NM_001177506.1 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:41001151 T>G maps to NM_009590.2 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:41003869 C>T maps to NM_003734.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:201478592 C>T maps to NM_001159.3 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:201467061 C>T maps to NM_001159.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:201477408 C>T maps to NM_001159.3 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr2:201531407 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr2:201531429 C>T maps to NM_001159.3 V1188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:201505840 C>T maps to NM_001159.3 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:201501716 G>A maps to NM_001159.3 K810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr2:201501704 G>A maps to NM_001159.3 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr2:201468738 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:113174396 G>A maps to NM_018569.4 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:113189432 G>A maps to NM_018569.4 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:29755830 G>A maps to NM_001127.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:29745218 G>A maps to NM_001127.3 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:29754897 G>A maps to NM_001127.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:29735104 G>A maps to NM_001127.3 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:29736836 G>A maps to NM_001127.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:29752475 G>A maps to NM_001127.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:29750664 G>A maps to NM_001127.3 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:29754900 G>A maps to NM_001127.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:29754807 G>A maps to NM_001127.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:29747753 G>A maps to NM_001127.3 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:29754816 T>C maps to NM_001127.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:29737716 G>T maps to NM_001127.3 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr16:71823367 G>A maps to ENST00000423132 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:71799412 A>G maps to ENST00000423132 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:71803537 C>T maps to ENST00000423132 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:71779113 C>T maps to ENST00000423132 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:24033018 G>A maps to NM_003917.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:16319906 C>T maps to NM_001130524.1 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:10694656 G>A maps to ENST00000453102 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:15864107 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:15845478 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:50302682 G>A maps to NM_014203.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr19:50285900 C>A maps to NM_014203.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:50270388 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:50303256 C>T maps to NM_014203.2 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr19:50309019 G>A maps to NM_014203.2 W879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:972111 C>T maps to ENST00000332231 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:970289 C>T maps to ENST00000332231 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:1009120 C>T maps to ENST00000332231 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:33963433 A>G maps to NM_001030006.1 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:33984641 T>C maps to NM_001030006.1 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:33954502 A>C maps to NM_001030006.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:33998861 G>A maps to NM_001030006.1 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:183901268 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:183899532 C>T maps to ENST00000411763 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:183900574 G>A maps to ENST00000411763 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:47341796 C>T maps to NM_004069.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:47342017 G>A maps to NM_004069.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:77523224 A>G maps to NM_003664.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr15:83331473 G>A maps to NM_004644.3 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:83349405 G>A maps to NM_004644.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr15:83349606 G>A maps to NM_004644.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:83348968 G>A maps to NM_004644.3 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:2129319 C>T maps to ENST00000355272 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:2132553 G>A maps to ENST00000355272 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:2118677 G>A maps to ENST00000355272 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:75897993 G>A maps to NM_207012.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:42023052 C>T maps to NM_006803.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:114437749 C>T maps to NM_006594.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:51260461 A>G maps to NM_007347.3 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:99702714 C>T maps to ENST00000429084 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:99703163 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:99700405 T>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:99121027 C>A maps to NM_181861.1 G1178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:99093196 G>A maps to NM_181861.1 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:72082834 G>A maps to NM_001163.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr9:72131001 T>C maps to NM_001163.3 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:72056031 C>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr9:72047538 C>T maps to NM_001163.3 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:72071228 C>T maps to NM_001163.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:72067196 G>T maps to NM_001163.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:72131388 G>A maps to NM_001163.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:72131748 G>A maps to NM_001163.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:29398919 G>A maps to NM_005503.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr15:29346158 T>A maps to NM_005503.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr15:29346437 C>T maps to NM_005503.3 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:29346437 C>T maps to NM_005503.3 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr15:29346254 C>T maps to NM_005503.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:29406143 C>T maps to NM_005503.3 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:29385351 C>T maps to NM_005503.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr15:29346254 C>T maps to NM_005503.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr15:29409284 C>T maps to NM_005503.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:3753762 G>A maps to NM_004886.3 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:3760157 G>A maps to NM_004886.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:3759908 G>A maps to NM_004886.3 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:3751225 G>A maps to NM_004886.3 H539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:6424924 G>T maps to ENST00000389906 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr11:6422614 G>T maps to ENST00000389906 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr11:6432343 C>T maps to ENST00000389906 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:6416781 C>T maps to ENST00000389906 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr11:6432421 G>A maps to ENST00000389906 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:6432421 G>A maps to ENST00000389906 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr11:6416886 G>C maps to ENST00000389906 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr10:26789969 T>A maps to NM_019043.3 L128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:26800782 T>C maps to NM_019043.3 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr10:26800821 G>A maps to NM_019043.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:40832594 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:41016407 T>C maps to NM_004307.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:139941252 G>A maps to ENST00000354402 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:112162833 C>T maps to NM_001127510.2 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr5:112174601 C>A maps to NM_001127510.2 S1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:112174392 G>A maps to NM_001127510.2 E1034E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:112174915 G>T maps to NM_001127510.2 E1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr5:112111435 T>G did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:112176016 G>T maps to NM_001127510.2 E1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr5:112174681 C>T maps to NM_001127510.2 Q1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:112102934 A>G maps to NM_001127510.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:112174377 T>G maps to NM_001127510.2 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:112178968 C>T maps to NM_001127510.2 R2560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:112174113 A>G maps to NM_001127510.2 E941E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr5:112175677 A>C maps to NM_001127510.2 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr5:112176357 C>T maps to NM_001127510.2 T1689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:112178040 C>T maps to NM_001127510.2 G2250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:112174359 A>G maps to NM_001127510.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:112174056 T>C maps to NM_001127510.2 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr5:112179025 G>T maps to NM_001127510.2 E2579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr5:112174493 C>A maps to NM_001127510.2 S1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:1460306 C>T maps to NM_005883.2 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:1465618 C>T maps to NM_005883.2 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:1468459 C>T maps to NM_005883.2 F1720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:1460270 C>T maps to NM_005883.2 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:1461987 C>T maps to NM_005883.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:10468631 C>T maps to ENST00000423585 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr18:10487674 C>A maps to ENST00000423585 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:10487647 C>T maps to ENST00000423585 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr18:10471556 C>A maps to ENST00000423585 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr18:10471814 C>T maps to ENST00000423585 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr20:57045663 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:57042215 C>T maps to NM_153360.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr20:57036310 G>A maps to NM_153360.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:57042224 G>A maps to NM_153360.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:57042281 C>T maps to NM_153360.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:49713594 C>T maps to ENST00000438011 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr14:20923812 G>A maps to NM_080649.1 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:55029533 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:55026948 G>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:55026916 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:55028041 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:55033429 A>G did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:43356826 G>T did not map to a codon.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr11:43342465 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:43345125 G>A maps to NM_001142930.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:57004211 C>T maps to NM_005161.4 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:57004322 G>A maps to NM_005161.4 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr11:57003368 G>T maps to NM_005161.4 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr11:57004340 G>A maps to NM_005161.4 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:36363448 T>C maps to NM_001024807.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:36362644 T>G maps to NM_001024807.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:116707012 G>A maps to NM_000039.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:116706799 C>T maps to NM_000039.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:116706603 G>A maps to NM_000039.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:156562002 T>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:156563291 C>T maps to ENST00000446584 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr1:156563292 C>T maps to ENST00000446584 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:161193166 G>A maps to NM_001643.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr11:116692383 C>T maps to NM_000482.3 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr11:116691969 C>T maps to NM_000482.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:116691980 G>A maps to NM_000482.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:116691960 G>A maps to NM_000482.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:116661767 G>A maps to NM_052968.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:116661359 G>A maps to NM_052968.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:116660972 G>A maps to NM_052968.4 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:116661296 G>A maps to NM_052968.4 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:116660972 G>A maps to NM_052968.4 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr11:116661338 G>A maps to NM_052968.4 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:21234947 G>A maps to NM_000384.2 L1598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr2:21229929 G>A maps to NM_000384.2 F3270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:21231015 G>A maps to NM_000384.2 N2908N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:21227275 G>A maps to NM_000384.2 T3984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:21225675 C>T maps to NM_000384.2 G4206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:21225915 G>A maps to NM_000384.2 I4126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:21242776 G>T maps to NM_000384.2 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr2:21226008 G>A maps to NM_000384.2 L4095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:21232206 T>C maps to NM_000384.2 K2511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:21228375 C>T maps to NM_000384.2 E3788E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr2:21233526 G>A maps to NM_000384.2 L2071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr2:21241933 G>A maps to NM_000384.2 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:21233211 T>C maps to NM_000384.2 T2176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr2:21229170 G>C maps to NM_000384.2 S3523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr2:21224622 T>C maps to NM_000384.2 G4557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr2:21230874 A>C maps to NM_000384.2 T2955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr2:21252825 C>A maps to NM_000384.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr2:21228759 G>A maps to NM_000384.2 D3660D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:21245797 G>A maps to NM_000384.2 H907H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr2:21247840 C>G maps to NM_000384.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:28508860 G>A maps to NM_018690.2 E824E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:28507726 A>G maps to NM_018690.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:7805321 G>A maps to NM_001644.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr22:39387488 A>G maps to ENST00000402182 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:39381947 G>A maps to ENST00000402182 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:39421134 C>T maps to NM_152426.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:39418982 G>A maps to NM_152426.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:39421595 T>C maps to NM_152426.3 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:39441118 G>C maps to NM_145298.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:39482480 T>C maps to NM_021822.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:183617810 G>A maps to NM_203454.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:116701501 C>T maps to ENST00000360377 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:195295824 A>G maps to ENST00000421243 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:45412332 G>A maps to NM_000041.2 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:45412437 C>T maps to NM_000041.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:56755797 G>T maps to NM_001638.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:56755503 G>A maps to NM_001638.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr22:36661727 C>T maps to NM_145343.2 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:36624091 G>A maps to ENST00000451256 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr22:36623749 C>T maps to ENST00000451256 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr22:36624136 G>A maps to ENST00000451256 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:36541534 C>T maps to NM_145640.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr22:36537682 G>A maps to NM_145640.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:36123048 C>T maps to NM_030642.1 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:36122609 C>G maps to NM_030642.1 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr22:36054691 C>T maps to NM_030641.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:23876802 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:84310875 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:84258930 A>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr21:27347534 G>A maps to NM_000484.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr21:27264117 A>G maps to NM_000484.3 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr21:27254028 G>A maps to NM_000484.3 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr21:27264120 G>A maps to NM_000484.3 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:57274551 T>C maps to NM_012096.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:57283435 G>A maps to NM_012096.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:105601754 A>G maps to NM_018171.3 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:105600916 G>T maps to NM_018171.3 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:105601799 G>A maps to NM_018171.3 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:88876189 G>A maps to NM_000485.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:32984852 A>G maps to NM_001195248.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:32987826 G>T maps to NM_001195248.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:32973608 G>A maps to NM_001195248.1 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:154294497 C>T maps to NM_080429.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr11:77314622 A>C maps to NM_173039.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:77301361 C>T maps to NM_173039.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:241622122 C>T maps to NM_001102467.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:50348486 C>T maps to NM_000486.5 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr18:24436276 A>G maps to NM_001650.4 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:50358887 G>A maps to NM_001651.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:50357291 G>A maps to NM_001651.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr12:50367277 C>T maps to NM_001652.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:33386119 G>A maps to NM_001170.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:33386191 C>T maps to NM_001170.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:33385029 A>G maps to NM_001170.1 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr9:33385750 G>A maps to NM_001170.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr16:25235897 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:25232873 C>T maps to NM_001169.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:25228610 G>A maps to NM_001169.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:115298523 G>A maps to NM_173800.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:115298451 G>A maps to NM_173800.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr5:115298412 C>T maps to NM_173800.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:115336318 C>T maps to NM_173800.4 N537N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:115298778 C>T maps to NM_173800.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:115298724 C>T maps to NM_173800.4 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:35210477 A>G maps to NM_014691.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr15:35196620 G>A maps to NM_014691.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:35174731 G>A maps to NM_014691.2 R1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:35198752 A>G maps to NM_014691.2 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:66942786 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:66765157 T>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:66937332 A>G did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:66765697 A>G did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:66765080 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:66941795 T>C did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:66765884 A>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:66766152 C>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:66766583 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:66765882 G>A did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:66765644 T>G did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:66766241 T>A did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr23:66905929 G>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:66941679 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:66905887 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:66941795 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:66942765 T>G did not map to a codon.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr23:66941726 C>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:66765795 G>A did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:66941795 T>G did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:66765864 T>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:66765196 A>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:66765199 A>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:66765202 A>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:66765719 G>T did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr23:66863122 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:66765825 C>T did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:66765881 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr23:66905851 G>A did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr23:66765157 T>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:66931468 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:66765717 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:66941782 A>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:47430410 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:47426531 T>C did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:47422725 G>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:47424261 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:47426491 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:47426714 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:47430394 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:47428171 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:47424203 C>T did not map to a codon.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr23:47429312 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:72415277 C>T maps to NM_001040118.2 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:72422545 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:72423532 G>A maps to NM_001040118.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr11:72398782 G>A maps to NM_001040118.2 C1357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:72423490 G>A maps to NM_001040118.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:36179565 C>T maps to NM_015230.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr4:36189097 A>C maps to NM_015230.2 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:36081867 C>T maps to NM_015230.2 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:36179454 G>A maps to NM_015230.2 N617N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:36081900 C>T maps to NM_015230.2 W1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:36121277 G>A maps to NM_015230.2 D1319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:36160349 A>G did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr5:141033761 C>A maps to NM_022481.5 E1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:141051819 C>T maps to NM_022481.5 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:141051786 G>A maps to NM_022481.5 Y489Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr5:141053170 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:141052583 G>A maps to NM_022481.5 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:143694606 G>T maps to NM_015193.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:118454615 A>G maps to ENST00000359415 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:118451977 G>A maps to ENST00000359415 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:118454012 G>A maps to ENST00000359415 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr11:118452181 C>T maps to ENST00000359415 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:75312383 T>C maps to NM_001657.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:50360591 T>G maps to NM_001663.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr20:61910325 C>T maps to NM_175609.1 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr20:61919113 C>T maps to NM_175609.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:47196628 A>G maps to NM_032389.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr22:43195059 G>A maps to NM_014570.4 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:43219660 C>T did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr22:43195134 G>A maps to NM_014570.4 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:43231436 A>G maps to NM_014570.4 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:68169964 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:68111166 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:68208815 G>A maps to NM_006421.3 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:68208821 T>C maps to NM_006421.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:68150671 T>C maps to NM_006421.3 K1065K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr8:68123820 A>T maps to NM_006421.3 I1572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:68172073 T>C maps to NM_006421.3 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:68170429 G>A maps to NM_006421.3 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:68138269 A>G maps to NM_006421.3 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:68112695 G>A maps to NM_006421.3 R1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:47614882 C>T maps to NM_006420.2 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:47601973 C>T maps to NM_006420.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:47630222 A>G maps to NM_006420.2 V1347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr20:47611100 A>T maps to NM_006420.2 T1029T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr20:47633819 C>T maps to NM_006420.2 C1450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:47567867 C>T maps to NM_006420.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:47635530 C>T maps to NM_006420.2 Y1540Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr11:6499102 G>A maps to NM_012402.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:62333551 G>A maps to NM_003224.3 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr20:62331792 G>C did not map to a codon.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr20:62331988 T>G maps to NM_003224.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr14:68086711 C>T maps to NM_001172.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:46700718 G>A maps to NM_004308.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr11:46700613 G>A maps to NM_004308.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:148744109 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:148984397 G>A maps to NM_024605.3 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:32926191 C>T maps to NM_014783.3 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:30919027 G>A maps to NM_001039841.1 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr15:30926470 T>C maps to NM_001039841.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:32097964 A>G maps to NM_018287.5 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:32150541 A>G maps to NM_018287.5 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:32097969 C>A maps to NM_018287.5 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:32197423 C>T maps to NM_018287.5 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:144525620 T>C maps to NM_018460.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:144194564 C>T maps to NM_018460.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:144461009 A>G maps to NM_018460.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:24950788 T>C maps to NM_001006634.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:24955128 T>C maps to NM_001006634.1 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr16:24946806 C>T maps to NM_001006634.1 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:24950836 C>T maps to NM_001006634.1 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:24965986 G>A maps to NM_001006634.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:24971013 G>A maps to NM_001006634.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:99016072 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:110485314 G>T maps to NM_020809.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:110451041 A>C maps to NM_020809.2 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr11:110450219 A>C maps to NM_020809.2 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:110494968 C>T maps to NM_020809.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr11:110450333 A>G maps to NM_020809.2 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:24909044 C>T maps to NM_020824.3 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:24874036 T>C maps to NM_020824.3 A1727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr10:24874801 G>A maps to NM_020824.3 I1472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr10:24874723 C>T maps to NM_020824.3 T1498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:49654564 G>A maps to ENST00000417912 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:49654544 C>T maps to ENST00000417912 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr4:86863360 C>A maps to NM_001025616.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:86916255 C>T maps to NM_001025616.2 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:86916681 T>C maps to NM_001025616.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr4:86921731 C>T maps to NM_001025616.2 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr4:86491781 G>T maps to NM_001025616.2 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr4:86643069 T>G maps to NM_001025616.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:69034513 C>A maps to NM_001007231.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:69002506 G>A maps to NM_001007231.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr2:69040464 C>T maps to NM_001007231.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:142513669 C>T maps to NM_015071.4 Q613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:43481990 G>A maps to ENST00000428638 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:43475403 G>A maps to ENST00000428638 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:43474297 G>A maps to ENST00000428638 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:6876204 A>T maps to ENST00000400091 K430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr18:6859865 G>C maps to ENST00000400091 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:6868233 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:94651014 A>G maps to NM_004815.3 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:161039354 G>A maps to NM_001025598.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:161018409 C>A maps to NM_001025598.1 G801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:161018314 C>T maps to NM_001025598.1 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr1:161023087 G>A maps to NM_001025598.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:161019225 T>A maps to NM_001025598.1 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:161017912 C>T maps to NM_001025598.1 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:161018110 A>G maps to NM_001025598.1 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:161026240 G>A maps to NM_001025598.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr1:161018191 G>A maps to NM_001025598.1 D873D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:161018866 A>G maps to NM_001025598.1 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:161022269 A>G maps to NM_001025598.1 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:119133472 G>A maps to NM_020754.2 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr3:119087338 T>G maps to NM_020754.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr3:119133442 C>T maps to NM_020754.2 D889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr3:119133997 C>T maps to NM_020754.2 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:119121137 G>A maps to NM_020754.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:119134093 C>A maps to NM_020754.2 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:119121095 C>T maps to NM_020754.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:119121035 C>T maps to NM_020754.2 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:119120903 C>T maps to NM_020754.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:128842509 A>G maps to NM_001142685.1 A1283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:128840676 T>C maps to NM_001142685.1 Q1463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr11:128839749 T>C maps to NM_001142685.1 Q1772Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:128842461 C>T maps to NM_001142685.1 T1299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:128840481 G>T maps to NM_001142685.1 A1528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:128839758 G>A maps to NM_001142685.1 V1769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:128840448 G>T maps to NM_001142685.1 A1539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:128838936 G>A maps to NM_001142685.1 G2043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:128851442 C>A maps to NM_001142685.1 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:128844088 C>T maps to NM_001142685.1 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:128840871 G>A maps to NM_001142685.1 R1398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:128840295 C>T maps to NM_001142685.1 P1590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:128840496 C>T maps to NM_001142685.1 R1523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:128840928 C>T maps to NM_001142685.1 Q1379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:128843130 C>T maps to NM_001142685.1 A1076A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:36272094 C>T maps to ENST00000007510 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:36269463 G>A maps to ENST00000007510 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:36277955 G>T maps to ENST00000007510 G862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:130222705 C>T did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:130218984 T>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:130222660 G>T did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:130217932 G>A did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:130222706 G>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:130218271 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:130220337 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:130217916 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr23:130219890 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:130215787 T>C did not map to a codon.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr23:130219899 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:145771182 G>A maps to NM_025251.1 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr8:145772549 G>A maps to NM_025251.1 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:145763108 C>T maps to NM_025251.1 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:145757726 C>T maps to NM_025251.1 W981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:145773653 C>T maps to NM_025251.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:145770864 T>C maps to NM_025251.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:145755904 G>A maps to NM_025251.1 D1082D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:145759524 G>A maps to NM_025251.1 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:153184642 T>C did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:153176005 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:153173236 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:153174919 G>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:153175254 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:32623919 A>G maps to NM_001030055.1 R1425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:32561821 G>A maps to NM_001030055.1 W649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:32562223 C>T maps to NM_001030055.1 C783C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:32562667 T>C maps to NM_001030055.1 F931F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr14:32561827 C>T maps to NM_001030055.1 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:32562838 A>G maps to NM_001030055.1 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:32561513 G>T maps to NM_001030055.1 G547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:11157335 C>T did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:11157184 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:11162013 G>T did not map to a codon.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr23:11162203 C>T did not map to a codon.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr23:11162251 A>C did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:11682499 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:11162129 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:11157457 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:11206973 T>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:11682887 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:11187742 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:11682374 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr23:11162140 G>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:11157228 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:11272738 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:45255645 C>T maps to ENST00000352766 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr22:45182487 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:45210626 G>A maps to ENST00000352766 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:332055 G>A maps to NM_001176.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:332696 G>A maps to NM_001176.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:42398309 C>T maps to NM_199002.1 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:42396119 C>T maps to NM_199002.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr19:42396406 C>T maps to NM_199002.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:1877547 G>A maps to ENST00000398564 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:1904933 C>T maps to ENST00000398564 Y1205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:1905203 C>T maps to ENST00000398564 S1295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:1842725 C>A maps to ENST00000398564 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:1876636 G>A maps to ENST00000398564 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:1900958 G>A maps to ENST00000398564 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:1833851 C>T maps to ENST00000398564 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:1851508 A>C maps to ENST00000398564 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:1853832 C>T maps to ENST00000398564 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:1871716 G>A maps to ENST00000398564 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:1833845 G>A maps to ENST00000398564 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:1842671 C>T maps to ENST00000398564 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:1857613 C>T maps to ENST00000398564 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:17952450 C>T maps to NM_018125.3 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:18014123 G>A maps to NM_018125.3 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:18014075 C>T maps to NM_018125.3 F1006F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:156909340 T>C maps to NM_198236.1 K1365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:156909361 T>C maps to NM_198236.1 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:156917126 G>A maps to NM_198236.1 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:156921410 G>A maps to NM_198236.1 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:156909625 G>A maps to NM_198236.1 P1270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:120343775 G>A maps to NM_015313.2 Q991Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr11:120335950 C>T maps to NM_015313.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:120298859 G>A maps to NM_015313.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr11:120352119 C>A maps to NM_015313.2 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr11:120302616 A>T maps to NM_015313.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr17:8218456 T>G maps to NM_173728.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr17:8216417 C>T maps to NM_173728.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:8222198 C>T maps to NM_173728.3 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:8222916 T>C maps to NM_173728.3 P790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:8215770 G>A maps to NM_173728.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:3395095 C>T maps to NM_014448.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:3395176 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:3396445 G>A maps to NM_014448.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:73071552 C>A maps to NM_014786.3 A1465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:73076912 C>T maps to NM_014786.3 H1972H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr11:73021582 G>T maps to NM_014786.3 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr11:73022571 C>T maps to NM_014786.3 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:73068355 C>T maps to NM_014786.3 D1357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:16534231 G>A maps to NM_153213.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:155935498 C>T maps to NM_001162383.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:56766422 C>T maps to NM_001128615.1 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:56771218 C>T maps to NM_001128615.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:143885365 C>T maps to NM_001003702.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:149003663 A>G maps to NM_001001669.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:144068397 C>T maps to NM_005435.3 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr7:144060682 G>A maps to NM_005435.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:135751672 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:135790866 T>C did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:135789066 C>A did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:135825840 G>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:135750187 T>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:135763008 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:135754266 C>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:135862979 T>G did not map to a codon.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr23:135770112 A>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:135750257 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:135861600 A>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:111926265 T>C maps to NM_001113511.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:111935538 G>A maps to NM_001113511.1 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr13:111927979 C>T maps to NM_001113511.1 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:62893976 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:62893982 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:62944563 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:62893973 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr23:62944557 C>T did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr1:27100311 C>T maps to NM_006015.4 Q1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:27099052 G>T maps to NM_006015.4 G1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:27099007 C>T maps to NM_006015.4 Q1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:27106860 C>T maps to NM_006015.4 R2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr1:27097693 C>T maps to NM_006015.4 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:27101098 C>T maps to NM_006015.4 R1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:27105512 G>A did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr1:27107179 C>A maps to NM_006015.4 S2264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:27105609 C>T maps to NM_006015.4 Q1741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr1:27057729 C>T maps to NM_006015.4 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr1:27057795 C>T maps to NM_006015.4 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:27058096 T>C did not map to a codon.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr1:27059175 C>T maps to NM_006015.4 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:27087442 C>T maps to NM_006015.4 Q673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr1:27101053 C>T maps to NM_006015.4 R1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr1:27056213 C>T maps to NM_006015.4 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:27107150 C>A maps to NM_006015.4 Y2254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr1:27100356 C>T maps to NM_006015.4 Q1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr1:27100389 G>C did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:27100150 C>A maps to NM_006015.4 S1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr1:27099123 G>A did not map to a codon.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr1:27023419 C>T maps to NM_006015.4 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr1:27106860 C>T maps to NM_006015.4 R2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:27097629 G>A maps to NM_006015.4 W1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr1:27058047 C>T maps to NM_006015.4 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr1:27089593 T>G maps to NM_006015.4 Y850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:27059166 G>T maps to NM_006015.4 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr6:157527344 C>A maps to ENST00000367148 C1730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:157522468 C>T maps to ENST00000367148 Q1621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:157511234 G>T maps to ENST00000367148 R1291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:157528928 C>T maps to ENST00000367148 H2258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:157488278 G>A maps to ENST00000367148 P982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:157488171 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:157517408 C>T maps to ENST00000367148 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:157522084 C>T maps to ENST00000367148 Q1493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:46245032 C>T maps to NM_152641.2 Q1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:46246349 C>T maps to NM_152641.2 Q1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr12:46298715 G>C did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:46245343 G>A maps to NM_152641.2 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr12:46245719 C>T maps to NM_152641.2 R1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:46246048 T>G maps to NM_152641.2 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr12:46245191 C>T maps to NM_152641.2 Q1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr12:46231348 C>T maps to NM_152641.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:46285561 G>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:46287411 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr12:46245026 C>T maps to NM_152641.2 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr15:74836808 C>T maps to ENST00000395077 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr15:74882323 C>G maps to ENST00000395077 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr9:34623473 G>T maps to NM_001017363.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:34623961 G>A maps to NM_001017363.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:58814544 C>T maps to NM_002892.3 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:58831855 C>T maps to NM_002892.3 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr14:58795011 C>T maps to NM_002892.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:235377280 C>T maps to NM_016374.5 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:235377331 C>T maps to NM_016374.5 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:235377280 C>T maps to NM_016374.5 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:235383750 C>A maps to NM_016374.5 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:235377280 C>T maps to NM_016374.5 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:235386557 G>A maps to NM_016374.5 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:97217701 A>C maps to NM_212481.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:97217935 G>A maps to NM_212481.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:97217887 C>T maps to NM_212481.1 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr2:97215164 C>T maps to NM_212481.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:97215158 G>A maps to NM_212481.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:63759913 G>A maps to NM_032199.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:63851102 C>T maps to NM_032199.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:63810737 C>T maps to NM_032199.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:72837172 A>G maps to NM_005744.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:49004709 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:48965062 G>A maps to NM_006321.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:49006040 G>T maps to NM_006321.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:49004694 C>T maps to NM_006321.2 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:175793504 G>A maps to NM_173664.4 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:100243451 G>C did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:100242441 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:93768343 G>A maps to NM_182896.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:93755578 C>T maps to NM_182896.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:93755587 C>T maps to NM_182896.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:53409091 A>G maps to NM_019087.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:79649137 G>A maps to NM_001040025.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:57282447 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:104445596 T>C maps to NM_004311.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr10:104436692 G>A maps to NM_004311.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr10:104459162 G>C maps to NM_004311.2 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:12727923 G>A maps to NM_005738.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:235405083 G>A maps to ENST00000339728 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr17:41477309 C>T maps to NM_001661.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:152663339 G>A maps to NM_012097.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:152670733 A>G maps to NM_012097.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:18957476 T>C maps to NM_178815.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:18948571 G>A maps to NM_178815.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:18806788 C>T maps to NM_015161.1 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:18810042 A>G maps to NM_015161.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:69153702 G>A maps to NM_006407.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr3:69134224 C>T maps to NM_006407.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:202107100 G>A maps to NM_138795.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:66534565 G>A maps to NM_018120.4 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:102738780 C>T maps to NM_031905.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:102738804 A>G maps to NM_031905.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:109285401 G>A maps to NM_032131.4 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr6:109274510 G>A maps to NM_032131.4 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:23319584 A>G maps to NM_173081.3 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:23257330 A>T maps to NM_173081.3 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:23287214 C>T maps to NM_173081.3 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:23292306 T>C maps to NM_173081.3 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr10:23270359 T>C maps to NM_173081.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr10:23295907 C>T maps to NM_173081.3 Y609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr10:23321870 G>C maps to NM_173081.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:23295907 C>T maps to NM_173081.3 Y609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr10:28260194 G>T maps to NM_018076.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:28284023 A>G maps to NM_018076.2 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr10:28225653 C>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:28274086 C>A maps to NM_018076.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:28272791 C>A maps to NM_018076.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8210-01A-11D-2340-08 chr10:28250634 A>C maps to NM_018076.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr10:28225712 A>G maps to NM_018076.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:28283977 T>A maps to NM_018076.2 K32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr10:28233855 A>G maps to NM_018076.2 C474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:31476458 G>A maps to NM_024742.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:19153681 G>A maps to ENST00000392336 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:19154849 C>T maps to ENST00000392336 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr17:73124925 C>G maps to NM_024585.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:137991840 A>G maps to ENST00000469044 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr3:137983021 C>T maps to ENST00000469044 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:137942278 T>G maps to ENST00000469044 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:232156154 C>T maps to ENST00000359743 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:232091512 T>C did not map to a codon.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr2:232100084 C>T maps to ENST00000359743 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:232079590 C>T maps to ENST00000359743 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100808784 T>C did not map to a codon.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr23:100808143 G>T did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr23:100809058 T>G did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:100808486 T>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:100808254 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:100808096 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:100808035 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:100911087 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:100911472 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:100911456 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:100911644 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:100912154 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:100911495 C>A did not map to a codon.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr23:100911183 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:100880022 T>C did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr23:100880289 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:100880571 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:100880629 C>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:101857230 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:101857119 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:101858243 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:101858526 G>A did not map to a codon.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr23:100871323 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:100871577 C>T did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr23:100871541 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:100871446 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:150784537 C>A maps to NM_001668.3 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr15:80743251 G>A maps to NM_014862.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:80869225 C>T maps to NM_014862.3 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:13402722 G>A maps to ENST00000403290 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:13388246 G>A maps to ENST00000403290 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:13393878 C>T maps to ENST00000403290 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:13402722 G>A maps to ENST00000403290 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:13381931 T>G maps to ENST00000403290 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:13398204 C>T maps to ENST00000403290 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:13393795 G>T maps to ENST00000403290 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:27543173 T>C did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr7:98985725 G>A maps to NM_005720.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:98988635 C>T maps to NM_005720.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:98988839 G>A maps to NM_005720.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr2:219110153 A>G maps to NM_005731.2 E187E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4G8-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:110873941 G>A maps to NM_005719.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:127637423 C>T maps to NM_030978.1 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:127637423 C>T maps to NM_030978.1 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:169486059 T>A maps to NM_032487.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:169485576 A>G maps to NM_032487.4 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:169485672 G>A maps to NM_032487.4 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:35748562 G>T maps to ENST00000458225 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr3:35835431 T>A maps to ENST00000458225 G808G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr3:35758838 C>T maps to ENST00000458225 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr3:35723287 A>G maps to ENST00000458225 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:69496057 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:69500124 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:4620984 C>T maps to ENST00000412477 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr17:4621943 C>G maps to ENST00000412477 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:140507930 G>A maps to NM_152285.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:18121387 T>C maps to NM_015683.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr19:18119571 C>T maps to NM_015683.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:18119241 C>T maps to NM_015683.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:90669529 G>A maps to NM_020801.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr15:98514380 C>T maps to NM_183376.2 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:4902690 G>A maps to NM_001080523.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:4891414 G>A maps to NM_001080523.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:51065134 G>A maps to ENST00000395624 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:51065608 C>T maps to ENST00000395624 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:78280983 G>A maps to NM_000046.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:2825514 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:2840008 G>A did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:2825509 G>T did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr23:2832781 C>T did not map to a codon.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr23:2825402 A>G did not map to a codon.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr23:2836083 C>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:2836107 G>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:2838723 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:2878424 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:2854852 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:2873549 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:2856149 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:2861127 A>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:2867492 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr23:2867423 G>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:2867385 C>T did not map to a codon.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr23:2867486 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:2856236 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:2856187 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:3021855 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:3002315 C>T did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:3002504 G>A did not map to a codon.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr23:3002362 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:2998954 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:66303762 C>T maps to NM_014960.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:66391297 C>T maps to NM_014960.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:2936679 G>A did not map to a codon.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr23:2951148 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:2936657 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:149681756 G>A maps to NM_001012301.2 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr5:149677829 G>T maps to NM_001012301.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr5:149677328 C>T maps to NM_001012301.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:114824716 C>T maps to NM_024590.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:3681162 G>A maps to NM_004314.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:77003336 A>T maps to NM_001130016.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:77003515 C>T maps to NM_001130016.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr4:77033593 C>A maps to NM_001130016.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr1:44401760 G>A maps to NM_057090.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:231126010 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:19960546 G>A maps to NM_001670.2 R817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:19961271 C>T maps to NM_001670.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr22:19960456 C>T maps to NM_001670.2 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr22:19960697 C>A maps to NM_001670.2 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:19969122 C>T maps to NM_001670.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:25033797 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:25033730 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:25033713 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr23:25033777 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:17915117 T>C maps to NM_004315.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:122955286 G>A maps to NM_024769.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:131226855 C>T maps to NM_018482.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:131226881 G>A maps to NM_018482.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:131414174 G>T maps to NM_018482.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:9541416 T>A maps to NM_003887.2 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:9508630 C>T maps to NM_003887.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:9515027 T>G maps to NM_003887.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:9525430 C>T maps to NM_003887.2 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:9437477 C>T maps to NM_003887.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:9491024 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr2:9525430 C>T maps to NM_003887.2 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:9531278 G>A maps to NM_003887.2 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:9543425 G>A maps to NM_003887.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:23760792 G>T maps to NM_017707.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr1:23763701 C>T maps to NM_017707.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:23763746 G>A maps to NM_017707.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:239344627 G>T maps to NM_001040445.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:239342240 G>A maps to NM_001040445.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:150883647 G>A maps to ENST00000422024 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:150878202 G>A maps to ENST00000422024 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:150883947 G>A maps to ENST00000422024 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:150883992 C>T maps to ENST00000422024 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:15307686 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:15306010 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:15306175 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:15306057 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:15333599 C>T did not map to a codon.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr23:15315755 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:15311389 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:63445206 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:63445478 T>C did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:63444309 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:63444305 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:63444966 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:63445345 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:57312677 C>T maps to ENST00000295941 P2756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:123267252 C>T maps to NM_080928.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr7:123276951 A>T maps to NM_080928.3 K562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:123269133 C>T maps to NM_080928.3 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:76384669 A>G maps to NM_080868.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:76397949 A>G maps to NM_080868.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr2:237123061 C>T maps to NM_212556.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:94417564 G>A maps to ENST00000434324 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr14:94413762 G>A maps to ENST00000434324 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:94420792 G>A maps to ENST00000434324 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:94405675 C>T maps to ENST00000434324 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr14:94405615 G>A maps to ENST00000434324 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:94417546 C>T maps to ENST00000434324 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:94413726 C>T maps to ENST00000434324 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:95157167 G>A maps to NM_016116.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:95157218 C>T maps to NM_016116.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr4:177142386 C>A maps to NM_080874.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:177146477 G>A maps to NM_080874.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr15:101170068 C>T maps to NM_198243.2 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr15:101188576 T>C maps to NM_198243.2 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr15:101169957 C>T maps to NM_198243.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:48543595 G>A maps to NM_024095.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:48547246 G>A maps to NM_024095.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:15268631 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:15267047 A>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:15287931 A>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:15287957 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:30221724 C>T maps to NM_032204.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr22:30218381 G>A maps to NM_032204.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:30188436 G>A maps to NM_032204.3 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:30221195 A>C maps to NM_032204.3 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:101109777 C>T maps to NM_006828.2 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:101099510 T>C maps to NM_006828.2 E1000E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:101037584 C>T maps to NM_006828.2 K1825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr6:100960673 G>A maps to NM_006828.2 R2066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:101077032 C>T maps to NM_006828.2 V1411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:101246681 A>G maps to NM_006828.2 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:101054867 G>A maps to NM_006828.2 R1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:101296425 A>G maps to NM_006828.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:103352642 G>A maps to NM_004316.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr12:103352564 C>T maps to NM_004316.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:103352663 G>A maps to NM_004316.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:8959398 G>A maps to NM_020646.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:8959357 G>T maps to NM_020646.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:108169150 C>T maps to NM_203436.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:108169228 C>T maps to NM_203436.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:108169060 C>T maps to NM_203436.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:108169015 G>A maps to NM_203436.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:119226903 G>T maps to NM_014034.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:7077549 C>T maps to NM_001671.3 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr17:7077073 G>A maps to NM_001671.3 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr17:7010447 G>T maps to NM_080912.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:155308102 T>C maps to ENST00000368346 E2865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:155448744 G>A maps to ENST00000368346 R1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:155322512 A>G maps to ENST00000368346 G2455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:155451949 C>T maps to ENST00000368346 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:155451337 A>G maps to ENST00000368346 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr1:155408473 G>A maps to ENST00000368346 D1824D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:155307501 C>T maps to ENST00000368346 R2953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr1:155340377 C>A maps to ENST00000368346 G2206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:155451724 A>C maps to ENST00000368346 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:37964604 C>T maps to NM_004674.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:37974226 T>C maps to NM_004674.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr8:37964666 A>T maps to NM_004674.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1748789 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:1742125 C>T did not map to a codon.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr23:1748788 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:1748727 G>A did not map to a codon.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr23:1743213 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:1734119 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr23:1755355 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:1752145 C>A did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:1522322 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1522302 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1540733 A>G did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:1537978 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:1536898 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:1546792 C>A did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr23:1522377 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:1537917 C>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:1557991 C>T did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr23:1546728 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:1546684 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:1561149 C>T did not map to a codon.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr23:1551237 A>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:1531639 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:1540580 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:1551187 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:12856291 C>T maps to NM_004317.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:12858228 C>T maps to NM_004317.2 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:97482431 A>G maps to NM_183356.3 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:97488684 C>T maps to NM_183356.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:97483923 A>G maps to NM_183356.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:190532198 C>T maps to NM_019048.2 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr2:190531619 G>A maps to NM_019048.2 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:190531820 T>C maps to NM_019048.2 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:3402246 G>A maps to NM_000049.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr14:104570727 C>T maps to NM_001080464.1 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:104570672 C>T maps to NM_001080464.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:104575629 G>T maps to NM_001080464.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr14:104575604 C>T maps to NM_001080464.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:62555984 A>G maps to NM_004318.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:62430154 C>T maps to NM_004318.3 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:62465664 G>A maps to NM_004318.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:62475335 T>C maps to NM_004318.3 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:62416019 G>A maps to NM_004318.3 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr16:29916254 C>T maps to NM_181718.3 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:26830108 G>A maps to NM_020437.4 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:197098314 A>G did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:197053459 A>T maps to NM_018136.4 P3476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:197093356 A>G maps to NM_018136.4 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:197108942 G>A maps to NM_018136.4 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:197059337 A>G maps to NM_018136.4 L3273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:197057535 A>G maps to NM_018136.4 Y3337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr1:197097720 G>T maps to NM_018136.4 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:197101438 A>C maps to NM_018136.4 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:197111557 C>T maps to NM_018136.4 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:197087071 G>T maps to NM_018136.4 I1304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:197093436 G>A maps to NM_018136.4 Q1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:197070760 T>C maps to NM_018136.4 A2540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:197097796 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:197099129 A>G maps to NM_018136.4 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr1:197072530 C>T maps to NM_018136.4 A1950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:95228783 G>A maps to NM_017680.4 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:70188637 C>T maps to NM_152792.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:70188544 A>G maps to NM_152792.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:70188556 G>A maps to NM_152792.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:79954544 G>A maps to ENST00000306729 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:79954319 C>T maps to ENST00000306729 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:62159698 C>T maps to NM_025080.3 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr9:133333963 C>T maps to NM_000050.4 G117G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-7707-01A-11D-2053-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr3:130733116 G>A maps to ENST00000514044 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:130743232 T>C maps to ENST00000514044 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:96798441 C>T maps to NM_001002036.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:96789627 A>G maps to NM_001002036.3 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:96789816 T>G maps to NM_001002036.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr2:96795680 T>C maps to NM_001002036.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:96789645 T>C maps to NM_001002036.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:96798408 C>T maps to NM_001002036.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:96795653 G>A maps to NM_001002036.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr1:176999972 G>A maps to ENST00000281881 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:176998869 G>A maps to ENST00000281881 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:176853604 G>A maps to ENST00000281881 H1040H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:177133689 C>T maps to ENST00000281881 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:176857270 G>A maps to ENST00000281881 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:176903369 G>A maps to ENST00000281881 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:176918358 C>T maps to ENST00000281881 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:176926900 C>T maps to ENST00000281881 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:119413812 T>C maps to ENST00000313400 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:119582953 G>A maps to ENST00000313400 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:119188282 G>A maps to ENST00000313400 R1289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:119188189 C>T maps to ENST00000313400 T1320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr9:119203071 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:119495676 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:119382590 C>T maps to ENST00000313400 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr9:119770443 G>A maps to ENST00000313400 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:119495738 C>T maps to ENST00000313400 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr9:119858380 G>A maps to ENST00000313400 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:31021710 G>A maps to ENST00000375687 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:31024633 T>C maps to ENST00000375687 F1373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:31022317 G>A maps to ENST00000375687 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:31022896 T>G maps to ENST00000375687 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr20:31022998 C>T maps to ENST00000375687 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr20:31024756 C>T maps to ENST00000375687 P1414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr20:31023115 G>A maps to ENST00000375687 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:25966040 G>A maps to NM_018263.4 H1055H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:25965809 G>A maps to NM_018263.4 G1132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:25964954 G>A maps to NM_018263.4 C1417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:25966040 G>A maps to NM_018263.4 H1055H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:25991623 T>C maps to NM_018263.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr2:25967339 C>T maps to NM_018263.4 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr18:31326438 G>A maps to NM_030632.1 L2209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr18:31326156 C>T maps to NM_030632.1 F2115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr18:31325577 C>T maps to NM_030632.1 D1922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr18:31319395 G>A maps to NM_030632.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr18:31319839 G>A maps to NM_030632.1 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:31325871 A>G maps to NM_030632.1 P2020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:31263450 A>G maps to NM_030632.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:31325871 A>G maps to NM_030632.1 P2020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:31325826 T>C maps to NM_030632.1 T2005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr18:31322937 T>C maps to NM_030632.1 S1042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr18:31326039 T>C maps to NM_030632.1 C2076C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr18:31325874 G>A maps to NM_030632.1 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:117067502 G>A maps to NM_130768.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:117067495 G>A maps to NM_130768.2 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:124382181 A>G maps to NM_014109.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:124335284 T>A maps to NM_014109.3 K1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:124361577 G>A maps to NM_014109.3 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr8:124357231 T>C maps to NM_014109.3 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:124382181 A>G maps to NM_014109.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:124348742 T>C maps to NM_014109.3 Q1027Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:124382193 A>G maps to NM_014109.3 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:124338213 C>T maps to NM_014109.3 Q1307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:124371573 T>C maps to NM_014109.3 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:124373884 G>A maps to NM_014109.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:24046212 C>T maps to NM_017552.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:1451390 G>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr1:1423269 C>T maps to NM_031921.4 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:1424618 C>T maps to NM_031921.4 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr1:1420547 C>A maps to NM_031921.4 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:1391274 C>T maps to NM_001039211.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr1:1391199 C>T maps to NM_001039211.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:29220337 G>A maps to NM_024857.3 W1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:29221132 T>C maps to NM_024857.3 N1754N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr17:29220646 G>A maps to NM_024857.3 L1592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:29161689 C>A maps to NM_024857.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:29161233 A>G maps to NM_024857.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr17:29182286 G>A maps to NM_024857.3 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:3907774 C>T maps to NM_033064.4 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr19:3905588 C>T maps to NM_033064.4 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr12:51203289 C>T maps to NM_005171.4 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:175962205 A>T maps to NM_001880.2 L315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr2:175976307 T>C maps to NM_001880.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:175994916 C>T maps to NM_001880.2 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:212788566 C>T maps to NM_001674.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:161753837 C>G maps to NM_007348.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:161928323 G>A maps to NM_007348.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:161816298 G>A maps to NM_007348.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:161748106 G>A maps to NM_007348.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:32087701 G>A maps to NM_004381.4 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:32093996 C>T maps to NM_004381.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:14649273 T>C maps to NM_018179.3 H1130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr12:14614025 C>A maps to NM_018179.3 S919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:14577700 C>A maps to NM_018179.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:14649258 A>C maps to NM_018179.3 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:14589053 C>T maps to NM_018179.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:14650877 T>C maps to NM_018179.3 C1228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:14591098 G>A maps to NM_018179.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:14577286 C>T maps to NM_018179.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:14650664 C>T maps to NM_018179.3 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:10524905 C>T maps to NM_024997.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr16:10567832 C>T maps to NM_024997.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:10527500 G>T maps to NM_024997.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr5:81474360 T>A maps to NM_031482.4 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:72540425 C>T maps to NM_033388.1 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:64666106 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:64681810 T>C maps to ENST00000421419 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr11:64664313 G>A maps to ENST00000421419 G1728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr14:96798978 G>A maps to NM_018036.5 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:96756088 C>T maps to NM_018036.5 E1970E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:96794866 A>G maps to NM_018036.5 N660N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:96781918 G>A maps to NM_018036.5 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:96797966 T>C maps to NM_018036.5 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:96770924 C>T maps to NM_018036.5 S1583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:96769565 C>T maps to NM_018036.5 P1623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:96811654 A>G maps to NM_018036.5 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:96797723 G>A maps to NM_018036.5 H573H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr14:96798639 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:107395054 A>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:107372042 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:107374534 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:107396917 A>C did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:107381174 G>A did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:242598543 G>A maps to ENST00000337606 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:242606144 C>T maps to ENST00000337606 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:242608087 G>A maps to ENST00000337606 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:63329808 G>A maps to NM_032852.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:63269478 G>T maps to NM_032852.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr19:10657621 C>T maps to NM_032885.4 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:11372821 T>C maps to NM_006395.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:11372884 C>T maps to NM_006395.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:11340891 T>C did not map to a codon.
Multiple mappings detected for codon TCGA-CG-4300-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:220090248 G>A maps to NM_024085.3 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr2:220088826 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr7:150714338 A>G maps to NM_173681.5 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr7:150721408 A>T maps to NM_173681.5 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr11:290920 C>G maps to ENST00000409479 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:216209519 C>T maps to NM_004044.6 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:216197138 C>T maps to NM_004044.6 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:51094792 G>A maps to ENST00000358385 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:38546106 G>A maps to NM_001135673.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:63414020 G>A maps to NM_015459.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:108098362 A>G maps to NM_000051.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:108155160 C>A maps to NM_000051.3 V1318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr11:108163406 C>T maps to NM_000051.3 Q1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:108203491 C>T maps to NM_000051.3 R2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:108213966 C>T maps to NM_000051.3 R2763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr11:108128224 A>T maps to NM_000051.3 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr11:108235868 C>T maps to NM_000051.3 Q2971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr11:108192026 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:108114792 G>T maps to NM_000051.3 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:108129783 A>C maps to NM_000051.3 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:108170453 C>T maps to NM_000051.3 S1673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:108202190 A>G maps to NM_000051.3 P2512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:108121686 C>T maps to NM_000051.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr11:108196195 A>G maps to NM_000051.3 R2244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:81077065 C>T maps to NM_015251.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:81075941 G>A maps to NM_015251.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:81076064 C>T maps to NM_015251.2 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:7046277 G>A maps to NM_001940.3 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr12:7045878 C>T maps to NM_001940.3 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:7046280 C>T maps to NM_001940.3 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:7046301 G>A maps to NM_001940.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr12:7045884 A>G maps to NM_001940.3 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:7045896 G>A maps to NM_001940.3 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:7044831 T>C maps to NM_001940.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:7045908 G>A maps to NM_001940.3 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:7044972 T>C maps to NM_001940.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr4:94750922 G>A maps to NM_005172.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:94750178 G>A maps to NM_005172.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:94751045 G>A maps to NM_005172.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:69991317 C>T maps to NM_145178.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr2:85981536 G>A maps to NM_032827.6 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:85981554 G>A maps to NM_032827.6 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr15:25972388 G>A maps to NM_024490.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr15:25924997 G>A maps to NM_024490.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:25926194 A>G maps to NM_024490.3 F1173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:25971229 C>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr15:25953352 G>A maps to NM_024490.3 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:25961951 G>A maps to NM_024490.3 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr15:25958992 C>T maps to NM_024490.3 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:25958890 G>A maps to NM_024490.3 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr15:25924925 A>G maps to NM_024490.3 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr15:25966921 C>T maps to NM_024490.3 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:25928618 G>A maps to NM_024490.3 L1102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:25959169 G>A maps to NM_024490.3 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr15:25924925 A>C maps to NM_024490.3 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr15:25925359 C>T maps to NM_024490.3 P1258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr15:25953237 T>C maps to NM_024490.3 K820K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:25966951 C>T maps to NM_024490.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:25971229 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:26107940 C>T maps to NM_024490.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr15:25924925 A>G maps to NM_024490.3 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:160113245 A>G maps to NM_025153.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr5:160047921 C>T maps to NM_025153.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr5:160033904 T>C maps to NM_025153.2 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:160044941 G>A maps to NM_025153.2 R819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr5:159992887 G>A maps to NM_025153.2 Q1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:160042878 A>G maps to NM_025153.2 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr4:47514785 C>T maps to NM_020453.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr4:47559904 C>T maps to NM_020453.3 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:47593304 A>C maps to NM_020453.3 G1396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr4:47582420 T>C maps to NM_020453.3 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr4:47565664 G>A maps to NM_020453.3 A912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr4:47559778 G>A maps to NM_020453.3 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:47525166 G>A maps to NM_020453.3 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr4:47578875 C>T maps to NM_020453.3 F1151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:113508591 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:138844224 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:138811116 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:138882247 G>T did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:138845547 G>T did not map to a codon.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr23:138880883 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:138878613 T>C did not map to a codon.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr23:138864762 A>G did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:138856897 G>A did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr23:138856960 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:138828011 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:138857047 G>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr13:25265210 G>A maps to NM_001185085.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr13:25262593 C>T maps to NM_001185085.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:19766901 G>A maps to NM_020410.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:19767527 G>A maps to NM_020410.2 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:19762528 G>A maps to NM_020410.2 H768H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:17313104 C>A maps to NM_022089.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:17318353 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:17331317 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:17314701 C>T maps to NM_022089.2 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:17316762 C>T maps to NM_022089.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:17313390 G>A maps to NM_022089.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:17316726 G>A maps to NM_022089.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:194147838 C>T maps to NM_024524.3 Q1030Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:194169308 C>A maps to NM_024524.3 G343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:194147931 C>T maps to NM_024524.3 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr3:193080198 C>T maps to NM_198505.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:192997202 T>A maps to NM_198505.2 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr3:193031863 G>A maps to NM_198505.2 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr3:193002748 G>A maps to NM_198505.2 F1060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr3:192992920 G>A maps to NM_198505.2 N1189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr3:193042673 T>C maps to NM_198505.2 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:116946595 C>T maps to NM_000701.7 G1014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:116935564 C>T maps to NM_000701.7 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:160094923 A>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:42474391 C>T maps to ENST00000441343 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:42474439 C>T maps to ENST00000441343 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:42482920 G>A maps to ENST00000441343 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:42492105 G>A maps to ENST00000441343 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:42489309 C>T maps to ENST00000441343 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:42480633 G>A maps to ENST00000441343 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:42482398 C>T maps to ENST00000441343 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:42485960 C>T maps to ENST00000441343 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:42471892 G>A maps to ENST00000441343 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:42486240 G>A maps to ENST00000441343 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:42482413 G>A maps to ENST00000441343 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:42492086 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr19:42479895 C>T maps to ENST00000441343 K716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:42490288 G>T maps to ENST00000441343 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:160151794 C>T maps to NM_144699.3 D981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:160125848 C>T maps to NM_144699.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:160134081 G>T maps to NM_144699.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:160145891 C>A maps to NM_144699.3 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:160147328 G>T maps to NM_144699.3 G871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:160156152 G>A maps to NM_144699.3 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:169080736 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:7557198 T>C maps to NM_001678.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:141626114 A>G maps to NM_001679.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:141626090 T>C maps to NM_001679.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:119504980 G>A did not map to a codon.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr23:119505007 G>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:119509227 T>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:119504683 G>T did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:119505006 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:28912048 C>T maps to NM_173201.3 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:28898954 C>T maps to NM_173201.3 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr16:28909607 C>A maps to NM_173201.3 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:28911960 G>A maps to NM_173201.3 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:110734411 T>C maps to NM_170665.3 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:3850714 C>T maps to NM_174953.1 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr17:3854670 C>A maps to NM_174953.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:3844375 G>A maps to NM_174953.1 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr17:3854674 G>A maps to NM_174953.1 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:3850768 C>T maps to NM_174953.1 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:3851104 G>T maps to NM_174953.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:3840882 G>A maps to NM_174953.1 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:3831308 C>T maps to NM_174953.1 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:89997946 G>A maps to ENST00000428670 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:90028813 T>C maps to ENST00000428670 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:90004245 G>A maps to ENST00000428670 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:89998029 G>A maps to ENST00000428670 R846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:10382233 G>A maps to NM_001001331.2 D1024D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:10387132 G>A maps to NM_001001331.2 Q880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:10491113 C>T maps to NM_001001331.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:10382278 G>A maps to NM_001001331.2 N1009N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:10370623 C>T maps to NM_001001331.2 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:10430086 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:10387765 G>A maps to NM_001001331.2 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:10370623 C>T maps to NM_001001331.2 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:10401789 G>A maps to NM_001001331.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:10452320 C>T maps to NM_001001331.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:152830540 C>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:152814983 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:152813441 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:152813344 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:152845657 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:152814245 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:152821584 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:152835150 A>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:152818574 G>A did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr23:152821534 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:152807797 G>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:152823641 G>A did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:152825249 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:152815581 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:152822454 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:152818527 G>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:152830477 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:152807869 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:152845525 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:152815143 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:152821866 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:152825263 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:152818541 C>T did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:152807853 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:152813386 C>T did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr23:152813387 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:152813353 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:152801811 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:152823743 G>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:152835117 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:152845746 G>A did not map to a codon.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr23:152807374 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:152814999 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:152813343 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:152813422 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:203672792 C>T maps to NM_001001396.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:203668686 T>A maps to NM_001001396.1 L164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr1:203680139 C>T maps to NM_001001396.1 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:203677054 C>T maps to NM_001001396.1 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:203691675 C>A maps to NM_001001396.1 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr1:203672792 C>T maps to NM_001001396.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:203683365 C>T maps to NM_001001396.1 D789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:84459365 G>A maps to ENST00000416219 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr16:84456239 C>T maps to ENST00000416219 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:36050940 G>A maps to NM_000704.2 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:36051499 G>A maps to NM_000704.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:36045886 G>A maps to NM_000704.2 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:36046362 G>T maps to NM_000704.2 I712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:36046104 A>G maps to NM_000704.2 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:36046155 G>A maps to NM_000704.2 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr19:36050081 G>A maps to NM_000704.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:36049991 C>T maps to NM_000704.2 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:36043936 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:36053495 C>A maps to NM_000704.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:36051331 G>T maps to NM_000704.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:114304804 G>A maps to NM_000705.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr18:43666115 G>A maps to NM_001001937.1 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:7838093 C>T maps to NM_001001973.1 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:1241935 G>A maps to NM_001687.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:46973022 G>A maps to NM_005175.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:46973103 C>T maps to NM_005175.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:176046085 A>T maps to NM_001689.4 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:176043782 A>G maps to NM_001190329.1 *106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:27096988 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:50788252 A>G maps to NM_001003803.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:153664117 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:153662012 A>G did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr23:153664187 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:153663741 G>A did not map to a codon.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr23:153661990 C>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:153663735 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:153660653 G>A did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr5:81613992 C>T maps to NM_001017971.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:81613881 G>A maps to NM_001017971.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:40456499 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:40448347 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:40456805 T>C did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:40450528 G>A did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr23:40464995 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:40450602 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:40464918 T>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:40460099 G>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:40666352 C>T maps to NM_001130020.1 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:40652942 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:40632728 C>T maps to NM_001130020.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr17:40650952 T>C maps to NM_001130020.1 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:124228802 C>T maps to NM_012463.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:138418957 C>T maps to NM_130840.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr7:138437554 G>A maps to NM_130840.2 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:138455993 T>C did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:138394385 G>A maps to NM_130840.2 H804H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:138394472 G>A maps to NM_130840.2 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr7:138447125 C>T maps to NM_130840.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:138434047 G>T maps to NM_130840.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:44442497 T>C did not map to a codon.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr1:44442010 G>T maps to NM_004047.3 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:2569559 C>T maps to NM_001694.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:67477082 T>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:87111212 C>T maps to NM_152565.1 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr8:87165043 G>A did not map to a codon.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr8:87165112 G>A maps to NM_152565.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr8:87165115 G>A maps to NM_152565.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:87111267 C>T maps to NM_152565.1 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:87165085 C>T maps to NM_152565.1 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr7:149576435 C>G maps to NM_001100592.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:149576654 G>A maps to NM_001100592.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:113503562 C>T maps to NM_001690.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:113503219 G>T maps to NM_001690.3 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:71189996 G>A maps to NM_001692.3 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:71192184 C>T maps to NM_001692.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:71190411 C>T maps to NM_001692.3 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:20070373 T>C maps to NM_001693.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr8:104068161 C>T maps to NM_001695.4 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:10918695 A>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:10908852 G>A maps to NM_001039362.1 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:10917838 C>T maps to NM_001039362.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:18082819 G>A maps to NM_001696.3 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr2:46739556 C>T maps to NM_080653.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:117359932 G>A maps to NM_004888.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:31514300 C>T maps to NM_130463.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:54656162 G>A maps to NM_015941.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:77243894 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:77227164 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:77254040 A>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:77284766 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:77267083 T>C did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:77245352 T>C did not map to a codon.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr23:77298825 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:77266708 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:77284890 C>T did not map to a codon.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr23:77245090 T>A did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:77267113 T>C did not map to a codon.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr23:77243796 G>C did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr23:77245136 C>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:77253978 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:77301977 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:77258619 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr23:77245412 G>A did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:77245438 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:77294452 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:77296163 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr23:77243897 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:52523919 G>A maps to NM_000053.2 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:52511797 G>T maps to NM_000053.2 V1239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:52518370 G>T maps to NM_000053.2 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:52548155 T>C maps to NM_000053.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:52548992 G>A maps to NM_000053.2 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:52532476 G>A maps to NM_000053.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr13:52532475 G>A maps to NM_000053.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:52518246 C>A maps to NM_000053.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr13:52544778 C>A maps to NM_000053.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr4:42580303 T>C maps to NM_006095.2 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr4:42583691 T>A maps to NM_006095.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:42581863 C>T maps to NM_006095.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:42414995 G>A maps to NM_006095.2 I1144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:42416686 G>A maps to NM_006095.2 H1118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr4:42416719 C>T maps to NM_006095.2 A1107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr4:42524203 G>A maps to NM_006095.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:42509099 C>T maps to NM_006095.2 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:42545945 G>A maps to NM_006095.2 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:26163836 T>C maps to NM_016529.4 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr13:26343261 C>T maps to NM_016529.4 D821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:26273358 C>T maps to NM_016529.4 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:26153032 G>A maps to NM_016529.4 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr13:26125596 G>A maps to NM_016529.4 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr13:26163783 C>T maps to NM_016529.4 R720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:55322535 G>A maps to NM_005603.4 R941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:55315854 C>T maps to NM_005603.4 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr18:55338740 G>A maps to NM_005603.4 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr18:55362737 G>C maps to NM_005603.4 S242*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D7-A6F0-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:55338812 C>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:154313482 C>A maps to NM_020452.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:1802600 G>A maps to NM_138813.2 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:1784889 A>G maps to NM_138813.2 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr15:50152451 A>T maps to NM_024837.2 L1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr15:50339640 C>T maps to NM_024837.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:50235531 C>T maps to NM_006045.1 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:50221452 C>T maps to NM_006045.1 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr20:50244186 G>A maps to NM_006045.1 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:50245608 A>G maps to NM_006045.1 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:50346504 C>T maps to NM_006045.1 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:50287726 G>A maps to NM_006045.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr20:50287726 G>A maps to NM_006045.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:50290783 C>T maps to NM_006045.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:50241844 C>T maps to NM_006045.1 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:77037167 C>T maps to NM_198531.3 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:77133949 C>T maps to NM_198531.3 H1041H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr18:77107846 C>T maps to NM_198531.3 H920H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:77067104 C>T maps to NM_198531.3 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:77089272 G>T maps to NM_198531.3 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:77133943 C>T maps to NM_198531.3 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:77089289 C>T maps to NM_198531.3 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr18:77107819 G>A maps to NM_198531.3 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:17931620 G>A maps to NM_145691.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:142266698 C>T maps to NM_001184.3 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:142242990 G>T maps to NM_001184.3 I1332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:142281951 C>A did not map to a codon.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr3:142275391 C>T maps to NM_001184.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr3:142297489 G>A maps to NM_001184.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr3:142268401 T>G maps to NM_001184.3 I1030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:142217518 C>T maps to NM_001184.3 V1826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr3:142215232 G>A maps to NM_001184.3 Y1956Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr3:142275399 G>A maps to NM_001184.3 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:142231105 T>C maps to NM_001184.3 S1616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:48506345 G>A maps to NM_130384.1 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:48500803 G>A maps to NM_130384.1 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:3584893 G>A maps to NM_139321.2 W1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr20:3543987 A>G maps to NM_139321.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr20:3540126 C>T maps to NM_139321.2 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:3556540 C>T maps to NM_139321.2 C720C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr10:117486772 C>T maps to NM_207303.2 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:116881570 A>G maps to NM_207303.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:116930923 C>T maps to NM_207303.2 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr10:117026351 T>C maps to NM_207303.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:76875931 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:76937944 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:76938508 T>C did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:76888865 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:76937065 G>A did not map to a codon.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr23:76937283 G>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:76814140 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:76920195 T>C did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:76918943 G>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:76939710 A>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:76855268 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:76938400 T>G did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:76939921 A>C did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:76938018 T>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:76938180 C>T did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:76944358 T>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:76918896 T>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:76939969 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:76939917 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr23:76907601 A>C did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:76907835 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:76763846 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:76776389 T>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:16306661 C>A maps to NM_000332.3 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:16307006 C>T maps to NM_000332.3 Q667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr6:16326834 C>T maps to NM_000332.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:16328199 C>T maps to NM_000332.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:16306823 G>A maps to NM_000332.3 N728N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:16327473 G>A maps to NM_000332.3 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr6:16326660 G>A maps to NM_000332.3 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:46096162 T>C maps to NM_013236.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr22:46114328 G>A maps to NM_013236.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:111895131 C>T maps to NM_002973.3 A1134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:111893895 C>T maps to NM_002973.3 T1227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:111893937 C>T maps to NM_002973.3 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:28847719 G>A maps to NM_148414.1 P1071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:28845902 T>A maps to NM_148414.1 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:28845453 G>T maps to NM_148414.1 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:28843628 A>G maps to NM_148414.1 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:92560112 A>G maps to ENST00000359819 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:92555088 G>A maps to ENST00000359819 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:13337534 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:13337199 T>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:13337423 T>C did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:13337596 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:13337234 A>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:63965618 G>A maps to NM_001177387.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:63975974 C>T maps to NM_001177387.1 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:63973913 G>A maps to NM_001177387.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:63965642 A>G maps to NM_001177387.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:63898588 T>C maps to NM_001177387.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:105516959 A>G maps to NM_020725.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:105429098 G>A maps to NM_020725.1 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr1:110030426 G>A did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr1:110028718 G>A maps to NM_153340.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:110032912 G>A maps to NM_153340.4 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:110033759 C>T maps to NM_153340.4 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr1:110030319 C>T maps to NM_153340.4 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:42274611 G>A maps to NM_020218.1 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:42274990 C>T maps to NM_020218.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:42272169 G>A maps to NM_020218.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr9:93983131 C>T maps to NM_001698.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:93983208 G>A maps to NM_001698.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:74754075 G>A maps to ENST00000258081 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:54959345 C>T maps to NM_198437.1 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr20:54948570 C>T maps to NM_198437.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:54961463 G>A maps to NM_198437.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:54956590 A>G maps to NM_198437.1 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:1309706 C>T maps to NM_001127230.1 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr19:57743415 C>T maps to NM_001015878.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr19:57743526 G>A maps to NM_001015878.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:57746682 C>A maps to NM_001015878.1 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:57743928 C>T maps to NM_001015878.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:69064857 G>A maps to NM_015570.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:70255175 C>T maps to NM_015570.2 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:70255699 G>A maps to NM_015570.2 R1166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:70252291 G>A maps to NM_015570.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:70254988 G>A maps to NM_015570.2 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:70255372 C>T maps to NM_015570.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:69599556 C>T maps to NM_015570.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr7:70252342 G>A maps to NM_015570.2 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:34168181 G>A maps to NM_020371.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:34295365 A>G maps to NM_020371.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:34159951 C>T maps to NM_020371.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:34163231 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:58197056 G>A maps to NM_006576.3 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:58203442 G>T maps to NM_006576.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:58207050 A>G maps to NM_006576.3 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:58193643 A>G maps to NM_006576.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:3065236 G>A maps to NM_000490.4 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:99439419 C>T maps to NM_021732.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:63544334 G>A maps to NM_000706.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:63543830 C>T maps to NM_000706.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:63543908 G>A maps to NM_000706.3 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:63544007 G>T maps to NM_000706.3 C203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:206225357 G>A maps to NM_000707.3 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:206230973 C>T maps to NM_000707.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:206224691 G>A maps to NM_000707.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153171084 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153171978 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:153171713 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:153171757 G>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:153172146 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153171979 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:153171112 G>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:153171221 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:153171567 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:153170623 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:69455638 C>A did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:69454558 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:69261774 T>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:69261762 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:69261724 C>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:69261761 C>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:396308 C>T maps to NM_003502.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr16:347939 C>T maps to NM_003502.3 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:364604 G>A maps to NM_003502.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:338226 G>A maps to NM_003502.3 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:396380 C>T maps to NM_003502.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr16:347813 C>T maps to NM_003502.3 W564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:63526099 G>A maps to NM_004655.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:63554009 A>G maps to NM_004655.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:63533494 C>T maps to NM_004655.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr17:63554147 G>C maps to NM_004655.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:41726604 C>T maps to NM_021913.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:41765751 C>T maps to NM_021913.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:41744381 G>T maps to NM_021913.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:41749583 C>A maps to NM_021913.3 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr19:41758856 C>G maps to NM_021913.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:79166623 G>A maps to ENST00000269392 Q784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:79173614 G>A maps to ENST00000269392 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr17:79167922 C>T maps to ENST00000269392 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:79167877 C>T maps to ENST00000269392 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:28379464 T>C maps to NM_022461.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:28382054 A>G maps to NM_022461.3 H18H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:103855873 C>A maps to NM_148174.2 G3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:103840906 C>A did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr19:829666 C>T maps to NM_001700.3 Y107Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:45003811 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:45007618 A>G did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr15:45007739 G>T maps to NM_004048.2 G63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr15:45007718 G>T maps to NM_004048.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr15:45007693 G>A maps to NM_004048.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:160803765 G>A maps to NM_033168.2 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:168726163 C>T maps to NM_020981.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr1:193149666 T>C maps to NM_003783.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:33245429 C>T maps to NM_003782.3 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:33246149 G>T maps to NM_003782.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:41032851 G>A maps to NM_033172.1 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr21:41033307 C>T maps to NM_033172.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr21:41032653 T>C maps to NM_033172.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr21:41033163 G>A maps to NM_033172.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr13:31891747 G>A maps to NM_194318.3 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:134253717 G>A maps to NM_054025.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:134253810 C>T maps to NM_054025.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:134253987 G>A maps to NM_054025.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:71665874 C>T maps to NM_080742.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:17919074 G>A maps to NM_014256.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:17922435 C>T maps to NM_014256.3 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:182988415 C>A maps to NM_032047.4 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:182987867 A>G maps to NM_032047.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:76751335 C>T maps to ENST00000354301 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:76750654 C>T maps to ENST00000354301 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:76750723 G>A maps to ENST00000354301 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:76751074 G>A maps to ENST00000354301 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:232263296 C>T maps to NM_145236.2 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:232262513 T>C maps to NM_145236.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:232263029 C>T maps to NM_145236.2 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:232263161 C>T maps to NM_145236.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:41932374 G>A maps to NM_198540.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:67183689 G>A maps to NM_033309.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:67183704 G>A maps to NM_033309.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:67183797 G>A maps to NM_033309.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:80919006 G>A maps to NM_001009905.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:58024082 G>A maps to NM_001478.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr12:58024984 C>G maps to NM_001478.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:58022555 G>A maps to NM_001478.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:47247083 C>T maps to NM_153446.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr17:47219489 G>C maps to NM_153446.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:47236550 G>A maps to NM_153446.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:47233955 C>T maps to NM_153446.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:47210512 C>A maps to NM_153446.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:47246251 G>T maps to NM_153446.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:657407 C>T maps to NM_173593.3 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr12:666772 G>C did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr12:659022 T>C maps to NM_173593.3 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:667190 C>T maps to NM_173593.3 Y848Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:662789 G>A maps to NM_173593.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:665814 C>T maps to NM_173593.3 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:373263 T>C maps to NM_178537.4 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:376349 C>T maps to NM_178537.4 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:373456 C>T maps to NM_178537.4 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:377225 C>T maps to NM_178537.4 N701N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:375711 G>A maps to NM_178537.4 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr11:376087 C>T maps to NM_178537.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:372923 C>T maps to NM_178537.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:33120580 A>G maps to NM_001497.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:44447484 G>A maps to ENST00000309519 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr1:44450679 C>T maps to ENST00000309519 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:44447439 C>T maps to ENST00000309519 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:161141818 T>C maps to NM_003779.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:161143510 C>T maps to NM_003779.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:118937519 G>A maps to NM_212543.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:118943092 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:118945805 C>T maps to NM_212543.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:118937617 A>G maps to NM_212543.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:48252914 G>A maps to NM_004776.3 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr18:29218624 C>T maps to NM_004775.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:177031389 C>T maps to NM_007255.2 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr19:41863922 C>T maps to NM_030578.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr19:41860823 C>T maps to NM_030578.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:104125183 G>A maps to NM_001701.3 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:104133521 G>A maps to NM_001701.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:117186301 C>T maps to NM_012104.3 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:117161684 G>A maps to NM_012104.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:117161233 G>A maps to NM_012104.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:117162425 A>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr21:42629206 C>T maps to NM_012105.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr21:42647385 C>T maps to NM_012105.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:42647469 G>A maps to NM_012105.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr21:42647424 C>T maps to NM_012105.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:30693750 C>T maps to NM_206866.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:90718449 G>A maps to NM_001170794.1 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:90661317 C>T maps to NM_001170794.1 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:90661242 G>A maps to NM_001170794.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:90660303 G>A maps to NM_001170794.1 C507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:90661191 G>A maps to NM_001170794.1 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:90660297 G>A maps to NM_001170794.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:90642333 G>A maps to NM_001170794.1 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr6:90661068 A>C maps to NM_001170794.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr11:64037707 G>A maps to NM_032989.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr9:33264405 G>A maps to NM_004323.5 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:57048630 C>T maps to NM_004282.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:121429559 G>A maps to NM_004281.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:121436098 G>T maps to NM_004281.3 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr10:121429412 G>A maps to NM_004281.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:121429487 C>T maps to NM_004281.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:121436121 C>A maps to NM_004281.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:38065193 T>G maps to NM_004874.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:38034593 C>T maps to NM_004874.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:38034485 T>G maps to NM_004874.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:104026838 C>T maps to NM_001015049.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:11098731 C>T maps to NM_181704.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:11098711 C>T maps to NM_182482.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr21:11098718 T>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:40758301 C>T maps to NM_014952.3 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:40756211 C>T maps to NM_014952.3 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:40751844 G>A maps to NM_014952.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:40756080 C>T maps to NM_014952.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:143623647 C>T maps to NM_001702.2 A1351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:143603465 C>T maps to NM_001702.2 C1055C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr8:143623494 C>T maps to NM_001702.2 P1300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr8:143569805 G>A maps to NM_001702.2 W797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:143602198 G>A maps to NM_001702.2 E979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:143570402 T>C maps to NM_001702.2 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr8:143558755 C>G maps to NM_001702.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr8:143562904 C>T maps to NM_001702.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:32207515 C>T maps to NM_001703.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr1:32207042 G>A maps to NM_001703.2 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:32221678 G>A maps to NM_001703.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:32221744 G>A maps to NM_001703.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:32222254 G>A maps to NM_001703.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:69665994 G>A maps to NM_001704.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:70098713 A>G maps to NM_001704.2 P1500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:70070836 T>C maps to NM_001704.2 D1224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr6:70064151 A>C maps to NM_001704.2 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr6:70071175 T>C maps to NM_001704.2 H1337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:69758077 G>C maps to NM_001704.2 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:70064144 C>T maps to NM_001704.2 C1160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:69653792 A>C maps to NM_001704.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:70071268 A>G maps to NM_001704.2 A1368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:69349253 C>A maps to NM_001704.2 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr6:69348662 T>G maps to NM_001704.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr6:70065745 C>T maps to NM_001704.2 R1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr6:70042816 C>T maps to NM_001704.2 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr6:69772894 G>A maps to NM_001704.2 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr6:69653786 A>C maps to NM_001704.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr6:69685129 C>A maps to NM_001704.2 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr6:70071193 C>G maps to NM_001704.2 Y1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:70040442 A>G maps to NM_001704.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:69666663 C>T maps to NM_001704.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:69653881 C>T maps to NM_001704.2 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr6:69653786 A>C maps to NM_001704.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:79077501 C>T maps to NM_017451.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:79077411 C>T maps to NM_017451.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr17:79077492 G>T maps to NM_017451.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:97946560 G>A maps to NM_018842.4 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:97944909 A>G maps to NM_018842.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:97984431 G>A maps to NM_018842.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:38484912 C>T maps to NM_025045.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:38493073 G>A maps to NM_025045.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:38484756 G>A maps to NM_025045.4 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:38484858 G>A maps to NM_025045.4 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr22:38494144 C>A maps to NM_025045.4 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:1394699 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:1394669 C>A maps to NM_003933.4 C611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:1397757 G>A maps to NM_003933.4 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:1398108 C>T maps to NM_003933.4 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr16:1392040 C>A maps to NM_003933.4 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr16:1398108 C>T maps to NM_003933.4 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:1392601 C>T maps to NM_003933.4 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr16:1398099 C>T maps to NM_003933.4 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:1392007 C>A maps to NM_003933.4 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:28971177 T>C maps to NM_012342.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:28971305 G>A maps to NM_012342.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr4:102776246 T>C maps to NM_017935.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr4:102984240 C>T maps to NM_017935.4 R720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:102946458 G>T maps to NM_017935.4 G463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:102984240 C>T maps to NM_017935.4 R720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:88105721 G>A maps to NM_001173543.1 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:88066730 C>T maps to NM_001173543.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:88052118 G>A maps to NM_001173543.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:88014675 C>T maps to NM_001173543.1 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr16:88017671 C>T maps to NM_001173542.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:52439831 G>A maps to NM_004656.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:52439910 C>T maps to NM_004656.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:52437204 C>T maps to NM_004656.2 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr3:52443592 G>T maps to NM_004656.2 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:52439241 G>A maps to NM_004656.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr2:215593708 G>A maps to NM_000465.2 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:135464749 G>A maps to NM_020064.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr9:135458243 C>T maps to NM_020064.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:135464716 G>A maps to NM_020064.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:135458534 C>T maps to NM_020064.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:135464698 G>A maps to NM_020064.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:91180131 G>A maps to NM_020063.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:91180161 C>T maps to NM_020063.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:91180281 C>T maps to NM_020063.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:96715467 G>A maps to NM_021570.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:96715440 C>T maps to NM_021570.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:17275855 G>A maps to NM_006317.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:17275414 G>A maps to NM_006317.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr6:31506923 C>T maps to ENST00000417556 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr6:31599479 G>A maps to NM_080686.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:31593068 C>T maps to NM_080686.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:31602534 T>C maps to NM_080686.2 S1647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:31599956 C>T maps to NM_080686.2 R1169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:31593817 C>G maps to NM_080686.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:31600250 C>T maps to NM_080686.2 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:31602657 A>G maps to NM_080686.2 G1688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:31593588 G>A maps to NM_080686.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:31600179 C>T maps to NM_080686.2 R1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:31594920 A>G maps to NM_080686.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr6:31591674 C>T maps to NM_080686.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr6:31593817 C>G maps to NM_080686.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:31594893 G>A maps to NM_080686.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr9:134305593 C>G maps to NM_013318.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:134350980 C>T maps to NM_013318.3 N1155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:134351151 C>T maps to NM_013318.3 C1212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:134319683 G>A maps to NM_013318.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:171509406 G>A maps to ENST00000392078 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:171494055 A>G maps to ENST00000392078 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:171510624 G>A maps to ENST00000392078 E1340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:171494088 A>G maps to ENST00000392078 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:171537432 C>T maps to ENST00000392078 T2202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:31611971 C>A did not map to a codon.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr6:31606972 C>A maps to ENST00000404765 E1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr6:31631742 C>T maps to NM_033177.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:31668788 G>A maps to ENST00000375842 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:31655073 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:76012902 C>T maps to NM_006399.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr11:64757200 C>T maps to NM_138456.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr11:64757254 G>A maps to NM_138456.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:49464182 C>T maps to NM_004324.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:35276668 G>A maps to NM_013448.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:35222776 G>A maps to NM_013448.2 H1536H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:35272176 C>T maps to NM_013448.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:35272163 C>A maps to NM_013448.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr7:72891795 A>G maps to NM_032408.3 D665D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:72892374 A>T maps to NM_032408.3 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:72925182 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:72892596 A>G maps to NM_032408.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr7:72879829 G>A maps to NM_032408.3 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr12:56993019 G>A maps to NM_013449.3 G1767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:56993983 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:57008966 G>T maps to NM_013449.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:160304906 C>T maps to NM_013450.2 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:160181326 A>G maps to NM_013450.2 S2116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr2:160206506 A>G maps to NM_013450.2 S1525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:160243033 G>A maps to NM_013450.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:160242866 G>A maps to NM_013450.2 Y1156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:160206341 A>C maps to NM_013450.2 T1580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:160335107 A>G maps to NM_013450.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:160229664 C>T maps to NM_013450.2 A1368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:160181407 T>C maps to NM_013450.2 V2089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:160182227 G>A maps to NM_013450.2 Q2049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:160310280 C>T maps to NM_013450.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:47725008 G>A maps to NM_001127240.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:27148838 G>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:27114772 A>G maps to NM_003986.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:27141368 A>G maps to NM_003986.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66288770 G>T maps to NM_024649.4 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:66287194 C>T maps to NM_024649.4 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:76740998 G>A maps to NM_024685.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:123664250 C>T maps to NM_152618.2 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:123663067 C>T maps to NM_152618.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:123663985 A>G maps to NM_152618.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:123663196 C>T maps to NM_152618.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:56545130 A>G maps to NM_031885.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:56535331 C>T maps to NM_031885.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:56536264 C>T maps to NM_031885.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:56553705 G>T maps to NM_031885.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr15:73023933 C>G maps to NM_033028.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:170344507 C>T maps to ENST00000419050 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr4:122754404 G>A maps to NM_176824.1 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:122749571 T>C maps to NM_176824.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:122782656 A>G did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:122774170 G>A maps to NM_176824.1 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:33303971 G>T maps to NM_198428.2 G230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:33296947 T>G maps to NM_198428.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:33195314 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:33192463 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:107463487 C>T maps to NM_001142568.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:107491836 C>T maps to NM_001142568.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:107517481 C>T maps to NM_001142568.1 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:107491996 C>T maps to NM_001142568.1 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr3:107491965 A>G maps to NM_001142568.1 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:45321842 C>T maps to NM_005581.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:45321842 C>T maps to NM_005581.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr19:45322613 A>G maps to NM_005581.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:45322872 C>T maps to NM_005581.3 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:45317964 C>T maps to NM_005581.3 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:156622646 C>T maps to NM_021948.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:156622145 A>G maps to NM_021948.3 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:156621380 T>C maps to NM_021948.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:156621426 G>T maps to NM_021948.3 G415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr1:156622676 C>A maps to NM_021948.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:156627953 C>T maps to NM_021948.3 S776S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FP-A4BE-01A-12D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:156617399 G>A maps to NM_021948.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:156616836 G>A maps to NM_021948.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:107234460 C>T maps to NM_001008405.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:152988722 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:152968387 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:94033333 C>T maps to NM_003567.2 Q683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:94054954 G>A maps to NM_003567.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:94140237 C>T maps to NM_003567.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:52645320 G>A maps to NM_003657.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr20:52583567 T>A maps to NM_003657.2 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:52645023 G>A maps to NM_003657.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:52561535 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:52645509 G>A maps to NM_003657.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:52674651 C>T maps to NM_003657.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:115124131 A>G maps to NM_005872.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:59155836 G>A maps to ENST00000407086 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:58952025 C>T maps to ENST00000407086 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:59155773 A>G maps to ENST00000407086 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:49493048 G>A maps to NM_198799.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:25047226 A>C maps to NM_001178093.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:24995139 A>C maps to NM_001178093.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:25002717 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:25002730 G>A maps to NM_001178093.1 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr12:25047301 C>T maps to NM_001178093.1 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:49300466 G>A maps to NM_001190.3 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:127524752 A>G maps to NM_078468.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:127524803 C>T maps to NM_078468.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:165548071 C>T maps to NM_000055.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr3:165547876 T>C maps to NM_000055.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:165548647 T>G maps to NM_000055.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:165548071 C>A maps to NM_000055.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr3:165503996 C>T maps to NM_000055.2 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:165547356 C>A maps to NM_000055.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:165547537 G>A maps to NM_000055.2 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:41916540 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:41928570 C>T maps to NM_000709.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:80816556 G>A maps to NM_183050.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:80881108 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr16:31121523 A>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:85736474 G>A maps to NM_003921.4 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:60687880 C>T maps to NM_022893.3 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:60688702 C>T maps to NM_022893.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:60688651 G>T maps to NM_022893.3 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:60688522 G>A maps to NM_022893.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:60687748 G>A maps to NM_022893.3 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:60688450 C>T maps to NM_022893.3 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:60689539 G>A maps to NM_022893.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr14:99640529 C>T maps to NM_138576.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:99641327 G>A maps to NM_138576.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:99641912 C>T maps to NM_138576.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:99640504 G>A maps to NM_138576.2 Q890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:99641153 G>A maps to NM_138576.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:99642455 G>A maps to NM_138576.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:99641429 G>C maps to NM_138576.2 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:99697709 A>C maps to NM_138576.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:99642455 G>A maps to NM_138576.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr18:60985788 G>A maps to NM_000633.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:60985398 C>T maps to NM_000633.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:60985893 C>T maps to NM_000633.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:80263395 C>T maps to NM_004049.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:50173480 G>A maps to NM_138639.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr19:50172123 C>T maps to NM_138639.1 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:18209582 G>A maps to NM_015367.2 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:18185097 C>T maps to NM_015367.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:18210179 C>T maps to NM_015367.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:114424448 A>G maps to NM_001010922.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr1:114429945 G>A maps to NM_001010922.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr1:114429205 A>G maps to NM_001010922.2 L68L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4184-01A-01D-1126-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:187444606 G>T maps to NM_001706.4 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:6927587 C>T maps to NM_181844.3 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:6927124 C>T maps to NM_181844.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:6927449 C>T maps to NM_181844.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:6929845 T>C maps to NM_181844.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:6927488 C>T maps to NM_181844.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr17:6927473 C>T maps to NM_181844.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr17:6927899 G>A maps to NM_181844.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:6927842 A>G maps to NM_181844.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:122492807 C>T maps to NM_020993.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:122468686 C>T maps to NM_020993.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr12:122492798 G>A maps to NM_020993.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr7:72954380 G>A maps to NM_001707.3 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:72951687 C>T maps to NM_001707.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:72954299 C>T maps to NM_001707.3 Q116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:30899187 A>G maps to NM_004765.2 *218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:147084978 C>T maps to NM_004326.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr1:147090674 C>A maps to NM_004326.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr1:147096238 C>T maps to NM_004326.2 R1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:147091095 G>T maps to NM_004326.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:147096165 C>T maps to NM_004326.2 T1229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:147094246 T>C maps to NM_004326.2 H1026H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:147096051 A>G maps to NM_004326.2 A1191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr1:147091940 G>A maps to NM_004326.2 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:147092486 G>C maps to NM_004326.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:118772843 T>C maps to NM_182557.2 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:118773196 G>A maps to NM_182557.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:118773101 G>T maps to NM_182557.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:118769522 C>T maps to NM_182557.2 A1367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:118779231 G>A maps to NM_182557.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118769228 C>T maps to NM_182557.2 Q1465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118769411 G>A maps to NM_182557.2 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118771829 C>T maps to NM_182557.2 Q874Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:136597543 T>C maps to NM_014739.2 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:136589343 C>A maps to NM_014739.2 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:136599139 A>G maps to NM_014739.2 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:136600995 G>A maps to NM_014739.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr6:136599543 G>A maps to NM_014739.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:81279096 C>T maps to NM_017429.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:81320985 G>A maps to NM_017429.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:81303867 C>T maps to NM_017429.2 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr16:81314535 A>G maps to NM_017429.2 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:81320985 G>A maps to NM_017429.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:112050079 G>A maps to NM_031938.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:112071462 G>A maps to NM_031938.4 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:39911558 T>C did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:39933722 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:39932704 C>T did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr23:39933821 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:39932567 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:39934152 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:39931991 A>G did not map to a codon.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr23:39931762 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:39922030 C>A did not map to a codon.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr23:39923058 G>A did not map to a codon.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr23:39923603 G>A did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:39916462 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:39933821 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:39934411 T>C did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:39932569 C>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:39931849 T>C did not map to a codon.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr23:39932668 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:39911468 T>A did not map to a codon.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr23:39932170 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr23:39932986 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:39922089 C>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:39931666 T>A did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:39933150 G>A did not map to a codon.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr23:39921996 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:39914620 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:39933919 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:39931682 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:39932994 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:129147329 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:129159177 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:129148193 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:129149509 C>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:129147950 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:129147515 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:129159024 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:129185848 T>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:129147982 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:129185909 T>C did not map to a codon.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr23:129190050 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:129189906 G>A did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:129185951 T>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:129159090 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:129189981 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:129189947 G>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:129147950 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:129149139 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:129155064 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr23:129156939 C>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:23615882 C>T maps to NM_004327.3 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:23656167 G>A maps to NM_004327.3 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr22:23627246 G>A maps to NM_004327.3 W755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:23613759 G>A maps to NM_004327.3 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:23631788 G>A maps to NM_004327.3 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:219526162 C>T maps to NM_004328.4 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:219525790 A>C maps to NM_004328.4 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr3:197238849 G>A maps to NM_203315.2 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:197273281 T>C maps to NM_203315.2 S11S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GN-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:197241146 G>A maps to NM_203315.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:104003288 G>A maps to NM_020139.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:96730666 T>C maps to NM_000710.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:96730669 G>A maps to NM_000710.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:96730738 C>T maps to NM_000710.2 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:96707400 C>T maps to NM_000623.3 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:96707570 C>A maps to NM_000623.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:96706964 C>T maps to NM_000623.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr14:96706781 C>T maps to NM_000623.3 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:96707036 C>T maps to NM_000623.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:27695723 G>A maps to NM_001143810.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:27680042 T>C maps to NM_001143810.1 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:27679541 A>C maps to NM_001143810.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:27679426 G>A maps to NM_001143810.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:27679622 C>T maps to NM_001143810.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:70779722 C>T maps to NM_018429.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:70805291 C>T maps to NM_018429.2 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr5:70759923 G>A maps to NM_018429.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr5:70811941 T>C maps to NM_018429.2 T1568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:70751889 G>A maps to NM_018429.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr5:70818193 A>C maps to NM_018429.2 G1690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:70811959 C>G maps to NM_018429.2 G1574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:70791145 C>T maps to NM_018429.2 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:70855830 T>C maps to NM_018429.2 D2421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:70860615 T>C maps to NM_018429.2 Y2593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:70798602 C>T maps to NM_018429.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:101004413 A>C maps to NM_020836.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:101004527 G>A maps to NM_020836.3 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:18234720 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:18213470 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:18189250 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:18221756 T>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:18198716 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:18192242 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:18221768 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:18192291 A>G did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:18209165 C>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:107390837 G>A maps to NM_001080450.2 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr6:107390252 C>T maps to NM_001080450.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:107391956 C>T maps to NM_001080450.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:107389967 G>A maps to NM_001080450.2 C809C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:107391395 G>A maps to NM_001080450.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:107390933 C>T maps to NM_001080450.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:107391161 G>A maps to NM_001080450.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:107390479 G>A maps to NM_001080450.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr6:107391626 G>A maps to NM_001080450.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:42119702 C>T maps to NM_207406.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:42119656 G>A maps to NM_207406.3 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:49208297 G>T maps to NM_024603.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:49201944 T>C maps to NM_024603.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr1:49208339 G>A maps to NM_024603.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr1:49201941 G>A maps to NM_024603.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:49201992 G>A maps to NM_024603.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:49224923 C>T maps to NM_024603.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:49224932 G>A maps to NM_024603.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:13541862 C>T maps to ENST00000396900 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:13481459 C>T maps to ENST00000396900 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr10:13523094 G>A maps to ENST00000396900 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:13523007 C>T maps to ENST00000396900 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:13523007 C>T maps to ENST00000396900 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:13541999 G>T maps to ENST00000396900 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:61730440 C>A maps to NM_001139443.1 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:12866953 G>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:12866251 A>G maps to NM_017682.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:12866520 A>G maps to NM_017682.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:12865757 G>A maps to NM_017682.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:70066742 T>C maps to NM_032735.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:70070962 G>A maps to NM_032735.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr12:70049316 G>A maps to NM_032735.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:45251766 G>A maps to NM_153274.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:45250929 G>A maps to NM_153274.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:45250968 G>T maps to NM_153274.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:102318122 A>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:102317839 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:102318160 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:102564732 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:102564885 G>A did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr23:102471358 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:101409128 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:101409173 C>T did not map to a codon.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr20:17475309 C>A maps to NM_001195.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr20:17475018 G>A maps to NM_001195.3 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:133191256 C>T maps to NM_003571.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:133119256 C>T maps to NM_003571.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:152770092 T>C did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr23:152773818 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:102004165 G>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:102004718 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:102005016 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:102005118 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:102004813 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:102005179 A>G did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:102004546 A>G did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:102004034 G>C did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:102005401 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:102004166 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:65494006 T>C maps to NM_152414.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:65494210 C>T maps to NM_152414.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr8:65494390 G>A maps to NM_152414.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:65493460 G>A maps to NM_152414.3 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:65493745 G>A maps to NM_152414.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:65493418 C>T maps to NM_152414.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:65494178 C>T maps to NM_152414.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:61637535 C>T maps to NM_080606.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:61637727 G>A maps to NM_080606.3 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:5023159 G>A maps to NM_003670.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:5024983 C>T maps to NM_003670.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr12:26277451 C>T maps to NM_030762.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:78416204 C>T maps to NM_001713.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:78417156 C>T maps to NM_001713.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:78379532 C>T maps to NM_017614.4 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:60549122 G>A maps to NM_001080512.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:60273019 G>A maps to NM_001080512.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:60588641 C>T maps to NM_001080512.1 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr10:60546750 C>T maps to NM_001080512.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:60562875 T>C maps to NM_001080512.1 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr10:60588554 G>A maps to NM_001080512.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:60558306 T>G maps to NM_001080512.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:60588647 G>A maps to NM_001080512.1 W974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr10:60546813 G>A maps to NM_001080512.1 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr10:60566911 T>A maps to NM_001080512.1 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:32481125 A>G maps to NM_001714.2 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:32458628 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr12:32458845 C>T maps to NM_001714.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:95481492 G>A maps to NM_001003800.1 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:95491461 C>T maps to NM_001003800.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:95482662 C>T maps to NM_001003800.1 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:95481195 C>T maps to NM_001003800.1 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:95481240 G>A maps to NM_001003800.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:95477522 G>T maps to NM_001003800.1 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:95481294 G>T maps to NM_001003800.1 C544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:95481858 C>T maps to NM_001003800.1 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:127821514 C>T maps to NM_139343.1 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr2:127864486 C>G maps to NM_139343.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:127808728 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:127808728 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:51693444 G>A maps to NM_016293.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:22488002 C>T maps to NM_018688.4 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:102248748 G>A maps to NM_001166.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:102195542 C>T maps to NM_182962.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr11:102196268 G>A maps to NM_182962.1 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:76219622 T>C maps to NM_001012271.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr2:32724718 C>T maps to NM_016252.3 A2858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:32640461 G>A maps to NM_016252.3 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:32750028 G>T maps to NM_016252.3 E3900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:32824934 C>T maps to NM_016252.3 R4654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:32656152 C>T maps to NM_016252.3 T1081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr2:32715110 C>G maps to NM_016252.3 S2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:32658759 T>C maps to NM_016252.3 C1099C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:32800337 T>C maps to NM_016252.3 G4420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:32658786 C>T maps to NM_016252.3 F1108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:32740782 G>A maps to NM_016252.3 A3765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:32641160 T>C maps to NM_016252.3 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr2:32703758 G>A maps to NM_016252.3 V2375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:32626305 C>A maps to NM_016252.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr2:32750042 G>A maps to NM_016252.3 A3904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr20:61869318 C>T maps to NM_139317.1 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr19:53793014 C>A maps to NM_033341.3 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr19:53793269 G>A maps to NM_033341.3 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr20:36147486 G>C maps to NM_006698.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:11420557 C>T maps to ENST00000427279 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:11400774 G>A maps to ENST00000427279 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr8:11406592 T>C maps to ENST00000427279 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr8:11400774 G>A maps to ENST00000427279 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:91295077 A>G maps to NM_000057.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91292794 A>G maps to NM_000057.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91293253 T>G maps to NM_000057.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:91358409 T>C maps to NM_000057.2 T1385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:91292842 G>A maps to NM_000057.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:91333929 C>T maps to NM_000057.2 R959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:28601208 G>A maps to NM_000386.2 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr10:97983644 C>T maps to NM_013314.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:97987262 G>A maps to NM_013314.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:97987265 G>A maps to NM_013314.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:97987265 G>A maps to NM_013314.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:56113372 C>T maps to NM_001487.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:43846579 C>T maps to NM_000712.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:43830922 C>T maps to NM_000712.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:43840109 C>T maps to NM_000712.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:43843447 T>C did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:169338788 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr1:169349823 T>C maps to NM_003666.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:40384005 G>A maps to NM_001003940.1 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr10:22617554 C>T maps to NM_005180.6 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:22051619 C>T maps to NM_006129.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:22066961 C>T maps to NM_006129.4 C860C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:22053002 C>T maps to NM_006129.4 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr8:22064884 C>T maps to NM_006129.4 R811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:22054886 C>T maps to NM_006129.4 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr8:22037328 T>C maps to NM_006129.4 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:22064889 C>T maps to NM_006129.4 D812D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:22064991 G>A maps to NM_006129.4 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr8:22069238 T>G maps to NM_006129.4 *987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:22034148 C>A maps to NM_006129.4 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:69093326 T>C maps to NM_014482.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr2:69093086 G>A maps to NM_014482.1 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:69092786 G>A maps to NM_014482.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:69092996 G>A maps to NM_014482.1 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:50659439 G>A did not map to a codon.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr23:50659158 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:50659506 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:6759222 C>T maps to NM_001200.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:6759450 C>T maps to NM_001200.2 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:81967099 C>T maps to NM_001201.2 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr4:81967171 T>A maps to NM_001201.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:54417277 C>T maps to NM_130850.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:54417454 G>A maps to NM_130850.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:54418805 G>T maps to NM_130850.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr6:55659182 A>C maps to NM_021073.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr6:55639027 G>A maps to NM_021073.2 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr6:55638952 C>T maps to NM_021073.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr6:55638912 G>A maps to NM_021073.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:7727817 C>T maps to NM_001718.4 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:7727442 G>A maps to NM_001718.4 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr6:7880470 G>A maps to NM_001718.4 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:7727781 C>A maps to NM_001718.4 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:7862639 C>T maps to NM_001718.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr20:55746146 C>T maps to NM_001719.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr1:40253911 G>A maps to NM_001720.3 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:33945296 C>T maps to NM_133468.3 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:34097735 T>C maps to NM_133468.3 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:34118649 G>A maps to NM_133468.3 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr7:33946428 G>A did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr7:34118718 G>C maps to NM_133468.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr7:33976944 C>G maps to NM_133468.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr7:34118784 G>C maps to NM_133468.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8209-01A-11D-2340-08 chr7:34118718 G>C maps to NM_133468.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr7:34182862 T>C maps to NM_133468.3 C589C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:88676972 G>A maps to NM_004329.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr10:88681424 G>T maps to NM_004329.2 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr10:88683356 C>T maps to NM_004329.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:96025676 C>T maps to ENST00000440890 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:96035906 T>C maps to ENST00000440890 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:203384849 G>A maps to NM_001204.6 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:203383559 C>T maps to NM_001204.6 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:203383648 C>T maps to NM_001204.6 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr2:203383564 T>A maps to NM_001204.6 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:203329535 G>A maps to NM_001204.6 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:203242244 G>A maps to NM_001204.6 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:203407104 C>T maps to NM_001204.6 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:203384917 C>T maps to NM_001204.6 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:203329664 G>A maps to NM_001204.6 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:203384913 A>G maps to NM_001204.6 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:43326399 G>A maps to NM_014753.3 E1235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:43319099 G>A maps to NM_014753.3 A1108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:43318711 C>T maps to NM_014753.3 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr10:43312890 A>G maps to NM_014753.3 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:43316062 C>T maps to NM_014753.3 I959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:43292209 T>C maps to NM_014753.3 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:43287076 T>G maps to NM_014753.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:43318579 T>A maps to NM_014753.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:43326423 G>A maps to NM_014753.3 E1243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:15543415 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:15540631 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:15560310 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:15555365 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:15526523 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr15:83926568 G>A maps to NM_001717.3 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:83935707 G>A maps to NM_001717.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr15:83932805 T>C maps to NM_001717.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:83932511 C>T maps to NM_001717.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:83932175 G>A maps to NM_001717.3 C609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr15:83935596 G>A maps to NM_001717.3 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr15:83935596 G>A maps to NM_001717.3 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:16435989 G>A maps to NM_017637.5 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:16436811 G>T maps to NM_017637.5 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:16583062 T>C maps to NM_017637.5 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr9:16436585 G>A maps to NM_017637.5 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:16419574 C>T maps to NM_017637.5 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:16419598 G>A maps to NM_017637.5 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr9:16419499 G>A maps to NM_017637.5 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:172585848 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:59963458 A>T maps to NM_004330.2 Y331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:133787388 C>T maps to NM_004052.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:112969474 C>T maps to ENST00000273395 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr3:112969654 C>T maps to ENST00000273395 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:112998719 C>T maps to ENST00000273395 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:112998785 C>T maps to ENST00000273395 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:112991964 C>T maps to ENST00000273395 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr3:112998785 C>T maps to ENST00000273395 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:112991491 C>T maps to ENST00000273395 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:112969432 G>A maps to ENST00000273395 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:13603591 G>A maps to NM_148894.2 S1644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:13603609 G>A maps to NM_148894.2 I1638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:13604572 G>T maps to NM_148894.2 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr4:13606645 T>C maps to NM_148894.2 E626E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr4:13617044 C>T maps to NM_148894.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:13579111 C>A did not map to a codon.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr4:13602961 A>G maps to NM_148894.2 I1854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:13602538 T>C maps to NM_148894.2 E1995E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:13601692 G>A maps to NM_148894.2 G2277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:13601770 G>A maps to NM_148894.2 D2251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:242501856 G>A maps to NM_032515.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr2:198641827 G>A maps to NM_197970.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:134346582 T>C maps to NM_001724.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:3127584 C>T maps to NM_004332.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:3137677 C>A maps to NM_004332.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr20:31601628 C>T maps to NM_025227.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr22:32831744 C>T maps to NM_174932.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:31624278 C>T maps to NM_174897.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:31619461 G>A maps to NM_174897.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:220246278 C>A maps to NM_006085.4 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:65899997 G>A maps to ENST00000321892 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:65905704 T>C maps to ENST00000321892 N1066N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr17:65899994 A>G maps to ENST00000321892 Q1004Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:65889598 C>T maps to ENST00000321892 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:65889727 C>T maps to ENST00000321892 N892N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:65900945 G>A maps to ENST00000321892 S1060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:65942074 C>T maps to ENST00000321892 S2543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:140453127 G>A maps to NM_004333.4 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:140439718 G>A maps to NM_004333.4 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:140534519 T>C maps to NM_004333.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:140501255 A>G maps to NM_004333.4 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:140534453 T>C maps to NM_004333.4 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:140534519 T>C maps to NM_004333.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:140494167 T>C maps to NM_004333.4 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:112120994 G>A maps to NM_006768.3 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:112110575 A>G maps to NM_006768.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:112119463 A>G maps to NM_006768.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr12:112119583 C>T maps to NM_006768.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:41228548 A>G maps to ENST00000471181 S1502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:41219625 T>G maps to ENST00000471181 T1713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr17:41209094 G>A maps to ENST00000471181 R1773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr13:32972744 C>G maps to NM_000059.3 V3365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:32944627 G>A maps to NM_000059.3 S2807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr13:32911314 G>C maps to NM_000059.3 V941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:32914521 C>A maps to NM_000059.3 V2010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:32906994 T>C maps to NM_000059.3 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr13:32912229 T>C maps to NM_000059.3 N1246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:32913066 T>C maps to NM_000059.3 H1525H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:32914984 T>C maps to NM_000059.3 L2165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:32914236 G>A maps to NM_000059.3 T1915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:32915238 C>T maps to NM_000059.3 A2249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr13:32937422 C>A maps to NM_000059.3 S2695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:32913861 A>G maps to NM_000059.3 V1790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:32913951 C>T maps to NM_000059.3 C1820C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:154305517 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:154348416 C>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:50217866 G>A maps to ENST00000342989 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:50216753 G>A maps to ENST00000342989 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr22:50217323 G>A maps to ENST00000342989 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr22:50216630 C>T maps to ENST00000342989 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:50192335 T>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:32942488 C>T maps to ENST00000395289 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:32942266 C>T maps to ENST00000395289 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:136913402 G>A maps to NM_007371.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr9:136907049 G>C maps to NM_007371.3 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:136913252 G>A maps to NM_007371.3 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:136901427 G>A maps to NM_007371.3 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:136901430 G>A maps to NM_007371.3 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr9:136907001 C>T maps to NM_007371.3 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:136913402 G>A maps to NM_007371.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:15367879 C>T maps to NM_058243.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:15383720 G>A maps to NM_058243.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr19:15379808 T>A maps to NM_058243.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:15383772 C>T maps to NM_058243.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:15365023 C>T maps to NM_058243.2 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:15376437 G>A maps to NM_058243.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:15354287 G>A maps to NM_058243.2 N864N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr16:50354622 C>A maps to NM_001173984.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:50354204 C>T maps to NM_001173984.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:50357599 C>T maps to NM_001173984.2 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:50359753 C>T maps to NM_001173984.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:50384078 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:137492898 A>G maps to NM_006696.3 *952R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr5:137485476 G>A maps to NM_139199.1 Q1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:137486466 A>G maps to NM_139199.1 C1029C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:865541 G>A maps to NM_001009877.2 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:884058 G>A maps to NM_001009877.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:92428389 C>T maps to ENST00000347608 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:92457861 C>T maps to ENST00000347608 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:92469984 G>A maps to ENST00000347608 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:92445139 G>A maps to ENST00000347608 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:92443768 G>A maps to ENST00000347608 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr1:92467669 G>A maps to ENST00000347608 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr1:92442752 C>T maps to ENST00000347608 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:105688093 G>A maps to NM_001519.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:105683990 C>T maps to NM_001519.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:37702450 G>A maps to NM_018310.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr8:37704430 G>T maps to NM_018310.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:37704628 C>T maps to NM_018310.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:37702232 T>C maps to NM_018310.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:125497153 C>T maps to NM_080626.5 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr5:34915866 G>A maps to NM_018321.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:34922809 C>T maps to NM_018321.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:66109070 G>A maps to NM_001024957.1 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr14:36302312 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:36302196 C>T maps to NM_032352.3 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:166779544 C>T maps to ENST00000360961 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr6:166778940 C>T maps to ENST00000360961 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:9786076 G>C maps to NM_001003694.1 G935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr3:9781150 G>A maps to NM_001003694.1 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:9781015 T>C maps to NM_001003694.1 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr3:9780997 C>T maps to NM_001003694.1 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:9780730 C>T maps to NM_001003694.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr3:9788873 G>C maps to NM_001003694.1 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:9780730 C>T maps to NM_001003694.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:9782460 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:9780814 C>A maps to NM_001003694.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:135574169 T>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:135574495 A>G did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr23:135572289 A>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:55800908 A>T maps to NM_032430.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:55805593 T>G maps to NM_032430.1 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:55813017 A>C maps to NM_032430.1 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:55800868 C>T maps to NM_032430.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:1471020 C>T maps to NM_003957.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:40670382 C>T maps to NM_018963.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr21:40608630 G>A maps to NM_018963.3 R886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr21:40571562 A>G maps to NM_018963.3 C1593C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr23:79975124 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:79980462 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:79932588 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:79951475 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:79948490 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:79978163 A>T did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:79959052 C>A did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:79978188 A>C did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:79962955 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:80001090 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:79978258 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:79955466 T>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:79943585 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:79978129 G>A did not map to a codon.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr23:79939564 C>A did not map to a codon.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr23:79932137 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:79991558 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:79965050 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:79955508 T>C did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:79942371 A>C did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:79978217 C>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:32834082 G>A maps to NM_001143888.1 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:32842163 G>A maps to NM_001143888.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:580688 C>T maps to NM_001728.2 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:49694977 C>T maps to NM_003458.3 S2663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:49688508 G>A maps to NM_003458.3 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:49689427 C>T maps to NM_003458.3 D813D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr3:49688121 G>A maps to NM_003458.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:49699105 C>T maps to NM_003458.3 D3276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:49690675 T>G maps to NM_003458.3 Y1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr3:49698361 C>T maps to NM_003458.3 P3028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr3:49694710 C>T maps to NM_003458.3 P2574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:49700780 C>T maps to NM_003458.3 S3730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr3:49691692 G>A maps to NM_003458.3 Q1568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr3:49689340 C>T maps to NM_003458.3 D784D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr3:49688127 C>A maps to NM_003458.3 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:49699942 T>C maps to NM_003458.3 R3555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:49690306 G>A maps to NM_003458.3 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr3:49695568 C>T maps to NM_003458.3 A2860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:49699543 C>A maps to NM_003458.3 Y3422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:49700702 G>A maps to NM_003458.3 E3704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:55472852 C>T maps to NM_057176.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:55464927 G>A maps to NM_057176.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr4:15733453 A>C maps to ENST00000382346 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:17516267 C>T maps to NM_004335.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr11:122848365 G>A maps to NM_001098169.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:122848476 G>A maps to NM_001098169.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:122849971 C>T maps to NM_001098169.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:122848566 C>T maps to NM_001098169.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr11:122848401 G>A maps to NM_001098169.1 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:93749218 G>A maps to NM_003972.2 T912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:93726432 G>A maps to NM_003972.2 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:93744028 C>T maps to NM_003972.2 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:93740221 T>G maps to NM_003972.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:93786975 G>A maps to NM_003972.2 A1775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:93784637 T>C maps to NM_003972.2 D1663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:93749218 G>A maps to NM_003972.2 T912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:93756172 T>C maps to NM_003972.2 S1119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:93768863 G>A maps to NM_003972.2 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:108011204 C>T maps to NM_001018072.1 H741H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr12:108010927 G>A maps to NM_001018072.1 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:107713787 C>T maps to NM_001018072.1 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:3640236 C>T maps to NM_032444.2 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:3640515 C>T maps to NM_032444.2 Q1041Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:3632366 G>A maps to NM_032444.2 G1827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:3644516 G>A maps to NM_032444.2 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:3652116 A>G did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr16:3639114 C>T maps to NM_032444.2 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:3640548 C>T maps to NM_032444.2 P1030P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:3640611 G>A maps to NM_032444.2 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:3640332 C>T maps to NM_032444.2 E1102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr10:124089066 T>C maps to ENST00000368994 R329R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4184-01A-01D-1126-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-4370-01A-01D-1158-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CG-4460-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:72352846 C>T maps to ENST00000440684 Q445*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D7-A4YU-01A-21D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr17:72353344 C>T maps to ENST00000440684 R611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:72356373 G>A maps to NM_001080466.1 A32A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-A4G8-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MX-A5UJ-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-VQ-A8DZ-01A-11D-A364-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:72353593 G>T maps to ENST00000440684 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:1986915 G>A maps to NM_017797.3 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:1997458 G>A maps to NM_017797.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr20:11904023 G>T maps to NM_014962.2 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr20:11900475 T>A maps to NM_014962.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:11903866 C>T maps to NM_014962.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:105716186 C>T maps to NM_033271.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:105716435 C>T maps to NM_033271.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:105716568 C>T maps to NM_033271.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:93761248 G>A maps to NM_001002860.2 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:93717917 C>T maps to NM_001002860.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:93762391 A>G maps to NM_001002860.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:93723552 G>A maps to NM_001002860.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:92595318 C>T maps to NM_183242.3 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:38562048 G>T maps to NM_052893.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr6:38561910 C>T maps to NM_052893.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:38565762 G>A maps to NM_052893.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:38160321 G>A maps to NM_052893.1 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:75695291 C>A maps to NM_001729.2 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:15686553 G>A maps to NM_000060.2 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:15686847 C>T maps to NM_000060.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:72798356 A>G maps to NM_001037637.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr5:72798942 G>C did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:52551841 A>G maps to NM_152265.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:52530501 A>C maps to NM_152265.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:52551817 T>C maps to NM_152265.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:92539221 C>T maps to NM_001731.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr21:18966419 T>C maps to NM_001130914.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr11:111365982 A>G maps to NM_017589.2 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100608209 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:100613618 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:100613406 T>C did not map to a codon.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr23:100629565 T>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:100625040 G>A did not map to a codon.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr23:100615076 C>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:112198428 C>T maps to NM_181780.3 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:26501974 C>T maps to NM_001732.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:26508301 T>A maps to NM_001732.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:26392963 C>T maps to NM_001197237.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:26384102 C>G maps to NM_001197237.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:26392759 A>G maps to NM_001197237.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:26393113 T>C maps to NM_001197237.1 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:26388403 C>T maps to NM_001197237.1 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:26385501 C>T maps to NM_001197237.1 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:26390935 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:26392904 C>A maps to NM_001197237.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr6:26413838 C>T maps to NM_007048.5 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr6:26410258 T>C maps to NM_007048.5 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:26413634 A>G maps to NM_007048.5 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:26370757 C>T maps to NM_001197246.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:26370652 G>A maps to NM_001197246.1 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:26452044 T>C maps to NM_006994.4 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:26448536 G>A maps to NM_006994.4 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:26452152 C>T maps to NM_006994.4 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:26448644 C>T maps to NM_006994.4 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:32364032 A>G maps to ENST00000468270 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:180377102 C>T maps to NM_001040462.2 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:180475168 C>T maps to NM_152547.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:180486591 G>A maps to NM_152547.4 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:180485373 T>C maps to NM_152547.4 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:180475227 C>T maps to NM_152547.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:180486840 C>T maps to NM_152547.4 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:180486693 C>T maps to NM_152547.4 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr5:180472557 C>G maps to NM_152547.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:103292821 G>T maps to NM_033637.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:103294453 G>A maps to NM_033637.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:103221769 C>T maps to NM_033637.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr10:103292068 G>A maps to NM_033637.2 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr2:111415163 A>T maps to NM_004336.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:40504750 G>T maps to ENST00000412359 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:124914612 G>A maps to NM_004725.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr11:116619287 G>C maps to NM_032725.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr11:116643656 G>C maps to NM_032725.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:99015148 C>T maps to NM_003910.3 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr7:99015076 A>G maps to NM_003910.3 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:105577342 G>A maps to NM_007073.4 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:41900302 C>T maps to NM_004053.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:56389880 A>G maps to NM_004758.2 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:56389687 G>A maps to NM_004758.2 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:56386099 G>A maps to NM_004758.2 S1511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:56389307 G>A maps to NM_004758.2 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:56386606 G>A maps to NM_004758.2 D1342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:16714184 C>T maps to NM_014038.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr7:16722402 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:16705076 G>A maps to NM_014038.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr10:63520672 C>A maps to NM_173554.2 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr10:63441052 C>G maps to NM_173554.2 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr10:77795864 G>C maps to NM_032024.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:115917414 A>G maps to NM_018017.2 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:115896979 G>A maps to NM_018017.2 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:115917402 G>A maps to NM_018017.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:121607132 A>G maps to NM_024834.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:121602087 G>A maps to NM_024834.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:98742562 C>A maps to NM_015652.2 C472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr10:98744131 C>T maps to NM_015652.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:98742989 G>T maps to NM_015652.2 G615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:98744566 G>A maps to NM_015652.2 T1140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr10:98744029 A>G maps to NM_015652.2 E961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:98743673 A>T maps to NM_015652.2 K843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr10:98742709 A>G maps to NM_015652.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr10:98742232 C>A maps to NM_015652.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr10:98742241 A>G maps to NM_015652.2 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:124457677 T>C maps to NM_001010912.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr10:124457428 G>A maps to NM_001010912.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr10:96972613 G>C did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:127412447 A>G maps to ENST00000356792 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:127424223 C>T maps to ENST00000356792 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:127438078 C>T maps to ENST00000356792 C1074C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:127436238 G>A maps to ENST00000356792 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr10:127429071 A>C maps to ENST00000356792 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:127452031 C>T maps to ENST00000356792 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr10:21804402 T>C maps to NM_207371.3 T783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:21805319 G>A maps to NM_207371.3 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr10:21806718 C>T maps to NM_207371.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:21804936 A>G maps to NM_207371.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:5788413 G>A maps to NM_017782.4 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:5788344 G>A maps to NM_017782.4 Q987Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:5773003 C>T maps to NM_017782.4 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:5798694 G>A maps to NM_017782.4 L2242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr10:5766450 G>A maps to NM_017782.4 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:5800956 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:5791053 G>A maps to NM_017782.4 E1890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:5791572 G>A maps to NM_017782.4 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:5788818 G>A maps to NM_017782.4 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:5769036 G>A maps to NM_017782.4 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:102748164 G>A maps to NM_021830.4 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:102748966 C>T maps to NM_021830.4 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr10:102748497 T>C maps to NM_021830.4 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:104569764 C>T maps to NM_001083913.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:72539498 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:72539370 A>G maps to NM_152710.2 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:72531166 C>A maps to NM_152710.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:99968818 T>C maps to ENST00000314594 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:99991420 T>C maps to ENST00000314594 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr10:99969330 T>A maps to ENST00000314594 L487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:120489878 C>T maps to NM_153810.4 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:11908666 G>A maps to NM_153256.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr10:73521514 G>A maps to NM_022153.1 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:73521631 G>A maps to NM_022153.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr10:99350028 C>T maps to NM_001009997.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:33018338 C>T maps to ENST00000375025 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:32983819 A>G maps to ENST00000375025 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:50531159 T>C maps to NM_001135196.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr10:50532584 C>T maps to NM_001135196.1 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr10:50530847 G>A maps to NM_001135196.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:50532450 G>T maps to NM_001135196.1 G621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:50532146 C>A maps to NM_001135196.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:50227736 G>A maps to NM_001031746.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:50315771 C>T maps to NM_001031746.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:50315741 C>T maps to NM_001031746.3 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr10:50315891 G>A maps to NM_001031746.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:50315660 G>A maps to NM_001031746.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:103766309 C>T maps to NM_024541.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:103716444 G>A maps to NM_024541.2 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:105885350 T>C maps to ENST00000336358 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:105967429 C>T maps to ENST00000389588 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr10:115534092 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:124691942 T>G maps to NM_024942.3 *446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:124713678 C>A maps to NM_024942.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:128192843 G>A maps to NM_001004298.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr10:128192683 C>T maps to NM_001004298.2 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr10:128193339 C>T maps to NM_001004298.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:134742983 C>T maps to NM_173572.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:134743283 C>T maps to ENST00000368586 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr10:118084561 C>T maps to NM_198515.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:85936260 G>A maps to NM_207373.2 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr11:111750325 C>T maps to NM_022761.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr11:61557966 G>A maps to NM_014206.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:61558068 G>A maps to NM_014206.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr11:8951046 G>A maps to NM_020643.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr11:64876214 C>T maps to NM_013265.2 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:64875962 C>T maps to NM_013265.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr11:64863868 G>A maps to NM_013265.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:68031217 C>T maps to NM_022338.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:68030282 A>C maps to NM_022338.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:76207358 A>G maps to ENST00000393457 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:558938 G>A maps to NM_173573.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:33565469 G>A maps to ENST00000389726 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:33564425 C>G maps to ENST00000389726 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:33565322 A>G maps to ENST00000389726 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr11:33667476 G>A maps to ENST00000389726 S1594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:33667449 C>T maps to ENST00000389726 Y1585Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:33565883 T>C maps to ENST00000389726 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:33565124 G>A maps to ENST00000389726 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:6231597 C>T maps to NM_173525.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:6231117 A>G maps to NM_173525.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:6232265 C>T maps to NM_173525.2 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:128773395 G>T maps to NM_145013.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:30358284 G>A maps to NM_152316.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:47183173 C>T maps to NM_001003677.1 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr11:46958380 C>T maps to NM_001003677.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:71822200 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:71822258 G>A maps to NM_014042.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:111796698 G>T maps to NM_080659.2 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:93492963 G>A maps to ENST00000354421 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:122756902 T>C did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr11:122756769 C>T maps to NM_024806.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr11:122805453 C>G maps to NM_024806.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr11:122817500 G>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:122829966 C>T maps to NM_024806.2 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:122756889 C>T maps to NM_024806.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:122756781 C>T maps to NM_024806.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr11:122805640 G>T maps to NM_024806.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:122805597 G>A maps to NM_024806.2 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:108277567 A>G maps to NM_152587.3 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:108277839 G>A maps to NM_152587.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:61254448 C>T maps to NM_145017.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr11:61257334 C>T maps to NM_145017.2 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:61254060 T>C maps to NM_145017.2 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:65685481 G>A maps to NM_001135635.1 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:101953824 T>G maps to NM_032930.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:86048430 C>T maps to NM_016401.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:86048521 C>T maps to NM_016401.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr11:36654981 A>G maps to NM_138787.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:36669605 C>T maps to NM_138787.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66555667 G>A maps to ENST00000360962 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:82644689 A>G maps to NM_145018.3 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr11:82645280 T>C maps to NM_145018.3 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:63594574 T>C maps to NM_138471.1 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:63585421 C>T maps to NM_138471.1 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:63594445 C>T maps to NM_138471.1 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:64717263 A>T maps to NM_001037225.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:64717890 G>A maps to NM_001037225.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr11:109294781 C>T maps to NM_207645.3 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr11:109294442 C>T maps to NM_207645.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr11:61541498 C>T maps to NM_001127392.1 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:61543859 C>A maps to NM_001127392.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:61533178 C>T maps to NM_001127392.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:61539202 G>A maps to NM_001127392.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:61533537 A>G maps to NM_001127392.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr11:61548670 C>T maps to NM_001127392.1 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr11:45928155 G>C maps to NM_001080446.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:45928441 C>T maps to NM_001080446.2 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr12:27078741 G>C maps to NM_018164.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:91348141 G>A maps to NM_152638.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:91348378 C>T maps to NM_152638.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr12:91347820 G>A maps to NM_152638.2 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:91348306 G>A maps to NM_152638.2 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr12:91348075 G>A maps to NM_152638.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:91348254 C>A maps to NM_152638.2 G89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:91348465 G>A maps to NM_152638.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:91347925 G>A maps to NM_152638.2 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:110924486 G>A maps to NM_013300.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:82871070 A>G maps to NM_032230.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:110206267 C>T maps to NM_032829.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:110206228 G>A maps to NM_032829.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:32136018 C>T maps to NM_018169.3 N710N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:32138394 G>A maps to NM_018169.3 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:32134185 T>C maps to NM_018169.3 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr12:32138388 C>T maps to NM_018169.3 S1500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr12:32136201 C>T maps to NM_018169.3 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:4599041 A>T maps to NM_020374.2 Y530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:40076661 G>A maps to NM_001031748.2 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr12:40114806 C>T maps to NM_001031748.2 C571C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:40040224 T>C maps to NM_001031748.2 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:103696164 C>T maps to NM_001099336.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:103696140 G>A maps to NM_001099336.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:121448637 G>A maps to NM_022895.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:121448670 G>A maps to NM_022895.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr12:52470725 C>A maps to NM_021934.4 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:52467514 G>A maps to NM_021934.4 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:105388284 G>A maps to NM_152318.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:102572377 T>C maps to NM_017915.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr12:102589957 A>G maps to NM_017915.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:117158241 G>A maps to NM_024738.1 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:117158199 G>A maps to NM_024738.1 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:4460521 C>T maps to NM_020375.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:88380179 C>T maps to NM_152589.1 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:88390244 A>G maps to NM_152589.1 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr12:88379765 C>T maps to NM_152589.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:112657287 G>A maps to NM_001109662.2 R2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:112721040 G>A maps to NM_001109662.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:112696394 C>T maps to NM_001109662.2 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:112688018 C>T maps to NM_001109662.2 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:112638473 G>A maps to NM_001109662.2 V2673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:112721040 G>A maps to NM_001109662.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:112674830 G>A maps to NM_001109662.2 R1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr12:112630953 G>A maps to NM_001109662.2 S2827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:112622701 G>A maps to NM_001109662.2 R3184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:112630520 G>A maps to NM_001109662.2 L2873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:112690239 T>C maps to NM_001109662.2 T1008T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:112646327 G>A maps to NM_001109662.2 S2486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:112654719 C>T maps to NM_001109662.2 P2242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:6806942 C>T maps to NM_153685.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:64678529 T>C maps to NM_001170633.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:64784108 G>T maps to NM_001170633.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr12:64746806 C>T maps to NM_001170633.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:14976430 T>C maps to NM_175874.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:97098549 T>C maps to ENST00000342887 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:97051677 G>T maps to ENST00000342887 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr12:97158012 A>C maps to ENST00000342887 R1134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr12:97082747 G>A maps to ENST00000342887 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:80633159 C>T maps to NM_173591.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr12:80733020 C>G maps to NM_173591.3 S1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:80722858 A>G maps to NM_173591.3 T1427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:80633219 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:80722525 T>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:123738250 T>G maps to NM_001143905.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr12:64588302 C>T maps to ENST00000311915 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:64609627 G>A maps to ENST00000311915 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr12:64587771 G>C maps to ENST00000311915 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:64587876 C>T maps to ENST00000311915 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:31820593 T>A maps to NM_001135864.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr12:31820773 A>T maps to NM_001135864.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:31819051 G>T maps to NM_001135864.1 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:93100871 C>T maps to NM_001037671.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:25148943 G>A maps to NM_001101339.1 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr12:25148832 C>T maps to NM_001101339.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:111980579 C>T maps to NM_152324.1 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr13:46930567 A>C maps to NM_025113.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr13:46924337 C>A maps to NM_025113.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:46933763 G>A maps to NM_025113.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:46917573 C>T maps to NM_025113.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:39585609 C>A maps to NM_025138.3 S909S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:39588011 G>A maps to NM_025138.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:39587654 T>C maps to NM_025138.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:39586877 G>A maps to NM_025138.3 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:39586970 G>A maps to NM_025138.3 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr13:39588423 G>C maps to NM_025138.3 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr13:39587975 C>T maps to NM_025138.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:103418897 T>C maps to NM_138779.3 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:103420631 T>C maps to NM_138779.3 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr13:103419820 T>C maps to NM_138779.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:103419620 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr13:113030764 T>G maps to NM_145248.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr13:113030731 C>A maps to NM_145248.4 C11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:44463068 C>T maps to NM_153218.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:44463028 A>G maps to NM_153218.2 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr13:44458067 C>T maps to NM_153218.2 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:31495958 C>T maps to NM_032849.3 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:31495897 G>A maps to NM_032849.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:73327857 G>T maps to ENST00000377815 G565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr13:73303149 T>A maps to ENST00000377815 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:37269457 C>T maps to NM_203451.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr13:37269502 C>G maps to NM_203451.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:37269460 C>T maps to NM_203451.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:57085367 T>C maps to NM_017799.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:57070531 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:57072361 C>T maps to NM_017799.3 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:90784356 C>T maps to NM_017970.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:90754928 C>T maps to NM_017970.2 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:90755330 C>T maps to NM_017970.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:90752829 G>A maps to NM_017970.2 D1055D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:50101027 G>A maps to NM_018139.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:50100340 G>T maps to NM_018139.2 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:57938105 G>A maps to NM_018168.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:45711563 G>A maps to NM_018353.4 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr14:45716198 G>A maps to NM_018353.4 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:45711578 C>T maps to NM_018353.4 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr14:74824118 C>T maps to NM_018228.2 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:74824568 G>A maps to NM_018228.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:74824124 C>T maps to NM_018228.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:74825384 G>A maps to NM_018228.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:76620991 C>T maps to NM_017926.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr14:76633038 T>C maps to NM_017926.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr14:76621075 C>T maps to NM_017926.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:96851948 C>T maps to NM_016472.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:60582090 G>A maps to ENST00000404681 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:60581847 T>C maps to ENST00000404681 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr14:50576419 C>T maps to NM_024558.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:77873100 C>T maps to NM_001113475.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:59950878 G>T maps to NM_144581.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr14:78183894 A>G maps to NM_031210.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:91691155 C>T maps to NM_001102368.1 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr14:52471143 A>G maps to NM_016039.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:77302605 C>T maps to NM_194287.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:77297612 A>G maps to NM_194287.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:73959332 G>A maps to NM_024644.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:77844360 A>G maps to NM_001010860.1 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr14:77844276 G>A maps to NM_001010860.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:77844528 A>G maps to NM_001010860.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr14:99182680 A>G maps to NM_182560.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr14:99182659 T>C maps to NM_182560.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:76542993 G>A maps to NM_052873.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:76549610 G>A maps to NM_052873.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:105054177 C>T maps to NM_001008404.1 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:24771313 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr14:24771557 G>A maps to NM_174913.1 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:58563559 G>T maps to ENST00000438670 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:58604792 G>A maps to ENST00000438670 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr14:58605155 G>T maps to ENST00000438670 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:60903607 A>C maps to NM_174978.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr14:60923729 C>T maps to NM_174978.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr14:60903741 C>A maps to NM_174978.2 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:60938345 A>G maps to NM_174978.2 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:77492632 G>A maps to NM_024496.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:77492224 C>T maps to NM_024496.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr14:77491777 C>G maps to NM_024496.2 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:74186093 T>C maps to NM_001043318.1 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:74203799 G>A maps to NM_001043318.1 D550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:74205490 C>T maps to NM_001043318.1 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:74206624 G>T maps to NM_001043318.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:74206173 G>A maps to NM_001043318.1 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:74514755 T>C maps to NM_025057.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:95922034 G>A maps to NM_152592.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:95923564 G>A maps to NM_152592.3 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:95884237 G>A maps to NM_152592.3 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:95934205 G>A maps to NM_152592.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr14:95905453 C>T maps to NM_152592.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:95932330 G>A maps to NM_152592.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:65054920 C>T maps to NM_172365.1 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:65054950 C>T maps to NM_172365.1 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:65019529 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:65053590 C>T maps to NM_172365.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr14:100793682 G>A maps to NM_207117.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:103571410 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:103566846 C>T maps to NM_001077594.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:103573762 G>A maps to NM_001077594.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:103568554 G>A maps to NM_001077594.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr14:105960170 G>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:105958492 G>A maps to ENST00000392523 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr15:24921097 G>A maps to NM_018958.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:24921854 C>T maps to NM_018958.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:24921892 G>T maps to NM_018958.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:24923623 A>G maps to NM_018958.2 Q870Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:24923731 G>A maps to NM_018958.2 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr15:24921535 C>T maps to NM_018958.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr15:24923083 A>T maps to NM_018958.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr15:24923221 C>T maps to NM_018958.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr15:24923623 A>G maps to NM_018958.2 Q870Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr15:24921280 T>C maps to NM_018958.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr15:24921475 A>G maps to NM_018958.2 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr15:24922990 T>C maps to NM_018958.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr15:40675071 T>A maps to NM_033286.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr15:81440852 C>A maps to ENST00000458088 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr15:76467993 G>A maps to NM_152335.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr15:76484306 A>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:76462154 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:76496085 C>T maps to NM_152335.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr15:76430194 G>A maps to NM_152335.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr15:34440951 C>G did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr15:93015417 T>C maps to NM_153040.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:93015407 A>G maps to NM_153040.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr15:93015605 A>G maps to NM_153040.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:49903458 G>A maps to NM_152647.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr15:75498436 C>T maps to NM_015492.4 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:37100596 C>T maps to NM_001130010.1 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr15:90164759 G>A maps to NM_152259.3 S1097S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:90169243 C>T maps to NM_152259.3 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:90125981 C>T maps to NM_152259.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:90159666 C>T maps to NM_152259.3 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr15:90118930 C>T maps to NM_152259.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:90169246 C>T maps to NM_152259.3 L1853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:90167737 G>A maps to NM_152259.3 Q1399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:90137717 C>T maps to NM_152259.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:45253730 A>G maps to NM_152448.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:65871778 C>T maps to ENST00000420799 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:65891301 G>A maps to ENST00000420799 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr15:65871769 A>C maps to ENST00000420799 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:39544626 A>G maps to NM_207445.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:39544752 C>T maps to NM_207445.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:34648762 C>T maps to ENST00000438749 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:34648161 T>C maps to ENST00000438749 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr15:34648353 C>T maps to ENST00000438749 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:34649311 A>T maps to ENST00000438749 K1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr15:90784209 C>T maps to NM_001013657.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:90784506 C>T maps to NM_001013657.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr15:90785030 G>A maps to NM_001013657.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:73852106 G>A maps to NM_001042367.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:73766201 T>G maps to NM_001042367.1 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:614328 G>A maps to ENST00000293874 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:684594 G>A maps to NM_001040160.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:1400976 G>A maps to NM_001001410.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:81095509 G>A maps to NM_152337.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr16:81094819 C>T maps to NM_152337.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:67699036 C>T maps to NM_032140.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:67697557 A>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:4562626 C>T maps to ENST00000359075 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:4563766 C>T maps to ENST00000359075 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr16:29828031 C>T maps to NM_024516.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:29828528 A>G did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr16:89735829 G>A maps to NM_153025.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:89735848 C>A maps to NM_153025.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr16:58048231 T>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:31504365 G>T maps to NM_022744.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:31512029 G>A maps to NM_022744.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:2512522 G>A maps to NM_025108.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:15977963 G>A maps to NM_144600.2 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:8722947 G>A maps to NM_024109.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:8719647 G>A maps to NM_024109.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:89783003 A>G maps to NM_004913.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:89783150 C>T maps to NM_004913.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:67168348 C>T maps to NM_025187.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:67179282 C>T maps to NM_025187.3 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr16:4790602 C>A maps to NM_139170.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:9210616 A>C maps to NM_014117.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr16:1891974 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:49407987 A>G maps to NM_144602.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:49430586 C>T maps to NM_144602.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr16:49430496 C>T maps to NM_144602.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:19726315 C>T maps to NM_001012991.2 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:3544553 G>A maps to NM_001080524.1 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr16:30771692 C>T maps to NM_001014979.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr17:42744529 C>A maps to NM_001145080.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr17:42744388 G>A maps to NM_001145080.2 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:42745516 C>A maps to NM_001145080.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:72948428 C>T maps to NM_030630.2 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:72947724 A>G maps to NM_030630.2 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:72956279 G>A maps to NM_030630.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:72959142 G>A maps to NM_030630.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:72956335 G>A maps to NM_030630.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:72951938 C>T maps to NM_030630.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr17:37886534 G>T maps to NM_032339.3 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:29231313 G>A maps to NM_024683.3 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:29233198 G>T maps to NM_024683.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:43332689 G>A maps to NM_152343.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:43334551 G>A maps to NM_152343.2 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr17:56620385 C>A maps to NM_001038704.1 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:56620623 G>A maps to NM_001038704.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:56620548 G>A maps to NM_001038704.1 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:10608782 C>T maps to NM_020233.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:42225347 G>A maps to NM_024032.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:79202745 G>A maps to NM_144679.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:79207477 C>T maps to NM_144679.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:79202796 C>T maps to NM_144679.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:45421628 A>G maps to NM_152347.4 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr17:45468803 G>A maps to NM_152347.4 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:65989052 T>A maps to NM_181656.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:8092990 G>A maps to NM_017622.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:58506847 C>G maps to NM_181707.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:8141901 G>A maps to NM_025099.5 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:8138087 T>C maps to NM_025099.5 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:8136251 A>G maps to NM_025099.5 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:8139579 G>A maps to NM_025099.5 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr17:8139247 G>A maps to NM_025099.5 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:79512906 G>A maps to NM_025161.5 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:79514274 G>A maps to NM_025161.5 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:79514604 C>T maps to NM_025161.5 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:79508400 G>A maps to NM_025161.5 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:57289172 T>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:57289052 C>T maps to NM_018149.6 Y547Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:57288692 C>T maps to NM_018149.6 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:57292309 C>T maps to NM_018149.6 Q975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:57290391 C>T maps to NM_018149.6 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:57287462 G>A maps to NM_018149.6 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:57290862 A>G maps to NM_018149.6 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:7330105 C>T maps to NM_175734.4 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:7329687 C>T maps to NM_175734.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:7329094 C>T maps to NM_175734.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7329687 C>T maps to NM_175734.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7330143 G>A maps to NM_175734.4 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7330755 G>A maps to NM_175734.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr17:72588199 G>A maps to NM_152460.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:72588247 G>A maps to NM_152460.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:72588511 G>A maps to NM_152460.2 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:71232595 G>A maps to NM_017941.4 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:71232727 G>A maps to NM_017941.4 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr17:59489995 G>T maps to NM_203425.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:3724564 C>T maps to NM_001114118.1 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr17:36997468 G>A maps to NM_001080465.2 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:36997561 G>A maps to NM_001080465.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr18:13621227 C>T maps to NM_181481.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:34376818 A>C maps to NM_015476.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr18:34408645 C>A maps to NM_015476.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:13682034 G>A maps to NM_152352.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:13666625 C>T maps to NM_152352.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:33554883 G>A maps to NM_031446.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:77798608 G>A maps to NM_024805.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:77806127 C>T maps to NM_024805.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr18:43843011 T>C maps to NM_145055.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:52262273 C>T maps to NM_173629.1 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr18:30554567 C>T maps to NM_001105528.1 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr18:30847186 T>A maps to NM_001105528.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr18:30672723 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:30792019 C>A did not map to a codon.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr18:30928929 A>C maps to NM_001105528.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:20889669 C>T maps to NM_032933.4 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:51887089 C>T maps to ENST00000382911 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:51886947 G>A maps to ENST00000382911 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr18:51904588 G>A maps to ENST00000382911 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr18:71825637 C>T maps to NM_014177.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:21109231 C>T maps to NM_013326.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:30193762 G>A maps to NM_001031726.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr19:30193720 G>A maps to NM_001031726.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:58485725 C>T maps to NM_152474.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:30462125 C>T maps to NM_003796.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:518966 C>T maps to NM_033513.2 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:758559 G>A maps to NM_173481.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:758106 C>T maps to NM_173481.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr19:758148 G>A maps to NM_173481.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:899641 G>A maps to NM_138774.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr19:1235848 G>T maps to ENST00000382477 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:1230903 T>C maps to NM_152769.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:3551145 G>A maps to NM_021731.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:3546151 G>A maps to NM_021731.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:3551130 C>T maps to NM_021731.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:3544812 G>A maps to NM_021731.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:3624135 C>T maps to NM_021231.1 W64*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4292-01A-01D-1126-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-4361-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr19:3623841 C>T maps to NM_021231.1 T162T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CD-A4MJ-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:3623940 C>T maps to NM_021231.1 A129A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8DU-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:3624072 G>T maps to NM_021231.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:2278642 G>A maps to NM_198532.2 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:2280891 G>A maps to NM_198532.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:2099001 T>C maps to NM_001039846.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:2098791 C>T maps to NM_001039846.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr19:33464168 G>T maps to NM_152266.3 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr19:33464170 G>A maps to NM_152266.3 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:50655901 A>G maps to NM_152358.2 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:16612313 C>A maps to NM_032207.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:7569088 A>G maps to NM_198534.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:7571037 G>A maps to NM_198534.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr19:36498122 C>A maps to ENST00000455847 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:40834365 C>T maps to ENST00000357884 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr19:40827890 C>A maps to ENST00000357884 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:40829911 C>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:55672678 G>A maps to ENST00000301249 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:11040107 C>T maps to NM_138358.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:41250030 G>A maps to NM_198476.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:41249852 C>T maps to NM_198476.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:12779184 C>T maps to NM_016145.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr19:12779423 C>T maps to NM_016145.3 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:14001116 G>A maps to ENST00000454313 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:18700330 C>T maps to NM_001100418.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr19:44237014 C>T maps to NM_019108.2 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:50983972 C>T maps to ENST00000376920 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:50985201 T>C maps to NM_175063.4 *255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:51767343 G>A maps to NM_173635.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:51768880 T>G maps to NM_173635.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr7:7283246 T>G maps to NM_020156.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr7:7283231 C>T maps to NM_020156.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:119760636 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:119760211 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:119760098 A>G did not map to a codon.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr23:119760592 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:119760721 G>A did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:119761011 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:119760806 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:22964156 G>A maps to NM_015991.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:22965797 T>C maps to NM_015991.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:22987548 C>T maps to NM_000491.3 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:22987797 C>T maps to NM_000491.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:22974056 G>A maps to NM_172369.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:22973963 G>A maps to NM_172369.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr1:22974056 G>A maps to NM_172369.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:43044867 G>A maps to NM_006688.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:43037708 G>A maps to NM_006688.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr17:43044867 G>A maps to NM_006688.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:119915380 G>A maps to NM_182528.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:16562695 C>T maps to NM_001010908.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:49729948 G>A maps to NM_001008223.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr12:49729918 C>T maps to NM_001008223.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr5:159781799 G>A maps to NM_031908.4 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:34033498 G>A maps to NM_181435.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:34043140 G>A maps to NM_181435.4 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:34033498 G>A maps to NM_181435.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:47612347 C>T maps to NM_031909.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:47611774 C>T maps to NM_031909.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:47612293 C>T maps to NM_031909.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:47611585 G>A maps to NM_031909.2 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr22:37578650 C>T maps to NM_182486.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr22:37578512 A>C maps to NM_182486.1 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:15437603 A>G maps to NM_001135170.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:15437525 G>A maps to NM_001135170.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr16:1144783 G>A maps to NM_207419.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:1143887 G>A maps to NM_207419.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:1143668 G>A maps to NM_207419.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:24890299 C>T maps to NM_178540.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:24892995 G>A maps to NM_178540.3 T69T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CD-5800-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr13:24895860 C>T maps to NM_178540.3 D319D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-8602-01A-11D-2394-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-6566-01A-11D-1800-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-7703-01A-11D-2053-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HU-8602-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:24465775 A>G maps to NM_001135816.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:24470981 C>T maps to NM_001007537.1 A48A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:7244122 C>A maps to ENST00000290575 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:7242709 G>A maps to ENST00000290575 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:7249729 G>A maps to NM_016546.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:7249742 G>A maps to NM_016546.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:7177813 T>C maps to NM_001734.3 N642N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:244552295 G>A maps to NM_001012970.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:244756859 G>A maps to NM_001130957.1 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:244716100 C>G maps to NM_001130957.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr1:244735821 T>A maps to NM_001130957.1 Y566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr1:111494911 C>T maps to NM_018372.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:111490688 C>T maps to NM_018372.3 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:155290688 T>C maps to NM_001039517.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:200880841 C>T maps to NM_018265.2 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:200880604 T>C maps to NM_018265.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr1:200867551 C>T maps to NM_018265.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr1:200876965 C>T maps to NM_018265.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:210004281 G>A maps to NM_014388.6 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:210024593 G>A maps to NM_014388.6 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr1:210008471 T>A maps to NM_014388.6 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:162825103 G>T maps to NM_178550.4 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr1:162344041 G>A maps to NM_182581.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:162343897 G>T maps to NM_182581.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:169790901 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:169772332 T>G maps to NM_018186.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr1:169819473 C>A maps to NM_018186.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:169772366 C>T maps to NM_018186.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:169816850 G>A maps to NM_018186.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:36785373 C>T maps to NM_001162530.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:169366586 T>A maps to ENST00000367806 K420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:169391107 T>C maps to ENST00000367806 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:207196178 G>A maps to NM_023938.5 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr1:53684565 C>T maps to NM_017887.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:53680368 C>A maps to NM_017887.1 G149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr1:53681695 C>T maps to NM_017887.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:231487132 G>A maps to NM_032018.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:179414260 C>T maps to NM_144696.4 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:179364322 G>A maps to NM_144696.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:24113775 C>T maps to NM_020362.4 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:170940929 G>A maps to NM_001163629.1 E174E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-7707-01A-11D-2053-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:170967483 C>T maps to NM_025063.2 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:170955772 A>G maps to NM_001163629.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:170934366 A>C maps to NM_001163629.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:170967432 T>C maps to NM_025063.2 C538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:231374788 C>T maps to ENST00000421623 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr1:231362781 C>T maps to ENST00000421623 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:26164012 T>C maps to NM_024037.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:26185788 C>T maps to NM_024037.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr1:182873395 T>A maps to ENST00000287709 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:182908621 A>G maps to ENST00000287709 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:67559155 G>A maps to NM_001013674.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:67561066 C>A maps to NM_001013674.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:67558858 A>G maps to NM_001013674.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:92707842 A>G maps to NM_001012425.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:92711098 T>C maps to NM_001012425.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:92707766 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:92707798 C>T maps to NM_001012425.1 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:247719753 T>C maps to NM_145278.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:247737542 T>C maps to NM_145278.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr1:169762815 G>A maps to NM_033418.1 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:116663674 G>A maps to NM_152367.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr1:116670947 C>T maps to NM_152367.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:53153822 G>A maps to NM_023077.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:57258263 A>G maps to NM_001004303.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:57258128 T>C maps to NM_001004303.4 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:57257957 C>A maps to NM_001004303.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:27278022 C>T maps to NM_152365.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:27277974 G>A maps to NM_152365.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:27278808 C>T maps to NM_152365.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr1:27278472 T>G maps to NM_152365.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:75055516 C>T maps to NM_001002912.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:75097396 C>T maps to NM_001002912.4 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:75108708 A>G did not map to a codon.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:75037595 G>A maps to NM_001002912.4 V1266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr1:75038060 A>T maps to NM_001002912.4 A1111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr1:75038609 C>T maps to NM_001002912.4 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:75037867 C>A maps to NM_001002912.4 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:75037016 A>G maps to NM_001002912.4 T1459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:3809467 C>T maps to NM_207356.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:3809520 G>A maps to NM_207356.2 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:3809518 T>C maps to NM_207356.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:3807423 G>A maps to NM_207356.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:55119780 C>A maps to ENST00000454855 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:55161147 C>T maps to ENST00000454855 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:55175637 T>C maps to ENST00000454855 H1279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:55118745 G>A maps to ENST00000454855 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:55119765 G>A maps to ENST00000454855 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:55139381 G>A maps to ENST00000454855 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:55151959 C>T maps to ENST00000454855 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:55279515 C>T maps to NM_001110533.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:112298320 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:11769434 G>A maps to NM_198545.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:46669227 C>T maps to NM_001013615.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:46685585 G>A maps to NM_001013615.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:161334772 T>C maps to NM_001013625.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:109649217 A>G maps to NM_001122961.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:230979462 C>T maps to NM_032800.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:24685104 C>T maps to ENST00000374409 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr1:184567567 C>T maps to NM_030806.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:23695954 T>C maps to ENST00000507744 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:162351993 G>A maps to NM_001135240.1 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:185106735 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:185112527 G>A maps to NM_030934.4 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:185113147 T>C maps to NM_030934.4 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:185171821 T>C maps to NM_001105518.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:185143596 T>C maps to NM_001105518.1 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr1:185153426 G>C maps to NM_001105518.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:186357571 A>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:228290070 G>A maps to NM_024319.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:28208950 C>T maps to NM_001105556.1 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:154179927 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:154185101 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:150259050 T>C maps to NM_144697.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:150252085 G>A maps to NM_024579.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:226175748 C>A maps to NM_152608.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:151021159 C>T maps to NM_017860.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:233091412 G>T maps to NM_032324.1 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:233091396 G>A maps to NM_032324.1 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:222898865 C>T maps to NM_144695.2 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:109191325 C>T maps to ENST00000370031 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:156704045 C>T maps to NM_015997.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:228362617 G>A maps to NM_001010867.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:209956975 A>G maps to NM_152485.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:153609081 G>A maps to NM_015607.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:156264627 T>C maps to NM_144580.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:156264770 G>A maps to NM_144580.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr1:156264606 G>A maps to NM_144580.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:2125139 C>T maps to ENST00000359030 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:2125205 G>A maps to ENST00000359030 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:60506704 C>T maps to NM_152377.2 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:60491136 G>A maps to NM_152377.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:60521110 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:60456443 C>T maps to NM_152377.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr1:60499177 G>T maps to NM_152377.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:60499174 C>T maps to NM_152377.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:16558725 C>T maps to NM_030907.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:16559402 G>A maps to NM_030907.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:16559402 G>A maps to NM_030907.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:172558185 C>T maps to ENST00000367723 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:172522401 T>C maps to NM_014283.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:172539807 A>G maps to ENST00000367723 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:172579317 G>A maps to ENST00000367723 P1380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr1:172558820 T>G maps to ENST00000367723 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:156899199 C>T maps to NM_144702.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:156899079 C>A maps to NM_144702.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:156902757 C>A maps to NM_144702.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:34666584 C>T maps to NM_001134734.1 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:34666580 C>T maps to NM_001134734.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:31901480 G>A maps to ENST00000437789 S117S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-4306-01A-01D-1158-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CG-5728-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr20:55100040 A>G maps to NM_001012971.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:55100070 G>C maps to NM_001012971.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:55100859 G>T maps to NM_001012971.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:42825844 G>A maps to NM_016470.6 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:42826090 C>T maps to NM_016470.6 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:42825819 G>T maps to NM_016470.6 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:31040054 T>C maps to NM_080616.3 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr20:31044127 C>T maps to NM_080616.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:31044121 G>A maps to NM_080616.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:31041274 G>A maps to NM_080616.3 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr20:31062419 G>A maps to NM_080616.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr20:31876652 C>T maps to NM_033197.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr20:35507502 G>A maps to NM_080628.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr20:35506354 G>A maps to NM_080628.1 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr20:18407802 C>A maps to NM_001099407.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:18370424 G>A maps to NM_001099407.1 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:18365043 T>C maps to NM_001099407.1 *753W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:62493363 C>T maps to NM_080622.3 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr20:62493708 C>T maps to NM_080622.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr20:62493609 G>A maps to NM_080622.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:2796243 C>T maps to NM_080739.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr20:60986023 C>T maps to NM_080833.2 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:60991217 A>G did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr20:34568409 C>A maps to ENST00000373973 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr20:30602747 C>T maps to ENST00000300415 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:44515245 C>T maps to NM_080608.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr20:44515368 G>C maps to NM_080608.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:44515479 G>A maps to NM_080608.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr20:58519081 C>T maps to NM_022106.2 H28H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:58519369 A>G maps to NM_022106.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:58519318 T>G maps to NM_022106.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:31652620 C>T maps to NM_182658.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:31656728 C>T maps to NM_182658.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr20:31652353 C>T maps to NM_182658.1 N248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:31656643 A>G maps to NM_182658.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr20:31652536 G>T maps to NM_182658.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:31676771 G>A maps to NM_182519.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr20:31678529 G>A maps to NM_182519.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:3262380 G>A maps to NM_001009984.1 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:3299035 G>A maps to NM_001009984.1 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:3362032 T>C maps to NM_001009984.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr20:3262287 T>A maps to NM_001009984.1 R871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:3274886 G>A maps to NM_001009984.1 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:3306888 A>C maps to NM_001009984.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr20:3236669 C>A maps to NM_001009984.1 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:3329231 G>A maps to NM_001009984.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:3362098 A>G maps to NM_001009984.1 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr20:3355773 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:61430898 C>T maps to NM_018270.4 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:35240457 T>C maps to NM_199483.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:20257972 G>A maps to ENST00000389655 A892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:20180468 C>T maps to ENST00000389655 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr20:20232237 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:20258056 C>T maps to ENST00000389655 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr20:20257981 C>T maps to ENST00000389655 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr20:20243712 C>T maps to ENST00000389655 N817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr20:20056253 A>G maps to ENST00000389655 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:20226820 A>G maps to ENST00000389655 K710K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:20278850 G>A maps to ENST00000389655 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:20037345 C>T maps to ENST00000389655 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:20232280 C>A maps to ENST00000389655 C737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr20:20279000 C>T maps to ENST00000389655 Y1134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr20:3804850 C>T maps to NM_018347.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr20:3802808 T>A maps to NM_018347.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:24944640 C>T maps to NM_020531.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:34827849 T>C maps to NM_015511.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr20:34832802 C>T maps to NM_015511.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:34832790 C>T maps to NM_015511.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:34832707 C>A maps to NM_015511.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:55059246 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:55059238 C>T maps to ENST00000357348 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr20:55048422 C>T maps to ENST00000357348 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:1161599 G>A maps to NM_018354.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:746208 G>A maps to NM_033409.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:744158 G>A maps to NM_033409.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr20:741723 G>A maps to NM_033409.3 N452N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:745872 C>T maps to NM_033409.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:741783 G>A maps to NM_033409.3 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr20:744554 G>A maps to NM_033409.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:13773857 T>C maps to NM_024120.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr20:13797518 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:31756983 C>T maps to NM_080574.2 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr20:31756983 C>T maps to NM_080574.2 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:31813011 C>T maps to NM_178466.3 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr20:18794851 C>T maps to NM_178483.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr20:56730597 G>A maps to NM_178456.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:45752927 G>A maps to ENST00000397956 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:45953665 G>A maps to ENST00000443468 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr21:45953800 G>A maps to ENST00000443468 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr21:45924735 C>A maps to ENST00000443468 G599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:45941906 G>A maps to ENST00000443468 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr21:45929122 G>A maps to ENST00000443468 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:45949812 G>A maps to ENST00000443468 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr21:33651280 G>A maps to NM_018944.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr21:33642776 C>T maps to NM_018944.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:47711298 T>C maps to NM_058181.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:47706910 G>A maps to NM_058181.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:33984412 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:33976432 A>G did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr21:33887130 G>A maps to NM_058187.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr21:33840139 G>A maps to NM_058187.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:30532269 G>A maps to NM_020152.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr21:30464855 G>A maps to NM_020152.2 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:19839619 G>A maps to NM_024627.5 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr22:19839007 C>A maps to NM_024627.5 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr22:19839751 A>T maps to NM_024627.5 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:19839609 G>A maps to NM_024627.5 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr22:37387546 C>T maps to NM_001163857.1 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:24982309 C>T maps to NM_207644.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:46643045 C>T maps to NM_207327.4 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:32546323 G>A maps to NM_001010859.1 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:45595910 G>T maps to NM_001009880.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:45599827 G>T maps to NM_001009880.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr22:45599791 C>T maps to NM_001009880.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:45599791 C>T maps to NM_001009880.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:45601543 G>A maps to NM_001009880.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:45608161 G>T maps to NM_015264.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr21:43342110 G>A maps to NM_015500.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr21:43327822 C>T maps to NM_015500.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr21:43327792 C>T maps to NM_015500.1 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:118982337 C>T maps to NM_014807.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:118984694 C>T maps to NM_014807.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:73844001 A>G maps to ENST00000334126 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:73806438 T>C maps to ENST00000334126 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:73820093 T>C maps to ENST00000334126 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:73820179 G>A maps to ENST00000334126 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:73824825 T>C maps to ENST00000334126 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:73811694 T>C maps to ENST00000334126 K869K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr11:73849765 T>C maps to ENST00000334126 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr11:73803554 G>C maps to ENST00000334126 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:99767056 A>T maps to NM_144706.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr2:27801238 C>T maps to NM_032266.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:27804550 T>A maps to NM_032266.3 G1704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:27802996 A>G maps to NM_032266.3 R1186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr2:27804748 T>A maps to NM_032266.3 S1770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:27803795 C>T maps to NM_032266.3 R1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:27001126 C>T maps to NM_017877.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:26998045 G>A maps to NM_017877.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:26999330 G>A maps to NM_017877.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:26999342 C>T maps to NM_017877.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:101881314 C>T maps to NM_017546.4 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:75921498 G>A maps to NM_003203.4 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr2:26677607 C>T maps to NM_145038.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:26667582 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:26672937 G>T maps to NM_145038.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr2:106694259 C>T maps to NM_032411.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr2:106690498 G>A maps to NM_032411.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:70392253 C>A maps to NM_017880.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:70408873 G>T maps to NM_017880.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:20939808 G>A maps to ENST00000381090 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr2:24253803 C>G maps to NM_025203.2 *722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:24262142 A>G maps to NM_025203.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr2:105959478 G>A maps to NM_024093.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:11284095 G>A maps to NM_182500.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:11273483 G>A maps to NM_182500.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:88828730 C>A maps to NM_152670.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:88828700 C>T maps to NM_152670.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr2:27361134 A>C maps to NM_178553.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:241831148 C>T maps to NM_001085437.1 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:99439343 C>T maps to NM_207362.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:99448876 G>A maps to NM_207362.2 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr2:99449453 C>T maps to NM_207362.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:99454682 C>T maps to NM_207362.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:99439595 C>T maps to NM_207362.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:99439661 C>T maps to NM_207362.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:99439883 G>A maps to NM_207362.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:99413926 A>G maps to NM_207362.2 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:37459357 T>A maps to NM_144736.4 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:37468909 C>T maps to NM_144736.4 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:37474648 A>G maps to NM_144736.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:232458156 G>A maps to NM_152614.2 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:232458075 G>A maps to NM_152614.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:232458552 C>T maps to NM_152614.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:232458510 C>T maps to NM_152614.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:200797993 G>T maps to NM_001039693.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr2:200820175 G>C maps to NM_001039693.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:200813093 A>G maps to NM_001039693.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:200820113 A>G did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr2:219231773 C>T maps to NM_198559.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:219229424 C>T maps to NM_198559.1 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:197672181 A>G maps to NM_213608.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:210887768 T>C maps to NM_152519.2 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:210887887 G>A maps to NM_152519.2 R917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:210896238 T>A maps to NM_152519.2 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:85836154 C>T maps to NM_001013649.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:200789975 A>C maps to NM_153689.5 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:73456644 G>A maps to NM_032319.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:73456017 G>A maps to NM_032319.1 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:73455924 G>A maps to NM_032319.1 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:29293518 C>T maps to NM_001029883.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:29296326 C>T maps to NM_001029883.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:29296020 G>A maps to NM_001029883.1 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr2:29295777 C>A maps to NM_001029883.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:29295108 G>A maps to NM_001029883.1 N673N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:74042615 C>T maps to NM_001080474.1 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr2:74042216 G>T maps to NM_001080474.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:209035782 G>A maps to NM_001099334.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:209045982 G>A maps to NM_001099334.2 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:242814492 G>A maps to NM_173821.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:242815104 G>A maps to NM_173821.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr2:242814201 C>T maps to NM_173821.2 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:242815401 C>T maps to NM_173821.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:63631684 C>T maps to NM_015910.4 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:63540406 G>A maps to NM_015910.4 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:85051309 G>T maps to ENST00000409520 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:85049039 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:6684607 G>A maps to NM_000064.2 F1361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:6707488 G>A maps to NM_000064.2 R679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:6718270 G>A maps to NM_000064.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr19:6711198 C>T maps to NM_000064.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:6690639 G>A maps to NM_000064.2 N1163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:6697782 G>A maps to NM_000064.2 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:6694538 C>T maps to NM_000064.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:8212286 A>G maps to NM_004054.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:8211842 A>G maps to NM_004054.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:8211427 C>A maps to NM_004054.2 G452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:8211803 G>A maps to NM_004054.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr3:62317025 A>G maps to NM_020685.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:62319058 C>T maps to NM_020685.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:119466107 C>T maps to NM_033364.3 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:119452223 T>C maps to NM_033364.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:119434406 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:119459416 C>T maps to NM_033364.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:112732834 G>T maps to NM_015412.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:112730202 A>T maps to NM_015412.3 L201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:50597096 G>T maps to NM_001171741.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:14693375 G>T maps to NM_016474.4 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:14799159 C>T maps to NM_032137.4 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr3:14770024 C>T maps to NM_032137.4 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:14744718 C>T maps to NM_032137.4 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr3:14744670 G>A maps to NM_032137.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:14769958 T>C maps to NM_032137.4 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:194790464 G>A maps to NM_152531.4 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:44434452 C>T maps to NM_173826.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:10146116 C>T maps to NM_001164839.1 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:99890706 C>T maps to NM_032359.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:128292137 G>A maps to NM_007354.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr3:118865645 C>T maps to NM_152539.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:11851060 T>C maps to ENST00000444133 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr3:8673780 G>T maps to NM_015931.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:8671347 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:8675522 G>A maps to NM_015931.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr3:155485297 C>T maps to ENST00000340171 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:196435396 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:133647491 C>T maps to NM_025041.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:133647383 C>T maps to NM_025041.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:133647419 C>T maps to NM_025041.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:129009634 C>T maps to NM_001006109.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:43122149 G>A maps to NM_032806.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:50324509 T>C maps to NM_153215.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:50316561 C>T maps to NM_153215.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr3:50324174 G>A maps to NM_153215.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:111828412 G>A maps to NM_024616.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr3:157271103 G>T maps to NM_001130002.1 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:143708551 G>T maps to NM_173552.3 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:192516330 T>A maps to NM_178496.3 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:192516462 G>A maps to NM_178496.3 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:192516768 G>A maps to NM_178496.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:56657580 G>A maps to ENST00000447900 N1499N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:56657214 C>T maps to ENST00000447900 G1621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:56674011 A>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:56658876 G>A maps to ENST00000447900 R1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:56681219 C>T maps to ENST00000447900 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:69053563 C>T maps to ENST00000383701 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:69026834 A>T maps to ENST00000383701 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr3:58849419 G>C maps to ENST00000482387 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:184870602 C>T maps to NM_001025266.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:184801193 A>G maps to NM_001025266.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:153203895 T>C did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr3:153220202 C>T maps to NM_001101337.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr3:153203808 C>T maps to NM_001101337.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:31994881 C>T maps to NM_001002029.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:31962393 G>A maps to NM_007293.2 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:207300064 C>A maps to NM_000715.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:207287496 G>A maps to NM_000715.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr1:207300152 C>T maps to NM_000715.3 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:207307749 G>A maps to NM_000715.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:57834642 A>C maps to NM_032313.2 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr4:57842917 C>G maps to NM_032313.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr4:57843169 C>A maps to NM_032313.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:100460467 A>C maps to NM_032149.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr4:113539454 A>G maps to NM_018392.4 C581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:113544978 G>A maps to NM_018392.4 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:113524696 G>A maps to NM_018392.4 Q987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:113524721 T>C maps to NM_018392.4 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:81866026 C>T maps to ENST00000508675 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr4:81884684 C>T maps to ENST00000508675 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:81284035 A>G maps to ENST00000508675 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:76489613 A>C maps to NM_178497.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:76489372 C>T maps to NM_178497.2 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:170652928 G>A maps to NM_017867.2 Q279*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4G6-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr4:121957571 G>A maps to NM_024574.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr4:121966923 G>A maps to NM_024574.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr4:121958018 A>T maps to NM_024574.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr4:121966863 C>T maps to NM_024574.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr4:121957511 G>T maps to NM_024574.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:130023785 C>T maps to NM_001099783.1 H7H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr4:130030828 T>G maps to ENST00000502887 *166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:71201856 T>C maps to NM_033122.3 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:71201046 C>A maps to NM_033122.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:71201538 T>C maps to NM_033122.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr4:71200842 G>T maps to NM_033122.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr4:71200810 A>T maps to NM_033122.3 K19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:87809322 C>T maps to NM_144645.3 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr4:98902358 A>T maps to NM_174952.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:98762071 C>T maps to NM_174952.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr4:98761986 T>G maps to NM_174952.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:184585025 C>T maps to NM_021942.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:184614171 G>A maps to NM_021942.4 W703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:184622880 A>G maps to NM_021942.4 E961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:184585064 G>A maps to NM_021942.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:184589195 C>T maps to NM_021942.4 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:184614801 T>C maps to NM_021942.4 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:184606267 G>A maps to NM_021942.4 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr4:184615857 T>C maps to NM_021942.4 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:5981912 C>T maps to ENST00000324058 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr4:5975439 G>A maps to ENST00000324058 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr4:5966822 T>C maps to ENST00000324058 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:123723808 A>G maps to NM_001735.2 N1513N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:123776295 G>A maps to NM_001735.2 C704C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:123783954 C>T maps to NM_001735.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:123725006 G>T maps to NM_001735.2 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr9:123785723 A>C maps to NM_001735.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:123723778 G>A maps to NM_001735.2 A1523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr19:47823123 T>C maps to ENST00000355085 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:133292615 A>G maps to NM_020199.2 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:133304224 C>T maps to NM_020199.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:133295583 A>T maps to NM_020199.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr5:134782297 G>A maps to NM_130848.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:134782378 C>T maps to NM_130848.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:31538589 G>T maps to NM_018356.2 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr5:32789794 T>G maps to NM_024563.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr5:134190925 C>T maps to NM_152409.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:175772237 T>C maps to ENST00000443967 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:175772211 C>T maps to ENST00000443967 R795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:43446518 G>T maps to NM_022483.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:102611814 G>A maps to NM_033211.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:43494676 A>G maps to NM_198566.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:56208889 G>A maps to NM_153706.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr5:93856181 T>A maps to ENST00000513200 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:2752843 G>A maps to NM_178569.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr5:2752816 C>T maps to NM_178569.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:43039977 A>G maps to NM_001014279.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:156770018 G>A maps to NM_001001343.3 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:156769911 C>A maps to NM_001001343.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr5:156770403 G>A maps to NM_001001343.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:156770202 C>T maps to NM_001001343.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:172513562 G>A maps to NM_153607.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:172513526 G>A maps to NM_153607.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:172513515 G>T maps to NM_153607.2 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:37183091 C>A maps to NM_023073.3 E1731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:37183563 G>A maps to NM_023073.3 D1573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr5:37170432 G>A maps to NM_023073.3 L2058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:37198875 C>T maps to NM_023073.3 A1200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:37183478 G>A maps to NM_023073.3 R1602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr5:37198820 T>G maps to NM_023073.3 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr5:37142582 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:37169399 A>G maps to NM_023073.3 H2242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:37184972 T>C maps to NM_023073.3 G1466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:7851035 C>T maps to NM_001089584.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr5:159821851 C>A maps to NM_022090.3 G216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:159821323 G>A maps to NM_022090.3 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:131796356 T>C maps to NM_001013717.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:41142989 C>A maps to NM_001115131.1 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:41149541 G>A maps to NM_001115131.1 N808N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr5:41149448 G>A maps to NM_001115131.1 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:41176625 G>A maps to NM_001115131.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:34214512 A>G maps to NM_178508.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr6:34214425 G>A maps to NM_178508.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:34214602 G>A maps to NM_178508.3 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:32261735 G>A maps to ENST00000447241 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:32261426 A>G maps to ENST00000447241 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:32307385 C>A maps to ENST00000447241 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:32261098 G>A maps to ENST00000447241 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr6:43197128 G>A maps to ENST00000509253 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr6:13470335 A>C maps to NM_033069.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:165706905 T>A maps to NM_144980.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:165715714 C>T maps to NM_144980.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr6:165712985 T>C maps to NM_144980.3 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr6:165711566 C>T maps to NM_144980.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:165693543 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr6:165715540 G>A maps to NM_144980.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr6:30596122 G>A maps to ENST00000376485 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:30615106 G>A maps to NM_001161376.1 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr6:47846506 G>A maps to NM_001013732.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:54095591 G>A maps to ENST00000502396 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:54025581 T>C maps to ENST00000502396 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr6:54034363 C>A maps to ENST00000502396 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:4073577 T>G did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr6:31079709 C>T maps to NM_014070.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:31079952 C>T maps to NM_014070.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:74138430 C>A did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr6:74161871 T>C maps to NM_138441.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr6:42995124 C>T maps to NM_033112.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:42996915 C>T maps to NM_033112.2 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr6:43475389 G>T maps to NM_001012974.1 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:88049952 G>A maps to NM_020425.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:88049877 C>T maps to NM_020425.4 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:88173832 T>C maps to NM_001031743.2 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:88120334 C>T maps to NM_001031743.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:88123614 C>T maps to NM_001031743.2 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:88170801 G>A maps to NM_001031743.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:97720927 T>C maps to NM_198468.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:97679387 A>T maps to NM_198468.2 Y481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:97597751 G>A maps to NM_198468.2 G1209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:99739595 G>T maps to NM_032511.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:99771428 C>T maps to NM_032511.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:99771410 G>A maps to NM_032511.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr6:121576499 A>G maps to ENST00000275159 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:121434206 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr6:121412188 T>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:121577346 C>T maps to ENST00000275159 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:127797298 G>A maps to NM_001012279.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:127837611 G>A maps to NM_001012279.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr6:127834068 T>C maps to NM_001012279.2 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:127837735 G>A maps to NM_001012279.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr6:127837075 T>C maps to NM_001012279.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr6:127837555 A>G maps to NM_001012279.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:127797589 G>A maps to NM_001012279.2 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:127797066 G>A maps to NM_001012279.2 Q702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr6:127836183 G>A maps to NM_001012279.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:127797442 G>A maps to NM_001012279.2 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:109471408 A>G maps to NM_173830.4 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:110620348 C>A maps to NM_001123364.1 G188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:130164726 C>A maps to NM_001010876.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr6:130164749 T>G did not map to a codon.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr6:130164744 C>T maps to NM_001010876.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:130166946 G>A maps to NM_001010876.1 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:133092042 A>G maps to NM_052831.2 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:133097496 T>C maps to NM_052831.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:118801651 G>A maps to NM_001042475.2 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:118886985 G>A maps to NM_001042475.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:118844969 G>A maps to NM_001042475.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr6:118953694 A>G maps to NM_001042475.2 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr6:118813010 A>C maps to NM_001042475.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:118845080 A>G maps to NM_001042475.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:118804976 G>A maps to NM_001042475.2 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:151790161 C>T maps to NM_024573.1 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:74072842 C>T maps to NM_001017361.2 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr6:74072893 C>T maps to NM_001017361.2 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:74072893 C>T maps to NM_001017361.2 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr6:74073315 G>A maps to NM_001017361.2 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:74073495 G>A maps to NM_001017361.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:36288973 A>C maps to NM_001010903.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:36291214 C>T maps to NM_001010903.4 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:42858502 T>C maps to NM_001008739.1 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr6:31692808 G>A maps to NM_138272.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:31734482 C>T maps to NM_025258.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr6:31736827 C>T maps to NM_025258.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:31740842 G>A maps to NM_025258.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:157739924 C>T maps to NM_018452.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:31627517 A>G maps to NM_021184.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:31627031 C>G maps to NM_021184.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr6:31627481 C>T maps to NM_021184.3 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:31807421 A>G maps to NM_001040438.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:71298400 C>T maps to NM_145267.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:170176101 T>A maps to NM_018341.1 Y487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:170162627 G>C did not map to a codon.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr6:149893481 T>C did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr6:149903625 G>A maps to NM_138785.3 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:35704935 C>T maps to NM_145028.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:35706177 G>A maps to NM_145028.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:36867234 C>T maps to NM_152734.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:151857472 G>A maps to ENST00000367290 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:40981653 T>G maps to NM_000587.2 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr7:31735215 C>T maps to NM_006658.4 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:86827313 C>T maps to NM_024315.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:42949773 G>A maps to NM_001099858.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:42950001 G>A maps to NM_001099858.1 I224I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:2583342 G>A maps to NM_152743.3 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr7:2594050 G>A maps to NM_152743.3 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:5959525 C>T maps to NM_015622.5 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr7:5944825 C>T maps to NM_015622.5 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:6864281 T>C maps to NM_198097.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:150027621 C>T maps to NM_138434.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:150028035 C>T maps to NM_138434.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr7:150027912 C>T maps to NM_138434.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:23339093 G>A maps to NM_138446.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:25182373 G>A maps to NM_138811.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:25194711 C>T maps to NM_138811.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:25194756 G>A maps to NM_138811.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:148311381 C>T maps to NM_145304.2 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:148288103 C>A maps to NM_145304.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:142636663 A>T maps to NM_178829.4 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:30185809 C>T maps to NM_152793.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:30197085 G>A maps to NM_152793.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:30185809 C>T maps to NM_152793.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr7:66413648 C>A maps to NM_017994.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:66415980 G>A maps to NM_017994.4 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:43687182 G>A maps to NM_018224.2 H22H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:43684885 G>A maps to NM_018224.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr7:129847884 T>A maps to NM_145268.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:23724153 T>A maps to NM_199136.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:134851434 G>T maps to NM_024033.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:134852549 C>T maps to NM_024033.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr7:134852516 C>T maps to NM_024033.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:100087128 C>T maps to ENST00000423930 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:100085811 C>T maps to ENST00000423930 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr7:100087128 C>T maps to ENST00000423930 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:100086957 G>A maps to ENST00000423930 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:100815806 G>A maps to NM_198571.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr7:112129967 C>T maps to NM_182597.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:112127026 C>T maps to NM_182597.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:139026219 C>T maps to NM_197964.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:120629692 G>A maps to NM_024913.4 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr7:120770265 C>T maps to NM_024913.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr7:120781019 T>C maps to NM_024913.4 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:120704357 A>C maps to NM_024913.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:120739988 G>A maps to NM_024913.4 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:120935616 C>T maps to NM_024913.4 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:120629902 T>C maps to NM_024913.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr7:120876820 T>G maps to NM_024913.4 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:120740006 T>C maps to NM_024913.4 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:120770303 A>G maps to NM_024913.4 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:120767142 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:112535787 G>A maps to NM_152556.2 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:112472731 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr7:112461938 G>A maps to NM_152556.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:112472681 G>T maps to NM_152556.2 C174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:89936276 T>C maps to NM_001039706.2 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr7:89909172 A>T maps to NM_001039706.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:92163896 T>C maps to NM_032120.2 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr7:92164115 G>A maps to NM_032120.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr7:108524087 A>C maps to NM_001024607.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr7:6370485 C>T maps to NM_001037163.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr1:57349319 C>A maps to NM_000562.2 S274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:57340750 C>T maps to NM_000562.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:57420405 A>T maps to NM_000066.2 C162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr1:57399076 C>A maps to NM_000066.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:139840986 T>C maps to NM_000606.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr9:139840618 G>A maps to NM_000606.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:146278794 C>T maps to ENST00000444534 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:146278737 C>A maps to ENST00000444534 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr8:69434188 C>T maps to NM_052958.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:69351823 C>T maps to NM_052958.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr8:69728124 C>T maps to NM_052958.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:69358681 G>A maps to NM_052958.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr8:69552689 T>G maps to NM_052958.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr8:69434169 G>A maps to NM_052958.2 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:69552648 C>T maps to NM_052958.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:96044274 C>T maps to NM_152416.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:96047720 C>T maps to NM_152416.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:96053841 C>T maps to NM_152416.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:42401750 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:33369576 G>A maps to NM_001102401.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:33367394 G>A maps to NM_001102401.1 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:33367404 C>T maps to NM_001102401.1 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:67809146 C>T maps to NM_173518.4 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:67425870 G>T maps to NM_152765.3 G147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr8:22458518 C>T maps to ENST00000450780 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr8:22459489 C>T maps to ENST00000450780 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:144650730 G>A maps to NM_001100878.1 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:10555406 C>T maps to NM_001040032.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr8:10555328 C>T maps to NM_001040032.1 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr8:12878835 C>A maps to NM_020844.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:12863854 C>T maps to NM_020844.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:12879198 T>C maps to NM_020844.2 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:27922179 G>A maps to ENST00000341513 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:27925084 C>T maps to ENST00000341513 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:27922053 G>A maps to ENST00000341513 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr8:27925084 C>T maps to ENST00000341513 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:117950592 C>T maps to NM_001025357.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:117950577 C>T maps to NM_001025357.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:117950646 G>A maps to NM_001025357.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:117950598 C>T maps to NM_001025357.2 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:38386080 A>C maps to NM_207412.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:39341718 C>T maps to NM_001737.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:39316122 G>A maps to NM_001737.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:39311416 G>A maps to NM_001737.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:39311446 A>G maps to NM_001737.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr9:98691032 G>A maps to NM_001010895.2 A557A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B7-A5TI-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:98678045 C>G maps to NM_001010895.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr9:86258433 A>C maps to NM_001001551.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr9:132084373 T>C maps to NM_001012715.3 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:132084349 T>C maps to NM_001012715.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:131591431 A>G maps to NM_016390.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:138387440 C>T maps to NM_001048265.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr9:138387362 G>A maps to NM_001048265.1 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:130475025 G>A maps to NM_001012502.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:131038510 C>T maps to NM_001040011.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr9:104238825 C>T maps to NM_032342.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr9:35825635 C>A maps to NM_001012446.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:96080727 C>T maps to NM_001098808.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:96097785 G>A maps to NM_001098808.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:35043237 C>T maps to NM_203299.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr9:72521030 T>C maps to NM_001010940.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:72435827 G>A maps to NM_001010940.1 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:72501761 T>A maps to NM_001010940.1 L153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:139888235 C>T maps to NM_183241.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:12775776 C>T maps to NM_203403.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:112963472 A>G maps to NM_001012993.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:100672389 C>T maps to NM_016481.3 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100678462 T>C maps to NM_016481.3 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:139379475 C>A maps to NM_152571.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:89771627 C>T maps to NM_001001709.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr9:135374804 C>T maps to NM_207417.1 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:135285798 C>T maps to NM_207417.1 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:139740977 C>T maps to NM_001080482.2 D704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr9:139741625 C>T maps to NM_001080482.2 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:140147665 G>A maps to ENST00000388931 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:140147689 C>T maps to ENST00000388931 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:140147653 G>A maps to ENST00000388931 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:34611197 A>G maps to NM_148179.1 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:34379097 G>T maps to ENST00000412555 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr9:34401081 G>A maps to NM_001184940.1 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:97555116 C>T maps to NM_001193329.1 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr9:97563248 C>T maps to NM_001193329.1 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:103204336 G>A maps to NM_001198812.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:103204420 C>T maps to NM_001198812.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:103213193 T>C maps to NM_001198805.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:111911986 A>G maps to NM_014334.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:111899875 C>T maps to NM_014334.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr9:77598769 A>G maps to NM_152420.1 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:77614758 T>C maps to NM_152420.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr9:116185754 G>A maps to ENST00000451722 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:116187628 A>C maps to ENST00000451722 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr9:116191235 T>C maps to ENST00000451722 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr9:5431896 C>T maps to NM_018465.2 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:132375433 C>T maps to NM_199350.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:132375721 G>A maps to NM_199350.3 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:132382796 A>G maps to NM_199350.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:111697918 T>C maps to NM_017832.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:111701921 G>T maps to NM_017832.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:111698718 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:86570364 A>G maps to NM_032307.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:214856 C>T maps to NM_152569.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:4625437 C>T maps to ENST00000454239 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:139008559 T>C maps to NM_152833.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:139008451 G>T maps to NM_152833.2 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:136330476 G>A maps to NM_017586.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:132591761 G>A maps to NM_016520.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:90500034 G>A maps to NM_178828.4 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:90501321 C>A maps to NM_178828.4 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr9:90503232 G>A maps to NM_178828.4 R1277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr9:90500004 C>T maps to NM_178828.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:90497877 C>G maps to NM_178828.4 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr9:90500145 G>C maps to NM_178828.4 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:26884836 A>G maps to NM_024828.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:26842610 A>G maps to NM_024828.3 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr9:114464485 A>G maps to NM_173521.3 Y932Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:114453906 T>C maps to NM_173521.3 Q1386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:114462247 C>A maps to NM_173521.3 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:114453876 C>T maps to NM_173521.3 R1396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:117405500 C>T maps to ENST00000374049 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr9:15971635 C>T maps to NM_173550.2 S1261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:15678795 G>T maps to NM_173550.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:77684722 A>G maps to NM_017881.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:136256455 G>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:136268948 C>T maps to NM_153710.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:136265619 G>A maps to NM_153710.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:136270003 G>A maps to NM_153710.3 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:135739049 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:135742311 G>A maps to NM_152572.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:49825028 C>T maps to NM_001082534.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr17:50008433 C>A maps to NM_001082534.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:63632624 C>T maps to NM_001218.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:86171713 C>T maps to NM_198584.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr1:150234695 A>C maps to NM_012113.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:150234015 C>T maps to NM_012113.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr8:86386596 A>G maps to NM_000067.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:86357401 C>T maps to NM_005181.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr8:86352124 T>G maps to NM_005181.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:86358462 G>A maps to NM_005181.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:9005998 G>A maps to ENST00000413627 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr1:9009385 G>A maps to ENST00000413627 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:9027745 C>T maps to ENST00000413627 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr1:9030996 G>A maps to ENST00000413627 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr1:9030987 C>A maps to ENST00000413627 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr1:9017325 G>T maps to ENST00000413627 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:66881123 C>T maps to NM_005182.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:61121465 G>A maps to NM_004056.4 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:61192347 C>T maps to NM_004056.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:35676070 C>A maps to NM_001216.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:231657992 T>C maps to NM_001130850.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr2:231624773 A>T maps to NM_001130850.1 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr13:49906109 G>A maps to NM_001079670.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr13:49924992 G>A maps to NM_001079670.1 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:227165156 C>T maps to NM_020247.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:227152741 C>T maps to NM_020247.4 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:227152948 C>T maps to NM_020247.4 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:227169737 C>T maps to NM_020247.4 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:227152798 C>T maps to NM_020247.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:24573538 C>A maps to NM_012295.3 P2091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:24459470 T>C maps to NM_012295.3 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr22:24530288 C>T maps to NM_012295.3 D1551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr22:24515544 G>A maps to NM_012295.3 Q1504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:24574127 C>T maps to NM_012295.3 S2209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:24456570 G>A maps to NM_012295.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:24472127 G>A maps to NM_012295.3 E881E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:24439496 C>A maps to NM_012295.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:24562755 C>T maps to NM_012295.3 P1719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:24483488 G>A maps to NM_012295.3 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:24560390 C>T maps to NM_012295.3 D1590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:24463059 G>T maps to NM_012295.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr22:24562605 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:20814616 T>C maps to NM_001100619.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:60969278 G>T maps to NM_031215.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:60966360 G>A maps to NM_031215.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:121093978 G>A maps to ENST00000453000 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:67287282 G>A maps to NM_016366.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr11:67287393 G>A maps to NM_016366.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:67287381 G>A maps to NM_016366.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr11:67225879 G>A maps to NM_145200.3 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:67225915 G>A maps to NM_145200.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr11:67223082 C>T maps to NM_145200.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:67225876 G>T maps to NM_145200.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:67222962 G>A maps to NM_145200.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:67223139 C>T maps to NM_145200.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:48543979 G>A maps to NM_019855.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr19:48543883 G>A maps to NM_019855.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:30116481 G>A maps to NM_182527.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:21739457 A>T maps to NM_138644.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr18:21739565 C>T maps to NM_138644.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:65143940 C>T maps to ENST00000371073 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr1:65139146 G>A maps to ENST00000371073 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr1:65098383 C>T maps to ENST00000371073 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:65143850 T>C maps to ENST00000371073 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:13368349 C>T maps to NM_023035.2 S1472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:13418631 G>A maps to NM_023035.2 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:13410046 G>A maps to NM_023035.2 D804D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:13372360 G>A maps to NM_023035.2 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:13470613 C>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:13409875 G>A maps to NM_023035.2 F861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr19:13411395 A>G maps to NM_023035.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:13386662 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:13409914 G>A maps to NM_023035.2 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:13323305 G>A maps to NM_023035.2 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:13414686 G>A maps to NM_023035.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:13470494 G>A maps to NM_023035.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:13409812 G>A maps to NM_023035.2 D882D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:13414692 C>T maps to NM_023035.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:13394194 G>T maps to NM_023035.2 C1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:13397764 G>A maps to NM_023035.2 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:13387909 G>A maps to NM_023035.2 G1289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:13414686 G>A maps to NM_023035.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:140968004 C>T maps to ENST00000277549 R1581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:140777296 C>T maps to ENST00000277549 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:140852062 G>A maps to ENST00000277549 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:140777317 C>T maps to ENST00000277549 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:140777197 C>T maps to ENST00000277549 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr9:140777326 C>T maps to ENST00000277549 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:140968056 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:141016369 T>C maps to ENST00000277549 G2314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:140773592 G>A maps to ENST00000277549 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr9:140904510 C>T maps to ENST00000277549 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr9:140772534 G>A maps to ENST00000277549 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:141016147 G>T maps to ENST00000277549 L2240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:140773592 G>A maps to ENST00000277549 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:140946567 T>C maps to ENST00000277549 N1246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:140777194 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:2566786 C>T maps to NM_199460.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr12:2706663 T>C did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr12:2558190 T>A maps to NM_199460.2 L176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:2795378 C>T maps to NM_199460.2 R1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr12:2719811 G>T maps to NM_199460.2 E1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr12:2566825 G>A maps to NM_199460.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:2800301 C>T maps to NM_199460.2 R2201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:2714867 C>T maps to NM_199460.2 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:2224702 C>T maps to NM_199460.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:2602491 C>T maps to NM_199460.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:2797863 G>A maps to NM_199460.2 R2095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:2676927 C>T maps to NM_199460.2 C621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:2705038 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:2789627 G>T maps to ENST00000399634 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:2659184 C>T maps to NM_199460.2 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr12:2676927 C>T maps to NM_199460.2 C621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:2760795 C>T maps to NM_001129829.1 D1334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:2795386 A>G maps to NM_199460.2 G1995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:2800253 C>T maps to NM_199460.2 D2185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr12:2795344 C>T maps to NM_199460.2 S1981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr12:2719828 C>T maps to NM_199460.2 V1247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:53766110 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:53783468 T>C maps to NM_001128840.1 Y1163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr3:53778853 G>A maps to NM_001128840.1 K1002K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:53700369 C>T maps to NM_001128840.1 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr3:53757545 C>T maps to NM_001128840.1 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:53806909 G>A maps to NM_001128840.1 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:53694219 C>T maps to NM_001128840.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:53694204 C>T maps to NM_001128840.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:181680203 A>C maps to ENST00000357570 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr1:181695295 C>T maps to ENST00000357570 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:181680123 C>T maps to ENST00000357570 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:181764121 T>A maps to ENST00000357570 R2050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr1:181724449 C>T maps to ENST00000357570 I1302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:181453005 G>A maps to ENST00000357570 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr1:181724428 G>C maps to ENST00000357570 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:181754545 G>T maps to ENST00000357570 E1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:181690988 T>C maps to ENST00000357570 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr1:181726081 T>C maps to ENST00000357570 D1383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:181706741 C>T maps to ENST00000357570 I1168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:181693654 C>T maps to ENST00000357570 N708N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:181688961 C>T maps to ENST00000357570 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr1:181706750 G>A maps to ENST00000357570 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:49083446 C>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:49071805 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:49081338 G>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:49061779 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:49078998 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:49079418 G>A did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:49076975 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:49082528 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:49067891 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:49065044 T>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:49066135 C>A did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:49066461 G>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:49086759 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr23:49079192 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:48678109 G>A maps to NM_018896.3 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:48703769 G>A maps to NM_018896.3 E2264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr17:48674154 G>A maps to NM_018896.3 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:48653058 C>A maps to NM_018896.3 C432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:48696323 G>A maps to NM_018896.3 A1912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:48680218 C>T maps to NM_018896.3 T1318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr17:48681642 G>C did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr16:1250558 T>C maps to NM_021098.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:1250470 G>A maps to NM_021098.2 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:1255202 C>T maps to NM_021098.2 C847C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr16:1252243 C>T maps to NM_021098.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:1250558 T>C maps to NM_021098.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr16:1259297 G>A maps to NM_021098.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr22:40055733 C>T maps to NM_021096.3 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr22:40037133 A>T maps to NM_021096.3 K335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:39966798 C>A maps to NM_021096.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr22:40057992 C>T maps to NM_021096.3 Y975Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr22:40043923 G>A maps to NM_021096.3 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr22:40064343 C>T maps to NM_021096.3 N1384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:40064364 T>C maps to NM_021096.3 D1391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr22:40036886 C>T maps to NM_021096.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr22:40069983 G>A maps to NM_021096.3 K1600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:40080307 A>G maps to NM_021096.3 A1944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr22:40045824 G>A maps to NM_021096.3 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr22:40037180 C>A maps to NM_021096.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:201027619 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:201058526 C>T maps to NM_000069.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:201022685 G>A maps to NM_000069.2 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:201047119 G>A maps to NM_000069.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:201039449 G>A maps to NM_000069.2 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr1:201039500 C>T maps to NM_000069.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:201012449 G>T maps to NM_000069.2 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:201043695 C>T maps to NM_000069.2 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:201022612 G>A maps to NM_000069.2 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:201054638 G>A maps to NM_000069.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr1:201061118 C>T maps to NM_000069.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:201054151 C>T maps to NM_000069.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:201058502 G>A maps to NM_000069.2 C261C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:81588644 A>G maps to NM_000722.2 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:81591313 C>T maps to NM_000722.2 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:81598281 T>C maps to NM_000722.2 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr7:82072712 G>A maps to NM_000722.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:81588671 A>G maps to NM_000722.2 S1026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:81643726 A>G maps to NM_000722.2 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:81588628 G>A maps to NM_000722.2 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:50418198 G>A maps to ENST00000435965 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:50402902 C>T maps to ENST00000435965 E1001E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:50414939 G>A maps to ENST00000435965 D528D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:50417406 G>A maps to ENST00000435965 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:55038846 C>T maps to NM_018398.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:54157557 G>A maps to NM_018398.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:54922022 G>A maps to NM_018398.2 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:54933813 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:54157602 T>C maps to NM_018398.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr3:54604064 C>T maps to NM_018398.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr3:54871250 C>T maps to NM_018398.2 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:54661851 A>G maps to NM_018398.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr3:55107474 C>G maps to NM_018398.2 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:54603874 C>T maps to NM_018398.2 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:54914834 G>A maps to NM_018398.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr3:54798282 G>T maps to NM_018398.2 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:2024073 G>A maps to NM_172364.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:1983838 C>T maps to NM_172364.4 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:1992104 G>A maps to NM_172364.4 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr12:2019092 G>A maps to NM_172364.4 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:2024024 G>A maps to NM_172364.4 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr12:1983838 C>T maps to NM_172364.4 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:1987495 G>A maps to NM_172364.4 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:2017137 G>A maps to NM_172364.4 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:37333584 C>T maps to NM_199247.1 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:37341051 C>T maps to NM_000723.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:37343782 C>T maps to NM_000723.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:18828509 C>T maps to NM_201596.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr10:18789767 C>T maps to NM_201596.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:18828394 C>A maps to NM_201596.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:49220202 C>T maps to NM_000725.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:49220258 G>A maps to NM_000725.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr12:49220833 C>T maps to NM_000725.2 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:49220150 G>A maps to NM_000725.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:152695679 G>A maps to NM_000726.3 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:152709979 T>C maps to NM_000726.3 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr2:152737346 G>A maps to NM_000726.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr2:152727080 C>T maps to NM_000726.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:65040889 C>T maps to NM_000727.3 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:65040928 C>T maps to NM_000727.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:65052272 C>A maps to NM_000727.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:65040805 C>T maps to NM_000727.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr22:36960742 C>T maps to NM_006078.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:36983539 G>A maps to NM_006078.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr22:36962409 G>A maps to NM_006078.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:24372934 G>A maps to NM_006539.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr16:24372727 C>T maps to NM_006539.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr16:24372787 C>T maps to NM_006539.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:65026894 G>A maps to NM_014405.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr17:64881014 G>A maps to NM_014404.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:64873461 C>T maps to NM_014404.1 C4C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr17:64880741 G>A maps to NM_014404.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:54515274 G>A maps to NM_145814.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:54418709 G>A maps to NM_031896.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:54444844 C>A maps to NM_031896.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr19:54445294 C>T maps to NM_031896.4 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:54466536 G>A maps to NM_031895.5 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr19:54483127 C>T maps to NM_031895.5 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:54481412 C>T maps to NM_031895.5 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:27458192 C>T maps to NM_004341.3 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:27449762 T>A maps to NM_004341.3 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:27446502 C>T maps to NM_004341.3 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:27444117 A>G maps to NM_004341.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr2:27454961 C>T maps to NM_004341.3 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:27447222 G>A maps to NM_004341.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:86028311 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:85932471 C>T maps to NM_153184.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr3:86114776 G>A maps to NM_153184.3 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:86114764 T>G maps to NM_153184.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr1:159162372 C>T maps to NM_021189.3 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:44130297 C>T maps to NM_145296.1 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:44130990 C>T maps to NM_145296.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr3:62739190 C>T maps to ENST00000383709 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:62860689 C>T maps to ENST00000383709 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:62860296 C>T maps to ENST00000383709 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:122269328 C>T maps to NM_001167940.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:122194637 G>A maps to NM_001167940.1 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:7370299 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:91072925 G>A maps to NM_004929.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:91094853 G>A maps to NM_004929.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr8:91094289 G>A maps to NM_004929.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr8:91094294 A>G maps to NM_004929.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:14989261 G>T maps to NM_001033953.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:54115378 C>T maps to NM_020898.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr12:54109687 G>A maps to NM_020898.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:93072951 T>A maps to NM_001164737.1 K290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:134632498 C>T maps to NM_033138.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:134635159 G>A maps to NM_033138.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:134618717 C>T maps to NM_033138.3 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr7:134617999 C>T maps to NM_033138.3 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr7:134632474 G>A maps to NM_033138.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:105215351 C>T maps to NM_001001412.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:105218346 C>T maps to NM_001001412.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr10:105218370 C>T maps to NM_001001412.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:105209698 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:105209488 G>A maps to NM_015916.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:105207115 C>T maps to NM_015916.4 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:47111799 A>C maps to NM_005184.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:5567440 G>A maps to NM_005185.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:68489898 G>A maps to NM_033429.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:68491893 G>A maps to NM_033429.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:5541218 G>A maps to NM_017422.4 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:5541224 G>A maps to NM_017422.4 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:71252834 G>A maps to NM_031468.3 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr19:13051266 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:16593515 C>T maps to NM_145046.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:16601325 C>T maps to NM_145046.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:16591433 G>A maps to NM_145046.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:16593572 G>A maps to NM_145046.3 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:128394339 C>T maps to ENST00000342367 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr3:9804848 C>A maps to NM_003656.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr3:9804597 C>T maps to NM_003656.3 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:9799261 C>T maps to NM_003656.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr10:12803036 C>T maps to NM_153498.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr5:149636153 C>T maps to NM_015981.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr5:149602667 G>A maps to NM_015981.3 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:149602646 G>A maps to NM_015981.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:44286736 G>A maps to NM_001220.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:44260281 C>T maps to NM_001220.4 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:44260471 C>A maps to NM_001220.4 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:114473242 T>C maps to ENST00000515496 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr10:75612947 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:183978983 C>T maps to NM_033259.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:183978962 G>A maps to NM_033259.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:110730431 T>C maps to NM_001744.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:110560282 C>T maps to NM_001744.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr5:110679801 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:3779600 G>A maps to ENST00000381771 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr17:3787703 G>A maps to ENST00000381771 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:3786410 C>T maps to ENST00000381771 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:121678609 A>G maps to NM_006549.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr12:121712173 G>A maps to NM_006549.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:49898997 C>T maps to NM_024046.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:134077002 G>A maps to NM_001745.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:138713713 C>T maps to ENST00000409386 R942R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:138710920 G>A maps to ENST00000409386 A1309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:138712717 G>A maps to ENST00000409386 G1274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:200816801 T>G maps to ENST00000236925 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:200730171 T>C maps to ENST00000236925 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:200818149 G>A maps to ENST00000236925 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:200817780 G>A maps to ENST00000236925 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:7721915 C>T maps to NM_015215.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:7723545 C>T maps to NM_015215.2 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:7737719 G>A maps to NM_015215.2 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:7724487 C>T maps to NM_015215.2 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:7527915 C>T maps to NM_015215.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr1:7792607 C>T maps to NM_015215.2 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:7725120 C>T maps to NM_015215.2 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:7806100 G>T maps to NM_015215.2 E1523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:7792622 C>T maps to NM_015215.2 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr1:7151398 C>T maps to NM_015215.2 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr1:7724184 C>T maps to NM_015215.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:7723845 C>A maps to NM_015215.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:7737776 C>T maps to NM_015215.2 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:4880350 A>G did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:4889532 G>T maps to NM_001171168.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr17:4875790 G>T maps to NM_015099.3 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:4875559 G>A maps to NM_015099.3 D925D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:4886165 G>A maps to NM_015099.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:4876899 G>A maps to NM_015099.3 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:4883428 T>C maps to NM_015099.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:4876496 G>A maps to NM_015099.3 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:4883673 G>A maps to NM_015099.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:4883673 G>A maps to NM_015099.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:4885434 A>G maps to NM_015099.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:67698441 C>T maps to NM_018448.3 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:12875477 C>T maps to NM_001162499.1 S1236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:12858332 T>C maps to NM_001162499.1 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:12858122 G>A maps to NM_001162499.1 E564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:12858542 C>T maps to NM_001162499.1 N704N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr3:12858629 T>C maps to NM_001162499.1 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr3:12858314 G>T maps to NM_001162499.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:76989802 C>T maps to NM_138793.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:40533258 C>T maps to NM_001105530.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:40537206 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:17543141 C>T maps to NM_006366.2 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:17507410 C>T maps to NM_006366.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:17421845 G>A maps to NM_006366.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:85628440 C>T maps to NM_001747.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr2:85622746 G>T maps to NM_001747.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:64977873 C>T maps to NM_005186.3 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:64977873 C>T maps to NM_005186.3 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:64972289 C>T maps to NM_005186.3 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:64977870 G>A maps to NM_005186.3 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:64950207 T>C maps to NM_005186.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:64953461 C>T maps to NM_005186.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:241537369 C>T maps to NM_023083.3 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr2:241530407 A>G maps to NM_023083.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:241533992 A>G maps to NM_023083.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:44148517 C>T maps to NM_007058.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:44148735 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:39229237 C>T maps to NM_144691.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr19:39228253 G>C maps to NM_144691.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr19:39233130 A>G maps to NM_144691.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr19:39233064 G>A maps to NM_144691.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:39229237 C>T maps to NM_144691.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:39229237 C>T maps to NM_144691.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:39224421 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:31010092 C>T maps to ENST00000295055 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr2:30985950 C>T maps to ENST00000295055 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr2:30966279 G>A maps to ENST00000295055 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:30974114 C>A maps to ENST00000295055 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr1:223958165 C>T maps to NM_001748.4 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:223954099 C>T maps to NM_001748.4 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:42681201 G>T maps to NM_000070.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:110489889 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:110494316 T>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:110489859 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:110495723 C>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:110497631 C>T did not map to a codon.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr23:110496245 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:110491973 A>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:15269406 C>T maps to NM_014296.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:230903328 C>T maps to NM_006615.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:36637135 C>T maps to NM_001749.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr11:34107865 T>C maps to NM_005898.4 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:34093452 C>T maps to NM_005898.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:34098104 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:30887987 A>G maps to NM_001002259.1 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:30863195 C>T maps to NM_001002259.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:5915018 C>T maps to ENST00000394521 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:75687144 A>G maps to NM_032606.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:75692520 A>G maps to NM_032606.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr5:35921153 G>A maps to NM_144647.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:35921186 C>T maps to NM_144647.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:116544379 A>G maps to NM_006136.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:116544410 G>T maps to NM_006136.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:18891438 C>T maps to NM_033328.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:37912252 C>T maps to NM_014550.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:2962767 G>A maps to NM_032415.4 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:2984022 C>T maps to NM_032415.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:2974164 C>T maps to NM_032415.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:2985498 T>C maps to NM_032415.4 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr7:2962951 C>T maps to NM_032415.4 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:2946427 G>A maps to NM_032415.4 C1103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:2951925 G>A maps to NM_032415.4 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr7:2977627 C>T maps to NM_032415.4 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:2974155 T>C maps to NM_032415.4 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:2984022 C>T maps to NM_032415.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:2959064 C>T maps to NM_032415.4 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:2959214 G>A maps to NM_032415.4 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:78176085 C>T maps to NM_024110.2 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr17:78176189 C>A maps to NM_024110.2 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:78169018 G>A maps to NM_024110.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:78169063 G>A maps to NM_024110.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:104915353 A>G maps to NM_001017534.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:104912363 G>A maps to NM_001017534.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:40853350 A>G maps to NM_032587.3 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr19:48715026 G>A maps to NM_001184900.1 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:139265580 T>C maps to NM_052813.4 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:139265833 C>T maps to NM_052813.4 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:67191612 C>T maps to NM_001166222.1 N798N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:67191325 C>T maps to NM_001166222.1 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr11:67191315 C>T maps to NM_001166222.1 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:67192056 G>A maps to NM_001166222.1 L946L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FP-8099-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:3028184 A>G maps to NM_001014437.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:3062130 G>A maps to NM_001014437.2 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:3040467 C>A maps to NM_001014437.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:3069061 G>A maps to NM_001014437.2 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:111329448 C>T maps to NM_024537.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:111335428 G>A maps to NM_024537.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:38318389 C>T maps to NM_007359.4 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:38323833 C>T maps to NM_007359.4 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:38324585 C>T maps to NM_007359.4 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:38325680 C>T maps to NM_007359.4 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:38320385 C>T maps to NM_007359.4 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr17:38324585 C>T maps to NM_007359.4 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr17:38325680 C>T maps to NM_007359.4 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr17:38323765 C>T maps to NM_007359.4 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:38318389 C>T maps to NM_007359.4 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:38323755 C>T maps to NM_007359.4 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:38323833 C>T maps to NM_007359.4 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:38324585 C>T maps to NM_007359.4 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:38325680 C>T maps to NM_007359.4 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:40937928 G>T maps to NM_170589.3 G2015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:40912958 T>A maps to NM_170589.3 L192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:40895137 G>T maps to NM_170589.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr15:40921538 G>A maps to NM_170589.3 Q1910Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:94168364 T>C maps to NM_022900.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:94146969 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:94184853 C>A maps to NM_022900.4 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:94174900 A>G maps to NM_022900.4 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:94168364 T>C maps to NM_022900.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:41379719 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:41413003 T>C did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr23:41446215 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:41712438 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:41390260 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:41394179 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:41524622 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:2231517 G>T maps to NM_020764.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:2237062 C>T maps to NM_020764.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:2231825 C>T maps to NM_020764.3 W578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:73500971 C>T maps to NM_020753.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:73504337 G>A maps to NM_020753.3 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:73498688 G>A maps to NM_020753.3 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr2:202050847 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:15166244 C>T maps to NM_012114.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15164408 C>T maps to NM_012114.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:15164692 C>T maps to NM_012114.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:142997068 G>A maps to NM_032982.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr7:142989723 C>T maps to NM_032982.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr7:143000937 C>T maps to NM_032982.2 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:142989723 C>T maps to NM_032982.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr7:143001809 C>T maps to NM_032982.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr7:143001854 C>T maps to NM_032982.2 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr7:143002037 C>T maps to NM_032982.2 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:104825630 C>T maps to NM_001225.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:104825594 A>G maps to NM_001225.3 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:104825728 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:115481531 A>T maps to NM_033338.4 K157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:115451792 T>C maps to NM_033338.4 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr10:115489259 G>T maps to NM_033338.4 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:202123106 T>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:202149987 G>T maps to NM_001080125.1 G477*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-4363-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:90577949 T>C maps to NM_012115.3 C1647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:90577061 C>T maps to NM_012115.3 C1351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:90577061 C>T maps to NM_012115.3 C1351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:90577010 T>C maps to NM_012115.3 S1334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:90573827 G>A maps to NM_012115.3 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:90572132 C>T maps to NM_012115.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:90572999 C>T maps to NM_012115.3 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr6:90572157 A>T maps to NM_012115.3 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:121981175 C>T maps to NM_001178065.1 Q432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:121981055 C>T maps to NM_001178065.1 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr3:121980734 C>A maps to NM_001178065.1 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:121980560 C>T maps to NM_001178065.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:121980529 C>T maps to NM_001178065.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr3:122003878 C>T maps to NM_001178065.1 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:121980769 C>T maps to NM_001178065.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:122003038 G>A maps to NM_001178065.1 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:121981055 C>T maps to NM_001178065.1 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:122002807 C>T maps to NM_001178065.1 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr20:55027311 T>C maps to NM_020356.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:55012386 C>T maps to NM_020356.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:96064901 G>T maps to ENST00000508830 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:10706295 C>T maps to NM_001079843.1 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:10714073 G>T maps to NM_001079843.1 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:10725239 G>A maps to NM_001079843.1 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:10713536 G>A maps to NM_001079843.1 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:10713857 A>G maps to NM_001079843.1 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:10705022 T>C maps to NM_001079843.1 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:10720567 G>A maps to NM_001079843.1 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:10713998 C>T maps to NM_001079843.1 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:10720567 G>A maps to NM_001079843.1 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr1:10700033 C>T maps to NM_001079843.1 R1415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr1:10718605 G>A maps to NM_001079843.1 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:10725421 G>T maps to NM_001079843.1 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:10719928 C>T maps to NM_001079843.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:10699613 G>A maps to NM_001079843.1 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:10725587 G>A maps to NM_001079843.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:10699616 G>A maps to NM_001079843.1 S1554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:10708132 C>T maps to NM_001079843.1 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:34485650 G>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:34489884 G>A maps to NM_001752.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:65788643 G>A maps to NM_053054.3 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:65788381 G>A maps to NM_053054.3 D609D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:65792902 G>A maps to NM_053054.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:43925049 C>A maps to NM_172095.1 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:43924969 G>T maps to NM_172095.1 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:43924969 G>T maps to NM_172095.1 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:43924999 C>T maps to NM_172095.1 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr15:43932663 C>T maps to NM_172095.1 W140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:134305634 C>T maps to NM_178019.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:134305721 G>A maps to NM_178019.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:134346088 T>C maps to NM_178019.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:26524486 C>A maps to NM_198137.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:26527937 T>C maps to NM_198137.1 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:26517330 G>A maps to NM_198137.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:26526467 C>T maps to NM_198137.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:92102821 C>T maps to NM_024764.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:38855583 C>T maps to NM_021185.4 H843H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:32199011 A>G maps to NM_005093.3 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:32232388 G>A maps to NM_005093.3 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:32232205 C>T maps to NM_005093.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr20:32232208 G>A maps to NM_005093.3 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr20:32224500 T>C maps to NM_005093.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:32232181 C>T maps to NM_005093.3 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:32232400 G>A maps to NM_005093.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:88945787 C>A maps to NM_005187.5 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr16:88951474 G>A maps to NM_005187.5 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr16:67100582 A>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:119156152 T>C maps to NM_005188.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:119146845 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr11:119155731 G>A maps to NM_005188.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:105400356 C>T maps to NM_170662.3 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:105400356 C>T maps to NM_170662.3 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:105378038 T>C maps to NM_170662.3 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:105378017 T>A maps to NM_170662.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:105377981 C>T maps to NM_170662.3 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:105470338 A>G maps to NM_170662.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:105422837 T>C maps to NM_170662.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:45296786 C>T maps to NM_012116.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:107398608 A>G maps to NM_024814.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr16:49315160 G>A maps to NM_004352.3 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr16:49313470 G>A maps to NM_004352.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:49315262 G>A maps to NM_004352.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:70209263 G>A maps to NM_182511.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:70209281 C>T maps to NM_182511.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:70209140 G>A maps to NM_182511.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:24897593 G>A maps to NM_001039771.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:24897156 T>C maps to NM_001039771.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:24897542 G>C maps to NM_001039771.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:24897096 G>T maps to NM_001039771.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr20:54573660 T>C maps to NM_080617.4 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr20:54575873 T>A maps to NM_080617.4 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:37442655 C>T maps to NM_001757.2 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr21:44488616 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr9:178909 A>T maps to NM_018491.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:173280 G>A maps to NM_018491.3 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:114195462 A>T maps to NM_172003.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:114210716 T>C maps to NM_172003.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:46154278 G>A maps to ENST00000442683 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:77758363 C>T maps to NM_005189.2 H374H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:77807928 C>T maps to NM_003655.2 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:77809002 C>T maps to NM_003655.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:77809107 C>T maps to NM_003655.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr12:54651320 T>G maps to NM_012117.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:39262534 G>A maps to NM_014292.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:39263008 C>T maps to NM_014292.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr22:39267746 C>T maps to NM_014292.3 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:77769923 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:14031641 C>T maps to NM_017721.4 D516D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:14037632 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:14020712 T>C maps to NM_017721.4 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:52821975 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:52822737 G>A maps to NM_032449.2 R611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr1:52825374 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:70500385 T>C maps to NM_018237.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr10:70509364 G>A maps to NM_018237.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:70516197 C>T maps to NM_018237.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:57106991 G>A maps to NM_133459.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr18:57107013 G>A maps to NM_133459.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:57103340 A>G maps to NM_133459.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:89408750 T>C maps to NM_001008661.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:89408687 T>C maps to NM_001008661.2 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:42906980 C>T maps to NM_001296.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr18:66513582 A>G maps to NM_024781.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr18:66504245 G>A maps to NM_024781.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:66678241 T>A maps to NM_024781.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr18:66721373 A>C maps to NM_024781.2 *514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:42979824 A>G maps to NM_213607.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:55756031 T>C maps to ENST00000339012 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:55771387 G>A maps to ENST00000339012 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr2:55756106 C>A maps to ENST00000339012 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr19:15121879 C>T maps to NM_173482.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:15133852 C>T maps to NM_173482.2 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:15132165 G>A maps to NM_173482.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15132650 G>T maps to NM_173482.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:15133897 G>A maps to NM_173482.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:56163821 C>A maps to NM_013301.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:56163868 G>A maps to NM_013301.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:56160816 C>T maps to NM_013301.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:56163919 G>A maps to NM_013301.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:35661183 A>G maps to NM_174923.2 *284W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:219893009 C>T maps to NM_194302.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:219895915 G>T maps to NM_194302.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:219878238 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:219900383 G>A maps to NM_194302.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:219900227 G>T maps to NM_194302.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr2:219875580 G>T maps to NM_194302.2 G1365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:219892514 G>A maps to NM_194302.2 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr2:219892491 C>T maps to NM_194302.2 W697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:219895548 G>A maps to NM_194302.2 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:219894816 C>T maps to NM_194302.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:219895873 G>A maps to NM_194302.2 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:74631232 G>A maps to NM_138357.1 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:74645549 G>A maps to NM_138357.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr4:110606495 C>T maps to NM_017918.4 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:186379493 G>A maps to NM_152775.3 Y749Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr4:186379712 A>G maps to NM_152775.3 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:186380473 G>A maps to NM_152775.3 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr4:186392203 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:186381014 G>A maps to NM_152775.3 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:186379289 C>T maps to NM_152775.3 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:185593325 G>T did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr4:185593357 T>G maps to NM_152683.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:185599424 C>A maps to NM_152683.2 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:185606593 C>A maps to NM_152683.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:114610996 G>A maps to NM_001040440.2 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr19:48807366 C>A maps to NM_144577.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:21988330 A>T maps to NM_152612.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr22:21989290 G>A maps to NM_152612.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:21989104 C>T maps to NM_152612.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr22:21988516 G>A maps to NM_152612.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr22:21989248 C>G maps to NM_152612.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr22:21989425 T>C maps to NM_152612.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr22:21991025 G>A maps to NM_152612.2 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:21989344 C>T maps to NM_152612.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:21989104 C>T maps to NM_152612.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:29169748 G>A maps to NM_173510.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:46963600 G>A maps to NM_144716.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:48922186 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:48923102 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:48925338 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:48921420 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:48925126 G>A did not map to a codon.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr23:48920040 G>A did not map to a codon.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr23:48925184 G>T did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:48921439 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:48922628 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:48923025 C>T did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr2:27850633 A>G maps to ENST00000435516 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr13:44443473 A>G maps to NM_144974.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:44434095 A>G maps to NM_144974.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:44411429 C>A maps to NM_144974.3 G270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:33424378 A>G maps to NM_032816.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:68590715 G>A maps to NM_176816.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:68581210 C>A maps to NM_176816.3 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:205672 G>A maps to NM_145265.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:205459 G>A maps to NM_145265.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr5:205696 G>T maps to NM_145265.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:31617484 C>T maps to NM_194300.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:31682345 G>A maps to NM_194300.2 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr7:31682399 G>A maps to NM_194300.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:31690790 A>T maps to NM_194300.2 I873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr7:31690787 G>A maps to NM_194300.2 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr7:31682577 G>T maps to NM_194300.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:31682654 A>G maps to NM_194300.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:42777196 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:42798651 G>A maps to NM_144719.3 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:42793518 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:42794102 C>T maps to NM_144719.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:42751225 G>T maps to NM_144719.3 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:42777360 C>T maps to NM_144719.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr3:42798564 G>A maps to NM_144719.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:92987642 G>A maps to NM_017667.2 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr7:92935137 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:57735852 G>A maps to NM_032269.5 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:57732055 G>A maps to NM_032269.5 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:57735978 G>A maps to NM_032269.5 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:57752347 C>T maps to NM_032269.5 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr16:57752257 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:128441249 T>C maps to NM_022742.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:79634812 T>C maps to NM_199287.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:109405347 G>A maps to NM_144978.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:109463339 A>G maps to NM_144978.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:123633802 G>A maps to NM_022757.4 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:123634042 T>C maps to NM_022757.4 G774G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8360-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:123667977 T>C maps to NM_022757.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:123633847 A>G maps to NM_022757.4 C839C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:223168941 G>A maps to NM_153038.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179730574 C>T maps to NM_173648.3 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:74701735 T>C maps to ENST00000393965 Q730Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr17:20799060 G>A maps to NM_001004306.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:76889458 C>T maps to NM_020879.2 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr7:76908082 C>T maps to NM_020879.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:106160653 G>T maps to NM_001008723.1 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:106209870 G>T maps to NM_001008723.1 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr10:106124544 C>A maps to NM_001008723.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:106160487 T>C maps to NM_001008723.1 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr2:159028731 G>A maps to NM_138803.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:24854801 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:24875301 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:124863120 T>C maps to NM_025004.2 N732N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:197521850 G>A maps to NM_001080539.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:197594734 C>T maps to NM_001080539.1 Q959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:197541383 C>T maps to NM_001080539.1 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr19:11531514 A>C maps to NM_145045.4 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:11531505 G>T maps to NM_145045.4 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr22:30762084 C>T maps to NM_001017437.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr22:30772517 A>T maps to NM_001017437.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:30766893 C>T maps to NM_001017437.2 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr22:30772688 G>A maps to NM_001017437.2 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:77255320 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:11460641 C>T maps to ENST00000427879 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:133379643 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:133379179 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:46086448 C>T maps to NM_001114938.2 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:93682303 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:93672694 G>T maps to NM_206886.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:93712496 G>T maps to NM_206886.2 E1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:93705384 A>G maps to NM_206886.2 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:93667455 C>T maps to NM_206886.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:93659211 A>G maps to NM_206886.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr1:159846398 G>A maps to NM_012337.2 H433H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:159860391 G>A maps to NM_012337.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr1:159858159 C>T maps to NM_012337.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr1:26566315 C>T maps to NM_022778.2 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:26597569 G>A maps to NM_022778.2 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:49093644 C>T did not map to a codon.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr23:49104739 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:49093688 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:49106177 G>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:3669275 C>T maps to NM_152492.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:3679949 G>A maps to NM_152492.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:3688086 G>T maps to NM_152492.2 *657Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:3680037 G>T maps to NM_152492.2 G441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr6:139097403 A>G maps to NM_015439.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr1:43119641 G>A maps to NM_001080850.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:74536489 G>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:74536465 C>T maps to ENST00000321288 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr11:27371795 T>G maps to NM_080654.2 *230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:49249251 T>C maps to NM_178173.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:126138587 G>A maps to ENST00000505024 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:126138521 C>A maps to ENST00000505024 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:96275316 G>A maps to NM_182496.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:96273420 C>G did not map to a codon.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr12:96330275 A>G maps to NM_182496.2 N4N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:96263269 T>C maps to NM_182496.2 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:180397080 G>A maps to NM_181426.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:180364953 A>G maps to NM_181426.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:180364905 A>G maps to NM_181426.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr3:180397168 G>A maps to ENST00000273654 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:180377344 T>C maps to NM_181426.1 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:78055727 C>T maps to NM_017950.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:78013750 A>G maps to NM_017950.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:78011978 C>T maps to NM_017950.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr17:78013900 A>G maps to NM_017950.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:78023883 C>A maps to NM_017950.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:94769790 A>G maps to NM_001042399.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:62527045 G>A maps to NM_138363.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr17:62504716 A>C maps to NM_138363.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr17:64059182 A>C maps to NM_145036.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:63923698 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:64049988 A>G maps to NM_145036.3 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:63685266 C>A maps to NM_145036.3 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:64171303 G>A maps to NM_145036.3 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:63685296 G>A maps to NM_145036.3 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:128757720 C>T maps to NM_024768.2 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:191097970 G>T maps to NM_178335.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:113176103 C>T maps to NM_144718.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:113169270 T>A maps to NM_144718.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr3:107097189 T>G maps to NM_032600.2 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:80136445 T>C maps to ENST00000445854 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:80159421 G>A maps to ENST00000445854 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:61564175 A>G did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:61552815 C>T maps to ENST00000395341 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:61665921 C>T maps to ENST00000395341 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:61572398 A>G maps to ENST00000395341 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr10:61566726 A>T maps to ENST00000395341 C319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:119773071 G>C did not map to a codon.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr12:119954426 G>T did not map to a codon.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr12:119926656 C>T maps to NM_178499.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:119773055 G>A maps to NM_178499.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:119943092 G>T maps to NM_178499.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr12:119943016 C>A maps to NM_178499.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr12:119960741 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:46498680 A>G did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:123270348 G>A maps to NM_201435.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:123285970 A>G maps to NM_201435.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:123297962 A>G maps to NM_201435.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:111291375 G>A maps to NM_152591.1 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr12:120502664 C>T maps to NM_207311.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:120530907 G>A maps to NM_207311.2 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:120509470 C>T maps to NM_207311.2 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:3085467 C>T maps to NM_001103175.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:49298821 G>T maps to NM_033124.4 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:49298863 C>T maps to NM_033124.4 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:49312164 T>C maps to NM_033124.4 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:56651195 G>T maps to NM_001141947.1 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:56651333 C>T maps to NM_001141947.1 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr3:56597953 C>T maps to NM_001141947.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:56651272 G>A maps to NM_001141947.1 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:93103270 G>A maps to NM_181645.3 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr11:93104247 G>A maps to NM_181645.3 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:32740785 T>C maps to NM_001026383.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr10:32742306 C>T maps to NM_001026383.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr10:32863355 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:49200837 C>T maps to NM_022903.3 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:49201173 A>G maps to NM_022903.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr3:49200782 G>A maps to NM_022903.3 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:32636060 G>A maps to NM_001008391.2 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:32676470 A>G maps to NM_001008391.2 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:32635337 A>G maps to NM_001008391.2 N842N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:132285714 C>T maps to NM_138770.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:132288335 G>A maps to NM_138770.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:132290600 G>A maps to NM_138770.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr2:130897229 G>A maps to NM_207310.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:130897828 G>A maps to NM_207310.1 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:100606012 C>T maps to NM_019083.2 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr1:100613740 G>A maps to NM_019083.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:520942 C>T maps to NM_032358.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:46915401 G>A maps to NM_032040.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:46915731 G>T maps to NM_032040.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr19:46915029 C>A maps to NM_032040.3 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:112357945 G>A maps to ENST00000447230 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:96117863 G>A maps to NM_024725.3 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:96117890 A>G maps to NM_024725.3 H7H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:96086842 C>T maps to NM_024725.3 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr2:56420318 C>T maps to NM_001080433.1 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:56420253 A>T maps to NM_001080433.1 K307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:56570050 A>G maps to NM_001080433.1 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr2:56420472 G>T maps to NM_001080433.1 G380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:65658544 G>A maps to NM_006848.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:60615435 G>A maps to NM_024098.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:60609968 A>G maps to NM_024098.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:60617770 G>A maps to NM_024098.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:60609935 C>T maps to NM_024098.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:55561384 T>A maps to ENST00000436346 K858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:55561247 C>T maps to ENST00000436346 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:55561432 G>A maps to ENST00000436346 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr11:64112238 G>A maps to NM_032251.5 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:64109147 G>A maps to NM_032251.5 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr11:64119678 G>A maps to NM_032251.5 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:64108423 C>T maps to NM_032251.5 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:91780227 G>A maps to NM_001080414.2 N644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:91787574 A>G maps to NM_001080414.2 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:91805635 G>T maps to NM_001080414.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr14:91806314 G>A maps to NM_001080414.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:91770130 G>A maps to NM_001080414.2 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:91787502 G>A maps to NM_001080414.2 C496C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:91780407 G>A maps to NM_001080414.2 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:85396903 G>A maps to NM_152723.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:47774661 T>C maps to NM_015603.2 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:13802558 T>C maps to NM_001031713.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:82996915 C>A maps to NM_021825.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:124421928 G>A maps to NM_025140.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:118732838 C>T maps to NM_019044.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:118766147 T>C maps to NM_019044.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr2:118766204 A>G maps to NM_019044.4 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr19:4249235 G>A maps to NM_018074.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:7043252 G>A maps to NM_153376.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:7043036 C>T maps to NM_153376.2 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:7044596 C>T maps to NM_153376.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:7043546 G>A maps to NM_153376.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:41822536 C>T maps to NM_052848.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:41822544 C>T maps to NM_052848.1 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:41822287 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:31116475 G>A maps to NM_001105564.1 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:31125290 A>G maps to NM_001105564.1 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:31124667 G>A maps to NM_001105564.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:36169822 T>G maps to NM_005893.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:36169948 C>T maps to NM_005893.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:26483547 G>A maps to NM_000730.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:26487446 G>A maps to NM_000730.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:26483748 G>A maps to NM_000730.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:26483559 G>T maps to NM_000730.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr4:26483540 G>T maps to NM_000730.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr4:26483295 C>T maps to NM_000730.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:6292298 C>T maps to NM_176875.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:6292724 G>A maps to NM_176875.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:6291483 C>T maps to NM_176875.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:6290929 C>T maps to NM_176875.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:6291064 T>G maps to NM_176875.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:6292283 G>A maps to NM_176875.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr11:6291351 G>A maps to NM_176875.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr11:6290929 C>T maps to NM_176875.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:32688802 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr17:32614136 C>T maps to NM_002986.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr17:32582394 C>T maps to NM_002982.3 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:228680263 C>A maps to NM_004591.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr17:34340328 G>A maps to NM_005064.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:34662076 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:43388543 C>T maps to NM_148672.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr5:43412388 G>C maps to NM_148672.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:32646549 G>A maps to ENST00000394620 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr17:32647375 C>A maps to ENST00000394620 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:45115622 G>A maps to NM_001029835.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:45104123 G>A maps to NM_001029835.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:45115559 G>A maps to NM_001029835.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:45067387 G>T maps to NM_001029835.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:37014190 A>G maps to NM_003914.3 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:37012842 C>T maps to NM_003914.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr13:37007219 A>C maps to NM_003914.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr13:37012965 A>G maps to NM_003914.3 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr13:37014127 G>A maps to NM_003914.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr13:37014259 G>A maps to NM_003914.3 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:37011902 G>A maps to NM_003914.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr4:122740664 C>T maps to NM_001237.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:20784645 G>A maps to NM_182849.1 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:50085218 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:50053727 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:50052658 C>T did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:50090652 C>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:50051703 A>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:50051988 A>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:50052636 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:50055600 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:50052148 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:50090754 T>C did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:50051782 C>T did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:50052015 T>G did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr23:50052273 T>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:50053306 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:50054262 G>A did not map to a codon.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr23:50056924 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:50090645 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:50052224 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:50054469 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:50055618 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:50053922 G>C did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:50085292 A>G did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:50052854 T>A did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr6:100009498 C>T maps to NM_005190.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:69456218 A>G maps to NM_053056.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr11:69462816 C>T maps to NM_053056.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:4385202 C>T maps to NM_001759.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:4409105 C>T maps to NM_001759.3 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:30313365 C>T maps to NM_001238.1 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:30313452 C>T maps to NM_001238.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:95906148 C>T maps to NM_057749.1 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr16:2499404 C>T maps to NM_001761.2 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:2503499 C>T maps to NM_001761.2 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr16:2482984 G>C maps to NM_001761.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:2489442 C>T maps to NM_001761.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:132086667 G>A maps to NM_001039780.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:97816980 G>A maps to NM_001134375.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:97817886 G>A maps to NM_001134375.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:97816674 C>T maps to NM_001134375.1 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:159680756 G>A maps to NM_024565.5 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:159738870 G>A maps to NM_024565.5 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:159680576 C>T maps to NM_024565.5 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:159686752 G>A maps to NM_024565.5 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:159707574 G>T maps to NM_024565.5 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:159680603 G>A maps to NM_024565.5 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:159680792 G>A maps to NM_024565.5 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:159680555 G>A maps to NM_024565.5 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:159680468 C>T maps to NM_024565.5 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:1328773 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:1326208 G>A maps to NM_030937.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr1:1330803 A>C maps to NM_030937.4 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:1322693 G>A maps to NM_030937.4 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:1330887 G>A maps to NM_030937.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:49086827 G>A maps to NM_001240.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:49087187 G>T maps to NM_001240.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:49087085 C>T maps to NM_001240.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:49110341 C>T maps to NM_001240.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:49087736 A>G maps to NM_001240.2 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:135711758 G>A maps to NM_058241.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:35842059 T>C maps to NM_145012.4 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr2:208611775 C>T maps to ENST00000295414 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr15:55651933 C>T maps to ENST00000442196 Q679Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:55652755 A>G maps to ENST00000442196 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr15:55652557 G>A maps to ENST00000442196 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr3:46245462 G>T maps to NM_001295.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:46245623 G>A maps to NM_001295.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:40832554 A>G maps to NM_016602.2 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:46306954 C>T maps to NM_178328.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:32995804 C>T maps to NM_005508.4 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:32995360 G>A maps to NM_005508.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:32995135 T>C maps to NM_005508.4 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr3:32995240 G>C maps to NM_005508.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:46415361 C>T maps to NM_001100168.1 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr6:167550722 G>A maps to NM_004367.5 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:167549867 G>A maps to NM_004367.5 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:167550437 C>A maps to NM_004367.5 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr17:38711206 G>A maps to NM_001838.3 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:38711959 T>C maps to NM_001838.3 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:39374652 G>A maps to NM_005201.3 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:39374055 C>A maps to NM_005201.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr3:45942858 C>T maps to NM_031200.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:45942736 A>T maps to NM_031200.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:66372814 C>T maps to NM_005125.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:66372847 C>T maps to NM_005125.1 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:156288679 T>C maps to NM_005998.4 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:62110668 T>C maps to NM_006430.2 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:62099381 T>C maps to NM_006430.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:10258613 C>T maps to NM_012073.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:10264814 C>T maps to NM_012073.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr5:10261760 G>A maps to NM_012073.3 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:56123450 T>C maps to NM_001762.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:56128608 T>C maps to NM_001762.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr7:56122108 C>T maps to NM_001762.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:33266704 G>A maps to NM_006584.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:33266713 A>G maps to NM_006584.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr17:33286635 G>A maps to NM_006584.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:33259421 G>A maps to NM_006584.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:73477493 C>T maps to NM_006429.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:73476279 T>G maps to NM_006429.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:73477496 C>T maps to NM_006429.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:73477499 G>A maps to NM_006429.3 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr2:73477514 G>A maps to NM_006429.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:30439210 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:17072816 C>G maps to NM_014406.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr22:17072885 G>T maps to NM_014406.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:117568455 A>T maps to NM_004258.3 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:117554379 C>A maps to NM_004258.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:74472142 G>A maps to NM_133493.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:74517819 G>A maps to NM_133493.3 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:74476734 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:74481261 T>C maps to NM_133493.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:74476678 G>A maps to NM_133493.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:74530183 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:74516796 T>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:74472142 G>A maps to NM_133493.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr6:74446227 G>T maps to NM_133493.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140011860 C>T maps to NM_001174105.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:836770 C>T maps to NM_139030.3 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr1:145699046 G>A maps to NM_007053.2 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:7649571 G>A maps to NM_004244.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:7649628 G>A maps to NM_004244.4 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr12:7639262 C>A maps to NM_004244.4 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr12:7639269 G>T maps to NM_004244.4 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr12:7632520 C>A maps to NM_004244.4 G1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr12:7640501 T>G maps to NM_004244.4 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:7586129 G>A maps to ENST00000416109 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:7522127 G>A maps to ENST00000416109 G1298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:7522058 A>G maps to ENST00000416109 D1321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:7527478 T>C maps to ENST00000416109 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:7527056 G>A maps to ENST00000416109 D1140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:7527910 A>G maps to ENST00000416109 C999C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr12:7551180 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:7548697 G>A maps to ENST00000416109 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:109690118 G>A maps to NM_006016.4 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr5:66480390 C>A maps to NM_005582.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:66478996 G>A maps to NM_005582.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:28948670 C>T maps to NM_001178098.1 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:28948646 C>T maps to NM_001178098.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr16:28943925 G>A maps to NM_001178098.1 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:158225972 C>T maps to NM_001763.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:158226061 C>A maps to NM_001763.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr1:158227220 T>C maps to NM_001763.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:158224874 G>A maps to NM_001763.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:158300853 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:158299692 G>A maps to NM_001764.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:158259868 G>A maps to NM_001765.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr1:158259915 G>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:158263002 A>G maps to NM_001765.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:158151347 G>A maps to NM_001766.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:158152734 T>C maps to NM_001766.3 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:158151368 G>A maps to NM_001766.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr1:158151308 G>A maps to NM_001766.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:158152041 C>T maps to NM_001766.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:158324299 T>C maps to NM_030893.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr3:112063821 C>G maps to NM_001004196.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:112063824 G>A maps to NM_001004196.2 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:112546412 G>A maps to NM_001008784.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr2:71058829 A>T did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr2:71058225 C>T maps to NM_015717.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr2:71060117 A>G maps to NM_015717.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:35828790 C>A maps to NM_001771.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:35831913 C>T maps to NM_001771.3 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:35832349 G>T maps to NM_001771.3 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr19:35836515 C>T maps to NM_001771.3 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr19:35823666 G>A maps to NM_001771.3 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:67562970 G>A maps to NM_006566.2 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr18:67563063 G>A maps to NM_006566.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr1:167404662 C>T maps to NM_198053.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:167400932 G>A maps to NM_198053.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr1:167400917 T>C maps to NM_198053.2 *165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:66084468 C>T maps to NM_020404.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr11:66083781 G>A maps to NM_020404.2 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:66083577 C>T maps to NM_020404.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:66083271 G>T maps to NM_020404.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:6559354 C>T maps to NM_001242.4 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:6554269 G>A maps to NM_001242.4 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:73995269 G>A maps to NM_001024736.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:204591491 G>A maps to NM_006139.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr6:47471061 A>G maps to NM_012120.2 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:47563666 T>C maps to NM_012120.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:30365562 C>T maps to NM_006110.2 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr17:72470704 G>A maps to NM_007261.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:72539079 T>G maps to NM_006678.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:72613482 G>A maps to ENST00000426295 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr17:72519040 T>A did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:72527552 T>C maps to NM_174892.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:72576252 C>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:72700806 G>T maps to ENST00000412086 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr17:72708984 G>T maps to ENST00000412086 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:41925965 C>T maps to NM_145273.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:41926250 C>T maps to NM_145273.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr2:160628361 T>G maps to NM_001198759.1 *1874Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr19:51742770 A>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:51742770 A>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr19:51742915 C>T maps to NM_001772.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:51728630 C>T maps to NM_001772.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr19:51742770 A>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:208061171 G>A maps to NM_001025109.1 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr1:208061154 G>A maps to NM_001025109.1 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:80292448 G>A maps to NM_001127444.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:15780066 C>T maps to NM_001775.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:15850202 C>A maps to NM_001775.2 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:15780177 C>T maps to NM_001775.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:15780075 A>G maps to NM_001775.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr11:118178015 G>A maps to NM_000733.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:45911522 G>A maps to ENST00000423698 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:45911616 C>T maps to ENST00000423698 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:6928488 C>A maps to NM_000616.4 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr12:6924048 G>T maps to NM_000616.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:6923958 G>A maps to NM_000616.4 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:6926428 T>C maps to NM_000616.4 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:6909476 C>A maps to NM_000616.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135732554 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:135741441 C>T did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:135738536 G>A did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr23:135741442 G>A did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:135736557 G>A did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr23:135741370 C>G did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:135741285 A>C did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:135738550 G>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:35229753 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr11:35201923 C>T maps to NM_000610.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr3:107798991 A>G maps to NM_001777.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:160654896 T>C maps to NM_001778.2 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:60885875 C>T maps to NM_014207.3 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:60886385 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:60892564 C>A maps to NM_014207.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:26646687 C>T maps to NM_001803.2 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:111437655 G>A maps to NM_000560.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:111440441 G>A maps to NM_000560.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:111439276 G>A maps to NM_000560.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr1:117087144 A>T maps to NM_001779.2 L51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:117078716 A>G maps to NM_001779.2 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:117064525 A>G maps to ENST00000369487 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:117078721 G>A maps to NM_001779.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:33731872 G>A maps to NM_203331.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr1:157804431 G>A maps to NM_005894.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:157804382 G>A maps to NM_005894.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:157803264 G>T maps to NM_005894.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:157805862 G>A maps to NM_005894.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:60785860 T>C maps to NM_006725.3 C646C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:60783257 G>A maps to NM_006725.3 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:60776003 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:60777347 T>C did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:9907699 T>C maps to NM_001781.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr12:9907795 A>C maps to NM_001781.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:80274771 C>T maps to NM_006137.6 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:35616087 C>T maps to NM_001782.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:42383114 C>T maps to NM_001783.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:119263418 A>G maps to NM_005191.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr11:2418060 C>T maps to NM_004356.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:14133941 C>T maps to NM_004233.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:6344709 A>G maps to NM_001769.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:6334635 C>T maps to NM_001769.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:23065848 C>T maps to NM_012072.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:23066076 G>A maps to NM_012072.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr20:23065701 G>A maps to NM_012072.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:23064996 C>T maps to NM_012072.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:23065494 G>A maps to NM_012072.3 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr20:23065098 G>A maps to NM_012072.3 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:111342619 A>G maps to NM_198196.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:111319600 A>G maps to NM_198196.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr3:111264124 G>A maps to NM_198196.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:14517535 C>T maps to NM_078481.2 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:14501874 C>T maps to NM_078481.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:14508024 C>A maps to NM_078481.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:14516663 G>A maps to NM_078481.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:2656272 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:149983361 G>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:149938841 T>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:149983347 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:149944760 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:149963933 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:149945927 T>C did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr15:43017427 G>A maps to NM_138477.2 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:43022950 G>A maps to NM_138477.2 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:43025361 G>A maps to NM_138477.2 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:43020418 C>A maps to NM_138477.2 E951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr15:43019869 G>A maps to NM_138477.2 R1015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:43021534 C>T maps to NM_138477.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr15:43021534 C>T maps to NM_138477.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:43023981 G>A maps to NM_138477.2 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr15:43018352 C>A maps to NM_138477.2 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:12291659 C>T maps to NM_006023.2 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:12238291 G>A maps to NM_006023.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr10:12259409 C>T maps to NM_006023.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:100964649 T>C maps to NM_033312.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:99284801 G>A maps to NM_033331.2 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:99272004 G>A maps to NM_033331.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:99285990 C>A maps to NM_033331.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:99284795 A>G maps to NM_033331.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:115022678 C>T maps to NM_003903.3 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:43825903 C>T maps to NM_001255.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:43825638 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:43824984 G>A maps to NM_001255.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:43824928 C>T maps to NM_001255.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:54420720 A>G maps to NM_001170402.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr5:54415674 C>A maps to NM_001170402.1 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr5:54420714 T>C maps to NM_001170402.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr5:137537840 C>A maps to NM_004661.3 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:137537823 G>A maps to NM_004661.3 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr3:48226153 G>A maps to NM_001789.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr20:3782935 C>T maps to NM_021873.2 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:3780932 A>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:3782593 C>A maps to NM_021873.2 C315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:137661708 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr5:137661569 C>T maps to NM_001790.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:116029554 A>G maps to NM_139286.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:4684899 G>A maps to NM_017913.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:110540592 C>T maps to NM_015891.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:110534290 C>T maps to NM_015891.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:110538951 C>T maps to NM_015891.2 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:227203898 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:227335095 C>T maps to ENST00000366766 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:103404709 G>A maps to NM_006035.3 P1622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:103449934 C>T maps to NM_006035.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:103447310 C>T maps to NM_006035.3 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr14:103435029 C>T maps to NM_006035.3 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:103447136 G>A maps to NM_006035.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:103478523 A>G maps to NM_006035.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:103470321 G>A maps to NM_006035.3 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:64606690 C>T maps to NM_017525.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:64601435 T>A maps to NM_017525.2 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:64606558 C>T maps to NM_017525.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:64597243 C>T maps to NM_017525.2 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:64597666 G>A maps to NM_017525.2 N1122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr11:64603907 T>C maps to NM_017525.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:64602413 T>C maps to NM_017525.2 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:64595038 G>A maps to NM_017525.2 T1370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:64597711 C>T maps to NM_017525.2 A1107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:64597000 G>A maps to NM_017525.2 G1303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:37873628 C>T maps to NM_006449.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:71282555 G>A maps to NM_012121.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:71282534 G>A maps to NM_012121.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:71281598 A>G maps to NM_012121.4 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:71281907 G>A maps to NM_012121.4 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:71282234 C>T maps to NM_012121.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr22:19484941 C>T maps to NM_001178010.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr22:19492983 A>G maps to NM_001178010.1 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:44376245 T>C maps to NM_001253.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:44376336 C>T maps to NM_001253.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:44392214 T>C maps to NM_001253.2 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr6:44413522 A>G maps to NM_001253.2 Q741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr17:38447832 T>A maps to NM_001254.3 C191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:91985808 G>T maps to NM_001134420.1 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:91985736 C>T maps to NM_001134420.1 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:91977450 C>T maps to NM_001134420.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr1:91977204 T>C maps to NM_001134420.1 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:91989925 T>C maps to NM_001134420.1 N553N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:193099371 G>A maps to NM_024529.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:193104570 C>T maps to NM_024529.4 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:193205391 C>T maps to NM_024529.4 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr8:25346198 G>A maps to ENST00000434814 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:25343306 C>T maps to ENST00000434814 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:25323824 C>T maps to ENST00000434814 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:6958313 C>A maps to NM_031299.4 G234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:174229537 C>T maps to NM_031942.4 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:21943868 C>T maps to NM_018719.4 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:21942600 C>T maps to NM_018719.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:21946037 G>A maps to NM_018719.4 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:21985415 A>G maps to NM_018719.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:38172655 C>T maps to NM_018101.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:45153658 C>A maps to NM_022842.3 G191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:45137007 G>A maps to NM_022842.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:45132791 G>A maps to NM_022842.3 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:54607089 G>C maps to NM_201546.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr16:68856128 G>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:68844098 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:68862116 G>A maps to NM_004360.3 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr16:68842594 G>T did not map to a codon.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr16:68846035 A>G did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:68862191 C>T maps to NM_004360.3 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:68844110 C>T maps to NM_004360.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:24511444 A>G maps to NM_006727.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:24498628 C>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:24509889 T>C maps to NM_006727.3 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:24509928 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:24509700 G>A maps to NM_006727.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:24511518 G>A maps to NM_006727.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr5:24498533 A>G maps to NM_006727.3 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:24505262 G>A maps to NM_006727.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:24593377 G>A maps to NM_006727.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:24537768 T>C maps to NM_006727.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:64981895 C>T maps to NM_001797.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr16:65038661 C>T maps to NM_001797.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:64981667 G>A maps to NM_001797.2 Y743Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:64981760 G>A maps to NM_001797.2 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:21802400 G>A maps to NM_004061.3 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr5:21751872 C>T maps to NM_004061.3 E786E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr5:21975260 A>G maps to NM_004061.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:21783500 C>T maps to NM_004061.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr5:21783539 G>A maps to NM_004061.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:21842350 G>A maps to NM_004061.3 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr5:21755817 G>T maps to NM_004061.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:21975260 A>G maps to NM_004061.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr5:21755927 G>A maps to NM_004061.3 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:21783499 G>A maps to NM_004061.3 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:83065684 C>T maps to ENST00000268613 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:83378582 C>T maps to ENST00000268613 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr16:83159045 G>A maps to ENST00000268613 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:83712049 C>T maps to ENST00000268613 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:83378553 C>T maps to ENST00000268613 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:89258291 C>T maps to NM_004933.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:89251635 C>T maps to NM_004933.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:89254626 C>T maps to NM_004933.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr16:89254539 A>G maps to NM_004933.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:66944196 C>T maps to NM_004062.2 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:66943991 G>A maps to NM_004062.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:66943281 G>A maps to NM_004062.2 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:66949215 G>A maps to NM_004062.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr16:66948277 G>A maps to NM_004062.2 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:66943185 G>A maps to NM_004062.2 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:66949215 G>A maps to NM_004062.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr16:66950202 C>A maps to NM_004062.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:95189850 G>T maps to NM_001144663.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:95178127 A>G maps to NM_001144663.1 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:95188799 G>A maps to NM_001144663.1 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr8:95186359 T>A maps to NM_001144663.1 K185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:95143160 A>G maps to NM_001144663.1 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:95164229 C>T maps to NM_001144663.1 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:95158306 C>T maps to NM_001144663.1 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr5:19473496 A>G maps to NM_004934.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr5:19591324 T>C maps to NM_004934.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:19838876 A>G maps to NM_004934.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr5:19721492 G>A maps to NM_004934.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:19747114 A>G maps to NM_004934.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr5:19721507 C>A maps to NM_004934.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr5:19520819 G>T maps to NM_004934.3 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:64176343 G>A maps to NM_021153.2 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:64176285 C>A maps to NM_021153.2 G592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr18:25572681 A>G maps to NM_001792.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:25568494 A>G maps to NM_001792.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr18:25583074 C>T maps to NM_001792.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr18:25593760 G>T maps to NM_001792.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr18:25543416 G>A maps to NM_001792.3 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr18:25582960 T>C maps to NM_001792.3 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr18:25532228 A>T maps to NM_001792.3 L870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:25589713 C>T maps to NM_001792.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr18:25585873 G>A maps to NM_001792.3 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr18:59221696 C>T maps to NM_031891.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:59158025 C>T maps to NM_031891.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:59206372 G>T maps to NM_031891.2 G509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:59221696 C>T maps to NM_031891.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:59157848 C>T maps to NM_031891.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:59195262 G>T maps to NM_031891.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:44869686 G>A maps to NM_021248.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:44869869 G>A maps to NM_021248.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:44815500 G>A maps to NM_021248.1 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:44839079 G>A maps to NM_021248.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:44845507 G>A maps to NM_021248.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:44806828 G>A maps to NM_021248.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:73538007 C>T maps to ENST00000398860 I1715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:73558150 G>A maps to ENST00000398860 T2295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:73537989 C>T maps to ENST00000398860 H1709H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr10:73269926 T>C maps to ENST00000398860 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:73501452 C>T maps to ENST00000398860 N1545N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr10:73574962 C>T maps to ENST00000398860 S3336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:73571098 G>A maps to ENST00000398860 K3040K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr10:73270758 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:73491780 C>T maps to ENST00000398860 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:73501578 C>T maps to ENST00000398860 S1587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:73491897 G>A maps to ENST00000398860 P1295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr10:73569610 C>T maps to ENST00000398860 L2924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:73553050 C>T maps to ENST00000398860 T2127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:23519066 G>A maps to NM_022478.3 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:23518335 G>A maps to NM_022478.3 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:58562545 C>T maps to NM_177980.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:58563984 G>A maps to NM_177980.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:58559742 T>C maps to NM_177980.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:68716320 T>C maps to NM_001793.4 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr16:68718509 C>T maps to NM_001793.4 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:68732230 C>T maps to NM_001793.4 Y806Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:68732296 C>T maps to NM_001793.4 D828D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr16:68718523 C>T maps to NM_001793.4 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:60448950 C>T maps to NM_001794.2 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:60448910 C>T maps to NM_001794.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:60508124 C>T maps to NM_001794.2 D774D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:60499481 C>T maps to NM_001794.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr20:60427820 C>T maps to NM_001794.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:60348096 T>C maps to NM_001794.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:60503308 C>T maps to NM_001794.2 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr20:60485494 C>T maps to NM_001794.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:60504829 C>T maps to NM_001794.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:60511883 C>T maps to NM_001794.2 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr20:60498760 A>C maps to NM_001794.2 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr20:60511940 C>T maps to NM_001794.2 N897N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:66436969 C>T maps to NM_001795.3 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr16:66422263 C>T maps to NM_001795.3 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:66413311 A>G maps to NM_001795.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:31297468 C>A maps to NM_004932.2 Y199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:31313499 G>A maps to NM_004932.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr5:31317786 G>A maps to NM_004932.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:31323339 C>T maps to NM_004932.2 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr5:31305339 T>G maps to NM_004932.2 Y353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr5:31313499 G>A maps to NM_004932.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:63477139 G>A maps to NM_004361.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:63547676 A>G maps to NM_004361.2 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr18:63530058 A>G maps to NM_004361.2 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr18:63481814 G>T maps to NM_004361.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:63530139 C>G maps to NM_004361.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:63548082 C>T maps to NM_004361.2 R771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr18:63489411 G>T maps to NM_004361.2 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:63547736 C>T maps to NM_004361.2 D655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr18:63477133 C>T maps to NM_004361.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr18:63530034 G>A maps to NM_004361.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr18:63511130 G>A maps to NM_004361.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr18:63525177 A>G maps to NM_004361.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr18:63547694 C>T maps to NM_004361.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr16:61935320 A>G maps to NM_001796.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr16:61687976 C>T maps to NM_001796.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr16:61935314 A>C maps to NM_001796.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr16:61761003 G>A maps to NM_001796.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:61891116 C>T maps to NM_001796.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:61687874 A>C maps to NM_001796.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:61747769 C>T maps to NM_001796.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr16:62055297 G>T maps to NM_001796.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr16:61823292 T>C maps to NM_001796.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:61689413 G>A maps to NM_001796.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr16:61851405 A>G maps to NM_001796.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:61851603 C>T maps to NM_001796.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:61761081 A>G maps to NM_001796.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:61851609 G>T maps to NM_001796.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:26881564 C>A maps to NM_016279.3 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:26885831 G>A maps to NM_016279.3 C591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr5:26915753 A>G maps to NM_016279.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:26885915 G>A maps to NM_016279.3 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr5:26988367 G>A maps to NM_016279.3 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr10:85955268 G>A maps to NM_033100.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:85974163 G>A maps to NM_033100.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr10:85968015 G>A maps to NM_033100.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:176011687 C>T maps to NM_001171976.1 N802N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:176017620 G>T maps to NM_001171976.1 G1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:176005479 C>T maps to NM_001171976.1 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:176011261 T>C did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr5:176016369 C>A maps to NM_001171976.1 Y1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr5:176011888 G>A maps to NM_001171976.1 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:176003173 C>T maps to NM_001171976.1 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr5:176003122 C>T maps to NM_001171976.1 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:176004425 G>A maps to NM_001171976.1 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:176016105 C>T maps to NM_001171976.1 D977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:176022600 G>A maps to NM_001171976.1 R1287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:105673076 C>T maps to NM_152750.4 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:105645091 C>T maps to NM_152750.4 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr7:105671266 T>C maps to NM_152750.4 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:105635243 C>T maps to NM_152750.4 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:105658314 C>T maps to NM_152750.4 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr11:618097 C>T maps to NM_021924.4 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:619025 C>T maps to NM_021924.4 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr16:89762155 C>T maps to ENST00000331006 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:1635564 C>T maps to NM_024011.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:1638925 G>A maps to NM_024011.2 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr1:1635781 C>A maps to NM_024011.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr1:1650866 G>T maps to NM_024011.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:37686959 C>T maps to NM_016507.2 S1288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:37650837 A>G maps to NM_016507.2 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr17:37649111 C>T maps to NM_016507.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:37687431 G>T maps to NM_016507.2 G1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:37676313 C>T maps to NM_016507.2 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr7:39991355 C>A maps to NM_003718.4 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr7:40132789 G>A maps to NM_003718.4 A1214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:40132831 G>C maps to NM_003718.4 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:40134335 T>C maps to NM_003718.4 G1432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:40134464 C>T maps to NM_003718.4 L1475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:40133991 G>T maps to NM_003718.4 E1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr7:40132774 A>C maps to NM_003718.4 G1209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:40132783 T>C maps to NM_003718.4 H1212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr7:40134359 C>T maps to NM_003718.4 S1440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:40118357 T>C maps to NM_003718.4 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:90675255 T>A maps to NM_012395.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:90741928 G>A maps to NM_012395.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:202755580 A>G maps to ENST00000450471 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:202737023 C>T maps to ENST00000450471 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:47086418 G>T did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:47088010 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:47087989 A>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:47085413 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:47086479 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:47088019 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:47085755 A>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:96674555 G>A maps to NM_001170464.2 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:96679897 A>G maps to NM_002595.4 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:96692659 T>G maps to NM_002595.4 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:110935839 G>A maps to NM_015076.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:110944513 A>G maps to NM_015076.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr9:90589343 G>A maps to NM_001039803.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:90585493 G>A maps to NM_001039803.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:90585725 G>A maps to NM_001039803.2 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:90585493 G>A maps to NM_001039803.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:90585537 G>A maps to NM_001039803.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:90589316 G>A maps to NM_001039803.2 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:90588856 C>A maps to NM_001039803.2 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:123749782 C>T maps to NM_004642.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:73998611 C>T maps to NM_001258.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:73998462 C>T maps to NM_001258.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:150754239 G>A maps to NM_004935.3 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:219825255 C>T maps to NM_003936.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:219824883 C>T maps to NM_003936.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:31954729 G>T maps to ENST00000357886 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:31980016 A>G maps to ENST00000357886 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:123222894 G>A maps to NM_018249.4 D719D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:123215732 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:123182138 G>T maps to NM_018249.4 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr9:123201861 G>A maps to NM_018249.4 Y1179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:92247478 A>C maps to NM_001145306.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:92247393 G>A maps to NM_001145306.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:92462454 C>T maps to NM_001145306.1 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:76521478 C>T maps to ENST00000307465 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:76522204 A>G maps to ENST00000307465 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr4:76551138 C>A maps to ENST00000307465 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:133657595 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:133634343 A>G maps to NM_001113575.1 *593Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:18668575 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:18622049 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:18622106 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:18631318 A>G did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr23:18671591 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:18646625 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:18622573 G>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:18598024 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:18606122 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:18622714 A>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:18622776 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:18646646 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:18622405 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:18602451 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:36651916 C>T maps to ENST00000448526 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:36652258 T>C maps to ENST00000448526 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:21970955 C>T maps to NM_001195132.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:21994369 G>A maps to ENST00000361570 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr9:21974694 G>T maps to NM_001195132.1 Y44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:21971138 G>T maps to NM_001195132.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:21971105 G>A maps to NM_001195132.1 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:21971132 G>A maps to NM_001195132.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr9:21974535 A>G maps to NM_058197.4 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:21974678 G>A maps to NM_001195132.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr9:21974678 G>A maps to NM_001195132.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr9:21971138 G>A maps to NM_001195132.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:21974514 G>A maps to NM_058197.4 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:184368552 A>G maps to NM_017632.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:51439923 A>G maps to NM_078626.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:10677826 G>A maps to NM_079421.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:10677792 G>A maps to NM_079421.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:54886792 A>G maps to NM_005192.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:14867475 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:14862005 T>C maps to NM_001029954.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr10:14867562 A>G maps to NM_001029954.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:115151944 G>A maps to NM_001801.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:125889550 G>A maps to ENST00000392693 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:125851194 C>A maps to ENST00000392693 G1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:125830914 A>G maps to ENST00000392693 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr11:125831724 G>A maps to ENST00000392693 S1175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:139866221 C>T did not map to a codon.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr23:139865817 A>C did not map to a codon.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr23:139865926 C>T did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:139866174 T>G did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:139865919 C>T did not map to a codon.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr23:139865799 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:22361161 C>T maps to NM_001802.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:22358597 C>T maps to NM_001802.1 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr17:14139300 G>A maps to NM_001007530.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr17:14140015 G>A maps to NM_001007530.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:15341230 C>T maps to ENST00000395926 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:85525439 A>C maps to NM_001263.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:85569712 C>T maps to NM_001263.3 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:5170379 G>T did not map to a codon.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr6:31084713 G>A maps to NM_001264.4 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:88871862 C>T maps to NM_030928.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:149546486 C>G maps to NM_001804.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:72667388 C>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:72674373 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:72667570 G>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:72667185 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:72667288 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:72667576 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:72667552 G>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:72667405 C>T did not map to a codon.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr6:4935818 G>C maps to ENST00000328908 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:4954277 C>T maps to ENST00000328908 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr6:4892401 C>T maps to ENST00000328908 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:4952570 G>A maps to ENST00000328908 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:4892425 C>T maps to ENST00000328908 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:4937915 C>T maps to ENST00000328908 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:80718774 T>C maps to NM_152342.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:80667008 A>G maps to NM_152342.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:80654763 G>A maps to NM_152342.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:80654799 G>A maps to NM_152342.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:80642063 C>T maps to NM_152342.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:80718447 C>T maps to NM_152342.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr16:80654772 C>A maps to NM_152342.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr16:80718954 G>A maps to NM_152342.2 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:43015773 G>A maps to NM_001712.4 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr19:43031283 G>A maps to NM_001712.4 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:43026352 C>T maps to NM_001712.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr19:51981862 G>A maps to NM_001080405.1 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:45026684 A>G maps to NM_001102597.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:42091828 G>A maps to NM_001098506.1 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:42301696 G>T maps to NM_001815.2 G81*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F1-6177-01A-11D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr19:42128058 G>A maps to NM_001817.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:42128058 G>T maps to NM_001817.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:42221554 A>G maps to NM_004363.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:42224050 C>T maps to NM_004363.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr19:42224896 G>A maps to NM_004363.2 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:42219620 G>A maps to NM_004363.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:42260652 C>T maps to NM_002483.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:42190984 G>A maps to NM_006890.3 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr19:42181399 G>A maps to NM_006890.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:42187806 G>A maps to NM_006890.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:43093692 T>G maps to NM_001816.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:43098934 G>A maps to NM_001816.3 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr19:43093140 T>C maps to NM_001816.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr19:33870288 C>T maps to NM_001806.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr2:37441096 T>A maps to NM_005760.2 K819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr2:37455879 A>G maps to NM_005760.2 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:37455663 C>T maps to NM_005760.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:37454736 T>C maps to NM_005760.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:17690429 C>G maps to NM_017424.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:17670867 T>C maps to NM_017424.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:17662441 C>T maps to NM_017424.2 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr22:17670887 G>A maps to NM_017424.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr22:17662906 C>T maps to NM_017424.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr22:17662741 C>T maps to NM_017424.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr22:17983976 C>T maps to ENST00000400579 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr22:18021538 A>G maps to ENST00000400579 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr22:18020104 T>A maps to ENST00000400579 Y479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr22:18016837 G>C maps to ENST00000400579 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr22:18022582 G>A maps to ENST00000400579 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:17976596 C>T maps to ENST00000400579 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr22:17622070 G>A maps to NM_033070.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:17601012 C>T maps to NM_031890.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:17601381 G>A maps to NM_031890.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:17601201 C>T maps to NM_031890.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:17601105 C>T maps to NM_031890.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:135942494 C>T maps to NM_001807.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:135940060 C>T maps to NM_001807.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:15788096 C>A maps to ENST00000375924 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:15813916 C>T maps to ENST00000442979 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:15809761 C>T maps to ENST00000442979 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:15817806 A>G maps to ENST00000442979 *307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:15813901 G>A maps to ENST00000442979 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:22336256 T>C maps to NM_005747.4 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr1:22336253 C>T maps to NM_005747.4 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr1:22336256 T>C maps to NM_005747.4 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:22307569 C>T maps to NM_007352.2 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:47504306 G>A maps to NM_001172639.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr11:47498888 G>C maps to NM_001172639.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:47510446 A>G maps to NM_001172639.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:11363284 G>A maps to NM_006561.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:11330378 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:11356214 C>T maps to NM_006561.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr10:11317063 C>T maps to NM_006561.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr10:11363206 C>T maps to NM_006561.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:151682224 G>A maps to NM_007185.4 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:34853108 C>T maps to NM_020180.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:34853048 G>A maps to NM_020180.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr18:34854282 G>A maps to NM_020180.3 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:34854291 G>A maps to NM_020180.3 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:72580691 A>G maps to NM_052840.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:46793715 G>A maps to NM_014246.1 N1852N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:46760631 C>T maps to NM_014246.1 G2852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr22:46931660 G>A maps to NM_014246.1 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:46794453 G>T maps to NM_014246.1 V1831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr22:46760029 C>T maps to NM_014246.1 T2966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr22:46776851 C>T maps to NM_014246.1 R2363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:46760451 G>A maps to NM_014246.1 G2912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr22:46835249 G>A maps to NM_014246.1 N1414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:46931759 C>T maps to NM_014246.1 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:46777834 G>A maps to NM_014246.1 D2332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:46786375 C>T maps to NM_014246.1 A2086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:46773145 G>A maps to NM_014246.1 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:46773155 G>A maps to NM_014246.1 N2462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:46932287 C>T maps to NM_014246.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:109813588 T>G maps to NM_001408.2 P2508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:109794578 C>T maps to NM_001408.2 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:109793561 T>C maps to NM_001408.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:109793003 T>C maps to NM_001408.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:109813579 C>T maps to NM_001408.2 Y2505Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:109808787 C>T maps to NM_001408.2 F1991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:109810579 C>T maps to NM_001408.2 S2072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:109801246 C>T maps to NM_001408.2 N1168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:109801081 C>T maps to NM_001408.2 C1113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:109815572 C>A maps to NM_001408.2 A2754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:109801411 C>T maps to NM_001408.2 R1223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr1:109811234 C>T maps to NM_001408.2 D2117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:48697745 A>G maps to NM_001407.2 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:48678952 C>A maps to NM_001407.2 V2943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:48699641 G>A maps to NM_001407.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:48691722 T>C maps to NM_001407.2 A1717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:48694578 G>A maps to NM_001407.2 N1317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:48685825 C>T maps to NM_001407.2 Q2282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr3:48696661 G>A maps to NM_001407.2 Q1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:48699590 G>T maps to NM_001407.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:48692474 A>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:48699497 G>A maps to NM_001407.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:48677915 T>G maps to NM_001407.2 A3034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:48691210 A>G maps to NM_001407.2 H1763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr3:48683605 C>T maps to NM_001407.2 E2460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:48697910 C>T maps to NM_001407.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:48683691 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:48697178 G>T maps to NM_001407.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:2581056 A>G maps to NM_001048212.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:788423 C>T maps to NM_016564.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:788285 A>G maps to NM_016564.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:788201 C>T maps to NM_016564.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:3765885 C>T maps to NM_001810.5 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:3766611 G>A maps to NM_001810.5 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:104106976 T>C maps to NM_001813.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr4:104101521 G>A maps to NM_001813.2 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr4:104030044 A>C maps to NM_001813.2 S2642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:104098056 T>C maps to NM_001813.2 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:104067057 T>C maps to NM_001813.2 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:104104377 T>C maps to NM_001813.2 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:104066409 G>A maps to NM_001813.2 Q1552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr4:104080415 T>A maps to NM_001813.2 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:104103996 G>A maps to NM_001813.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:214830279 T>C maps to NM_016343.3 T2830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:214832208 G>A maps to NM_016343.3 P2993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:214813867 T>C maps to NM_016343.3 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:214813765 C>A maps to NM_016343.3 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:214815832 G>A maps to NM_016343.3 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:214814767 T>C maps to NM_016343.3 C1029C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:214794278 G>A maps to NM_016343.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:214819368 T>G maps to NM_016343.3 L2152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr1:214816264 C>A maps to NM_016343.3 C1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr1:214792521 C>T maps to NM_016343.3 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:214815733 T>C maps to NM_016343.3 D1351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr1:214792554 C>T maps to NM_016343.3 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:214830481 C>T maps to NM_016343.3 R2898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr5:68498797 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:68492937 T>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:100387215 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:100400186 A>C did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:100417864 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:25480096 G>A maps to NM_018451.3 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:25486836 C>T maps to NM_018451.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:173776422 C>T maps to NM_001127181.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:81053749 C>T maps to NM_001100624.1 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:67862747 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:67865768 G>A maps to NM_025082.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr17:16253330 G>A maps to NM_181716.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr6:126661512 C>T maps to ENST00000368325 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:123877366 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:123928389 C>T maps to NM_007018.4 R1863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:123907625 T>C maps to NM_007018.4 I1091I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr9:123931889 A>G maps to NM_007018.4 K2024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr9:123900944 T>C maps to NM_007018.4 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr5:122724214 T>A maps to NM_153223.3 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:122729095 A>G maps to NM_153223.3 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr5:122725675 T>C maps to NM_153223.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:56835227 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:56841069 C>T maps to NM_025009.3 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:56877591 A>G maps to NM_025009.3 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:49081123 A>G maps to NM_001194998.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr15:49044576 G>T maps to NM_001194998.1 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:49048375 A>G maps to NM_001194998.1 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:49076170 G>A maps to NM_001194998.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:49031105 C>T maps to NM_001194998.1 P1491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:117251376 C>T maps to NM_014956.4 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:117253640 G>A maps to NM_014956.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:117266306 G>A maps to NM_014956.4 E986E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:117241944 A>T maps to NM_014956.4 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:117280457 G>A maps to NM_014956.4 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:117253625 G>A maps to NM_014956.4 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:117261588 C>G maps to NM_014956.4 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr11:117261606 A>T maps to NM_014956.4 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:117214934 C>T maps to NM_014956.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:243319560 G>T maps to NM_014812.2 Y1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:243328763 A>C maps to NM_014812.2 L833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr18:13057733 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:34091279 C>T maps to NM_007186.3 R1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:34053897 C>T maps to NM_007186.3 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:34092702 G>A maps to NM_007186.3 W2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:34092290 C>T maps to NM_007186.3 R2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:34091279 C>T maps to NM_007186.3 R1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:88454772 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:88478557 A>G maps to NM_025114.3 N1503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:88505560 G>A maps to NM_025114.3 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:88477713 C>T maps to NM_025114.3 V1574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:88505482 T>C maps to NM_025114.3 K735K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:180062779 C>T maps to NM_014810.4 R2514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:179983258 A>G maps to NM_014810.4 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:179993661 G>A maps to NM_014810.4 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:179983021 C>T maps to NM_014810.4 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:65299969 C>T maps to NM_015147.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:65298712 C>A maps to NM_015147.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:65300080 A>G maps to NM_015147.2 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:65298796 C>T maps to NM_015147.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:65296838 C>T maps to NM_015147.2 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr3:138248264 G>A maps to NM_024491.2 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr5:653237 C>T maps to NM_018140.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:640664 C>T maps to NM_018140.3 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr5:653169 G>T maps to NM_018140.3 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:12678170 G>A maps to NM_024899.2 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:12701113 T>C did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr9:80851394 G>A maps to NM_001098802.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr3:101451438 C>T maps to ENST00000327230 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr3:101451489 G>A maps to ENST00000327230 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:101483743 G>A maps to ENST00000327230 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:101484232 G>A maps to ENST00000327230 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr1:111724891 C>T maps to NM_001007794.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:14722634 C>T maps to NM_005454.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr9:131186864 C>A maps to NM_016174.4 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr9:131186738 C>T maps to NM_016174.4 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:131186472 G>A maps to NM_016174.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr22:47091192 G>A maps to NM_022766.5 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:182468699 A>G maps to NM_001030311.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:182423343 G>A maps to NM_001030311.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:182468771 T>C maps to NM_001030311.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:55866922 C>T maps to NM_001025195.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr16:55857580 G>T maps to NM_001025195.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:66974141 C>T maps to NM_003869.5 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr16:66972138 G>A maps to NM_003869.5 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:55883566 A>G maps to NM_001143685.1 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:55907785 C>T maps to NM_001143685.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr16:55899940 G>A maps to NM_001143685.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:55893466 G>A maps to NM_001143685.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:55899901 G>A maps to NM_001143685.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:55886931 C>T maps to NM_001143685.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:55903557 G>A maps to NM_001143685.1 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:55903593 G>A maps to NM_001143685.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:55893482 G>A maps to NM_001143685.1 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:55905569 C>T maps to NM_001143685.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:67043038 A>G maps to ENST00000326686 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:67042891 G>A maps to ENST00000326686 G511G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HJ-7597-01A-21D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:67034812 C>T maps to ENST00000326686 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:580530 C>T maps to NM_004066.1 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr18:580812 G>A maps to NM_004066.1 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:580689 G>A maps to NM_004066.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr18:580881 C>T maps to NM_004066.1 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:151998217 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:151997190 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:151996413 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:57016120 C>T maps to NM_000078.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:57004960 C>T maps to NM_000078.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:31914249 C>T maps to ENST00000437789 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:31915552 C>T maps to ENST00000437789 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:131356287 G>A maps to NM_032545.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:131356242 C>T maps to NM_032545.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:131356242 C>T maps to NM_032545.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:860950 G>A maps to NM_001928.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:861775 A>G maps to NM_001928.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr19:861718 G>A maps to NM_001928.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:196716412 A>G maps to NM_000186.3 K1222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr1:196684774 A>G maps to NM_000186.3 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr1:196695762 A>C maps to NM_000186.3 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr1:196709922 G>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:196799763 C>T maps to NM_002113.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr1:196920147 C>T maps to ENST00000367421 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:196928060 A>T maps to ENST00000367421 K222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:196749077 T>C maps to NM_021023.5 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:196757391 C>T maps to NM_021023.5 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:196759280 G>A maps to NM_021023.5 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:196883715 C>T maps to NM_006684.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr1:196887427 G>A maps to NM_006684.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:196887412 T>G maps to NM_006684.2 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:196964967 A>T maps to ENST00000367414 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:196967333 T>C maps to ENST00000367414 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr1:196953136 A>C maps to ENST00000367414 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr1:196971771 G>A maps to ENST00000367414 W460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:196965191 C>T maps to ENST00000367414 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr1:196964970 C>T maps to ENST00000367414 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr4:110681531 G>A maps to ENST00000394635 C259C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr4:110663683 G>T maps to ENST00000394635 Y507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:110682736 A>G maps to ENST00000394635 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:110667423 G>A maps to ENST00000394635 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr14:35182275 C>T maps to NM_138638.4 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr14:35182761 A>C maps to NM_138638.4 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:202025303 C>A maps to NM_001127183.1 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:47485905 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:47486573 C>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:47486542 G>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:47485835 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:117232479 C>T maps to NM_000492.3 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr7:117232020 G>A maps to NM_000492.3 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:117232510 C>T maps to NM_000492.3 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:117282580 C>T maps to NM_000492.3 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:49536285 C>T maps to NM_033378.1 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:49551584 T>C maps to ENST00000448456 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:88104712 G>A maps to NM_001195308.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:151502449 G>A maps to NM_020770.2 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:151491112 C>T maps to NM_020770.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:151498177 A>C maps to NM_020770.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:151491486 T>G maps to NM_020770.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:151491195 G>A maps to NM_020770.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:151502488 G>A maps to NM_020770.2 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:151509231 G>A maps to NM_020770.2 K1111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:57730211 C>T maps to NM_032866.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr15:57808976 G>C did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr15:57838431 C>T maps to NM_032866.3 D1256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:57730400 G>A maps to NM_032866.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:57815763 G>A maps to NM_032866.3 Q931Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr14:55004832 C>A maps to NM_006568.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:90966739 G>A maps to NM_003956.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:41245678 A>T maps to NM_024111.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:41245900 C>T maps to NM_024111.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:41247665 C>T maps to NM_024111.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:53999075 T>A maps to NM_001008708.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:53999078 G>T maps to NM_001008708.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:4433466 G>A maps to NM_005483.2 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:4409293 C>T maps to NM_005483.2 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:4430583 C>T maps to NM_005483.2 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:4433427 C>T maps to NM_005483.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:4433181 G>A maps to NM_005483.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:37759987 T>C maps to NM_005441.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:37781129 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:37785235 T>C maps to NM_005441.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:50863203 C>T maps to NM_020549.4 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:50833608 G>A maps to NM_020549.4 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:50872971 A>G maps to NM_020549.4 K709K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:50835781 G>A maps to NM_020549.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:50830169 A>G maps to NM_020549.4 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr10:50857653 T>C maps to NM_020549.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr10:50830160 C>T maps to NM_020549.4 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:50863167 C>T maps to NM_020549.4 Y554Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:75541868 G>C maps to NM_203298.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr7:56171921 G>T maps to NM_016139.2 Y99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr7:132481336 G>A maps to ENST00000448878 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:14154632 G>A maps to NM_144636.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr5:98207889 G>A maps to NM_001270.2 C1242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:98221293 A>G maps to NM_001270.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:98206417 A>C maps to NM_001270.2 L1317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:98193930 A>G maps to NM_001270.2 S1580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:98232038 A>T maps to NM_001270.2 L534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:93521591 T>C maps to NM_001271.3 H902H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:93489427 C>T maps to NM_001271.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:93552394 C>T maps to NM_001271.3 P1478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:93489370 A>G maps to NM_001271.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:93528849 G>A maps to NM_001271.3 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:7812020 C>T maps to NM_001005271.2 G1815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr17:7802337 A>T maps to NM_001005271.2 K780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:7810227 G>A maps to NM_001005271.2 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7811329 C>T maps to NM_001005271.2 G1774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:6692235 C>A maps to ENST00000309577 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:6711239 G>A maps to ENST00000309577 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:6700955 G>A maps to ENST00000309577 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:6696651 G>A maps to ENST00000309577 D1259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:6703728 A>G maps to ENST00000309577 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:6715476 A>G maps to ENST00000309577 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:6691862 G>A maps to ENST00000309577 R1458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:6203989 C>A maps to NM_015557.2 E646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:6169954 G>A maps to NM_015557.2 N1826N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:6215762 C>T maps to NM_015557.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:6215729 G>A maps to NM_015557.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:6209392 G>A maps to NM_015557.2 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr1:6209392 G>A maps to NM_015557.2 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:6170002 C>T maps to NM_015557.2 A1810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:6208970 G>A maps to NM_015557.2 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:6212525 G>A maps to NM_015557.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:6206378 G>A maps to NM_015557.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:6171884 G>A maps to NM_015557.2 Y1733Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:6206877 C>T maps to NM_015557.2 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:6211188 C>T maps to NM_015557.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:40033289 T>C maps to NM_032221.3 E2697E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:40102042 C>T maps to NM_032221.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:40112159 C>A did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr20:40143544 T>G maps to NM_032221.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr20:40049346 G>A maps to NM_032221.3 A1976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr20:40081525 C>T maps to NM_032221.3 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr20:40033523 A>C maps to NM_032221.3 P2619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr20:40043912 C>T maps to NM_032221.3 T2284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:40034021 A>G maps to NM_032221.3 A2453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:40081513 G>A maps to NM_032221.3 D1063D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr20:40116397 C>T maps to NM_032221.3 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:61765391 G>A maps to NM_017780.2 P2036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:61743113 C>T maps to NM_017780.2 C1252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:61654350 C>T maps to NM_017780.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:61769042 A>C maps to NM_017780.2 R2402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:61757810 T>C maps to NM_017780.2 L1685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:61693638 G>A maps to NM_017780.2 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:61734585 C>T maps to NM_017780.2 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:61777840 A>C maps to NM_017780.2 T2781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr8:61757605 C>T maps to NM_017780.2 A1678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:61654299 G>A maps to NM_017780.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:61754313 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:61764677 C>T maps to NM_017780.2 R1922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:61654074 T>C maps to NM_017780.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:61743071 A>G maps to NM_017780.2 V1238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:61765391 G>A maps to NM_017780.2 P2036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:61769374 G>A maps to NM_017780.2 R2512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr8:61655157 T>G maps to NM_017780.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:61763085 C>T maps to NM_017780.2 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:61743068 C>T maps to NM_017780.2 N1237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:61778056 G>A maps to NM_017780.2 E2853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:61655257 G>T maps to NM_017780.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:61742916 T>C maps to NM_017780.2 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:21861974 A>C maps to NM_001170629.1 T1993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:21882508 A>C maps to NM_001170629.1 L698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:21860060 C>T maps to NM_001170629.1 A2272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:21868763 G>A maps to NM_001170629.1 R1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:21896122 G>A maps to NM_001170629.1 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr14:21899097 A>G maps to NM_001170629.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:21861838 G>A maps to NM_001170629.1 Q2039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:21897485 C>T maps to NM_001170629.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:53358047 A>T maps to ENST00000219084 A2645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:53276822 T>A maps to ENST00000219084 C983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr16:53243431 T>C maps to ENST00000219084 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr16:53296900 G>A maps to ENST00000219084 A1404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr16:53321898 C>T maps to ENST00000219084 A1740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr16:53190618 T>C maps to ENST00000219084 H206H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:53269095 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:53358200 C>T maps to ENST00000219084 T2696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:53852073 T>C maps to NM_018397.4 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:53857837 G>A maps to NM_018397.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:53852022 G>A maps to NM_018397.4 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:53854582 G>A maps to NM_018397.4 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr3:53856655 G>A maps to NM_018397.4 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:53851804 T>C maps to NM_018397.4 *595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr3:53851804 T>A maps to NM_018397.4 *595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr3:53857456 C>T maps to NM_018397.4 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:125505411 C>T maps to NM_001274.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:125499187 G>T maps to NM_001274.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:29120962 A>G did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr22:29121016 G>T maps to NM_001005735.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr22:29091861 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:16646276 G>A maps to NM_006387.5 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr19:16641680 G>A maps to NM_006387.5 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:16630059 G>C maps to NM_006387.5 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:133435664 G>A maps to NM_001161344.1 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:133428222 C>T maps to NM_001161344.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:93398721 G>A maps to NM_001275.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:5904214 T>C maps to NM_001819.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:5903915 C>T maps to NM_001819.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr1:111862928 G>T maps to NM_201653.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr1:111861743 C>A maps to NM_201653.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr1:111862019 C>T maps to NM_201653.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:111857900 C>T maps to NM_201653.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:203186139 C>T maps to NM_003465.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr22:51019913 C>T maps to NM_005198.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:51020279 G>A maps to NM_005198.4 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr22:51018796 G>A maps to NM_005198.4 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr3:403457 C>T maps to NM_006614.2 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr3:370002 C>T maps to NM_006614.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:402042 G>A maps to NM_006614.2 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr3:382573 T>G maps to NM_006614.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:431056 G>A maps to NM_006614.2 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:440832 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:403380 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:85149201 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:85218945 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:85213975 A>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:85219035 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:85119780 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:85155674 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:85211342 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:85211331 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:85166341 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:85128194 T>C did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:241798363 T>C maps to NM_001821.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:241798633 T>C maps to NM_001821.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:89713099 G>A maps to NM_001083314.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr19:59065482 G>A maps to NM_014453.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:32439983 C>A maps to NM_176812.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr20:32436451 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr20:32439896 G>A maps to NM_176812.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:82644966 C>T maps to NM_152284.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:33271163 A>G maps to NM_016410.5 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:33280823 T>C maps to NM_016410.5 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:78971092 T>C maps to NM_024591.4 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr8:23114091 C>T maps to NM_152272.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:175676302 T>C maps to NM_001822.4 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:175676245 G>A maps to NM_001822.4 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:175664963 G>A maps to NM_001822.4 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:29552338 C>T maps to NM_004067.2 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:89947183 A>G did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:89939415 C>A maps to NM_012124.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:89951323 C>T maps to NM_012124.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:23767236 C>T maps to NM_022097.2 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:220404686 C>T maps to NM_024536.5 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:220404386 G>A maps to NM_024536.5 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:220406867 G>A maps to NM_024536.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:220405040 C>T maps to NM_024536.5 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:220404725 G>A maps to NM_024536.5 H569H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:220405700 C>A maps to NM_024536.5 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:150932241 G>A maps to NM_019015.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:150934479 C>T maps to NM_019015.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:150932673 C>T maps to NM_019015.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:150935107 C>T maps to NM_019015.1 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:184101308 A>G did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr3:184101336 G>A maps to NM_003741.2 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:184104635 C>T maps to NM_003741.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:184104512 C>T maps to NM_003741.2 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr3:184101157 C>T maps to NM_003741.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:184104712 C>T maps to NM_003741.2 C759C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:184104635 C>T maps to NM_003741.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:110005995 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:109964645 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:109937470 C>T did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:109924714 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:109924818 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:110035369 A>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:109937471 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:109924727 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:109937510 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:109937439 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:109922616 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:109964641 G>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:74421902 G>A maps to NM_015424.3 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:74421941 C>T maps to NM_015424.3 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:74415528 A>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:30654960 G>A maps to NM_139320.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:30659641 G>A maps to NM_139320.1 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:62677432 C>T maps to NM_000738.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:136700457 C>T maps to NM_001006628.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr7:136699938 C>G maps to NM_001006628.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:136700604 C>G maps to NM_001006628.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:136700064 T>G maps to NM_001006628.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:240071147 C>T maps to NM_000740.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:240072103 G>A maps to NM_000740.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:240071797 C>T maps to NM_000740.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:240070843 G>A maps to NM_000740.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:240071897 T>C maps to NM_000740.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:46407255 C>T maps to NM_000741.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:46406883 G>T maps to NM_000741.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:46407804 G>A maps to NM_000741.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:46406888 G>A maps to NM_000741.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:46407531 G>A maps to NM_000741.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr11:46407612 C>T maps to NM_000741.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:46406736 G>A maps to NM_000741.2 N457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:34355235 G>A maps to NM_012125.3 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:34355211 C>T maps to NM_012125.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:175618366 G>A maps to NM_001039523.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:175618333 G>A maps to NM_001039523.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:175622358 G>A maps to NM_001039523.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:175613393 G>A maps to NM_001039523.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:3688708 G>A maps to NM_020402.2 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr8:27320906 A>G maps to NM_000742.3 N351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr8:27319265 C>T maps to NM_000742.3 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:27320681 T>C maps to NM_000742.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr8:27320870 G>A maps to NM_000742.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:27327343 C>T maps to NM_000742.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:27321014 A>G maps to NM_000742.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:27320972 G>A maps to NM_000742.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr15:78894524 G>A maps to NM_000743.4 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr15:78888986 C>A maps to NM_000743.4 G493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:61981775 G>A maps to NM_000744.5 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr20:61978134 C>T maps to NM_000744.5 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:61981736 G>T maps to NM_000744.5 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:61981127 C>T maps to NM_000744.5 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:61981655 C>T maps to NM_000744.5 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr20:61982141 G>A maps to NM_000744.5 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:78873305 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr15:32460280 G>A maps to NM_001190455.1 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:32460268 C>T maps to NM_001190455.1 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr15:32460292 C>T maps to NM_001190455.1 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:32460418 C>T maps to NM_001190455.1 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr4:40356536 G>T maps to NM_017581.2 *480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:7351976 A>T maps to NM_000747.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:154543724 C>T maps to NM_000748.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:154544123 G>A maps to NM_000748.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr1:154544027 C>A maps to NM_000748.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:154543739 G>A maps to NM_000748.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:154544414 C>T maps to NM_000748.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:154544435 C>A maps to NM_000748.2 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:42587313 G>A maps to NM_000749.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:42586905 C>A maps to NM_000749.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:42586932 G>A maps to NM_000749.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr8:42591673 C>T maps to NM_000749.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:78921668 G>T maps to NM_000750.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:78921323 G>A maps to NM_000750.3 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr15:78922232 G>A maps to NM_000750.3 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:233393280 C>T maps to NM_000751.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:233392149 G>T maps to NM_000751.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr2:233398997 G>T maps to NM_000751.1 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr17:4805382 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:4802328 G>T maps to NM_000080.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:233408081 G>A maps to NM_005199.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:233409276 G>A maps to NM_005199.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:233407733 C>T maps to NM_005199.4 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:233405096 C>T maps to NM_005199.4 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:233405107 C>T maps to NM_005199.4 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:45671303 C>T maps to NM_003654.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:45672029 G>A maps to NM_003654.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:45671504 C>T maps to NM_003654.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:45672101 C>T maps to NM_003654.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:45672344 G>A maps to NM_003654.4 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:45671375 G>A maps to NM_003654.4 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr11:45671645 G>A maps to NM_003654.4 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:45672340 G>A maps to NM_003654.4 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:45671831 G>A maps to NM_003654.4 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr11:45671861 G>A maps to NM_003654.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:45671279 C>T maps to NM_003654.4 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:2473128 C>T maps to NM_018641.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:2472942 C>T maps to NM_018641.3 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:2473446 G>A maps to NM_018641.3 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:2472429 C>T maps to NM_018641.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:126261177 C>T maps to NM_152889.1 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr3:126261237 G>A maps to NM_152889.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr3:126260823 G>A maps to NM_152889.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr3:126260802 C>T maps to NM_152889.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr3:126261405 C>G maps to NM_152889.1 Y337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:125805493 G>A maps to NM_015892.3 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:125780848 G>A maps to NM_015892.3 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr10:125804384 A>G maps to NM_015892.3 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:125780885 G>A maps to NM_015892.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:125769711 G>A maps to NM_015892.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:142840395 G>A maps to NM_004267.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr3:142840281 C>T maps to NM_004267.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr3:142840710 G>A maps to NM_004267.3 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:73767274 C>T maps to NM_004273.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:73767331 C>T maps to NM_004273.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:73767292 C>T maps to NM_004273.4 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:73767280 G>A maps to NM_004273.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr10:73767622 G>T maps to NM_004273.4 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:71570900 C>T maps to NM_001166395.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:71571011 T>C maps to NM_001166395.1 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:71570699 C>T maps to NM_001166395.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:75563451 G>A maps to NM_024533.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr16:75563964 G>A maps to NM_024533.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:75563649 G>A maps to NM_024533.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:75563933 G>A maps to NM_024533.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr16:75563385 C>T maps to NM_024533.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr16:75563319 G>A maps to NM_024533.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:75563610 G>A maps to NM_024533.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:75512961 G>A maps to NM_021615.4 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:75512631 G>A maps to NM_021615.4 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:75513507 C>T maps to NM_021615.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:75512691 C>T maps to NM_021615.4 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:75513513 C>T maps to NM_021615.4 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr16:75513135 G>T maps to NM_021615.4 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:46433916 C>T did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:46433918 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:46433661 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:46433911 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:46434159 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:46434040 C>T did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:46433893 C>G did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:46433818 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:46434068 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:46434729 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:34263262 C>T maps to NM_022467.3 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:34263385 C>T maps to NM_022467.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:34263826 G>A maps to NM_022467.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr19:34263937 C>T maps to NM_022467.3 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:34263277 C>T maps to NM_022467.3 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr18:24496987 G>A maps to NM_031422.4 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:24722665 T>C maps to NM_031422.4 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr18:24722721 G>A maps to NM_031422.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr18:24722743 G>T maps to NM_031422.4 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:101775511 C>T maps to NM_014918.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr15:101717817 G>T maps to NM_014918.4 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:129243848 T>C maps to NM_175856.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:129521084 T>C maps to NM_175856.4 Y750Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:129244010 C>T maps to NM_175856.4 C348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:129521237 A>G maps to NM_175856.4 Q801Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr5:129243980 G>T maps to NM_175856.4 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:847004 T>C maps to ENST00000317063 I1091I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:847076 G>A maps to ENST00000317063 A1115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:842343 C>T maps to ENST00000317063 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr16:845785 C>A maps to ENST00000317063 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr10:101979083 G>C maps to NM_001278.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr15:78398115 G>A maps to NM_006383.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:78398175 G>A maps to NM_006383.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:78398175 G>A maps to NM_006383.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:78401631 C>T maps to NM_006383.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:42791716 G>A maps to NM_015125.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:42796287 G>A maps to NM_015125.3 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:42794849 G>T maps to NM_015125.3 G644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:42795870 C>T maps to NM_015125.3 Q954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:42791320 G>A maps to NM_015125.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:42791308 G>A maps to NM_015125.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:12274123 G>A maps to ENST00000342845 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr18:12274117 G>A maps to ENST00000342845 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:24776699 C>T maps to NM_014430.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:9911627 A>C maps to ENST00000430427 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:11000845 C>T maps to NM_000246.3 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:11000683 C>T maps to NM_000246.3 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:10998601 G>A maps to NM_000246.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:11000929 G>A maps to NM_000246.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:11012338 C>T maps to NM_000246.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:11000899 G>A maps to NM_000246.3 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:65489718 G>A maps to NM_003613.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr15:65489128 C>T maps to NM_003613.3 Q1165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr15:65489068 T>G maps to NM_003613.3 *1185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:19654937 C>T maps to NM_153221.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:19656296 C>T maps to NM_153221.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr19:19656263 C>T maps to NM_153221.2 Y970Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:19655135 C>T maps to NM_153221.2 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:19653319 C>T maps to NM_153221.2 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr19:19655210 G>A maps to NM_153221.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr2:175216445 C>T maps to NM_004882.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:175213407 G>A maps to NM_004882.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:175216390 G>A maps to NM_004882.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr16:69201030 A>G maps to NM_032830.2 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr10:60029032 C>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:120295413 A>G maps to ENST00000392521 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:120172993 G>A maps to ENST00000392521 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr12:120150500 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:120295461 C>T maps to ENST00000392521 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:71522014 T>C did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:71521801 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:71522038 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:71521649 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:71522050 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr9:130940662 C>T maps to NM_012127.2 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr9:130940033 G>A maps to NM_012127.2 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:130941407 G>A maps to NM_012127.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr9:130931345 C>T maps to NM_012127.2 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:113520090 G>A maps to NM_152515.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:113513702 T>C maps to NM_152515.3 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:113514491 C>T maps to NM_152515.3 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:113504146 T>C maps to NM_152515.3 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:113509870 C>T maps to NM_152515.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr2:113514602 C>T maps to NM_152515.3 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:106632987 G>T maps to NM_006825.3 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr12:106633278 G>A maps to NM_006825.3 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:46797802 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:46829613 G>A maps to ENST00000415402 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:46829625 T>C maps to ENST00000415402 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:46776614 G>A maps to ENST00000415402 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:46804909 T>C maps to ENST00000415402 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:46819662 C>T maps to ENST00000415402 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:46818454 G>A maps to ENST00000415402 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:46765728 T>C maps to ENST00000415402 K1988K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:46812088 G>A maps to ENST00000415402 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:46810324 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:103986379 C>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:103986326 G>A maps to NM_001823.3 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:45810785 C>T maps to NM_001824.3 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:45810166 G>A maps to NM_001824.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr19:45815133 G>A maps to NM_001824.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:80547073 C>A maps to NM_001825.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:122144774 C>T maps to NM_015282.2 T1099T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:122273334 G>A maps to NM_015282.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:33617675 C>T maps to ENST00000359576 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:33729800 G>A maps to ENST00000359576 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:33644480 A>G maps to ENST00000359576 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr3:33600815 G>A maps to ENST00000359576 Q1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr1:86965517 G>A maps to NM_001285.3 Q845Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:86900198 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:87031501 C>T maps to ENST00000263723 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:87025637 G>A maps to ENST00000263723 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:87045139 A>G maps to ENST00000263723 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:87012847 C>T maps to ENST00000263723 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr1:87033225 G>A maps to ENST00000263723 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:87029440 C>T maps to ENST00000263723 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:109479917 T>C maps to NM_001048210.1 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:67133086 G>A maps to NM_013246.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:67133074 G>A maps to NM_013246.2 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:143047659 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:143039040 T>C maps to NM_000083.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:143047728 C>T maps to NM_000083.2 G859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:184069836 A>G maps to NM_004366.4 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr4:170557217 T>C maps to NM_173872.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:10201603 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:10166024 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:10181870 T>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:10182014 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:10180665 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:10176509 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr23:10176606 A>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:10176510 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:49856841 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:49837185 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:49855015 C>A did not map to a codon.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr23:49834604 C>A did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr23:49855540 C>T did not map to a codon.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr23:49854897 C>T did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:49846486 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:49851323 A>C did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:49837206 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:49851172 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:11898429 C>T maps to ENST00000376496 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:11888654 C>T maps to ENST00000376496 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:11897526 C>T maps to ENST00000376496 R756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:11900198 G>C did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:11896035 C>T maps to ENST00000376496 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:1510841 G>A maps to ENST00000382745 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr16:1505132 A>G did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr16:1498391 G>A maps to ENST00000382745 N659N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:1524891 C>G maps to ENST00000382745 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:1498367 G>A maps to ENST00000382745 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:1502842 G>A maps to ENST00000382745 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:16355670 G>A maps to NM_004070.3 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:16380241 C>T maps to NM_000085.3 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr1:16377481 G>A maps to NM_000085.3 W389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:16375036 G>A maps to NM_000085.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr1:16374442 C>T maps to NM_000085.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:190030817 C>T maps to NM_021101.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:96212482 C>T maps to NM_182848.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr13:96086275 G>A maps to NM_182848.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr13:96230168 G>A maps to NM_182848.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:96086248 C>T maps to NM_182848.3 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:96229571 T>C maps to NM_182848.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr21:37833791 G>T maps to NM_001146077.1 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr21:37833699 G>A maps to NM_001146077.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr3:190127743 C>T maps to NM_006580.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr21:31538769 G>A maps to NM_012131.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr21:31538304 T>G maps to NM_012131.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:137729093 G>A maps to NM_016369.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:137742516 C>T maps to NM_016369.3 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:43204116 G>A maps to NM_148960.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:43205545 C>T maps to NM_148960.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:184240789 T>C maps to NM_001111319.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:184240708 T>G maps to NM_001111319.1 *221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr7:73183779 C>T maps to NM_001306.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:19511289 C>T maps to NM_003277.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:19511313 C>T maps to NM_003277.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:19511394 G>A maps to NM_003277.3 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr16:3065602 C>T maps to NM_021195.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr21:31587610 G>A maps to NM_199328.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:3063872 G>T maps to NM_020982.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr16:3063533 G>A maps to NM_020982.3 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:3063377 C>A maps to NM_020982.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:3063461 C>T maps to NM_020982.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr16:3063437 C>T maps to NM_020982.3 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr16:3063441 C>T maps to NM_020982.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:3063713 C>T maps to NM_020982.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:3063539 G>C maps to NM_020982.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr17:6978393 C>T maps to NM_182906.2 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:6978441 G>A maps to NM_182906.2 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr19:51228702 C>T maps to NM_002975.2 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr19:51228684 C>A maps to NM_002975.2 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr19:51227347 C>T maps to NM_002975.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:10131995 G>A maps to ENST00000355690 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr12:10124212 T>G maps to ENST00000355690 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr12:10133332 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:10137480 C>T maps to ENST00000355690 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:10163384 A>G maps to NM_001129998.1 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr12:10163367 G>T maps to NM_001129998.1 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr12:10168245 G>A maps to NM_001129998.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:38724732 G>A maps to NM_175060.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:38724746 G>A maps to NM_175060.1 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr14:38724435 G>A maps to NM_175060.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:38724534 G>A maps to NM_175060.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:38724675 G>A maps to NM_175060.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr16:11114065 C>T maps to ENST00000409790 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:11154826 G>A maps to ENST00000409790 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:11214577 G>A maps to ENST00000409790 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr16:11114107 C>T maps to ENST00000409790 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr16:11066811 C>T maps to ENST00000409790 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr19:14705595 T>C maps to ENST00000417570 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:14705583 C>T maps to ENST00000417570 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr16:69988259 G>A maps to NM_182619.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr16:70211289 T>C maps to NM_173619.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:70219799 C>T maps to NM_173619.2 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr12:10228174 A>G maps to NM_016511.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr12:10233965 A>G maps to NM_016511.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:10225944 A>C maps to NM_016511.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:10147758 G>A maps to NM_016509.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:10149516 T>C maps to NM_016509.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr12:10005898 T>G maps to NM_005127.2 *150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:10010105 G>A maps to NM_005127.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr12:10005930 T>G maps to NM_005127.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr12:10005913 C>T maps to NM_005127.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:10010141 C>T maps to NM_005127.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr12:9840549 C>T maps to NM_001004419.3 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:139228975 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:78064351 C>T maps to NM_005752.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:78064633 C>T maps to NM_005752.3 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:45077416 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:45077253 C>T maps to NM_003278.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:45077049 C>T maps to NM_003278.2 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:8281917 T>C maps to NM_016184.3 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:8288247 T>C maps to NM_016184.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:8673740 C>T maps to NM_080387.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr12:8670760 G>A maps to NM_080387.4 V41V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8588-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr12:8672847 A>G maps to ENST00000382064 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr12:8688702 A>T maps to NM_014358.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr12:8687404 G>A maps to NM_014358.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:71036893 T>C maps to NM_173535.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:71043194 G>A maps to NM_173535.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:71043873 G>A maps to NM_173535.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:7796188 C>T maps to NM_198492.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:7831061 T>G maps to NM_014257.4 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:7833780 G>A maps to NM_014257.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:141635625 C>T maps to NM_013252.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:8628797 G>A maps to NM_001007033.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:10206942 C>T maps to NM_207345.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:141317346 T>C maps to NM_004362.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:141310437 G>A maps to NM_004362.2 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:141321661 T>C maps to NM_004362.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:141315153 G>A maps to NM_004362.2 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:31698702 G>A maps to NM_001288.4 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:154528223 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:154507294 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:154563726 G>T did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:154508536 G>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:139889994 G>A maps to NM_004669.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr1:25153586 C>G maps to NM_013943.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr6:45870857 G>A maps to NM_001114086.1 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr21:36081084 G>A maps to ENST00000360731 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr12:122825398 G>A maps to ENST00000302528 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:122763598 G>A maps to ENST00000302528 A1247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:73753186 G>A maps to NM_003388.4 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:73790713 G>A maps to NM_003388.4 Q661Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:73753282 C>T maps to NM_003388.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:73771800 T>C maps to NM_003388.4 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:73753105 G>A maps to NM_003388.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr7:73768229 C>T maps to NM_003388.4 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:36518141 C>T maps to NM_015526.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:36517911 G>A maps to NM_015526.2 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:29404572 C>T maps to ENST00000379543 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:29386757 T>C maps to ENST00000379543 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:29404623 C>A maps to ENST00000379543 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:29356671 G>A maps to ENST00000379543 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:29404512 C>T maps to ENST00000379543 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:29404680 C>T maps to ENST00000379543 N682N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:29404450 T>C maps to ENST00000379543 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:201726527 C>A maps to NM_001162407.1 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:201718646 T>C maps to NM_001162407.1 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr2:201722525 G>A maps to NM_001162407.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:201722491 G>A maps to NM_001162407.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:155239458 G>A maps to ENST00000368361 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:155233107 C>T maps to ENST00000368361 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:74919714 C>T maps to NM_001130028.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:74911552 C>T maps to NM_001130028.1 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:74922172 C>T maps to NM_001130028.1 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:74911639 C>T maps to NM_001130028.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr12:92814940 G>A maps to NM_001025232.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:95690183 T>C maps to NM_024734.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:95670278 A>G maps to NM_024734.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:95669172 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:28497796 C>T maps to NM_000086.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr13:77574733 T>G maps to NM_006493.2 L285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:68500591 C>T maps to NM_017882.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:68506645 C>T maps to NM_017882.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:1719552 G>A maps to NM_018941.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:77336816 A>G maps to NM_001293.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr11:77340916 T>C maps to NM_001293.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr4:56319949 G>A maps to NM_004898.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr4:56336881 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:56316279 G>A maps to NM_004898.2 H442H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:57427133 G>A maps to NM_006831.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:57428562 T>C maps to NM_006831.2 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:57426971 C>T maps to NM_006831.2 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:72013355 G>A maps to NM_030813.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:72083975 G>A maps to NM_030813.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:72004578 C>A maps to NM_030813.3 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:72006683 C>T maps to NM_030813.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:72091322 A>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:6364535 C>T maps to NM_006012.2 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:6361915 C>T maps to NM_006012.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:45490449 C>T maps to NM_001294.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:45477799 C>T maps to NM_001294.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:45476380 C>T maps to NM_001294.2 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:45493704 C>T maps to NM_001294.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:45477832 T>C maps to NM_001294.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:45480717 G>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:45493785 C>T maps to NM_001294.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:1344506 G>A maps to NM_030782.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:1334415 G>A maps to NM_030782.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:65444826 G>A maps to NM_006660.3 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:65447359 T>C maps to NM_006660.3 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:65458980 A>G maps to NM_006660.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:65448094 G>A maps to NM_006660.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr3:150690402 C>T maps to NM_001195794.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:36203692 C>T maps to NM_022111.3 Q1188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:36217105 A>G maps to NM_022111.3 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:36212439 T>C maps to NM_022111.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:36204832 G>A maps to NM_022111.3 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:9795562 C>T maps to NM_001009566.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:9804681 G>A maps to NM_001009566.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:9790619 C>T maps to NM_001009566.1 Q964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:9811555 G>A maps to NM_001009566.1 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:9791936 C>A maps to NM_001009566.1 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:9809939 G>A maps to NM_001009566.1 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:140167436 C>T maps to NM_022131.2 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:140281686 A>G maps to NM_022131.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr3:140122502 G>T maps to NM_022131.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:140275380 C>T maps to NM_022131.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr3:140122507 G>T maps to NM_022131.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:140277616 C>G maps to NM_022131.2 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:140251227 C>T maps to NM_022131.2 Y469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:140122477 C>T maps to NM_022131.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:7286178 C>T maps to NM_014718.3 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:7295558 C>T maps to NM_014718.3 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:7303158 G>A maps to NM_014718.3 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:7295597 C>T maps to NM_014718.3 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr12:7301585 C>A maps to NM_014718.3 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:7303191 G>A maps to NM_014718.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr12:7290620 T>C maps to NM_014718.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr12:7293960 C>T maps to NM_014718.3 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:175819789 C>T maps to NM_007097.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:57725722 G>A maps to NM_004859.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:57744279 T>C maps to NM_004859.3 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:57752156 T>C maps to NM_004859.3 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:57759075 G>A maps to NM_004859.3 A1106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:57760779 G>A maps to NM_004859.3 W1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:57741234 G>A maps to NM_004859.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr22:19207438 G>A maps to NM_007098.3 H958H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:19221115 C>T maps to NM_007098.3 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:19211488 C>T maps to NM_007098.3 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr16:3586165 C>T maps to NM_015041.1 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:3582813 G>A maps to NM_015041.1 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:62412011 A>G did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr8:62212730 T>C maps to NM_173519.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr8:62212793 C>T maps to NM_173519.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr12:22208519 C>T maps to NM_018686.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:22218103 C>T maps to NM_018686.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:28357872 C>A maps to NM_182523.1 C53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr16:81739132 G>A maps to NM_198390.2 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:81685953 G>A maps to NM_198390.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr16:81641287 C>T maps to NM_198390.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:81740616 A>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:81730262 C>T maps to NM_198390.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:81712152 C>T maps to NM_198390.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:81735406 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:81712191 C>T maps to NM_198390.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:108686283 G>A maps to NM_001142344.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr12:108686190 C>T maps to NM_001142344.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:47840874 G>A maps to NM_016308.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:7001505 C>T maps to NM_207315.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:7005401 G>T maps to NM_207315.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:66600505 C>T maps to NM_052999.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:66643408 G>A maps to NM_181553.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr14:23848584 C>G maps to ENST00000339180 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:23847613 C>T maps to ENST00000339180 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr14:23848305 C>A maps to ENST00000339180 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:32544162 G>A maps to NM_017801.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:32529528 C>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:79027503 C>T maps to NM_153610.3 C972C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:79025397 G>A maps to NM_153610.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:79031079 G>T maps to NM_153610.3 P2164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:79032519 T>C maps to NM_153610.3 D2644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:79027050 A>G maps to NM_153610.3 Q821Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:79025877 T>G maps to NM_153610.3 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:79029546 T>C maps to NM_153610.3 G1653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:79034640 T>C maps to NM_153610.3 R3351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:79028991 T>G maps to NM_153610.3 V1468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:79031469 C>T maps to NM_153610.3 I2294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr5:79026747 G>A maps to NM_153610.3 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:79089346 C>T maps to NM_153610.3 L3959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:79028805 T>C maps to NM_153610.3 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:79031640 C>T maps to NM_153610.3 I2351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:79034493 T>A maps to NM_153610.3 Y3302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:79095360 T>C maps to NM_153610.3 P4044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:79095309 C>T maps to NM_153610.3 S4027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:79034571 C>T maps to NM_153610.3 D3328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:79027095 C>T maps to NM_153610.3 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:79025668 C>T maps to NM_153610.3 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:79030431 G>A maps to NM_153610.3 P1948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:79058946 C>T maps to NM_153610.3 R3824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:79026525 C>T maps to NM_153610.3 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr8:88365872 C>T maps to NM_173538.2 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:88249236 C>A maps to NM_173538.2 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr3:128890518 C>A maps to NM_001127192.1 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:72223580 C>A maps to NM_032649.5 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr18:72228192 C>T maps to NM_032649.5 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:72173239 C>T maps to NM_018235.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:72186223 T>C maps to NM_018235.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:72185804 C>T maps to NM_018235.2 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr18:72187232 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:42893099 G>A maps to NM_032488.3 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:47939481 G>A maps to NM_001142564.1 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:47938554 C>T maps to NM_001142564.1 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:47954604 T>C maps to NM_001142564.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:47938809 A>G maps to NM_001142564.1 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:150912577 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:150911108 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:150907013 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:150911845 T>C did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:150912809 A>G did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:150912263 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:150911719 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:150908124 C>T did not map to a codon.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr23:150912736 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:150907031 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:150911644 G>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:150912332 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:150912588 T>C did not map to a codon.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr23:150912252 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:150912842 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:99008386 G>A maps to NM_001298.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr2:99013225 T>A maps to NM_001298.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr2:99008434 T>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr2:98996760 A>G maps to NM_001298.2 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:98994191 G>A maps to NM_001298.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:6262730 C>T maps to NM_001037329.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:6265539 G>A maps to NM_001037329.2 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:6261644 G>A maps to NM_001037329.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:57996883 C>T maps to NM_001297.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:57953024 G>A maps to NM_001297.4 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr16:58001052 G>A maps to NM_001297.4 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:87641194 G>A maps to NM_019098.4 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:87679358 G>A maps to NM_019098.4 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:224804896 G>A maps to NM_152495.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:224922303 C>T maps to NM_152495.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:224922300 C>A maps to NM_152495.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:26506987 C>T maps to ENST00000374253 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:26515311 T>G maps to ENST00000374253 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:26510764 C>T maps to ENST00000374253 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr1:26515311 T>G maps to ENST00000374253 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:26511554 C>A maps to ENST00000374253 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:21670628 C>T did not map to a codon.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr23:21581552 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:21545077 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:21627196 C>T did not map to a codon.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr23:21450740 G>T did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr23:21627333 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr23:21667116 G>A did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr23:21450740 G>T did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:21670582 G>C did not map to a codon.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr23:21581448 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:21581505 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:21508686 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr23:21444647 A>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:11651958 T>C maps to NM_001299.4 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:95368701 G>A maps to NM_001839.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr1:95367784 A>G maps to NM_001839.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:101147614 C>T maps to NM_020348.2 C793C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr10:101124190 G>A maps to NM_020348.2 E682E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr10:101147909 C>A maps to NM_020348.2 C842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:104679241 C>T maps to NM_017649.3 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr10:104679832 C>T maps to NM_017649.3 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:97483048 C>A maps to NM_017623.4 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr2:97463382 A>G maps to NM_020184.3 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:97462747 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:97462839 C>T maps to NM_020184.3 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:97427779 G>A maps to NM_020184.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:58570931 G>A maps to NM_016284.3 G1869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:58622735 G>A maps to NM_016284.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:58581499 T>C maps to NM_016284.3 T1203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:58581511 T>C maps to NM_016284.3 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:58617055 C>T maps to NM_016284.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:58608622 C>T maps to NM_016284.3 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:58576170 A>G maps to NM_016284.3 Y1548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr16:58562513 G>A maps to NM_016284.3 F2106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:58620473 G>A maps to NM_016284.3 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:58555204 A>G maps to NM_016284.3 L2312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:58592416 A>G maps to NM_016284.3 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr16:58554927 C>T maps to NM_016284.3 S2355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr16:58589378 G>A maps to NM_016284.3 N889N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:32769229 T>C maps to NM_015442.1 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:32804345 C>T maps to NM_015442.1 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:32806267 C>T maps to NM_015442.1 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr19:54647252 G>C did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:135122962 T>A maps to NM_001190850.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:135098335 G>A maps to NM_001190850.1 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr7:135079000 C>T maps to NM_001190850.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr7:135079153 T>C maps to NM_001190850.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:135079000 C>T maps to NM_001190850.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:135079024 G>A maps to NM_001190850.1 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr7:135095395 C>A maps to NM_001190850.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:135073646 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:179994128 G>A maps to NM_015455.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:40125659 C>T maps to NM_033133.4 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:40120396 G>A maps to NM_033133.4 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:40120333 C>T maps to NM_033133.4 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:155301696 C>T maps to NM_001103176.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr7:99722427 G>T maps to NM_152755.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:88854348 G>A maps to NM_016083.4 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:88853778 T>C maps to NM_016083.4 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:88854387 G>T maps to NM_016083.4 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr6:88854342 G>A maps to NM_016083.4 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr6:88854324 G>T maps to NM_016083.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr6:88854384 G>A maps to NM_016083.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr6:88854840 A>C maps to NM_016083.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr6:88854840 A>C maps to NM_016083.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr1:24201570 G>A maps to NM_001841.2 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr1:24201526 C>T maps to NM_001841.2 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:246810591 G>A maps to NM_152609.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:246797235 A>G maps to NM_152609.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:246810567 A>G maps to NM_152609.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr11:58391515 C>T maps to NM_000614.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr11:58391662 T>C maps to NM_000614.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:34568916 G>A maps to NM_147164.1 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:34557548 A>G maps to NM_147164.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:34552675 A>G maps to NM_147164.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:17394854 A>G maps to NM_017738.2 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:17394903 C>T maps to NM_017738.2 R818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:17466780 T>C maps to NM_017738.2 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:17330767 C>T maps to NM_017738.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:17394903 C>T maps to NM_017738.2 R818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr9:17135261 C>T maps to NM_017738.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr9:17394903 C>T maps to NM_017738.2 R818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr9:17466792 A>G maps to NM_017738.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr12:41333275 C>G maps to NM_001843.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:41421689 A>C maps to NM_001843.2 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr12:41387063 C>T maps to NM_001843.2 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:41422873 A>C maps to NM_001843.2 R945R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr12:41333215 C>T maps to NM_001843.2 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr12:41374759 T>G maps to NM_001843.2 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr12:41463800 G>T maps to NM_001843.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:205041112 G>A maps to NM_005076.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:205030996 G>A maps to NM_005076.3 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:205034948 C>T maps to NM_005076.3 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:205033874 C>T maps to NM_005076.3 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr3:74334555 G>A maps to NM_020872.1 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:74334501 G>A maps to NM_020872.1 G886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:74420383 C>T maps to NM_020872.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:74383945 A>G maps to NM_020872.1 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:74418378 G>A maps to NM_020872.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr3:74350897 T>C maps to NM_020872.1 Q615Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:74418406 A>C maps to NM_020872.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:74315770 G>A maps to NM_020872.1 N949N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr3:74351862 A>G maps to NM_020872.1 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr3:74349081 T>C maps to NM_020872.1 E701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr3:74385745 A>G maps to NM_020872.1 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr3:74385745 A>C maps to NM_020872.1 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr3:74411081 A>C maps to NM_020872.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:74548934 A>G maps to NM_020872.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:3095600 A>G maps to NM_175607.1 P974P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:3081932 G>A maps to NM_175607.1 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:3067852 G>A maps to NM_175607.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:3067807 C>A maps to NM_175607.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:100211319 T>G maps to NM_014361.2 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:100126490 G>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:100168423 G>A maps to NM_014361.2 W794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:99932039 A>G maps to NM_014361.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:100221599 A>G maps to NM_014361.2 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr11:100168354 A>C did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr11:100221601 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:99827583 G>A maps to NM_014361.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr3:1394006 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:1369238 A>T maps to NM_014461.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:1394069 C>A maps to NM_014461.2 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:1445014 A>G maps to NM_014461.2 R1000R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:1363375 G>A maps to NM_014461.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr3:1337483 T>G maps to NM_014461.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:1339642 A>C maps to NM_014461.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:1414031 C>T maps to NM_014461.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr3:1418725 A>G maps to NM_014461.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:1415423 G>A maps to NM_014461.2 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:1444069 T>A maps to NM_014461.2 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr3:1337471 A>G maps to NM_014461.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr3:1424636 A>G maps to NM_014461.2 E726E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr3:1363366 C>T maps to NM_014461.2 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:1363414 C>T maps to NM_014461.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:40849678 C>T maps to NM_003632.2 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:40840603 G>C maps to NM_003632.2 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:40844010 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr17:40839907 C>T maps to NM_003632.2 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:40845417 T>C maps to NM_003632.2 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr7:146536933 C>A maps to NM_014141.5 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:146805248 T>A maps to NM_014141.5 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr7:147092833 C>T maps to NM_014141.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:147092803 C>T maps to NM_014141.5 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:146741141 T>C maps to NM_014141.5 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:147844724 C>T maps to NM_014141.5 D899D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:147183035 C>T maps to NM_014141.5 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:148106549 G>A maps to NM_014141.5 S1261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr7:147092836 G>A maps to NM_014141.5 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:146997330 C>A maps to NM_014141.5 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:147600792 C>T maps to NM_014141.5 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr7:148080939 G>A maps to NM_014141.5 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:147815285 C>T maps to NM_014141.5 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:147259296 T>C maps to NM_014141.5 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr7:147964123 G>T did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr9:39178352 A>C maps to NM_033655.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr9:39103828 G>A maps to NM_033655.3 D816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr9:39177437 G>A maps to NM_033655.3 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:76569664 G>A maps to NM_033401.3 G992G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:76481945 T>C maps to NM_033401.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr16:76569646 T>G maps to NM_033401.3 T986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr16:76523742 T>G maps to NM_033401.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr16:76486610 A>T maps to NM_033401.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr16:76389293 C>A maps to NM_033401.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr16:76513435 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:76389239 G>A maps to NM_033401.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:76555094 C>A maps to NM_033401.3 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr16:76523742 T>C maps to NM_033401.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr16:76569470 C>T maps to NM_033401.3 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:125405386 G>A maps to NM_130773.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:125367426 C>T maps to NM_130773.2 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:125530569 C>T maps to NM_130773.2 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr2:125204447 G>A maps to NM_130773.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr2:125262119 T>C maps to NM_130773.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr2:125530442 T>G maps to NM_130773.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr2:125367441 C>T maps to NM_130773.2 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr2:125547587 G>A maps to NM_130773.2 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr2:125521593 T>A maps to NM_130773.2 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:125504944 C>T maps to NM_130773.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr17:7846797 G>A maps to NM_001037144.4 Q467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:7852791 G>A maps to NM_001037144.4 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr17:7843052 C>T maps to NM_001037144.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:7847811 G>A maps to NM_001037144.4 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:7847955 A>C maps to NM_001037144.4 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:40716141 C>T maps to NM_001042532.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr17:40716177 C>G maps to NM_001042532.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:51096608 G>A maps to ENST00000395542 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:51095675 G>A maps to ENST00000395542 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:51096632 G>A maps to ENST00000395542 Y802Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:51095666 G>A maps to ENST00000395542 R1124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:165548786 G>A maps to ENST00000392717 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:165557204 C>T maps to ENST00000392717 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:165551249 A>G maps to ENST00000392717 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:165584505 C>A maps to ENST00000392717 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:165600194 A>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:165551063 G>T maps to ENST00000392717 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:165551507 C>T maps to ENST00000392717 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr2:165584553 G>A maps to ENST00000392717 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr9:140151446 G>T maps to NM_015456.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:140161523 C>T maps to NM_015456.3 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:140166983 C>T maps to NM_015456.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:230827228 C>T maps to NM_007357.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:230795217 C>T maps to NM_007357.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:230805214 G>A maps to NM_007357.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:230819334 G>T maps to NM_007357.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:230798931 C>T maps to NM_007357.2 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr13:46083902 G>A maps to NM_031431.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:107198537 G>A maps to NM_006348.3 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:40268796 T>C maps to ENST00000255468 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr13:40251605 C>T maps to ENST00000255468 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:40229919 C>T maps to ENST00000255468 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr16:23453966 C>A did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr16:23415149 T>C maps to NM_153603.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:69368939 C>T maps to NM_032382.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:116442006 C>T maps to NM_000493.3 V424V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4362-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:116442888 T>A maps to ENST00000430695 G90G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8363-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr6:116442354 T>G maps to NM_000493.3 G308G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IN-A6RS-01A-12D-A34U-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:116442816 C>T maps to NM_000493.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr1:103471440 G>A maps to NM_080629.2 R612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:103385914 T>G maps to NM_080629.2 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr1:103544368 A>T maps to NM_080629.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:103491361 C>A maps to NM_080629.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:103379955 A>T maps to NM_080629.2 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:103387076 A>C maps to NM_080629.2 A1247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:103491151 A>G maps to NM_080629.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr1:103488309 A>G maps to NM_080629.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:103427469 T>C maps to NM_080629.2 A1052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:103427800 A>G maps to NM_080629.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr1:103470025 C>A maps to NM_080629.2 G652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:103379198 A>C maps to NM_080629.2 G1354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr1:103449729 T>C maps to NM_080629.2 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr1:103343694 G>T maps to NM_080629.2 V1779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:103354302 G>A maps to NM_080629.2 G1522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:103453254 A>C maps to NM_080629.2 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:103444433 A>G maps to NM_080629.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:103540263 C>T maps to NM_080629.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr1:103474066 C>T maps to NM_080629.2 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:103343574 T>G maps to NM_080629.2 *1819Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr1:103461562 C>T maps to NM_080629.2 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:33138610 C>T maps to NM_080680.2 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:33144777 G>A maps to NM_080680.2 D687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:33133488 C>T maps to NM_080680.2 P1529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:33133485 G>A maps to NM_080680.2 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:33133581 G>A maps to NM_080680.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr6:33136331 G>A maps to NM_080680.2 T1308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr6:33141498 G>T maps to NM_080680.2 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr6:33140866 G>T maps to NM_080680.2 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:33132046 G>A maps to NM_080680.2 C1689C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:75899337 C>T maps to ENST00000322507 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:75814987 A>G maps to ENST00000322507 P2733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:75827137 T>C maps to ENST00000322507 E2493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr6:75838045 T>C maps to ENST00000322507 G2102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr6:75865562 C>A maps to ENST00000322507 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:75890798 C>A maps to ENST00000322507 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr6:75862082 T>C maps to ENST00000322507 E1227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr6:75797365 T>C maps to ENST00000322507 G3036G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr6:75828816 G>T maps to ENST00000322507 V2432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr6:75797463 C>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:75799922 T>C maps to ENST00000322507 G2948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:75833998 G>T maps to ENST00000322507 S2232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:75875262 A>G maps to ENST00000322507 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr6:75797370 G>A maps to ENST00000322507 R3035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr6:75840613 C>T maps to ENST00000322507 L2007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr6:75893723 G>A maps to ENST00000322507 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:75812405 C>T maps to ENST00000322507 G2774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:75862091 A>G maps to ENST00000322507 R1224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:121256224 C>T maps to NM_021110.1 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:121259945 C>A maps to NM_021110.1 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:121354656 G>A maps to NM_021110.1 A1620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr8:121170388 A>C maps to NM_021110.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:121296017 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:121344952 G>A maps to NM_021110.1 P1588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr8:121322262 C>T maps to NM_021110.1 R1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:121327826 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:121292216 G>A maps to NM_021110.1 S1175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:121238899 T>C maps to NM_021110.1 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr8:121237325 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:101832035 G>A maps to NM_001855.3 A1345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:101824543 C>T maps to NM_001855.3 P1183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr9:101810102 T>C maps to NM_001855.3 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:101801000 C>T maps to NM_001855.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:101831993 C>T maps to NM_001855.3 G1331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:32131192 C>T maps to NM_001856.3 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:32157656 G>A maps to NM_001856.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:32145657 G>T maps to NM_001856.3 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:32145287 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:32131488 G>A maps to NM_001856.3 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:105793032 G>A maps to NM_000494.3 Y1419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:105798254 G>A maps to NM_000494.3 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:105816868 G>A maps to NM_000494.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:105799266 A>C maps to NM_000494.3 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:105815735 C>T maps to NM_000494.3 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:105797490 G>T maps to NM_000494.3 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr10:105794505 G>A maps to NM_000494.3 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IZ-01A-32D-A25D-08 chr10:105795286 C>T maps to NM_000494.3 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr10:105830280 C>T maps to NM_000494.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:105799275 C>A maps to NM_000494.3 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr21:46888204 G>A maps to ENST00000359759 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr21:46896329 C>T maps to ENST00000359759 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr21:46895394 C>T maps to ENST00000359759 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr21:46924391 C>T maps to ENST00000359759 G1345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr21:46888234 C>T maps to ENST00000359759 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr21:46876082 A>G maps to ENST00000359759 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:46875779 C>T maps to ENST00000359759 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr21:46910217 G>T maps to ENST00000359759 G1078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr21:46888630 C>T maps to ENST00000359759 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:46875500 G>A maps to ENST00000359759 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:70744134 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr6:70866608 C>T maps to NM_001858.4 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:70639373 G>T maps to NM_001858.4 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:70916935 C>T maps to NM_001858.4 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:48267693 G>A maps to NM_000088.3 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr17:48265260 G>T maps to NM_000088.3 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:48275324 G>A maps to NM_000088.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr17:48270354 G>A maps to NM_000088.3 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:48263138 C>T maps to NM_000088.3 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:48267439 G>A maps to NM_000088.3 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:48268237 G>A maps to NM_000088.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:94054965 C>T maps to NM_000089.3 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:94057006 C>T maps to NM_000089.3 Y1112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr7:94041405 C>T maps to NM_000089.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr7:94056958 C>T maps to NM_000089.3 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:94056366 T>C maps to NM_000089.3 G1051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr7:94054923 C>A maps to NM_000089.3 G928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:94038107 A>G maps to NM_000089.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr7:94047815 A>G maps to NM_000089.3 E659E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:61944530 C>T maps to ENST00000326996 Y720Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr20:61958162 C>T maps to ENST00000326996 T1211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:61959432 C>T maps to ENST00000326996 G1228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:61938878 T>C maps to ENST00000326996 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:61943271 C>A maps to ENST00000326996 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:61944225 G>A maps to ENST00000326996 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:61937335 G>A maps to ENST00000326996 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:55925814 A>G maps to NM_030820.3 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:56047376 G>A maps to NM_030820.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr6:55942346 G>A maps to NM_030820.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:55925688 G>A maps to NM_030820.3 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:55935557 C>A maps to NM_030820.3 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:139691880 T>C maps to NM_152888.1 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:139696665 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:139712354 G>A maps to NM_152888.1 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:139833453 G>A maps to NM_152888.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr8:139890164 C>T maps to NM_152888.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr8:139833570 G>A maps to NM_152888.1 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr8:139737659 G>T maps to NM_152888.1 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:139890449 G>T maps to NM_152888.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr8:139636016 G>A maps to NM_152888.1 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:139833474 C>T maps to NM_152888.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:139606332 G>A maps to NM_152888.1 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr8:139729079 T>A maps to NM_152888.1 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:139790594 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:139838990 G>A maps to NM_152888.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:139631708 G>A maps to NM_152888.1 R1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:139728472 G>A maps to NM_152888.1 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:177987734 T>C maps to ENST00000390654 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:177682015 G>A maps to ENST00000390654 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:177681964 G>T maps to ENST00000390654 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr5:177987740 G>A maps to ENST00000390654 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:86590959 A>G maps to NM_152890.5 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:86591703 C>T maps to NM_152890.5 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr1:86590761 G>A maps to NM_152890.5 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:86591325 A>C maps to NM_152890.5 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:86591184 T>C maps to NM_152890.5 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:86515848 G>T maps to NM_152890.5 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:86591466 T>C maps to NM_152890.5 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:86554889 T>A maps to NM_152890.5 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:109740458 T>C maps to ENST00000333642 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:109895712 G>A maps to ENST00000333642 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr4:110223040 G>A maps to ENST00000333642 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr4:109841760 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:109861693 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:110222904 C>A maps to ENST00000333642 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:117062909 G>A maps to NM_032888.2 P1548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:117050983 C>T maps to NM_032888.2 G1349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:116999991 C>A maps to NM_032888.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:116930506 C>T maps to NM_032888.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:116930722 G>A maps to NM_032888.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr9:116930113 C>G maps to NM_032888.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:7476082 T>C maps to NM_001037763.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8364-01A-11D-2340-08 chr7:7412685 G>A maps to NM_001037763.2 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr7:7484114 C>T maps to NM_001037763.2 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:7410436 C>T maps to NM_001037763.2 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:7514246 T>C maps to NM_001037763.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr7:7572473 C>G maps to NM_001037763.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr7:7530220 C>T maps to NM_001037763.2 Q361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:48369181 G>A maps to NM_001844.4 S1268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:48391985 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:48369118 G>A maps to NM_001844.4 C1289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr12:48387590 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr12:48371126 G>T maps to NM_001844.4 G1083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:48369229 G>A maps to NM_001844.4 D1252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:48391984 C>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:48380148 G>A maps to NM_001844.4 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:48376305 G>A maps to NM_001844.4 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr12:48370675 T>C maps to NM_001844.4 K1118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:48387249 C>T maps to NM_001844.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr2:189856393 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:189875615 G>A maps to NM_000090.3 T1418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr2:189859786 C>T maps to NM_000090.3 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:189861889 G>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:110838885 C>T maps to NM_001845.4 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:110804757 G>A maps to NM_001845.4 H1617H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:110857864 A>G maps to NM_001845.4 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr13:110850973 G>A maps to NM_001845.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:110831354 G>A maps to NM_001845.4 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:110833707 C>T maps to NM_001845.4 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:110828807 C>T maps to NM_001845.4 P1007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr13:110826861 G>A maps to NM_001845.4 L1113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr13:110831660 T>C maps to NM_001845.4 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr13:110822921 G>A maps to NM_001845.4 R1238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:110804805 G>A maps to NM_001845.4 P1601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:110814757 G>A maps to NM_001845.4 P1427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr13:110845207 A>T maps to NM_001845.4 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:110835355 C>G maps to NM_001845.4 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:110802778 C>T maps to NM_001845.4 P1647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:110804811 C>T maps to NM_001845.4 A1599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:110864213 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr13:111077208 C>T maps to NM_001846.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr13:111088641 C>T maps to NM_001846.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr13:110960439 C>T maps to NM_001846.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:111155629 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:111118410 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:111156562 C>A maps to NM_001846.2 R1452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:228128640 G>A maps to NM_000091.4 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr2:228128560 C>T maps to NM_000091.4 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr2:228173943 G>A maps to NM_000091.4 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:228141188 A>G maps to NM_000091.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:228153917 A>G maps to NM_000091.4 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:228162444 G>T maps to NM_000091.4 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:228158019 T>C maps to NM_000091.4 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:228157923 G>A maps to NM_000091.4 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:227920727 G>A maps to ENST00000396625 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:227946897 C>T maps to ENST00000396625 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:227919309 C>A maps to ENST00000396625 G954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:227872901 C>T maps to ENST00000396625 A1547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:227875128 C>T maps to ENST00000396625 T1474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr2:227898158 A>G maps to ENST00000396625 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:107868942 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:107935980 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:107866039 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:107925065 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:107863536 T>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:107867515 C>T did not map to a codon.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr23:107829937 C>A did not map to a codon.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr23:107802348 G>T did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:107936060 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:107783021 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:107834413 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:107938145 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:107850075 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:107812033 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:107938086 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:107867546 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:107909800 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr23:107838772 A>C did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr23:107911635 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:107683364 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr23:107936060 A>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:107422583 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:107457430 C>A did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:107430497 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:107448666 A>G did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:107412758 C>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:107423837 G>A did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr23:107412791 T>C did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr23:107403857 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:107423853 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:107402788 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:107408253 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:107406264 G>C did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr23:107400415 G>T did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr23:107413931 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:107406165 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:107418962 T>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:137674514 T>C maps to NM_000093.3 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr9:137734064 C>A maps to NM_000093.3 P1811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:137591896 C>T maps to NM_000093.3 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:137658310 T>C maps to NM_000093.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:137642652 C>T maps to NM_000093.3 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr9:137704500 T>G maps to NM_000093.3 A1265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:137622230 C>T maps to NM_000093.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8364-01A-11D-2340-08 chr9:137622101 G>A maps to NM_000093.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:137710578 G>A maps to NM_000093.3 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:137622200 G>A maps to NM_000093.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:137694780 G>A maps to NM_000093.3 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:137681047 C>T maps to NM_000093.3 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:137591896 C>T maps to NM_000093.3 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr9:137622252 C>T maps to NM_000093.3 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:137622155 C>T maps to NM_000093.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:137657579 C>T maps to NM_000093.3 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:137688236 C>T maps to NM_000093.3 D939D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:137653811 C>T maps to NM_000093.3 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr9:137582872 C>T maps to NM_000093.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:189933517 A>G maps to NM_000393.3 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:189953418 A>G did not map to a codon.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr2:189928717 T>C maps to NM_000393.3 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:189899728 A>C maps to NM_000393.3 A1422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:189917495 A>G maps to NM_000393.3 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr2:189933585 G>A maps to NM_000393.3 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr2:189933586 C>T maps to NM_000393.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:189916941 C>A maps to NM_000393.3 G909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:189975011 C>T maps to NM_000393.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:10090069 C>T maps to NM_015719.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:10073524 G>A maps to NM_015719.3 G1607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:10071324 A>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:10114728 C>T maps to NM_015719.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:10108052 A>C maps to NM_015719.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:10071115 C>A maps to NM_015719.3 E1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:10071439 C>A maps to NM_015719.3 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:10076988 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr19:10097409 G>A maps to NM_015719.3 Q724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:10078752 A>G maps to NM_015719.3 G1439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:10087904 C>T maps to NM_015719.3 A1096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:10089248 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:10097404 C>A maps to NM_015719.3 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:10083624 G>A maps to NM_015719.3 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr21:47422311 C>T maps to NM_001848.2 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:47423434 G>A maps to NM_001848.2 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:47423590 C>T maps to NM_001848.2 N917N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:47418319 G>A maps to NM_001848.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr21:47552252 C>T maps to NM_001849.3 D949D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr21:47552159 C>T maps to NM_001849.3 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr21:47539014 C>T maps to NM_001849.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr21:47549380 C>T maps to NM_058174.2 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr21:47531965 G>A maps to NM_001849.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr21:47549263 C>T maps to NM_058174.2 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr21:47532202 G>A maps to NM_001849.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr21:47546071 G>A maps to NM_001849.3 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr21:47545972 C>T maps to NM_001849.3 C748C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr21:47552309 C>T maps to NM_001849.3 N968N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:47532202 G>T maps to NM_001849.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:238253699 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:238285436 C>T maps to NM_004369.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:238289603 C>T maps to NM_004369.3 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:238253584 G>A maps to NM_004369.3 Y2391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:238296675 G>A maps to NM_004369.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:238283328 C>G maps to NM_004369.3 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:238287276 A>G did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:238274487 C>T maps to NM_004369.3 P1897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:238277491 G>A maps to NM_004369.3 D1538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:238277260 G>A maps to NM_004369.3 P1615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr2:238268748 C>T maps to NM_004369.3 P2088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:238303833 A>G maps to NM_004369.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:238277419 C>A maps to NM_004369.3 V1562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr2:238274400 C>T maps to NM_004369.3 T1926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr2:238280909 G>A maps to NM_004369.3 Y1250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr2:238234359 G>T maps to NM_004369.3 C3112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr2:238259790 G>A maps to NM_004369.3 T2266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:238303251 C>T maps to NM_004369.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr2:238280828 G>A maps to NM_004369.3 S1277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:238280504 G>A maps to NM_004369.3 P1385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr2:238303695 G>C maps to NM_004369.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:238280582 G>C maps to NM_004369.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:238277428 G>A maps to NM_004369.3 F1559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:238268728 A>G did not map to a codon.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr2:238274466 G>A maps to NM_004369.3 D1904D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr2:238285553 G>A maps to NM_004369.3 N977N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:238266485 C>A maps to NM_004369.3 G2171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr3:130095347 G>A maps to ENST00000312481 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:130311907 G>T maps to NM_001102608.1 E1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:130287371 T>C maps to NM_001102608.1 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:130284027 C>T maps to NM_001102608.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:130285765 G>A maps to NM_001102608.1 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:130284282 C>T maps to NM_001102608.1 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:130290172 T>G maps to NM_001102608.1 T971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:130361854 C>T maps to NM_001102608.1 R1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:130368015 T>G maps to NM_001102608.1 A1781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:130290187 G>A maps to NM_001102608.1 K976K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:130346188 T>C maps to NM_001102608.1 G1656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:130289968 G>A maps to NM_001102608.1 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:130285958 C>T maps to NM_001102608.1 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:130377518 G>T did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr3:130282134 G>A maps to NM_001102608.1 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:48628012 C>T maps to NM_000094.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:48630676 A>G maps to NM_000094.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr3:48621021 G>A maps to NM_000094.3 G1456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr3:48618350 C>T maps to NM_000094.3 P1648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:48626117 G>A maps to NM_000094.3 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:48625316 G>A maps to NM_000094.3 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:48604158 A>G maps to NM_000094.3 G2746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:48619156 G>A maps to NM_000094.3 T1568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr3:48630222 C>T maps to NM_000094.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:48629532 A>T did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr3:48604363 G>A maps to NM_000094.3 G2734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr3:48623396 C>T maps to NM_000094.3 E1245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr3:48618752 T>A maps to NM_000094.3 G1613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:48621989 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:99513552 G>T maps to ENST00000429802 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr3:99514978 A>G maps to ENST00000429802 *746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:99513938 A>G maps to ENST00000429802 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:99514655 A>G maps to ENST00000429802 K638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:99514688 G>A maps to ENST00000429802 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:99514601 C>T maps to ENST00000429802 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:36564120 T>A maps to NM_005202.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr1:36563352 C>T maps to NM_005202.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:70990715 C>T maps to NM_001851.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:70935701 T>A maps to NM_001851.4 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:70942394 A>G maps to NM_001851.4 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:71004217 C>T maps to NM_001851.4 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:70942331 C>T maps to NM_001851.4 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:71003923 A>G maps to NM_001851.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr1:40775782 C>T maps to NM_001852.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:40768857 C>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:40775806 G>A maps to NM_001852.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:61467684 G>T maps to NM_001853.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr20:61460838 G>A maps to NM_001853.3 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:120118225 C>T maps to NM_006438.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:120118381 C>T maps to NM_006438.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:3691527 C>T maps to ENST00000418971 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:3687868 T>C maps to ENST00000418971 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:3660907 G>A maps to ENST00000418971 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr18:346781 G>A maps to NM_130386.2 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:335078 G>A maps to NM_130386.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:346508 G>A maps to NM_130386.2 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr18:480755 G>A maps to NM_130386.2 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr18:357516 G>A maps to NM_130386.2 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr18:346721 G>A maps to NM_130386.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:115426819 G>A maps to NM_016144.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:115628183 T>C maps to NM_016144.2 *203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:149468596 T>C maps to NM_016094.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:76100730 C>T maps to NM_203497.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:31315723 T>A maps to NM_053041.2 K73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:47455197 G>A maps to NM_017845.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:36298657 G>A maps to NM_014186.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr19:18898330 G>A maps to NM_000095.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:18893912 G>A maps to NM_000095.2 C726C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:18899281 G>A maps to NM_000095.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:19951206 C>G maps to NM_001135162.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:19956138 C>T maps to NM_001135162.1 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:160261160 T>C maps to NM_001098398.1 L1137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:160264606 A>G maps to NM_001098398.1 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:160268778 T>C maps to NM_001098398.1 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:160293314 G>A maps to NM_001098398.1 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr1:160261190 G>A maps to NM_001098398.1 F1127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:160262392 T>C maps to NM_001098398.1 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:14498462 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:14490364 G>A maps to NM_001144061.1 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:14486520 G>A maps to NM_001144061.1 F782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:14515964 T>A maps to NM_001144061.1 K38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr11:14515847 A>G maps to NM_001144061.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:14496076 G>A maps to NM_001144061.1 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:14502624 G>A maps to NM_001144061.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:139094429 T>C maps to NM_004766.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:139092573 G>A maps to NM_004766.2 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:139096963 G>A maps to NM_004766.2 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr3:139078161 C>A maps to NM_004766.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:19017911 G>A maps to NM_007263.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:19010502 G>A maps to NM_007263.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:128990664 G>A maps to NM_016128.3 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:128973579 C>T maps to NM_016128.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:128979637 G>A maps to NM_016128.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:128982799 C>T maps to NM_016128.3 H394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:49425999 C>T maps to NM_001143887.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:17168288 A>G maps to NM_003653.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:67963488 C>T maps to NM_006837.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:67969635 G>A maps to NM_006837.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:6838465 G>A maps to NM_001164093.1 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr12:54741793 G>T maps to NM_016057.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:198327367 T>G maps to NM_025147.3 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr2:198327260 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:84194758 T>C maps to NM_015697.7 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:99819382 A>G maps to NM_017421.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:99819460 G>A maps to NM_017421.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:131095135 C>T maps to NM_016035.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:131087458 C>T maps to NM_016035.3 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:120954553 G>A maps to NM_032314.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:74428587 T>C maps to NM_182476.1 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:74427994 G>A maps to NM_182476.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:19083250 T>G maps to NM_016138.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:47597893 A>G maps to NM_006587.2 C991C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:47597785 G>A maps to NM_006587.2 V1027V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:47602260 G>A maps to NM_006587.2 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:47663850 C>A maps to NM_006587.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr4:47746512 C>T maps to NM_006587.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr4:47647107 C>T maps to NM_006587.2 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:47788850 A>G maps to NM_006587.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:47645223 T>G maps to NM_006587.2 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:30199689 G>A maps to NM_007074.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:30198387 C>T maps to NM_007074.3 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr16:30198028 C>T maps to NM_007074.3 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:67208619 C>T maps to NM_020441.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:67207817 G>A maps to NM_020441.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:67209478 G>A maps to NM_020441.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:109042422 G>A maps to ENST00000420959 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:109046094 A>G maps to ENST00000420959 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:109095025 G>A maps to ENST00000420959 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:100887135 G>A maps to NM_052820.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr9:100890975 G>A maps to NM_052820.3 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:68987582 G>A maps to NM_006091.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:69011526 G>T maps to NM_006091.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:27948259 G>A maps to ENST00000345068 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr17:27943175 G>A maps to ENST00000345068 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr17:27946704 G>A maps to ENST00000345068 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:27945882 G>A maps to ENST00000345068 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:4410337 G>A maps to NM_024535.3 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr16:4457672 G>A maps to NM_024535.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:4414844 G>A maps to NM_024535.3 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:14110235 G>A maps to NM_001303.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:13977691 C>A maps to NM_001303.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr17:13980158 A>G maps to NM_001303.3 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr17:14110523 C>T maps to NM_001303.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:101486817 G>A maps to NM_078470.4 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr10:101483724 G>A maps to NM_078470.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:101489440 A>G maps to NM_078470.4 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:73927615 C>A maps to NM_173827.2 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:85834823 A>C maps to NM_001861.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr16:85839411 C>T maps to NM_001861.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:30231300 A>T maps to NM_032609.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:36642421 C>T maps to ENST00000437291 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:42578376 C>T maps to NM_004718.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:42578468 G>A maps to NM_004718.2 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:77158162 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr23:77158138 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:77158169 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:46737010 G>A maps to NM_130902.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:93813697 C>T maps to NM_182971.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:148904519 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:148897375 T>C maps to NM_000096.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:148894076 A>G maps to NM_000096.3 H1047H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:148927156 C>A maps to NM_000096.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:148899804 A>T maps to NM_000096.3 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:148904460 C>T maps to NM_000096.3 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:19548586 G>A maps to NM_014711.4 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:19539341 C>T maps to NM_014711.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:130027746 G>A maps to NM_001868.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:130023574 C>A maps to NM_001868.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:129910556 G>T maps to NM_001869.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr3:148614410 G>T maps to NM_001870.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr7:129962449 C>G maps to NM_016352.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:129948149 C>T maps to NM_016352.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:129986352 G>A maps to NM_080385.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr7:129999461 G>A maps to NM_080385.4 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:68421814 T>C maps to NM_020361.4 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:17036024 G>A maps to ENST00000443236 T1233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:17091334 C>T maps to ENST00000443236 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:17119327 C>T maps to ENST00000443236 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr19:17038951 G>A maps to ENST00000443236 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:17108022 G>A maps to ENST00000443236 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr19:17085974 G>A maps to ENST00000443236 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr19:17108019 C>A maps to ENST00000443236 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:17091391 C>T maps to ENST00000443236 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr3:148575293 C>G maps to NM_001871.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:46638816 G>A maps to NM_001872.3 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:46661955 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:46653020 C>A maps to NM_001872.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr13:46632516 C>T did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr13:46656605 C>T maps to NM_001872.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:46661877 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:28788226 G>A maps to NM_001304.4 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:28754502 G>A maps to NM_001304.4 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:28712246 T>C maps to NM_001304.4 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:28772999 A>G maps to NM_001304.4 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:28769341 G>A maps to NM_001304.4 W749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:28783286 G>A maps to NM_001304.4 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:28712231 C>T maps to NM_001304.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr4:166388880 C>T maps to NM_001873.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr4:166405610 C>G maps to NM_001873.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:83296088 G>A maps to ENST00000261723 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:15060833 A>G maps to NM_001177382.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:15018810 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:15063797 C>T maps to NM_001177382.1 R931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:15054155 A>G maps to NM_001177382.1 E773E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:93999717 G>T maps to NM_014912.4 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:93841160 G>A maps to NM_014912.4 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:173383100 C>T maps to NM_030627.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:173317107 G>A maps to NM_030627.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:173317506 T>C maps to NM_030627.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:173378895 C>T maps to NM_030627.2 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:173380103 G>A maps to NM_030627.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:173378930 A>G maps to NM_030627.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:173378882 G>A maps to NM_030627.2 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:175306957 C>T maps to NM_001008220.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:56979988 A>G maps to NM_181654.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr12:69265718 C>T maps to NM_001874.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:69265646 A>G maps to NM_001874.4 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:101835694 G>T maps to NM_001308.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr10:101829527 G>A maps to NM_001308.2 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:101823470 G>A maps to NM_001308.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:101841262 G>A maps to NM_001308.2 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:101835808 G>A maps to NM_001308.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:194062822 G>A maps to NM_001080513.2 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr3:194063145 G>A maps to NM_001080513.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr20:34214213 G>T maps to NM_003915.5 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:34220120 T>C maps to NM_003915.5 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr20:34220232 C>T maps to NM_003915.5 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:34220779 G>A maps to NM_003915.5 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:34214276 G>A maps to NM_003915.5 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:57180124 C>T maps to NM_152727.5 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr8:87567197 C>T maps to NM_003909.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:87567193 G>A maps to NM_003909.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:131283120 G>A maps to ENST00000502818 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:131404726 G>A maps to ENST00000502818 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr3:131404726 G>A maps to ENST00000502818 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:36767772 G>A maps to NM_020939.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:36710077 C>T maps to NM_020939.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:36733116 G>A maps to NM_020939.1 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:24542859 C>T maps to NM_006032.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:24542842 C>T maps to NM_006032.2 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:89644041 C>T maps to NM_014427.4 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:89644071 C>T maps to NM_014427.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:89650440 C>T maps to NM_014427.4 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:39161513 C>T maps to NM_153634.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr12:39154658 G>A maps to NM_153634.2 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr12:39047738 G>T maps to NM_153634.2 S547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr12:39047803 T>C maps to NM_153634.2 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr12:39223182 T>A maps to NM_153634.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:9747736 C>T maps to ENST00000383832 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr3:9746658 C>T maps to ENST00000383832 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr3:9771351 G>A maps to ENST00000383832 P546P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-A4QL-01A-31D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:98300251 G>A maps to ENST00000512905 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr16:12875063 G>A maps to NM_018340.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:12758896 G>T maps to NM_018340.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr16:12758925 A>G maps to NM_018340.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:211540486 C>T maps to NM_001122633.1 N1405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:211442162 C>T maps to NM_001122633.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr2:211540486 C>T maps to NM_001122633.1 N1405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr2:211540528 A>G maps to NM_001122633.1 Q1419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:211465396 G>A maps to NM_001122633.1 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:211512693 C>T maps to NM_001122633.1 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:211464178 T>C maps to NM_001122633.1 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr2:211465310 G>T maps to NM_001122633.1 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:145626418 G>A maps to NM_013291.2 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr8:145622562 G>C maps to NM_013291.2 V817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr8:145619683 G>A maps to NM_013291.2 V1218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:145619857 C>T did not map to a codon.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr8:145623312 G>A maps to NM_013291.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr8:145621890 G>A maps to NM_013291.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:145619906 G>A maps to NM_013291.2 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:145619254 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr8:145623306 G>T maps to NM_013291.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr8:145622113 C>A maps to NM_013291.2 E875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:9611522 C>T maps to NM_016207.2 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:1247493 T>C maps to NM_017871.4 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:99042415 G>A maps to NM_006693.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr12:69656201 C>T maps to ENST00000266679 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:69652830 C>T maps to ENST00000266679 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:61179395 G>A maps to NM_024811.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:68579963 G>A maps to NM_001876.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr11:68566685 G>A maps to NM_001876.3 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:68525198 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:68566683 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr22:51014749 C>T maps to NM_152245.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:50195520 G>A maps to NM_152359.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:50208532 G>A maps to NM_152359.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:29111985 G>A maps to NM_031311.3 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr23:88009037 T>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:88008423 T>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:88008750 C>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:88009022 A>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:88008702 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr23:88009103 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:88008709 A>T did not map to a codon.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr23:88008871 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:88008655 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr23:88008811 C>T did not map to a codon.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr23:88008762 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:88008468 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:2776642 G>A maps to NM_019609.4 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:125601968 C>T maps to NM_198148.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:125601940 G>A maps to NM_198148.2 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:125526527 A>G maps to NM_198148.2 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr10:125521394 G>A maps to NM_198148.2 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:125526655 C>A maps to NM_198148.2 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:8613860 C>T maps to NM_001014447.2 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:8603003 G>A maps to NM_001014447.2 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:207679428 G>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:207851609 C>T maps to NM_175710.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:207890812 C>A maps to NM_175710.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:207881607 C>T maps to NM_175710.1 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr1:207857240 T>C maps to NM_175710.1 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr1:207871116 G>T maps to NM_175710.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:207649615 C>T maps to NM_001006658.2 N918N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:207648253 C>A maps to NM_001006658.2 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:207647065 G>T maps to NM_001006658.2 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:207646198 G>A maps to NM_001006658.2 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:78635881 G>A maps to NM_004378.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:156670691 G>A maps to NM_001878.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr12:94243992 C>T maps to NM_003805.3 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:1716092 C>T maps to NM_020825.3 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:1712578 G>A maps to NM_020825.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:1709951 G>A maps to NM_020825.3 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:131862873 G>A maps to NM_000755.3 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:131862206 G>A maps to NM_000755.3 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:131864219 G>A maps to NM_000755.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:131862837 G>A maps to NM_000755.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:131870224 C>T maps to NM_000755.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:131870212 G>A maps to NM_000755.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:197390880 C>A maps to NM_201253.2 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:197404526 C>T maps to NM_201253.2 I1178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:197404028 G>A maps to NM_201253.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:197390139 C>T maps to NM_201253.2 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr1:197391072 C>T maps to NM_201253.2 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:197411412 C>T maps to NM_201253.2 C1332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:197316595 T>C maps to NM_201253.2 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:197390427 C>T maps to NM_201253.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr1:197396611 T>C maps to NM_201253.2 D719D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:197390634 C>A maps to NM_201253.2 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:197396684 C>T maps to NM_201253.2 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:126133050 C>T maps to NM_173689.5 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:126132597 C>T maps to NM_173689.5 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:126125189 C>T maps to NM_173689.5 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:126132396 T>C maps to NM_173689.5 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:126128523 G>A maps to NM_173689.5 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:126128640 G>A maps to NM_173689.5 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:3192622 G>A maps to NM_016302.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr7:65579836 G>T maps to NM_001142414.1 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:152487939 G>A maps to NM_019060.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:208432252 C>T maps to NM_134442.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:208442361 C>T maps to NM_134442.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:35736485 G>A maps to NM_006368.4 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:4164622 C>T maps to NM_032607.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr19:4154996 C>T maps to NM_032607.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:153946094 G>T did not map to a codon.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr7:28844123 C>T maps to NM_182898.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:28848847 G>A maps to NM_182898.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:28858737 G>T maps to NM_182898.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr7:28858730 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr7:28610047 C>T maps to NM_182898.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:28844111 G>A maps to NM_182898.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:3778794 G>A maps to NM_004380.2 Q2085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:3781372 G>A maps to NM_004380.2 R1664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:3790454 G>A maps to NM_004380.2 R1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:3779698 G>A maps to NM_004380.2 C1783C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:3843432 G>A maps to NM_004380.2 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:3777886 G>A maps to NM_004380.2 L2387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:3778705 G>A maps to NM_004380.2 G2114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:3781198 C>T maps to NM_004380.2 V1722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr16:3778426 T>C maps to NM_004380.2 Q2207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr16:3779596 C>T maps to NM_004380.2 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:3781926 G>A maps to NM_004380.2 G1580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr16:3778852 G>A maps to NM_004380.2 S2065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:3778765 C>T maps to NM_004380.2 P2094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:3786096 T>C maps to NM_004380.2 L1556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr16:3900420 C>T maps to NM_004380.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:101967438 G>A maps to NM_153836.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:101971818 G>A maps to NM_153836.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:9982595 C>T maps to NM_001077415.2 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:9979761 C>T maps to NM_001077415.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:50313887 C>T maps to NM_001135101.1 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:50315991 G>T maps to NM_001135101.1 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:50316957 G>A maps to NM_001135101.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:35467885 G>T maps to ENST00000429130 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:67089244 C>T maps to NM_000756.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr5:76249962 C>T maps to NM_001882.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:43907537 G>A maps to NM_001145146.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:43912049 C>T maps to NM_001145146.1 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr7:30695258 G>A maps to ENST00000348438 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:36749337 C>T maps to NM_016441.2 D770D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:36740835 C>T maps to NM_016441.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:36583581 G>A maps to NM_016441.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:36704125 C>T maps to NM_016441.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr2:36749367 C>T maps to NM_016441.2 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:36726452 C>T maps to NM_016441.2 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:36740852 G>A maps to NM_016441.2 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr4:1388391 G>A maps to NM_175918.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:1389214 C>T maps to NM_175918.3 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:49676858 T>C maps to ENST00000211238 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr6:49667599 C>T maps to ENST00000211238 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr6:49704127 G>C maps to NM_001190986.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr8:75924708 T>A maps to NM_031461.5 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:75928930 C>T maps to NM_031461.5 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:75898438 C>T maps to NM_031461.5 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr8:75928830 A>G maps to NM_031461.5 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:84906599 G>A maps to NM_031476.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:84940241 G>A maps to NM_031476.3 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:21288078 A>T maps to NM_005207.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:21272474 C>T maps to NM_005207.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:21304060 C>T maps to NM_005207.3 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:18707567 G>T maps to NM_004750.4 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:1317545 T>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:1327750 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr17:29120653 G>A maps to NM_015986.3 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:6012657 C>T maps to NM_019095.4 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:5838617 G>A maps to NM_001014809.1 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr4:5838596 G>A maps to NM_001014809.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:5868420 G>A maps to NM_001014809.1 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:5862924 C>T maps to NM_001014809.1 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:5857878 G>A maps to NM_001014809.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr4:5853179 T>C maps to NM_001014809.1 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:20029027 C>T maps to NM_016652.4 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:152382675 G>A maps to NM_016190.2 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:152382564 G>A maps to NM_016190.2 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:152382675 G>A maps to NM_016190.2 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:17281944 C>T maps to NM_014675.3 R1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:17298922 C>T maps to NM_014675.3 S2012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:17295651 C>T maps to NM_014675.3 T1706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:159683557 A>C maps to NM_000567.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:159683389 A>G maps to NM_000567.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:159684247 A>G maps to NM_000567.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:99655719 G>A maps to NM_018058.4 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:99695978 G>A maps to NM_018058.4 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:99677299 C>T maps to NM_018058.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:99655722 G>A maps to NM_018058.4 F412F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-A4QL-01A-31D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:122722512 C>T maps to NM_019604.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:33174140 G>A maps to NM_006371.4 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr19:18886479 C>T maps to NM_001098482.1 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:18888053 C>T maps to NM_001098482.1 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr19:18871038 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:18886578 G>A maps to NM_001098482.1 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:18876241 G>A maps to NM_001098482.1 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:153923903 G>A maps to NM_181715.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:91181742 G>A maps to NM_022769.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:91182001 T>G maps to NM_022769.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr15:91184352 C>T maps to NM_022769.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:48339651 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:107391120 G>A maps to NM_004075.3 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:107395695 A>G maps to NM_004075.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:107386600 A>G maps to NM_004075.3 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:107393778 G>A maps to NM_004075.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr21:44589334 C>T maps to NM_000394.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr11:111782346 C>T maps to NM_001885.1 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr17:27581345 G>A maps to NM_005208.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:219855054 G>A maps to NM_057094.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:219856928 C>T maps to NM_057094.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:219856889 G>A maps to NM_057094.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr22:27019289 G>A maps to NM_001886.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:27019232 G>A maps to NM_001886.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr22:27003850 A>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:25597377 C>T maps to NM_004076.3 H5H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:25601263 C>T maps to NM_004076.3 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr22:25597377 C>T maps to NM_004076.3 H5H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:25601329 G>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:97596377 A>T maps to ENST00000182096 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:209025725 G>A maps to NM_014617.3 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr2:209027987 G>A maps to NM_014617.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:209025752 G>A maps to NM_014617.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr2:209025554 A>T maps to NM_014617.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr2:209028014 C>T maps to NM_014617.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:209025560 G>A maps to NM_014617.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:209028002 G>A maps to NM_014617.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:209010698 G>A maps to NM_005210.3 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:208993094 G>A maps to NM_020989.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:208993061 G>A maps to NM_020989.3 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr2:208989036 A>G maps to NM_006891.3 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:208988910 G>A maps to NM_006891.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:151135153 G>A maps to NM_144727.1 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:151135150 G>A maps to NM_144727.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:151135099 G>T maps to NM_144727.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr7:151133408 G>A maps to NM_144727.1 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:186257251 C>T maps to NM_017541.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:186256601 A>G maps to NM_017541.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr13:20978776 G>A maps to NM_015974.2 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr13:21006291 A>G maps to NM_015974.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr13:20978273 G>T maps to NM_015974.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:21278977 C>T maps to NM_001888.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr21:34962201 G>A maps to ENST00000416217 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr21:34997045 C>T maps to ENST00000416217 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:56669892 G>A maps to NM_004077.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:53564256 C>T maps to NM_015989.4 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr12:53564265 C>T maps to NM_015989.4 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr23:151904506 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:10865890 A>G maps to NM_003651.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr12:10868334 T>C maps to NM_003651.4 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:41970769 C>T maps to NM_014460.3 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr1:115268967 G>A maps to NM_001130523.1 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr1:115273233 G>A maps to NM_001130523.1 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:115261367 T>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:115276642 G>A maps to NM_001130523.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr1:115275416 G>A maps to NM_001130523.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr1:115266561 C>T maps to NM_001130523.1 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr20:47712899 G>A maps to NM_001316.2 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:149441337 C>T maps to NM_005211.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:149433760 G>A maps to NM_005211.3 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:149456863 G>A maps to NM_005211.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:149449475 G>A maps to NM_005211.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr5:149447873 C>T maps to NM_005211.3 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:149449433 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:149459828 G>T maps to NM_005211.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:149447810 C>G maps to NM_005211.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr5:149447882 C>T maps to NM_005211.3 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:1422884 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:1401633 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:1409327 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1428458 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:1413262 C>T did not map to a codon.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr23:1424539 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:1409360 G>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:1419417 A>G did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:1407665 G>A did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr23:1413314 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:1413253 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:1409307 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:1413262 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:1404702 A>G did not map to a codon.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr22:37319373 G>T maps to ENST00000262825 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:37332595 G>T maps to ENST00000262825 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr22:37322199 C>T maps to ENST00000262825 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr22:37329914 C>T maps to ENST00000262825 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:37325724 G>A maps to ENST00000262825 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr17:38173106 C>T maps to NM_000759.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:36934823 G>A maps to NM_156039.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:36940984 G>A maps to NM_156039.3 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:36938264 C>T maps to NM_156039.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:36935295 C>T maps to NM_156039.3 W477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:19263548 G>A maps to NM_018371.4 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:19263581 T>C did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr8:19362709 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:19362751 G>A maps to NM_018371.4 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr8:19362916 A>T maps to NM_018371.4 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:43656002 G>T maps to NM_018590.3 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:43678814 G>A maps to NM_018590.3 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:43651043 A>G maps to NM_018590.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:43659392 C>T maps to NM_018590.3 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr10:43659337 C>T maps to NM_018590.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr17:61972706 T>G maps to NM_022640.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr17:61949671 G>A maps to NM_020991.3 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:61988104 C>A maps to NM_022579.1 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:61987658 G>A maps to NM_022579.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr15:75091015 C>T maps to NM_004383.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:75090972 T>C maps to NM_004383.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:75094778 C>T maps to NM_004383.2 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr15:75091246 C>T maps to NM_004383.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:75094809 C>T maps to NM_004383.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:3474260 T>C maps to NM_033225.5 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:2830723 A>T maps to NM_033225.5 C2946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:3611464 G>A maps to NM_033225.5 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr8:3855477 T>C maps to NM_033225.5 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr8:2820742 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:3046480 G>A maps to NM_033225.5 G1817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:3855549 G>A maps to NM_033225.5 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr8:3432553 G>A maps to NM_033225.5 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr8:2820837 A>G maps to NM_033225.5 S3120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:2820917 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:3046506 G>A maps to NM_033225.5 R1809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr8:3611557 A>T maps to NM_033225.5 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr8:3432499 A>T maps to NM_033225.5 C437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:34006748 T>C maps to ENST00000373381 G3106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:34401358 A>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:34554618 C>T maps to ENST00000373381 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:33985138 G>A maps to ENST00000373381 S3585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr1:34180298 G>A maps to ENST00000373381 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:34037144 C>T maps to ENST00000373381 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:33988918 A>C maps to ENST00000373381 A3459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr1:34008457 G>A maps to ENST00000373381 R3007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:34049314 G>C maps to ENST00000373381 P2349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr1:34052209 G>A maps to ENST00000373381 I2275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr1:34312506 G>A maps to ENST00000373381 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:34088991 T>C maps to ENST00000373381 V1860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:34238272 G>A maps to ENST00000373381 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:34401394 G>A maps to ENST00000373381 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:33998767 G>T maps to ENST00000373381 P3311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr1:34128511 C>T maps to ENST00000373381 Q1371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr1:34312569 G>A maps to ENST00000373381 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:34046404 A>C maps to ENST00000373381 R2405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:33990500 G>A maps to ENST00000373381 G3419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:34052730 G>T maps to ENST00000373381 L2258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr1:33990532 T>A maps to ENST00000373381 K3409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr1:34070966 C>T maps to ENST00000373381 P2109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr1:33998788 G>A maps to ENST00000373381 N3304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:113243834 A>C maps to NM_198123.1 T3589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr8:113649202 G>T maps to NM_198123.1 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:114448936 G>A maps to NM_198123.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr8:113318349 G>A maps to NM_198123.1 R2653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr8:113529403 G>T maps to NM_198123.1 R1539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:113237025 A>G maps to NM_198123.1 L3700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:113237133 C>A maps to NM_198123.1 G3664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:113256731 C>T maps to NM_198123.1 G3431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:113657440 T>G maps to NM_198123.1 G1069G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr8:113304871 A>G maps to NM_198123.1 N2894N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr8:113702267 C>A maps to NM_198123.1 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr8:113418873 G>A maps to NM_198123.1 V1896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr8:113702268 T>C maps to NM_198123.1 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr8:113529325 T>G maps to NM_198123.1 R1565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr8:113353898 A>G maps to NM_198123.1 F2153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:113933928 G>A maps to NM_198123.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr8:113569061 G>A maps to NM_198123.1 H1388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr8:113702268 T>C maps to NM_198123.1 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr8:113988119 T>G maps to NM_198123.1 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr8:114326984 A>G maps to NM_198123.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr8:113259258 A>T maps to NM_198123.1 P3404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:113293469 A>G maps to NM_198123.1 L3147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:113364725 A>G maps to NM_198123.1 P2058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:113518987 C>T maps to NM_198123.1 P1609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:113332151 C>T maps to NM_198123.1 T2408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:113668503 C>T maps to NM_198123.1 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr8:113662441 G>A maps to NM_198123.1 P1047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr8:113256737 A>G maps to NM_198123.1 S3429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr8:113678504 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr8:114186068 C>G maps to NM_198123.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:113516057 C>A maps to NM_198123.1 G1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr8:113267522 T>C maps to NM_198123.1 Q3332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:113301690 A>G maps to NM_198123.1 V3017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:113569031 C>A maps to NM_198123.1 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:113988258 T>C maps to NM_198123.1 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:113585760 C>A maps to NM_198123.1 G1337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr8:113871375 T>A maps to NM_198123.1 K585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:113484861 C>A maps to NM_198123.1 G1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:113275936 G>A maps to NM_198123.1 L3265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:113301624 G>A maps to NM_198123.1 G3039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:113988177 C>T maps to NM_198123.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr4:71115169 G>A maps to NM_005212.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:71114944 T>C maps to NM_005212.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr5:148891430 G>A maps to NM_001025105.1 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:37679303 G>A maps to NM_145203.5 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr13:37679177 G>A maps to NM_145203.5 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr17:80231182 G>A maps to NM_001893.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr22:38699203 C>T maps to NM_001894.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:64495364 G>A maps to NM_022048.3 H341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:122941057 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:122926249 T>C maps to NM_001044723.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:122941057 T>C did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:473004 G>A maps to NM_177559.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:58201621 G>T maps to NM_001896.2 Y197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:31636367 C>T maps to ENST00000375885 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:75968835 G>A maps to NM_001897.4 G2008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:75968796 A>G maps to NM_001897.4 H2021H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:75968943 C>T maps to NM_001897.4 R1972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:75969123 G>A maps to NM_001897.4 S1912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr15:75970140 G>T maps to NM_001897.4 S1679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr15:75981656 C>T maps to NM_001897.4 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:75968880 G>A maps to NM_001897.4 G1993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr15:75981452 C>G maps to NM_001897.4 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:75981656 C>T maps to NM_001897.4 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:75982160 G>A maps to NM_001897.4 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:47619065 G>A maps to ENST00000383738 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:47604203 G>A maps to ENST00000383738 C529C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:47619164 G>A maps to ENST00000383738 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:68044278 G>A maps to ENST00000389042 Q627Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:68007919 T>C maps to ENST00000389042 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr8:67988733 G>A maps to ENST00000389042 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:68007637 T>A maps to ENST00000389042 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:51461488 C>T maps to NM_030809.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:51457852 C>T maps to NM_030809.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:166514296 C>T maps to ENST00000409420 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:166535368 G>A maps to ENST00000409420 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:166535233 C>T maps to ENST00000409420 C275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr2:166535276 G>T maps to ENST00000409420 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:166535566 C>T maps to ENST00000409420 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:166536037 C>T maps to ENST00000409420 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:166514421 C>T maps to ENST00000409420 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:166536085 T>C maps to ENST00000409420 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:77252785 C>T maps to NM_001321.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:77254061 A>G did not map to a codon.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr12:77254165 A>G maps to NM_001321.1 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:18163859 C>T maps to NM_020536.4 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:18143417 G>A maps to NM_020536.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:18142881 T>C maps to NM_020536.4 H367H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:18123411 G>A maps to NM_020536.4 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:18143417 G>A maps to NM_020536.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:18143543 G>A maps to NM_020536.4 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:18139824 G>T maps to NM_020536.4 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:19213980 G>A maps to NM_003476.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:23432461 C>T maps to NM_130794.1 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:23805951 G>A maps to NM_001322.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr20:23804665 T>C maps to NM_001322.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:23614627 G>A maps to NM_000099.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr20:23858243 C>A maps to NM_001900.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:65780822 C>A maps to NM_001323.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:65780295 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:23473617 T>C maps to NM_005492.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr20:23472507 G>T maps to NM_005492.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr20:23472435 C>T maps to NM_005492.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:23472414 C>A maps to NM_005492.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr20:23473665 T>G maps to NM_005492.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:23584227 G>A maps to NM_001008693.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr20:23586246 C>T maps to NM_001008693.2 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:45194121 C>T maps to NM_000100.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:100078881 T>C did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:100077379 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:100078930 A>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:100077248 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:100079176 T>C did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:100078952 G>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:100088273 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:53458058 C>T maps to NM_015235.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:53458832 T>G maps to NM_015235.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:33124658 T>C maps to NM_001326.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:33108545 G>A maps to NM_001326.2 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:23421090 C>T maps to NM_138283.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:134948041 C>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:120009202 A>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:120009110 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:120008857 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:120009088 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:120009385 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:120009220 C>T did not map to a codon.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr23:120009289 C>T did not map to a codon.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr23:120009062 C>A did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:120008994 G>A did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:120008777 C>T did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:120009283 C>T did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:120009352 C>T did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr23:120008810 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:120007853 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:120009304 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr23:120008962 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:120008972 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:153881607 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153880695 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153880811 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:153881526 A>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:153880627 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr23:153880702 C>T did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr18:19995682 C>A maps to NM_172241.2 G698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:19996085 G>T maps to NM_172241.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr18:19995824 G>A maps to NM_172241.2 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr14:39818101 T>C maps to ENST00000396158 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:39748654 C>T maps to ENST00000396158 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr14:39818140 A>G maps to ENST00000396158 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:39782646 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:39819468 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:126691652 G>A maps to NM_022802.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:126727586 G>A maps to NM_001083914.1 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:126716139 G>A maps to NM_022802.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:126682503 G>A maps to NM_022802.2 D817D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:126691912 G>A maps to NM_022802.2 H609H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:67650675 C>T maps to NM_006565.3 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:67660618 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:67660615 C>T maps to NM_006565.3 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:67662367 C>T maps to NM_006565.3 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr20:56098122 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:56078504 G>A maps to ENST00000423479 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:77475146 C>T maps to NM_004715.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:77475100 C>T maps to NM_004715.3 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:77456021 G>A maps to NM_004715.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr18:77456042 C>T maps to NM_004715.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr18:77477646 G>A maps to NM_004715.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:77477824 G>A maps to NM_004715.3 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:77489023 G>T maps to NM_004715.3 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:77475505 G>A maps to NM_004715.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:58240194 G>A maps to NM_005730.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr1:70899632 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:104390322 A>G maps to NM_138455.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:104388117 C>A maps to NM_138455.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr2:204735609 G>A maps to NM_005214.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:138253546 C>T maps to ENST00000355078 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:138160445 T>A maps to ENST00000355078 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:138118936 T>C maps to ENST00000355078 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:138145809 C>T maps to ENST00000355078 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr5:138269666 G>A maps to ENST00000355078 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:138269586 C>T maps to ENST00000355078 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr5:138145884 C>T maps to ENST00000355078 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:80101446 T>C maps to ENST00000402739 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:80646605 C>T maps to ENST00000402739 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:80101242 C>A maps to ENST00000402739 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:80773144 C>T maps to ENST00000402739 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:80835349 T>G maps to ENST00000402739 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:80085187 G>A maps to ENST00000402739 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr2:80835418 G>T maps to ENST00000402739 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:80101332 C>T maps to ENST00000402739 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr2:80646692 A>G maps to ENST00000402739 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr2:80096985 A>G maps to ENST00000402739 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr2:80874748 C>T maps to ENST00000402739 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr2:80097052 A>C maps to ENST00000402739 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr10:68940245 A>G maps to NM_013266.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:69407205 G>A maps to NM_013266.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:68138967 G>A maps to NM_013266.2 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:68280471 G>A maps to NM_013266.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr10:69299326 C>T maps to NM_013266.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:67829229 C>A maps to NM_013266.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:67748556 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr10:67748509 C>T maps to NM_013266.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr10:67726480 C>T maps to NM_013266.2 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:111741586 G>A maps to NM_003798.2 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr9:111755007 C>T maps to NM_003798.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:41267267 C>T maps to NM_001904.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr3:41275253 C>T maps to NM_001904.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:41266485 C>T maps to NM_001904.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr3:41266598 G>A maps to NM_001904.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr3:41266670 G>C maps to NM_001904.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:41275087 C>A maps to NM_001904.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:36431374 C>T maps to NM_030877.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:36500393 G>A maps to NM_030877.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr20:36488338 C>T maps to NM_030877.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr20:36406107 G>A maps to NM_030877.3 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:36488706 C>T maps to NM_030877.3 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr11:57575681 C>A maps to NM_001085458.1 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:57576002 G>T maps to NM_001085458.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:57569577 A>T maps to NM_001085458.1 K444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr11:57573376 T>A maps to NM_001085458.1 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr11:57577602 C>T maps to NM_001085458.1 R820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:57583473 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:57569619 C>T maps to NM_001085458.1 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr11:57575763 G>A maps to NM_001085458.1 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:11411701 T>G maps to NM_001332.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:10973726 G>A maps to NM_001332.2 F1172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr5:11346620 G>A maps to NM_001332.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr5:11364951 A>G maps to NM_001332.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr5:11111071 C>T maps to NM_001332.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:11159845 G>A maps to NM_001332.2 C667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:11117588 C>T maps to NM_001332.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:11023011 C>T maps to NM_001332.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:11082808 G>A maps to NM_001332.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:11236904 C>T maps to NM_001332.2 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr5:11411764 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:11117638 T>A maps to NM_001332.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:10988354 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr5:11098706 A>G maps to NM_001332.2 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr17:3552212 G>A maps to NM_001031681.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:41475180 C>A maps to NM_001905.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:16685650 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:16717192 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:10793116 G>T maps to NM_014633.3 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:10785738 T>C maps to NM_014633.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:10785221 T>C maps to NM_014633.3 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr11:10795680 G>A maps to NM_014633.3 E950E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr11:10785356 C>T maps to NM_014633.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr11:10777232 G>A maps to NM_014633.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:10800333 C>T maps to NM_014633.3 S1068S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:10800333 C>T maps to NM_014633.3 S1068S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:15771161 G>A maps to NM_007272.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr16:67964637 G>A maps to NM_001907.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:67965048 G>A maps to NM_001907.2 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:67964198 C>T maps to NM_001907.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:44521440 G>A maps to NM_000308.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:44527007 C>T maps to NM_000308.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:44527010 C>T maps to NM_000308.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:44526651 G>A maps to NM_000308.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:11703215 G>T maps to NM_147783.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:11705323 T>C maps to NM_147783.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:11702660 G>A maps to NM_147783.2 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:88027299 G>A maps to NM_001814.4 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr11:88027275 G>A maps to NM_001814.4 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:1780836 C>T maps to NM_001909.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:1774894 C>T maps to NM_001909.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:206327497 C>T maps to ENST00000361052 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:206328751 C>T maps to ENST00000361052 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:206320268 C>T maps to ENST00000361052 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:25043576 T>C maps to NM_001911.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr14:25042922 T>G maps to NM_001911.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:79229753 G>T maps to NM_004390.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:79224791 G>A maps to NM_004390.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:150769274 T>C maps to NM_000396.3 *330W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:150769316 G>A maps to NM_000396.3 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:150776622 G>A maps to NM_000396.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:99800232 C>T maps to NM_001333.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr9:99797108 T>C maps to NM_001333.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:99800268 T>C maps to NM_001333.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr4:156863521 T>G maps to NM_001334.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:156847208 G>A maps to NM_001334.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr4:156860570 A>G maps to NM_001334.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr4:156849530 T>C maps to NM_001334.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:65650816 G>A maps to NM_001335.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr11:65649649 G>A maps to NM_001335.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:65650134 C>T maps to NM_001335.3 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr11:65649721 T>A maps to NM_001335.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:57576649 G>A maps to NM_001336.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr11:70260668 C>T maps to NM_001184740.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:70266594 C>T maps to NM_001184740.1 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:70279810 C>T maps to NM_001184740.1 Y464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr7:117432070 A>G maps to NM_033427.2 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr7:117432037 G>A maps to NM_033427.2 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:117431986 T>C maps to NM_033427.2 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:117432424 G>A maps to NM_033427.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:117432217 G>A maps to NM_033427.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:112998887 C>T maps to NM_018704.2 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr16:88779163 G>A maps to ENST00000378384 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:88779163 G>A maps to ENST00000378384 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:88781637 C>T maps to ENST00000378384 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:7990264 C>T maps to NM_206833.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:126993260 C>T maps to NM_001048252.2 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:16932368 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:17147454 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:16967690 A>G maps to NM_001081.3 C2118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:16948349 G>A maps to NM_001081.3 D2588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr10:16867000 G>A maps to NM_001081.3 S3615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:17146511 A>G maps to NM_001081.3 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr10:16932368 C>T did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr10:16970302 C>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:17126368 G>A maps to NM_001081.3 C734C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:16932370 G>A maps to NM_001081.3 S2918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:16911749 G>A maps to NM_001081.3 C3113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:16918923 G>A maps to NM_001081.3 F3026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:17024529 A>G maps to NM_001081.3 L1550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:17147482 A>G maps to NM_001081.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:17165586 C>T maps to NM_001081.3 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr10:17153023 G>A maps to NM_001081.3 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr10:17087074 G>A maps to NM_001081.3 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr10:16932427 A>G maps to NM_001081.3 T2899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:17145207 A>G maps to NM_001081.3 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:17113595 C>A maps to NM_001081.3 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr10:16941011 G>A maps to NM_001081.3 Q2861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:16992002 G>A maps to NM_001081.3 R1693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr10:17113493 T>C maps to NM_001081.3 Q852Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:17151669 G>A maps to NM_001081.3 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:17083157 C>T maps to NM_001081.3 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr10:16996517 G>T maps to NM_001081.3 S1575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:16942693 G>A maps to NM_001081.3 V2780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr10:17061889 G>A maps to NM_001081.3 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr10:17032413 C>T maps to NM_001081.3 T1423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr10:17127596 A>C maps to NM_001081.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr10:16982236 C>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:55945509 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr17:55962640 G>A maps to NM_017949.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:104183601 G>A maps to NM_024040.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr10:104184489 G>T maps to NM_024040.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:148456728 C>T maps to NM_003592.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:148496425 C>T maps to NM_003592.2 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:148489849 G>A maps to NM_003592.2 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:148484178 C>T maps to NM_003592.2 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:148451197 C>T maps to NM_003592.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:148456393 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:148456447 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:148454073 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:225378309 G>A maps to NM_003590.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:113909113 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:113900349 G>A maps to NM_001008895.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr13:113887617 T>C maps to NM_001008895.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:113899469 C>T maps to NM_001008895.1 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:113914988 C>T maps to NM_001008895.1 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:119680425 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:119669714 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:119674405 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:119673162 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:119694324 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:119691797 T>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:119691803 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:119680455 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:107925672 C>T maps to NM_003478.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:107959317 T>C maps to NM_003478.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:107969211 G>T maps to NM_003478.3 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:43020463 A>G maps to NM_001168370.1 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:43020091 G>A maps to NM_001168370.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:43017367 G>A maps to NM_001168370.1 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:43013342 G>A maps to NM_001168370.1 R1032R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr6:43020259 G>A maps to NM_001168370.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:43008317 G>A maps to NM_001168370.1 Q1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:43020478 G>A maps to NM_001168370.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:43014339 C>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:43167105 C>T maps to ENST00000354495 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:43155500 C>T maps to ENST00000354495 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:43155581 G>A maps to ENST00000354495 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:43168554 C>T maps to ENST00000354495 H1210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:43190358 G>T maps to ENST00000354495 G2338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:43166426 G>T maps to ENST00000354495 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:43163826 C>T maps to ENST00000354495 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:43192050 C>T maps to ENST00000354495 P2475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr6:43155044 C>T maps to ENST00000354495 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:43191081 C>T maps to ENST00000354495 L2412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:43153239 C>T maps to ENST00000354495 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:43152293 G>A maps to ENST00000354495 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:43166453 C>T maps to ENST00000354495 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:43154153 C>T maps to ENST00000354495 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:43153718 G>A maps to ENST00000354495 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:43155716 C>T maps to ENST00000354495 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr6:33385862 C>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:101514331 A>G maps to NM_015960.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:101459367 C>T maps to ENST00000360264 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:101844764 C>T maps to ENST00000360264 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:101837171 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:101845105 C>T maps to ENST00000360264 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr7:101559468 C>T maps to ENST00000360264 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr7:101839971 G>A maps to ENST00000360264 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:101755047 C>T maps to ENST00000360264 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:101845474 C>T maps to ENST00000360264 F977F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr7:101839959 G>A maps to ENST00000360264 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:101821798 C>T maps to ENST00000360264 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:101845114 G>A maps to ENST00000360264 T857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:101845117 C>T maps to ENST00000360264 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:111729243 G>A maps to NM_015267.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:111746229 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:111701596 G>A maps to NM_015267.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:111731283 G>A maps to NM_015267.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:111758569 C>T maps to NM_015267.3 F919F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:111745052 G>A maps to NM_015267.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr12:111779617 C>T maps to NM_015267.3 T1140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr12:111758425 C>T maps to NM_015267.3 Y871Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:111779752 G>A maps to NM_015267.3 K1185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr12:111779779 G>A maps to NM_015267.3 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:111785627 G>A maps to NM_015267.3 E1320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr12:111734322 C>T maps to NM_015267.3 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr12:111729304 C>T maps to NM_015267.3 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:111785411 G>A maps to NM_015267.3 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:124594391 T>C maps to NM_022034.4 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:94704652 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:180815356 C>T maps to NM_020943.2 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:180809957 G>A maps to NM_020943.2 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:180815329 G>A maps to NM_020943.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:36971184 A>G maps to NM_017748.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr17:36963082 T>A maps to NM_017748.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr17:36977248 A>C maps to NM_017748.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:36962648 C>T did not map to a codon.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr10:101997882 C>A maps to NM_018294.4 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:107299919 C>T maps to NM_152434.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr11:107299859 A>G maps to NM_152434.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr4:49005980 C>T maps to NM_025087.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:49063826 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:48990683 T>C maps to NM_025087.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr4:49052743 G>C maps to NM_025087.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:49005980 C>T maps to NM_025087.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr4:49046858 G>C maps to NM_025087.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:39307058 G>A maps to NM_001171174.1 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:76944542 C>T maps to NM_001565.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:134910281 G>A maps to NM_004887.4 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:4638555 A>G maps to NM_001100812.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:42937209 C>T maps to NM_198477.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:42938008 C>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:76927392 G>A maps to NM_002416.1 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:76924825 A>G maps to NM_002416.1 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:219029292 C>T maps to NM_000634.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:219028908 C>T maps to NM_000634.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:219028908 C>T maps to NM_000634.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:218999631 C>T maps to NM_001168298.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:70836469 G>A did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:70836600 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:70836597 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:136872771 G>A maps to NM_001008540.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:136872936 G>A maps to NM_001008540.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:118764510 G>A maps to NM_001716.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr11:118764729 C>T maps to NM_001716.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr11:118764999 G>A maps to NM_001716.3 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118765083 C>T maps to NM_001716.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118765254 G>A maps to NM_001716.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:237489245 G>A maps to NM_020311.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr2:237489896 C>G maps to NM_020311.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr2:237489446 C>T maps to NM_020311.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:237489455 G>A maps to NM_020311.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:237489305 C>A maps to NM_020311.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr2:237489188 C>T maps to NM_020311.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:47811497 C>T maps to NM_001101654.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:105393492 G>A maps to NM_025212.1 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:139060722 G>A maps to NM_016463.7 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:139060341 G>A maps to NM_016463.7 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr5:139060617 G>A maps to NM_016463.7 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:139060821 G>A maps to NM_016463.7 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:144909327 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:144909306 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr23:144909273 A>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:35938121 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:35969404 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:35944203 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:35959398 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:35966530 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:35969364 T>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:36007457 A>C did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr23:36007613 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:36007569 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:35989783 G>A did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:35971835 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:35969307 G>A did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr23:35984818 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:35993833 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:35969460 C>T did not map to a codon.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr23:35988979 A>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:35937996 C>T did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:19947941 G>A did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:19973634 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:19983248 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:75395396 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:37850372 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:37850183 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:45010930 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:45059990 G>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:45051066 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:45060040 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:45051246 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:45013319 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:40496295 A>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:40506752 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:148627250 G>A did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:148627277 G>T did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr23:148627249 C>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:149101878 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:149101974 C>T did not map to a codon.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr23:149101840 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:149102067 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:106482224 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:134303671 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:134303568 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:134294463 C>T did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr23:134294424 C>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:118694254 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:118676476 C>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:118694233 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:118679450 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:118699279 G>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:118675298 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:105865879 G>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:105883943 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:105875883 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:105905497 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:105876386 G>A did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:23953369 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:23933869 G>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:23953370 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:23928488 C>T did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:23953496 C>T did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:36122738 A>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:36122656 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr23:36156549 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:115592930 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:70326211 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:70326402 A>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:70323882 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:139038104 A>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:139038892 T>G did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:139038689 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:139038549 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:50390757 C>T maps to NM_007022.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr18:71928149 C>T maps to NM_148923.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr16:69458603 G>T maps to NM_030579.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:69481061 G>T maps to NM_030579.2 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr17:7762764 C>A maps to NM_144607.4 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr17:4058070 G>A maps to NM_144611.3 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:202934504 C>A maps to NM_016243.2 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:7690879 T>C maps to NM_016229.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:7693999 C>T maps to NM_016229.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:7686757 G>T maps to NM_016229.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:7693998 G>A maps to NM_016229.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:7687769 A>G maps to NM_016229.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:84573932 C>T maps to NM_016230.3 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:37663264 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:37658287 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:37664355 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:37655251 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:37665698 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:37663303 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:37660535 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:37665661 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:37641361 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:172398263 C>T maps to NM_024843.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:172379171 C>T maps to NM_024843.3 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:145151104 G>A maps to NM_001916.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr8:145150851 G>C maps to NM_001916.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:22945146 G>A maps to NM_014608.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:22997825 C>T maps to NM_014608.2 H1024H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:22956391 A>G maps to NM_001033028.1 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:22997853 C>T maps to NM_014608.2 R1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:22956280 G>A maps to NM_001033028.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:22956317 C>A maps to NM_001033028.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:22926025 C>T maps to NM_014608.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:23002964 C>T maps to NM_014608.2 G1229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr5:156753274 G>A maps to ENST00000442283 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:156747708 C>T maps to ENST00000442283 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr5:156816393 C>T maps to ENST00000442283 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:156752562 A>T maps to ENST00000442283 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr5:156755027 C>A maps to ENST00000442283 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr8:145689776 G>C maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:145689776 G>A maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr8:145689776 G>C maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:145689776 G>C maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr8:145689776 G>C maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr8:145689776 G>C maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr8:145689776 G>C maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:145689986 T>C maps to NM_138496.1 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr8:145689776 G>C maps to NM_001129888.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:83129419 A>G did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:83128751 G>T did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr23:83127905 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:83128371 A>C did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:83127963 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:83128920 A>C did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:83129479 C>T did not map to a codon.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr23:83128122 G>C did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:83128878 A>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:83141585 G>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:83126519 C>T did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:83124878 A>C did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:83129287 T>C did not map to a codon.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr23:83128312 T>A did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr23:83129024 G>A did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:83128537 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:83129173 G>A did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr23:83128289 T>C did not map to a codon.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr23:83128441 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:83129238 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:83128424 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:83128394 T>G did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:83128516 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr23:83129189 T>A did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:83128279 T>C did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:83127905 A>C did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:83127911 C>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr23:83141581 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:105767050 T>A maps to NM_001340.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:105767609 G>T maps to NM_001340.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:50815287 G>A maps to ENST00000311559 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:50785591 C>T maps to ENST00000311559 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:50828187 C>T maps to ENST00000311559 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:50826537 C>T maps to ENST00000311559 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:50788336 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:50828339 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr16:50788309 A>G maps to ENST00000311559 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr15:74640299 G>A maps to NM_000781.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr15:74659824 A>G maps to NM_000781.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr15:74637520 G>T maps to NM_000781.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr15:74631600 G>A maps to NM_000781.2 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:143956468 G>A maps to ENST00000377675 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr8:143956697 T>A maps to ENST00000377675 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr8:143958290 C>T maps to ENST00000377675 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:143994780 G>A maps to NM_000498.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr8:143999226 G>A maps to NM_000498.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:143994278 A>G maps to NM_000498.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:143996495 G>A maps to NM_000498.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr8:143994278 A>G maps to NM_000498.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:143994861 C>T maps to NM_000498.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:143994023 G>A maps to NM_000498.3 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr15:51503058 G>A maps to NM_031226.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr15:51503067 C>T maps to NM_031226.2 E483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:51514615 G>A maps to NM_031226.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:51503147 G>A maps to NM_031226.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr15:51529165 G>A maps to NM_031226.2 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:75014766 G>A maps to NM_000499.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr15:75013663 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr15:75013992 G>A maps to NM_000499.3 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr15:75042261 G>A maps to NM_000761.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:38298185 C>T maps to NM_000104.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:38302369 C>T maps to NM_000104.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:204161588 A>G maps to ENST00000429815 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:204131349 T>C maps to ENST00000429815 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr6:32006336 C>A maps to NM_000500.5 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:32007840 G>A maps to NM_000500.5 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:52789527 G>A maps to NM_000782.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr20:52774693 C>T maps to NM_000782.4 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:52788145 T>C maps to NM_000782.4 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr20:52773732 C>T maps to NM_000782.4 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr20:52774058 C>T maps to NM_000782.4 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:94834180 C>T maps to NM_000783.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:94834723 G>A maps to NM_000783.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:72371261 G>A maps to NM_019885.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:72371141 G>A maps to NM_019885.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:72359685 C>T maps to NM_019885.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:72371249 C>T maps to NM_019885.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:72362527 G>A maps to NM_019885.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:72360352 G>A maps to NM_019885.2 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:94828126 G>A maps to NM_183374.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:94822673 G>A maps to NM_183374.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:94825963 C>T maps to NM_183374.2 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:94825738 C>T maps to NM_183374.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:219677013 G>A maps to NM_000784.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:58158952 C>A maps to NM_000785.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:41596363 C>T maps to NM_000766.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:41601773 C>T maps to NM_000766.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:41355867 G>A maps to NM_000762.5 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:41349732 G>A maps to NM_000762.5 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:41386387 C>T maps to NM_000764.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:41381629 G>A maps to NM_000764.2 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:41387590 A>G maps to NM_000764.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:41386387 C>T maps to NM_000764.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:41518215 G>A maps to NM_000767.4 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:41518643 C>T maps to NM_000767.4 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:41516002 C>T maps to NM_000767.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:41522635 C>T maps to NM_000767.4 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:41510200 G>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:96535237 T>C maps to NM_000769.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:96602621 C>T maps to NM_000769.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:96541726 T>C maps to NM_000769.1 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr10:96612637 G>A maps to NM_000769.1 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:96829105 T>G maps to NM_000770.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr10:96707654 T>C maps to NM_000771.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:42524800 C>T maps to NM_000106.4 S217S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr10:135340997 C>T maps to NM_000773.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:135350627 T>C maps to NM_000773.3 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:135342019 C>T maps to NM_000773.3 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:41630642 C>T maps to NM_000774.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:60375596 C>T maps to NM_000775.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:60381763 C>T maps to NM_000775.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:14901789 C>A maps to NM_024514.4 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr11:14902272 T>A maps to NM_024514.4 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr11:14913628 C>A maps to NM_024514.4 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:108870668 G>A maps to NM_183075.2 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:108866522 T>C maps to NM_183075.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:108870648 G>T maps to NM_183075.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:1026411 C>T maps to NM_017781.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:99366085 T>C maps to NM_017460.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr7:99359761 C>T maps to NM_017460.3 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:99461223 C>T maps to NM_022820.3 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr7:99459297 G>A maps to NM_022820.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:99447300 C>T maps to NM_022820.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:99262894 T>C maps to NM_000777.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:99313471 G>A maps to ENST00000292414 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:99315207 C>A maps to ENST00000292414 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:99308405 A>G maps to ENST00000292414 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:47407042 C>T maps to ENST00000371904 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:47400813 G>T maps to ENST00000371904 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:47399630 G>T maps to ENST00000371904 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:47400714 G>A maps to ENST00000371904 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr1:47609042 C>T maps to NM_001010969.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr1:47610316 C>T maps to NM_001010969.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:47280919 C>T maps to NM_001099772.1 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr1:47283635 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:16045143 A>G maps to NM_021187.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:16025590 G>A maps to NM_021187.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:16024661 G>C maps to NM_021187.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:16040265 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:15806781 C>T maps to NM_023944.2 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:15791215 C>T maps to NM_023944.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:15795636 G>A maps to NM_023944.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:15791223 C>T maps to NM_023944.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:16001192 A>G maps to NM_001082.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:15989613 G>A maps to NM_001082.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr19:15989715 C>T maps to NM_001082.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:16000361 C>T maps to NM_001082.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:16003187 C>T maps to NM_001082.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:15997109 G>A maps to NM_001082.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr19:15990166 C>T maps to NM_001082.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15658948 T>G maps to NM_173483.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:15651269 T>C maps to NM_173483.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:15752260 G>A maps to NM_000896.2 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15758135 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:15752233 G>A maps to NM_000896.2 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr19:15769187 C>T maps to NM_000896.2 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:15730503 C>A maps to NM_007253.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:15730572 G>C did not map to a codon.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr19:15739640 C>A maps to NM_007253.3 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:47515713 A>G maps to NM_178033.1 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:47489570 C>T maps to NM_178033.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr1:47501733 C>T maps to NM_178033.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr1:47564902 G>A maps to NM_178134.2 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:91752480 G>A maps to NM_000786.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr7:91761089 T>A maps to NM_000786.3 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:59407182 T>C maps to NM_000780.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:59409278 A>G maps to NM_000780.3 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:59409212 C>T maps to NM_000780.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr8:59407089 T>C maps to NM_000780.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:65528500 T>C maps to NM_004820.3 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:65517325 G>A maps to NM_004820.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:42916093 G>A maps to NM_004391.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:42916498 A>G maps to NM_004391.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:86047683 T>C maps to NM_001554.4 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:86047710 C>T maps to NM_001554.4 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:77528567 A>G did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:77529239 C>T did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:77529218 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:77528565 T>C did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:77528937 A>G did not map to a codon.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr23:77528390 C>A did not map to a codon.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr23:77529188 C>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:76696461 C>T maps to NM_004762.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:76704343 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:48982464 T>C maps to NM_017457.4 *401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:6210229 G>A maps to ENST00000396741 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:6210220 G>A maps to ENST00000396741 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:6210911 C>T maps to ENST00000396741 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:6210487 G>A maps to ENST00000396741 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:6205175 G>A maps to ENST00000396741 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:37695344 C>T maps to NM_013385.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr2:158272553 G>A maps to NM_004288.4 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr2:158272338 G>A maps to NM_004288.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr22:24717988 T>C maps to NM_015330.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:24810528 C>T maps to NM_015330.2 R1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:24730390 C>T maps to NM_015330.2 R804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:20108735 T>C maps to NM_001033553.1 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:19999987 G>A maps to NM_001033553.1 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr17:20108519 C>T maps to NM_001033553.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:20013855 C>T maps to NM_001033553.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:20108669 A>G maps to NM_001033553.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr21:27938628 C>T maps to ENST00000435845 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:242680463 G>A maps to NM_152783.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:59793692 G>A maps to NM_014992.1 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:59826193 C>T maps to NM_014992.1 R879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:59814283 A>G maps to NM_014992.1 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:39847177 C>T maps to ENST00000398904 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:39835354 C>T maps to ENST00000398904 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr6:39869750 C>T maps to ENST00000398904 R1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:39835330 A>G maps to ENST00000398904 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:57756703 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:39382947 G>T maps to NM_001343.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:39382875 C>T maps to NM_001343.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:39382875 C>T maps to NM_001343.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:39376962 T>C maps to NM_001343.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:39383286 G>A maps to NM_001343.2 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:124532968 C>T maps to ENST00000408936 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr9:124441060 G>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr9:124535254 G>A maps to ENST00000408936 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:124535065 C>T maps to ENST00000408936 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:124530797 C>A maps to ENST00000408936 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:124532937 G>A maps to ENST00000408936 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:124519333 G>A maps to ENST00000408936 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:124535230 C>A maps to ENST00000408936 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr9:124329505 C>T maps to NM_032552.2 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:124543793 G>A maps to ENST00000408936 A1122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:124441044 G>A maps to ENST00000408936 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:124535251 C>T maps to ENST00000408936 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:72049922 T>C maps to ENST00000359684 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:72146995 G>T maps to ENST00000359684 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:72255948 A>G maps to ENST00000359684 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:85950099 T>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:85906123 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:85769379 T>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:85404094 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:85404079 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:85403797 C>T did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:86069813 A>G did not map to a codon.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr23:86069698 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:85404008 C>T did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr23:85950028 A>T did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:86087114 A>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:85403700 A>G did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:85950164 A>T did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:86067872 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:85404034 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:85969555 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:86067898 G>C did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:85769379 T>G did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:85403711 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:59108338 G>T maps to NM_016651.5 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:59113576 C>T maps to NM_016651.5 Q746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr14:59113479 C>T maps to NM_016651.5 Y713Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:59113704 C>T maps to NM_016651.5 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:59112666 C>T maps to NM_016651.5 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:59112996 G>A maps to NM_016651.5 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr14:59113461 G>A maps to NM_016651.5 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr14:59113503 T>C maps to NM_016651.5 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:49570130 A>G maps to NM_004393.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:49570085 G>A maps to NM_004393.4 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:49568876 G>A maps to NM_004393.4 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:61488160 C>T maps to NM_006133.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:61511462 C>T maps to NM_006133.2 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:61488195 G>A maps to NM_006133.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:61502350 C>T maps to NM_006133.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:61511876 G>A maps to NM_006133.2 A1015A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:61511765 C>A maps to NM_006133.2 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:61490942 G>A maps to NM_006133.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr7:6485686 G>A maps to NM_139179.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:6464451 C>T maps to NM_139179.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:6456286 G>A maps to NM_139179.3 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:6449536 G>A maps to NM_139179.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:6449536 G>A maps to NM_139179.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:6449981 G>A maps to NM_139179.3 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr7:6456528 G>A maps to NM_139179.3 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:61110230 C>A maps to NM_015533.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:61110302 C>T maps to NM_015533.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:61111666 C>T maps to NM_015533.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:61110053 C>T maps to NM_015533.3 T233T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8081-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:13084381 C>A maps to NM_152654.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:13084267 C>A maps to NM_152654.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:13080608 A>G maps to NM_152654.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:109283295 G>T maps to NM_001917.4 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr12:109278976 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:109278976 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:109293173 C>T maps to NM_001917.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:109288082 A>G maps to NM_001917.4 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:106124903 G>T maps to NM_172370.3 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:90255317 T>C maps to NM_004938.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:90220045 C>T maps to NM_004938.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:90321378 C>T maps to NM_004938.2 I1131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:90313685 G>A maps to NM_004938.2 S909S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:90317954 C>T maps to NM_004938.2 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:90283522 G>A maps to NM_004938.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:90321729 C>T maps to NM_004938.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr9:90219937 C>T maps to NM_004938.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr15:64332385 G>A maps to NM_014326.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr15:64200766 G>A maps to NM_014326.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:3964787 G>A maps to NM_001348.1 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr19:3969676 C>T maps to NM_001348.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:3959299 G>A maps to NM_001348.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:3964934 G>A maps to NM_001348.1 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr4:100756881 G>C maps to NM_014395.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr4:100784979 C>T maps to NM_014395.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:100789326 G>A maps to NM_014395.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr1:159176044 G>T maps to NM_001122951.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:159176185 G>T maps to NM_001122951.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr1:159175315 C>A maps to NM_001122951.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:159175525 G>T maps to NM_001122951.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:159175708 C>A maps to NM_001122951.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:136670054 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:136673803 G>A maps to NM_001349.2 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:173826788 C>A maps to NM_018122.4 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:33287896 T>C maps to NM_001350.4 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:33288216 C>T maps to NM_001350.4 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:33287512 C>T maps to NM_001350.4 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:33289521 G>A maps to NM_001350.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:33288599 G>A maps to NM_001350.4 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:33288839 G>A maps to NM_001350.4 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:1428884 G>A maps to NM_018959.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:1421166 T>C maps to NM_018959.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:51636172 C>T maps to NM_014764.3 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:16638358 A>G maps to NM_001190811.1 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:122011370 G>A maps to NM_014618.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr9:122011415 A>T maps to NM_014618.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr9:121929577 C>T maps to NM_014618.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:121929406 C>T maps to NM_014618.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:121929811 G>A maps to NM_014618.2 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:87530093 C>T maps to NM_006716.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr7:87537264 A>G maps to NM_006716.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:42818724 T>C maps to NM_145663.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:42811491 G>A maps to NM_145663.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:42809587 C>T maps to NM_145663.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:136508674 C>T maps to NM_000787.3 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:136501525 C>T maps to NM_000787.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:136517396 G>A maps to NM_000787.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr9:136507402 C>T maps to NM_000787.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:136508638 C>T maps to NM_000787.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:136509380 T>C maps to NM_000787.3 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:136513044 G>T maps to NM_000787.3 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:136505113 A>G maps to NM_000787.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr9:136518072 C>T maps to NM_000787.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr5:176894258 G>A maps to ENST00000393565 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:176886117 C>T maps to ENST00000393565 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:90075743 G>A maps to ENST00000392973 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:44092476 C>T maps to NM_001122956.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:44091459 C>T maps to NM_001122956.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:44096384 C>T maps to NM_001122956.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:49140173 T>C maps to NM_001352.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:137886141 C>T maps to NM_016216.3 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:100672099 G>A maps to NM_001918.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:100684198 G>A maps to NM_001918.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:100684198 G>A maps to NM_001918.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:20177882 C>A maps to ENST00000227256 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr11:20177849 C>T maps to ENST00000227256 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr11:20181546 C>T maps to ENST00000227256 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:20177912 C>T maps to ENST00000227256 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:37861192 C>T maps to NM_024345.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:24590141 A>G maps to NM_025230.4 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr14:24584817 C>T maps to NM_025230.4 N5N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr9:34125188 G>T maps to NM_015397.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:125685831 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:125686327 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:125685931 C>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:125685489 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:125686436 G>A did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr23:125685820 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:125685583 C>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:125685808 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:125686322 C>T did not map to a codon.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr23:125685742 G>A did not map to a codon.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr23:125686435 C>T did not map to a codon.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr23:125685735 A>C did not map to a codon.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr23:125685966 C>T did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:125685427 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:125686396 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:125686357 G>A did not map to a codon.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr23:125685717 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:125686354 C>A did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:125685809 C>A did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:125685488 C>A did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:125685508 G>C did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:125686200 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr23:125686061 T>A did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:125686484 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:125685266 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:125685931 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:125686046 A>T did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:125686264 C>A did not map to a codon.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr23:125685391 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:125685221 T>G did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:125686208 C>T did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:125686534 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:125686483 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:125685199 T>G did not map to a codon.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr23:125299655 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:125299777 G>A did not map to a codon.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:125299116 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:125298897 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:125298618 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:125299871 T>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:125299633 G>T did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:125299258 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:125298903 C>T did not map to a codon.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr23:125299769 C>T did not map to a codon.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr23:125298873 C>A did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:125298906 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:125299307 G>A did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:125299836 G>A did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr23:125299288 C>T did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:125298574 C>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:125298772 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:125299137 C>T did not map to a codon.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr23:125298906 G>A did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:125299785 T>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:125299493 G>A did not map to a codon.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr23:125299535 G>A did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:125298617 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:125298765 T>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:125298658 A>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:125299568 G>A did not map to a codon.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr23:125299670 G>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:125299722 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:125299808 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:125299269 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr23:125299815 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:125299312 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:125299512 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:125299071 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:125298953 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:125299551 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:104427571 T>C maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr8:104427571 T>G maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr8:104427571 T>C maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:104432574 C>T maps to NM_015420.6 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:104427571 T>G maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr8:104427607 G>A maps to NM_015420.6 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:104427340 G>T maps to NM_015420.6 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:14067018 C>T maps to NM_138353.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr19:14067170 G>A maps to NM_138353.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:17805437 T>C maps to NM_017741.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:17805512 G>A maps to NM_017741.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:73409782 C>T maps to NM_015604.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr14:73425479 C>T maps to NM_015604.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:73425338 G>A maps to NM_015604.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:41984912 C>T maps to NM_001029955.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:41984732 C>T maps to NM_001029955.3 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:41984519 T>C maps to NM_001029955.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:41984201 C>T maps to NM_001029955.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr8:88885338 T>C maps to NM_152418.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr8:88885089 A>G maps to NM_152418.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:88885020 G>T maps to NM_152418.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr8:88886058 G>A maps to NM_152418.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr8:88885230 G>A maps to NM_152418.3 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:69521971 G>A maps to NM_003861.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:167962537 A>C maps to ENST00000367840 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr1:167974017 A>G maps to ENST00000367840 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:61657270 C>T maps to NM_005828.3 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:27997831 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:27997797 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:27998140 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:27998624 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:27998760 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:27998015 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:27999323 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:27999216 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:27998804 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:27998106 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:27999202 G>A did not map to a codon.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr23:27998137 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:27998684 A>G did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:27998644 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:27766834 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:27766823 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:27765107 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:27765793 G>T did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:27765042 T>C did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:27766118 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:27765736 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:117864338 G>A maps to ENST00000338728 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr6:117842709 A>C maps to ENST00000338728 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:117860469 T>C maps to ENST00000338728 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:98538223 G>A maps to ENST00000326857 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:98568317 A>G maps to ENST00000326857 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:98536720 T>C maps to ENST00000326857 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:98538223 G>A maps to ENST00000326857 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:50985667 T>C maps to NM_005215.3 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr18:50731694 C>G maps to NM_005215.3 Y561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr18:51013230 T>A maps to NM_005215.3 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:50985625 C>T maps to NM_005215.3 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr18:51013254 G>A maps to NM_005215.3 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:50976948 G>A maps to NM_005215.3 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr18:50976897 G>A maps to NM_005215.3 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr18:50976987 C>T maps to NM_005215.3 I1116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr18:51052984 A>G did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr18:51053125 C>A maps to NM_005215.3 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr18:51013308 C>T maps to NM_005215.3 F1293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr18:50961523 A>G maps to NM_005215.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr18:51013194 G>A maps to NM_005215.3 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:50734114 C>T maps to NM_005215.3 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr11:31349806 T>C maps to NM_181807.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:31327838 T>C maps to NM_181807.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:31327258 G>A maps to NM_181807.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:31312289 T>C maps to NM_181807.2 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:24178770 A>G maps to NM_016356.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:24289077 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:6661149 G>A maps to NM_003737.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:6661809 C>T maps to NM_003737.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:6645997 A>C maps to NM_003737.2 A2416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:6653649 A>G maps to NM_003737.2 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr11:6652091 C>G maps to NM_003737.2 V1311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:6644404 G>A maps to NM_003737.2 H2834H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:6648095 C>T maps to NM_003737.2 L2058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:6646078 T>G maps to NM_003737.2 T2389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:6661446 G>A maps to NM_003737.2 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:6662301 C>T maps to NM_003737.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:6662450 G>A maps to NM_003737.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:6662034 A>G maps to NM_003737.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:6648206 G>A maps to NM_003737.2 R2021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr11:6653348 G>A maps to NM_003737.2 R1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:6651074 G>T maps to NM_003737.2 A1621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:6653373 G>A maps to NM_003737.2 S1123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:155180906 T>C maps to NM_017639.3 G1738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:155219675 A>G maps to NM_017639.3 S1475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:155254485 T>C maps to NM_017639.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr4:155287503 C>T maps to NM_017639.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:155312365 G>T maps to NM_017639.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr4:155254425 C>T maps to NM_017639.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:155243494 A>T maps to NM_017639.3 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr4:155253741 G>A maps to NM_017639.3 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr4:155157787 G>T maps to NM_017639.3 T2217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:155226010 T>C maps to NM_017639.3 G1350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr4:155241792 T>A maps to NM_017639.3 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:155163924 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:155155839 C>A maps to NM_017639.3 E2867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:155157006 C>A maps to NM_017639.3 G2478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr4:155191052 T>A maps to NM_017639.3 S1737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:155241939 A>G maps to NM_017639.3 D1082D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:155156860 G>T maps to NM_017639.3 S2526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr4:155236957 T>C maps to NM_017639.3 K1279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr4:155254614 A>G maps to NM_017639.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr4:155155849 A>C maps to NM_017639.3 G2863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr16:2290018 C>A maps to NM_001919.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr4:71888181 C>G maps to ENST00000504952 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr13:36686251 A>C maps to NM_004734.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:36348793 G>A maps to NM_004734.4 D725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:36699986 C>T maps to NM_004734.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr13:36700070 G>A maps to NM_004734.4 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:36396958 G>A maps to NM_004734.4 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:36445471 G>A maps to NM_004734.4 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr13:36402444 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:36401864 A>G maps to NM_004734.4 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr13:36383189 A>C maps to NM_004734.4 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr13:36700073 T>A maps to NM_004734.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr4:151000235 G>A maps to NM_001040261.4 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:151000400 G>A maps to NM_001040261.4 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:151141892 C>T maps to NM_001040261.4 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr3:36778860 G>A maps to NM_033403.1 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr3:36779378 T>G maps to NM_033403.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:36759552 G>T maps to NM_033403.1 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:36779460 C>T maps to NM_033403.1 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:115602111 T>C maps to NM_014881.3 K885K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:115612923 G>A maps to NM_014881.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:115608931 C>T maps to NM_014881.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:114454002 C>T maps to NM_022836.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:114454044 C>A maps to NM_022836.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:14951066 C>T maps to NM_001033855.1 L473L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F1-6874-01A-11D-1882-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr10:14976746 C>T maps to NM_001033855.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:91550891 G>A maps to NM_133503.2 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr12:91572142 G>A maps to NM_133503.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:53326746 C>T maps to ENST00000480258 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:112327833 G>A maps to NM_152624.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:155020284 C>T maps to NM_152494.3 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:155019788 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr1:155023298 C>T maps to NM_152494.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:155005624 C>T maps to NM_144622.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:183836079 C>T maps to NM_001012732.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:183815663 G>A maps to NM_001012732.1 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:74597937 C>T maps to NM_004082.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:74597748 C>T maps to NM_004082.4 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:74597438 C>T maps to NM_004082.4 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:74594896 C>A maps to NM_004082.4 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:74589791 G>A maps to NM_004082.4 T1198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:74592785 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:74596302 A>G maps to NM_004082.4 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:57924554 G>A maps to ENST00000434715 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:57924555 C>T maps to ENST00000434715 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:150095167 G>A maps to NM_001135643.1 Y383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:150133161 C>T maps to NM_001135643.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:150110225 T>C maps to NM_001135643.1 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:23652874 C>T maps to NM_032486.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:23676951 C>T maps to NM_032486.3 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:30435736 G>A maps to NM_024096.1 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:182681717 G>A maps to NM_020640.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr4:52779532 C>T maps to ENST00000451288 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:110574172 C>T did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr23:110653314 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:110653322 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr23:110576314 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr23:110555880 G>A did not map to a codon.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr19:17424911 G>A maps to NM_024050.5 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:85817242 G>A maps to NM_012137.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:85816109 C>T maps to NM_012137.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:85824449 G>A maps to NM_012137.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:31696671 C>T maps to NM_013974.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:31696698 C>A maps to NM_013974.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:31696719 C>T maps to NM_013974.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr6:31695064 G>A maps to NM_013974.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:61094347 G>A maps to NM_001923.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:61094322 G>A maps to NM_001923.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:61079549 C>T maps to NM_001923.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:61081421 G>A maps to NM_001923.3 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:61071396 G>A maps to NM_001923.3 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:61081892 C>T maps to NM_001923.3 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr11:61076453 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:61089820 C>A maps to NM_001923.3 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:61079549 C>T maps to NM_001923.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr11:61081143 G>T maps to NM_001923.3 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr11:61094278 G>A maps to NM_001923.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:61070546 G>T maps to NM_001923.3 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:53513590 C>T maps to NM_001160148.1 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr14:53560061 T>C maps to NM_001160148.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:38092103 T>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:103908680 T>C maps to NM_001001711.2 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:103908221 A>G maps to NM_001001711.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:103908617 G>A maps to NM_001001711.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:103907840 T>C maps to NM_001001711.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:103908602 C>T maps to NM_001001711.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:103907756 C>T maps to NM_001001711.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:74034057 G>A maps to NM_019058.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:101108898 C>A maps to NM_145244.3 G173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:101108926 A>C maps to NM_145244.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:101108947 A>G maps to NM_145244.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr4:101109028 G>A maps to NM_145244.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr4:101109016 A>C maps to NM_145244.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:49391773 C>T maps to NM_015086.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:110714481 C>T maps to NM_003649.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:110714088 G>A maps to NM_003649.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:20987822 G>A maps to NM_005216.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:20987834 G>A maps to NM_005216.4 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:20979188 G>A maps to NM_005216.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:30860095 G>A maps to NM_013994.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr6:30861166 C>G maps to NM_013994.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:30861184 C>T maps to NM_013994.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:162745615 C>T maps to NM_006182.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:162724998 G>A maps to NM_006182.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:162743360 C>T maps to NM_006182.2 R611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:15760381 C>T maps to NM_004939.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:15746095 T>C maps to NM_004939.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:15771005 T>C maps to NM_004939.1 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:108577480 T>C maps to NM_004398.2 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:108593961 G>T maps to NM_004398.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:108709178 G>T maps to NM_004398.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:31245811 C>T maps to NM_030653.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:31242910 C>T maps to NM_030653.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr12:31254030 A>G maps to NM_030653.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:31254801 C>T maps to NM_030653.3 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:31249859 C>T maps to NM_030653.3 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:38897251 C>T maps to NM_001098504.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:118578755 G>A maps to NM_006773.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr16:70395363 C>A maps to NM_018332.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:112302122 T>C maps to NM_007204.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:112309019 T>C maps to NM_007204.4 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr10:70716037 A>G maps to NM_004728.2 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:49225893 G>A maps to NM_004818.2 C677C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:134711257 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:134680679 T>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:134703343 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:134713912 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:134709113 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr23:134681169 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:134711258 A>T did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr23:134709085 G>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:47858678 G>A maps to NM_017895.7 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:47852752 T>C maps to NM_017895.7 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:47858672 G>A maps to NM_017895.7 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:47851604 G>A maps to NM_017895.7 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:68055611 G>A maps to NM_018380.3 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:68055914 T>C maps to NM_018380.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:135537950 G>A maps to NM_022779.7 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:135493750 G>A maps to NM_022779.7 H702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:135522410 A>G maps to NM_022779.7 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:135493776 G>A maps to NM_022779.7 Q694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr9:135535139 C>T maps to NM_022779.7 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:135505769 A>G maps to NM_022779.7 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr19:14519888 A>G maps to ENST00000451994 N452N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:41203053 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:41203301 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:41206133 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr23:41205631 C>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:41201790 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:41205774 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:41203053 C>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:41201758 G>A did not map to a codon.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr23:41204466 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:41205841 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:41203551 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:41205859 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:41202519 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:41201757 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:41206254 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr24:15026498 C>A did not map to a codon.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr24:15029364 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr24:15026510 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:55082354 G>T maps to NM_024415.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:55110956 G>A maps to NM_024415.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr5:55088577 C>G maps to NM_024415.2 S471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:176943355 G>A maps to NM_016222.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:176940712 G>A maps to NM_016222.2 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:176940763 G>T maps to NM_016222.2 Y340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr17:61886997 C>T maps to NM_203499.1 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:61895286 C>A maps to NM_203499.1 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:74117731 A>T maps to NM_018665.2 K363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:134099623 T>C maps to ENST00000452510 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:12974331 T>C maps to ENST00000426619 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:12974262 T>C maps to NM_016355.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:12974622 A>G maps to NM_016355.3 Q135Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-6457-01A-21D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:19032667 G>A maps to NM_019070.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr17:62500355 A>C maps to NM_004396.3 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:62496889 A>G maps to NM_004396.3 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:70696827 C>T maps to NM_024045.1 R578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr10:70666567 A>G maps to NM_024045.1 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:132625271 G>A maps to NM_175066.3 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:132625023 G>A maps to NM_175066.3 Y539Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:132624230 C>T maps to NM_175066.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr12:132624650 G>A maps to NM_175066.3 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:35986895 C>T maps to NM_007010.3 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:35992178 C>T maps to NM_007010.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:36002138 C>A maps to NM_007010.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:23018526 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:23018419 A>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:23018778 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:23019629 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr23:23019988 G>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:113612540 A>T maps to NM_001111322.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr12:113603715 A>G maps to NM_001111322.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:113617007 G>A maps to NM_001111322.1 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:124103352 G>A maps to NM_020936.1 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:32466434 T>C maps to NM_014314.3 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:32485254 C>T maps to NM_014314.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr9:32467892 T>A maps to NM_014314.3 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:200635400 A>G maps to NM_001031725.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:200635697 G>A maps to NM_001031725.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:118625486 G>A maps to NM_004397.4 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:169227856 C>T maps to NM_017631.5 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:169194427 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:169197321 C>T maps to NM_017631.5 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr4:169138149 G>A maps to NM_017631.5 D1691D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:169393086 C>T maps to NM_001012967.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr4:169362497 C>T maps to NM_001012967.1 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:169337879 G>T maps to NM_001012967.1 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:169300532 G>T maps to NM_001012967.1 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:688397 G>A maps to NM_021008.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:644594 G>A maps to NM_021008.2 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:687962 G>A maps to NM_021008.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:91031390 A>T maps to NM_001359.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr8:91063918 C>T maps to NM_001359.1 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:91029548 C>A maps to NM_001359.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:91031384 T>C maps to NM_001359.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:461553 C>T maps to NM_020664.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:461403 G>A maps to NM_020664.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:161092086 T>C maps to ENST00000368005 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:42703763 G>A maps to NM_133328.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:42713927 C>T maps to NM_133328.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:42703892 C>T maps to NM_133328.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:42703805 C>T maps to NM_133328.2 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:90029778 C>A maps to NM_207514.1 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:90028533 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:90023995 C>T maps to NM_207514.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:6793619 G>A maps to NM_001925.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:6728298 G>A maps to NM_005218.3 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:6728282 G>A maps to NM_005218.3 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr6:49976973 A>G maps to NM_001037728.2 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr6:50011400 T>G maps to NM_001037498.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:29965050 A>G maps to NM_153289.2 *85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr20:29965224 G>A maps to NM_153289.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr20:29992808 A>G maps to NM_001011878.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:30053416 A>C maps to NM_001037500.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:126053 A>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:126314 C>T maps to NM_030931.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:11851515 G>A maps to NM_001033019.1 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:11842017 C>T maps to NM_001033017.2 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr8:11842017 C>T maps to NM_001033017.2 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:100615981 G>A maps to NM_206918.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr14:100615694 G>T maps to NM_206918.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:126214596 T>C maps to NM_020946.1 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr9:126146188 C>G maps to NM_020946.1 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:126202749 G>A maps to NM_020946.1 C459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:126144433 G>A maps to NM_020946.1 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr9:126439025 G>T maps to NM_020946.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:197564379 A>C maps to NM_001195215.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:197586802 C>T maps to NM_001195215.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:197611861 A>G maps to NM_001195215.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr19:6475578 G>A maps to NM_024898.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:6468316 G>A maps to NM_024898.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:6475353 C>T maps to NM_024898.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:6470365 G>A maps to NM_024898.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:6476975 C>T maps to NM_024898.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:140273679 G>T maps to NM_015689.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:140273780 G>A maps to NM_015689.3 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:115168269 T>G maps to ENST00000393274 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:115130547 G>A maps to ENST00000393274 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:115130364 G>A maps to ENST00000393274 D880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:115130456 C>A maps to ENST00000393274 E850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:111734908 G>A maps to NM_024901.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr1:111737246 G>A maps to NM_024901.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:142202651 G>T maps to NM_014957.2 G1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:65956733 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:65983415 A>G maps to ENST00000443035 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:65962412 G>A maps to ENST00000443035 F1526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr15:65989677 T>C maps to ENST00000443035 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:65983355 A>G maps to ENST00000443035 R1192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:65954189 T>C maps to ENST00000443035 *1908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr15:65994117 A>C maps to ENST00000443035 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:153904886 T>C maps to NM_014856.2 A1263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:153907389 G>A maps to NM_014856.2 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:153914788 C>T maps to NM_014856.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:153914361 G>A maps to NM_014856.2 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr1:153910297 C>A maps to NM_014856.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:19324396 C>T maps to NM_017925.4 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:9225342 G>A maps to NM_015213.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:9225549 G>A maps to NM_015213.2 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:9166554 C>A maps to NM_015213.2 G1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:31613304 G>A maps to NM_144973.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:68948217 C>A maps to NM_001114120.1 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:68947795 G>A maps to NM_001114120.1 C565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:68944832 C>T maps to NM_001114120.1 K702K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:59943278 A>G maps to NM_018369.2 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:59893630 T>C maps to NM_018369.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:59943344 T>C maps to NM_018369.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:59940656 G>A maps to NM_018369.2 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr5:59940670 C>A maps to NM_018369.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:32210984 C>T maps to NM_001136029.1 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:32200850 T>C maps to NM_001136029.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:121013831 C>T maps to NM_022783.2 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:120940663 T>C maps to NM_022783.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:120940799 C>A maps to NM_022783.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:121015279 C>T maps to NM_022783.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr8:120940687 C>T maps to NM_022783.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:33054299 G>T maps to NM_001077242.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:5383797 G>A maps to NM_016041.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr2:220286141 G>A maps to NM_001927.3 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:89074846 G>A maps to NM_017996.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:89074105 C>G maps to NM_017996.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr1:10527273 G>A maps to NM_004401.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:3775292 C>T maps to ENST00000430539 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr9:117266505 G>A maps to NM_015404.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:117266880 C>T maps to NM_015404.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:117266505 G>A maps to NM_015404.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr9:117240979 G>A maps to NM_015404.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:117266883 G>A maps to NM_015404.3 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:117266580 G>A maps to NM_015404.3 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:117165144 C>T maps to NM_015404.3 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179325709 T>C maps to NM_001042702.3 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr2:179325943 G>A maps to NM_001042702.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145542208 C>T maps to NM_012079.4 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:75511516 C>T maps to NM_032564.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:69420150 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr22:19130141 C>T maps to NM_022719.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:19121750 C>T maps to NM_022719.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:19130105 T>C maps to NM_022719.2 A115A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8081-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr22:19055631 C>T maps to NM_005137.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:19028715 G>A maps to NM_005137.2 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:20303652 G>A maps to NM_033257.3 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:20302310 G>A maps to NM_033257.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:20073608 A>G maps to NM_022720.6 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:20097585 G>A maps to NM_022720.6 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:56347163 C>T maps to NM_201554.1 D698D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:56332995 T>C maps to NM_201554.1 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:56333950 T>C maps to NM_201554.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr12:56334502 C>T maps to NM_201554.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr12:56335327 C>T maps to NM_201554.1 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:14724956 G>A maps to NM_004080.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr7:14613992 G>A maps to NM_004080.2 Y539Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr7:14775678 A>T maps to NM_004080.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:14880849 C>T maps to NM_004080.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:14378323 T>C maps to NM_004080.2 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:14722437 A>G maps to NM_004080.2 C286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:234368889 G>A maps to NM_152879.2 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:234299086 C>T maps to NM_152879.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:185867950 C>T maps to NM_001346.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:185879417 C>A maps to NM_001346.2 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:42793376 G>A maps to NM_178009.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:42729867 A>G maps to NM_178009.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:42784856 G>A maps to NM_178009.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr13:42793376 G>A maps to NM_178009.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr13:42701681 C>T maps to NM_178009.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr13:42772701 G>A maps to NM_178009.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr13:42784856 G>A maps to NM_178009.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr13:42734148 C>T maps to NM_178009.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:42734212 A>T maps to NM_178009.2 K266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:42748259 G>T maps to NM_178009.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:137293789 A>G maps to NM_004717.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:137270053 T>C maps to NM_004717.2 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:137270093 T>C did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr7:137170146 A>T maps to NM_004717.2 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr7:137096915 C>T maps to NM_004717.2 K941K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr7:137255995 A>T maps to NM_004717.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:50213509 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:50146590 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:50213089 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:50136225 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:50125580 A>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:50213597 G>A did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:50111945 T>G did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:50146110 C>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:50130605 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:50146512 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:50130582 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:50146495 T>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:50129457 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:50111964 G>T did not map to a codon.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr23:50213278 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:50213211 C>A did not map to a codon.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr11:46400599 G>A maps to NM_001105540.1 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:74177849 T>C maps to NM_080916.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr2:74173902 C>T maps to NM_080916.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr1:55337220 G>A maps to NM_014762.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr1:55349368 A>T maps to NM_014762.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:71146456 G>A maps to NM_001360.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:71155134 G>A maps to NM_001360.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:71146576 G>A maps to NM_001360.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr11:71153309 T>A maps to NM_001360.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:26795418 A>C maps to NM_024887.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:49442912 C>T maps to NM_014475.3 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:49447627 C>T maps to NM_014475.3 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:49488121 G>A maps to NM_021044.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:49485070 G>A maps to NM_021044.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:72055071 C>T maps to NM_001361.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:12792442 C>T maps to NM_001930.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:12790342 C>T maps to NM_001930.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:24113764 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr14:24114489 G>A maps to NM_182908.4 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:12640619 G>A maps to NM_004753.4 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr1:12677212 C>T maps to NM_004753.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr14:24424378 C>A maps to NM_021004.2 C88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr14:24507074 G>C maps to NM_001082488.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:21094442 G>T maps to NM_015510.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:9674987 G>A maps to ENST00000330255 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:9674987 G>A maps to ENST00000330255 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr2:169938294 T>C maps to NM_001142271.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr2:169938102 G>A maps to NM_001142271.1 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr2:169939854 C>T maps to NM_001142271.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:2161158 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:2343242 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:2139162 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:2139158 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:2326791 C>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:2343344 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:2209602 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:12136228 T>C maps to NM_018706.5 D439D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GT-01A-21D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:12162179 G>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:24541860 A>G maps to NM_001358.2 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:30633375 C>T maps to NM_003587.4 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:30627592 A>G maps to NM_003587.4 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:30630482 C>A maps to NM_003587.4 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:54579186 A>G maps to NM_019030.2 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:54573110 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:54579210 A>G maps to NM_019030.2 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:54579255 T>C maps to NM_019030.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:47870545 C>T maps to NM_138615.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:47889771 C>T maps to NM_138615.2 R797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:47891143 A>G maps to NM_138615.2 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:47889026 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:47890174 C>T maps to NM_138615.2 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:47891513 C>T maps to NM_138615.2 S1163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:47888256 C>T maps to NM_138615.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:47882644 C>A maps to NM_138615.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:127540970 C>T maps to NM_018180.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:127548545 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:127541199 C>T maps to NM_018180.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:47880429 C>T maps to NM_014681.5 Y891Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr19:47856910 G>A maps to NM_014681.5 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr19:47858522 G>A maps to NM_014681.5 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:47858522 G>A maps to NM_014681.5 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:47883178 G>A maps to NM_014681.5 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:47856679 T>C maps to NM_014681.5 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:47865841 G>A maps to NM_014681.5 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:47885294 C>T maps to NM_014681.5 Y1119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:37653970 C>A maps to NM_021931.3 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:37652367 C>T maps to NM_021931.3 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:37638971 T>C maps to NM_021931.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:37639047 G>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:37650574 C>T maps to NM_021931.3 H530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:37634850 C>T maps to NM_021931.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:154033047 A>G maps to NM_020865.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:154006669 T>C maps to NM_020865.2 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:154033825 A>G did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr3:154013118 A>T maps to NM_020865.2 L520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:154017705 C>T maps to NM_020865.2 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:154010349 G>A maps to NM_020865.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:154042019 G>T maps to NM_020865.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:125435019 T>C maps to NM_032656.3 E1020E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:125438495 G>A maps to NM_032656.3 C875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:125460029 C>T maps to NM_032656.3 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:72130837 G>A maps to NM_014003.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:72138431 G>A maps to NM_014003.3 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:72131585 T>C maps to NM_014003.3 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:72138491 C>T maps to NM_014003.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:72141379 G>A maps to NM_014003.3 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr16:72139929 T>C maps to NM_014003.3 D838D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:57679905 C>A maps to NM_024612.4 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:57684403 G>A maps to NM_024612.4 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:57679953 C>T maps to NM_024612.4 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:57682874 C>T maps to NM_024612.4 Y680Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:39083498 G>A maps to NM_198963.1 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:39095427 G>A maps to NM_198963.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:39095409 T>A maps to NM_198963.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr2:39029990 G>A maps to NM_198963.1 R1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:40255747 C>T maps to NM_024119.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:40255768 T>C maps to NM_024119.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:41584564 G>A maps to NM_004941.1 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:182856358 C>T maps to NM_001357.4 G1201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:182848382 A>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:182836114 A>G maps to NM_001357.4 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:182856559 C>T maps to NM_001357.4 G1268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:182853798 G>T maps to NM_001357.4 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:140955847 A>G maps to ENST00000398557 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:140908487 C>T maps to ENST00000398557 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140960324 C>T maps to ENST00000398557 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:140953601 A>G maps to ENST00000398557 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr23:96167526 C>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:96502818 A>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:96854259 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:96213148 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:96212938 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:96167390 G>A did not map to a codon.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr23:96136667 C>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:96212915 G>A did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:95993745 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:96013169 C>T did not map to a codon.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr23:96638968 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:96354736 A>G did not map to a codon.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr23:96369920 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:60413549 G>A maps to NM_001042517.1 Q924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:60240956 C>A maps to NM_001042517.1 E1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:60565364 C>A maps to NM_001042517.1 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:60590073 C>T maps to NM_001042517.1 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr13:60737723 C>T maps to NM_001042517.1 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr13:60707104 G>A maps to NM_001042517.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr13:60348382 C>A did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr14:95570114 C>T maps to NM_177438.2 K1206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:95599741 G>T maps to NM_177438.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:95569829 C>T maps to NM_177438.2 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:95574427 A>G maps to NM_177438.2 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:61542718 C>T maps to NM_033081.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:61512756 C>A maps to NM_033081.2 S1517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:61512858 G>A maps to NM_033081.2 N1483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:61512441 G>A maps to NM_033081.2 G1622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr20:61542172 G>A maps to NM_033081.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr20:61512786 G>A maps to NM_033081.2 V1507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr20:61526263 C>G maps to NM_033081.2 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:61513746 C>T maps to NM_033081.2 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr20:61538600 C>T maps to NM_033081.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:61542745 G>A maps to NM_033081.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr20:61512060 C>T maps to NM_033081.2 P1749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr20:61512753 G>A maps to NM_033081.2 D1518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr20:61513314 G>C maps to NM_033081.2 S1331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:61690433 C>T maps to NM_014473.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:54360029 T>C maps to NM_000792.5 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr21:47986479 C>T maps to ENST00000318711 H1450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:47975892 A>G did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr21:47987519 C>T maps to ENST00000318711 V1568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr21:47918693 G>A maps to ENST00000318711 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:47966859 C>T maps to ENST00000318711 D810D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr21:47976976 G>A maps to ENST00000318711 L1209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:47957384 C>A maps to ENST00000318711 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr21:47953471 C>A maps to ENST00000318711 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr21:47918651 G>A maps to ENST00000318711 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr21:47952044 G>A maps to ENST00000318711 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:47966844 C>T maps to ENST00000318711 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr21:47961667 G>T did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:51116997 C>T maps to NM_173602.2 I1060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:51076943 T>C maps to NM_173602.2 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr12:51138609 T>G maps to NM_173602.2 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:51117072 G>A maps to NM_173602.2 T1085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:429999 G>A maps to NM_014974.2 R615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:410318 C>T maps to NM_014974.2 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr10:402364 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:460033 C>T maps to NM_014974.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr10:486826 G>A maps to NM_014974.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:323320 G>A maps to NM_014974.2 R1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:410450 G>A maps to NM_014974.2 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:436260 C>T maps to NM_014974.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr19:2717372 G>A maps to NM_145173.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:68512290 T>C maps to NM_004675.2 *230W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:68512692 G>A maps to NM_004675.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr1:68512428 G>A maps to NM_004675.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:68512563 A>G maps to NM_004675.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr1:68512740 G>T maps to NM_004675.2 C80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr1:68512610 G>A maps to NM_004675.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:68512857 C>A maps to NM_004675.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:122545748 C>A maps to NM_032839.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:122591443 G>T maps to NM_032839.2 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr3:122552294 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:73350152 A>G maps to NM_014953.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:73349346 A>G did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:66587468 A>C maps to NM_001143688.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:66607509 C>T maps to NM_001143688.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:233194690 C>T maps to NM_152383.4 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:231906717 C>A maps to NM_001164537.1 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:231906663 G>A maps to NM_001164537.1 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:231954072 A>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:231902975 G>A maps to NM_001164537.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:231906636 G>A maps to NM_001164537.1 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr1:231885786 A>G maps to NM_001164537.1 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr1:231830064 C>A maps to NM_001164537.1 C187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:223177972 C>T maps to NM_032890.2 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:223178671 C>T maps to NM_032890.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:223177972 C>T maps to NM_032890.2 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr1:223164005 G>A maps to NM_032890.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:223177309 A>G maps to NM_032890.2 K857K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:223177426 G>A maps to NM_032890.2 E896E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:223177921 C>T maps to NM_032890.2 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:223156445 A>C maps to NM_032890.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:223177114 C>T maps to NM_032890.2 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:223176685 C>T maps to NM_032890.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:223178671 C>T maps to NM_032890.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:223176629 C>T maps to NM_032890.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:223177681 C>T maps to NM_032890.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:223177192 C>T maps to NM_032890.2 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:223178572 A>G maps to NM_032890.2 K1278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:223178509 A>G maps to NM_032890.2 E1257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:223177873 C>T maps to NM_032890.2 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr15:40661111 G>A maps to NM_033510.1 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:40656424 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:40656438 C>A maps to NM_033510.1 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr15:40659314 C>T maps to NM_033510.1 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:111888542 T>C maps to NM_001037954.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:111866266 G>A maps to NM_001037954.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:111855969 T>C maps to NM_001037954.2 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:154002964 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153993211 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153995638 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:154002901 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:153996671 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:65546325 C>T maps to NM_138368.3 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr11:65547033 C>T maps to NM_138368.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:65546370 C>T maps to NM_138368.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:54074208 C>T maps to NM_012242.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr10:54074382 G>A maps to NM_012242.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr10:54076174 C>A maps to NM_012242.2 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:107846992 T>C maps to NM_014421.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr4:107956603 G>A maps to NM_014421.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:107846974 G>T maps to NM_014421.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr4:107847028 G>T maps to NM_014421.2 C100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:11986088 C>T maps to ENST00000450094 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:12957787 C>T maps to NM_182643.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:12957439 T>G maps to NM_182643.2 P802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:13357406 A>G maps to NM_182643.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:12956977 G>A maps to NM_182643.2 N956N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:12943848 G>T maps to NM_182643.2 P1472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:13357187 T>C maps to NM_182643.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr8:13259101 C>T maps to NM_182643.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:12957274 G>A maps to NM_182643.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr8:13357277 T>C maps to NM_182643.2 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:12957274 G>A maps to NM_182643.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:12957760 G>A maps to NM_182643.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:12943848 G>T maps to NM_182643.2 P1472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:12957133 G>A maps to NM_182643.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:107559492 G>A maps to NM_000108.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr7:107557907 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:38158778 C>T maps to NM_007335.2 Y1462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:38149176 C>T maps to NM_007335.2 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:38125693 C>T maps to NM_007335.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:38163247 C>T maps to NM_007335.2 R1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:38163205 C>T maps to NM_007335.2 Q1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:51417425 G>A maps to ENST00000504404 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:196867104 C>A maps to NM_004087.2 G240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:196792609 T>C maps to NM_004087.2 E756E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:196792301 G>A maps to NM_004087.2 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:196793608 G>A maps to NM_004087.2 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr3:196842798 G>T maps to NM_004087.2 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:197023217 T>A maps to NM_004087.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:196842851 G>A maps to NM_004087.2 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:83770424 C>T maps to NM_001142699.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:83673938 G>A maps to NM_001142699.1 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:84996395 A>G maps to NM_001142699.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:83641390 T>C maps to NM_001142699.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:83544673 C>A maps to NM_001142699.1 G569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:84245741 A>G maps to NM_001142699.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:69719079 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:69712026 G>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:69669639 T>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:69720430 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:69669628 C>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:69719838 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:69669648 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:69669610 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:69669654 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:69670588 G>A did not map to a codon.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr23:69719089 C>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:69720349 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:69669272 C>A did not map to a codon.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr23:69719107 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:69713240 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:7106648 C>T did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr17:7106878 C>T maps to NM_001365.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:79554686 C>T maps to NM_004747.3 P1822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:79576780 G>A maps to NM_004747.3 V1286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr10:79614031 G>A maps to NM_004747.3 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:79579710 C>T maps to NM_004747.3 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr10:79581592 G>T maps to NM_004747.3 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:79589140 C>T maps to NM_004747.3 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:79581376 C>T maps to NM_004747.3 T955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:79556236 A>C maps to NM_004747.3 A1760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr18:3879723 G>A maps to NM_004746.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr18:3581871 C>G did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr18:3879956 C>A maps to NM_004746.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:3729291 C>T maps to NM_004746.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:3879561 G>A maps to NM_004746.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr18:3534260 G>A maps to NM_004746.2 R804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:35332720 G>A maps to NM_001080418.1 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:35370393 C>T maps to NM_001080418.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr1:35369892 A>G maps to NM_001080418.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:35369943 G>A maps to NM_001080418.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:35369999 G>A maps to NM_001080418.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:35334425 C>T maps to NM_001080418.1 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:35370417 C>T maps to NM_001080418.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:35334690 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:35370557 G>A maps to NM_001080418.1 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr20:35075293 C>T maps to ENST00000339266 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr20:35060140 C>T maps to ENST00000339266 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:35125393 A>G maps to ENST00000339266 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:35060902 T>C maps to ENST00000339266 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:35127676 G>A maps to NM_014902.4 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr20:35060578 G>A maps to ENST00000339266 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:35075282 C>T maps to ENST00000339266 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr20:35075101 A>G maps to ENST00000339266 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr20:35064591 G>A maps to ENST00000339266 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:35060239 C>T maps to ENST00000339266 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr20:35128037 C>T maps to ENST00000339266 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:55650366 G>A maps to NM_014750.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr14:55655675 C>T maps to NM_014750.4 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:101193446 G>A maps to NM_003836.5 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr14:101193434 C>T maps to NM_003836.5 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:170592773 G>A maps to NM_005618.3 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr6:170592162 G>A maps to NM_005618.3 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:170592159 C>T maps to NM_005618.3 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:170597465 G>A maps to NM_005618.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:170592536 C>T maps to NM_005618.3 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr6:170594139 G>A maps to NM_005618.3 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr6:170594224 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:170592535 G>A maps to NM_005618.3 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:170592752 G>A maps to NM_005618.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr19:39998198 C>T maps to NM_016941.3 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:39997970 G>A maps to NM_016941.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr19:39995912 C>T maps to NM_016941.3 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:39995900 G>A maps to NM_016941.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr15:41228486 C>T maps to NM_019074.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr15:41228735 C>T maps to NM_019074.3 C517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:41223734 C>T maps to NM_019074.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:75367833 C>T maps to NM_001933.4 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:172965309 G>A maps to NM_004405.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:48072104 A>G maps to NM_005220.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr17:48069009 G>A maps to NM_005220.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr17:48050494 C>A maps to NM_138281.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr7:96651604 A>C maps to NM_005221.5 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:96650071 C>T maps to NM_005221.5 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr7:96639181 C>T maps to NM_005222.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:96639202 G>A maps to NM_005222.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:96639256 G>T maps to NM_005222.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:44685743 C>T maps to NM_019100.4 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:44684005 G>A maps to NM_019100.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:124348499 T>A maps to ENST00000368915 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:124391374 C>T maps to ENST00000368915 N2117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:124396683 C>T maps to ENST00000368915 S2266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr10:124377557 A>G maps to ENST00000368915 R1639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:124402673 G>A maps to ENST00000368915 S2463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:124337330 C>A maps to ENST00000368915 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:124339283 C>T maps to ENST00000368915 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:124390711 G>A maps to ENST00000368915 T2087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:124348580 T>C maps to ENST00000368915 D635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr10:124339247 C>A maps to ENST00000368915 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:46977910 G>T maps to NM_147192.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr1:46972810 G>A maps to NM_147192.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:38934369 G>A maps to NM_007068.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:38948669 C>T did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:31947779 G>A did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:32834624 A>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:31676227 T>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:31792184 A>G did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:32429932 T>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:32613900 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:32613903 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:31496308 G>A did not map to a codon.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr23:32486746 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:31165401 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:31196844 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:32398783 T>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:32536156 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:32360318 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:32466738 G>A did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:32381008 A>G did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr23:32867865 T>A did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:31515044 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:31986497 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:32481586 A>C did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:31191668 G>T did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:32430013 T>C did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:32360277 T>C did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:32430013 T>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:32490320 G>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:32383292 T>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:32481580 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:31164478 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:32235104 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:32328263 G>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:32366551 G>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:32583887 T>G did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr23:31191683 G>A did not map to a codon.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr23:31496451 A>C did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:32490329 A>C did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:32490352 T>C did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:32381008 A>C did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:32430011 A>C did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:32662248 T>G did not map to a codon.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr23:31854891 C>A did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr23:31152235 G>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:31222112 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:31496458 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:31164460 C>T did not map to a codon.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr23:32429955 G>A did not map to a codon.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr23:31792189 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:31645907 T>G did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:32430013 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:32235151 G>A did not map to a codon.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr23:32360398 C>A did not map to a codon.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr23:32305762 T>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:32366533 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:31198592 C>A did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:31893327 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:32834688 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:32360293 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:32867884 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:32662331 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:31496272 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr23:32398720 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:32717314 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:32328289 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr23:32472904 A>G did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:31525439 T>G did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:32583831 T>C did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:32717348 T>A did not map to a codon.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr23:32591739 T>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:31496331 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:31515001 A>C did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:32563330 G>C did not map to a codon.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr23:31986467 T>A did not map to a codon.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr5:78340264 G>A maps to NM_013391.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr5:78329125 G>T maps to NM_013391.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:78359537 G>A maps to NM_013391.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr19:36002330 G>A maps to NM_033317.4 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:88583145 A>G maps to NM_004407.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr4:88584285 C>T maps to NM_004407.3 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:46281041 G>A maps to NM_004409.3 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:46280966 C>T maps to NM_004409.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:841906 G>A maps to NM_021951.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:841876 G>A maps to NM_021951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:847111 G>A maps to NM_021951.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr9:841906 G>A maps to NM_021951.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr9:841978 C>T maps to NM_021951.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:1057242 T>C maps to NM_181872.4 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:1056534 T>C maps to NM_181872.4 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:1053756 C>T maps to NM_181872.4 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:1056567 C>T maps to NM_181872.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:1056579 T>C maps to NM_181872.4 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:990215 C>T maps to NM_021240.2 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:990545 C>A maps to NM_021240.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:977246 C>T maps to NM_021240.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:990338 G>A maps to NM_021240.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:990065 C>T maps to NM_021240.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:977276 C>T maps to NM_021240.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:990660 C>T maps to NM_021240.2 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:22447573 T>C maps to NM_022160.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:50884408 C>T maps to NM_032110.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:53930371 G>A maps to NM_033067.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr1:53925617 G>A maps to NM_033067.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:53930410 C>T maps to NM_033067.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:53925242 G>A maps to NM_033067.1 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:42352906 G>A maps to ENST00000427618 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:42354688 A>G maps to ENST00000427618 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:42354595 C>A maps to ENST00000427618 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:42351522 C>T maps to ENST00000427618 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:86811624 C>T maps to NM_021145.3 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:86802918 A>G maps to NM_021145.3 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:86795919 A>G maps to NM_021145.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:46290089 G>A maps to NM_004943.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:118482974 G>A maps to NM_005509.4 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr5:118484728 A>G maps to NM_005509.4 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:118513829 G>A maps to NM_005509.4 E2342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr5:118533558 T>A maps to NM_005509.4 Y2551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:118485263 G>T maps to NM_005509.4 E1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr5:118470008 A>G maps to NM_005509.4 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:118433790 C>T maps to NM_005509.4 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:118485922 G>A maps to NM_005509.4 K1467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:118486081 C>T maps to NM_005509.4 S1520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr5:118533639 C>T maps to NM_005509.4 N2578N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:118485997 C>T maps to NM_005509.4 H1492H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:118485652 T>C maps to NM_005509.4 S1377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:118506773 A>G maps to NM_005509.4 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:51860756 T>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:51868357 A>G maps to NM_001174116.1 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:51827879 A>G maps to NM_001174116.1 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:51857351 G>A maps to NM_001174116.1 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:51792057 T>C maps to NM_001174116.1 Q1121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr15:51830520 G>A maps to NM_001174116.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:51792125 C>A maps to NM_001174116.1 E1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:70225563 A>G maps to NM_001080449.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:70204763 T>C maps to NM_001080449.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:70231680 G>A maps to NM_001080449.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:70196955 T>C maps to NM_001080449.1 E572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr10:70231546 C>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:52400870 G>A maps to ENST00000273600 L1911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:52429687 C>T maps to ENST00000273600 P3815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:52391955 G>A maps to ENST00000273600 S1341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr3:52380534 C>T maps to ENST00000273600 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:52395697 C>T maps to ENST00000273600 F1632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:52423499 C>T maps to ENST00000273600 Y3237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr3:52412795 G>A maps to ENST00000273600 E2459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr3:52404575 C>T maps to ENST00000273600 S2114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:52397012 G>A maps to ENST00000273600 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:52418980 C>T maps to ENST00000273600 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:52433039 A>G maps to ENST00000273600 S4152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:124270300 G>A maps to NM_207437.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:124341745 G>A maps to NM_207437.3 A2076A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:124268705 C>T maps to NM_207437.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:124297908 C>T maps to NM_207437.3 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:124270303 C>T maps to NM_207437.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:124359794 G>A maps to NM_207437.3 T2534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr12:124359953 G>A maps to NM_207437.3 S2587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:124323172 C>T maps to NM_207437.3 D1573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:124333362 C>A maps to NM_207437.3 L1894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:124377847 C>T maps to NM_207437.3 L2904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr12:124416549 C>T maps to NM_207437.3 I4279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr12:124409640 T>G maps to NM_207437.3 G3819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:124330239 G>A maps to NM_207437.3 A1700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:124359902 A>G maps to NM_207437.3 A2570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr12:124330646 C>T maps to NM_207437.3 N1802N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:124303576 G>A maps to NM_207437.3 E1169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr12:124330580 G>A maps to NM_207437.3 P1780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:124387564 C>T maps to NM_207437.3 A3122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr12:124352666 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:124289587 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:124395179 C>A maps to NM_207437.3 Y3247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:124402293 G>A maps to NM_207437.3 T3604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr12:124403315 C>T maps to NM_207437.3 L3658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:21751478 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:21627788 T>C maps to NM_003777.3 C606C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:21742377 T>A maps to NM_003777.3 A2084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:21747334 C>T maps to NM_003777.3 R2196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr7:21826306 C>A maps to NM_003777.3 A3228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:21583117 C>T maps to NM_003777.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr7:21621621 T>C maps to NM_003777.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr7:21654887 C>T maps to NM_003777.3 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:21641065 G>T maps to NM_003777.3 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr7:21908602 C>T maps to NM_003777.3 I3994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr7:21630894 G>A maps to NM_003777.3 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr7:21779254 G>A maps to NM_003777.3 P2633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr7:21654729 A>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:21639577 A>G maps to NM_003777.3 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:21778371 G>T maps to NM_003777.3 G2574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:21598617 T>C did not map to a codon.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr7:21598553 T>G maps to NM_003777.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr7:21784531 C>A maps to NM_003777.3 C2794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:21631030 A>T maps to NM_003777.3 K835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:21939610 G>A maps to NM_003777.3 T4399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr7:21598514 G>A maps to NM_003777.3 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:21654769 G>A maps to NM_003777.3 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:21628210 C>T maps to NM_003777.3 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr7:21695559 G>A maps to NM_003777.3 E1690E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr7:21784184 A>C maps to NM_003777.3 R2769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr7:21675578 T>C maps to NM_003777.3 L1536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:21659620 C>T maps to NM_003777.3 Y1480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr7:21730448 G>A maps to NM_003777.3 P2004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:21781603 T>C maps to NM_003777.3 Y2665Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:21940814 C>T maps to NM_003777.3 S4505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr7:21646302 T>A maps to NM_003777.3 Y1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:57493549 A>G maps to NM_178504.4 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:57496514 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:76548814 A>G maps to ENST00000389840 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:76490731 G>A maps to ENST00000389840 I2057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:76496428 G>A maps to ENST00000389840 T1852T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr17:76496419 G>A maps to ENST00000389840 Y1855Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:76471876 G>T maps to ENST00000389840 I2717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:76554207 G>A maps to ENST00000389840 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr17:76488799 C>T maps to ENST00000389840 P2138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr17:76471407 G>A maps to ENST00000389840 D2807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:76420018 G>A maps to ENST00000389840 L4476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:76533440 G>A maps to ENST00000389840 N933N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:76503863 G>A maps to ENST00000389840 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:76547693 G>A maps to ENST00000389840 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:76557879 G>A maps to ENST00000389840 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr17:76525610 G>A maps to ENST00000389840 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr17:76475573 C>T maps to ENST00000389840 A2617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr17:76471425 C>T maps to ENST00000389840 A2801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:76441725 G>A maps to ENST00000389840 L3736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:76446422 G>T maps to ENST00000389840 Y3637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:76521201 C>T maps to ENST00000389840 A1247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:76539983 G>A maps to ENST00000389840 Y829Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr17:7674724 G>A maps to NM_020877.2 W1480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:7674151 C>A maps to NM_020877.2 A1421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:7710588 C>T maps to NM_020877.2 R3188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:7681675 C>T maps to NM_020877.2 T1810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:7695577 A>G maps to NM_020877.2 V2354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr17:7671345 T>C maps to NM_020877.2 F1268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr17:7699900 C>T maps to NM_020877.2 T2598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:7705022 G>T maps to NM_020877.2 E2943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:7681429 G>A maps to NM_020877.2 T1761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:7721663 G>A maps to NM_020877.2 E3474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:7691221 G>A maps to NM_020877.2 P2216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:7710585 C>T maps to NM_020877.2 G3187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:7681429 G>A maps to NM_020877.2 T1761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:7710837 C>T maps to NM_020877.2 N3221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:7689439 A>G did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:7707736 C>T maps to NM_020877.2 L3046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7701544 A>G maps to NM_020877.2 G2767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7726935 G>A maps to NM_020877.2 A3773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr16:20975847 G>A maps to NM_017539.1 Q3120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:21123334 A>G maps to NM_017539.1 H633H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:21042528 G>A maps to NM_017539.1 C1759C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:21109951 C>T maps to NM_017539.1 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:21117877 T>C maps to NM_017539.1 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:21061242 G>T maps to NM_017539.1 A1445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:21151865 C>T maps to NM_017539.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:21008635 C>G maps to NM_017539.1 G2190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:20975791 G>A maps to NM_017539.1 I3138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr16:21073985 G>A maps to NM_017539.1 N1179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:21038346 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:21049196 G>A maps to NM_017539.1 A1612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:20975755 T>C maps to NM_017539.1 Q3150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:20996749 G>A maps to NM_017539.1 S2438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:20966222 A>G maps to NM_017539.1 C3661C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr16:21108729 G>A maps to NM_017539.1 Q871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr16:20996455 G>A maps to NM_017539.1 T2536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:20975851 C>T maps to NM_017539.1 A3118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:21060916 C>T maps to NM_017539.1 A1478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:20994155 C>T maps to NM_017539.1 S2582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr16:21109951 C>T maps to NM_017539.1 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:21053365 G>A maps to NM_017539.1 L1541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr16:21053504 G>A maps to NM_017539.1 V1494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr16:21073961 G>A maps to NM_017539.1 S1187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:13891147 C>T maps to NM_001369.2 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:13737439 G>A maps to NM_001369.2 A3792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:13919400 G>A maps to NM_001369.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:13817726 G>A maps to NM_001369.2 D2306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:13923469 G>A maps to NM_001369.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:13829792 C>T maps to NM_001369.2 R2090R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:13729643 A>G maps to NM_001369.2 A3929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:13809284 C>T maps to NM_001369.2 T2540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr5:13824439 A>C maps to NM_001369.2 V2149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:13876846 T>C maps to NM_001369.2 K1114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:13769651 C>T maps to NM_001369.2 A3226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr5:13754329 G>A maps to NM_001369.2 Q3513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:13817684 A>G maps to NM_001369.2 L2320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:13876894 G>T maps to NM_001369.2 P1098P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:13792324 A>T maps to NM_001369.2 G2742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:13786320 C>T maps to NM_001369.2 V2929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr5:13885263 C>T maps to NM_001369.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:13719114 C>T maps to NM_001369.2 A4125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:13809167 A>G maps to NM_001369.2 I2579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:13811782 G>A maps to NM_001369.2 N2460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr5:13719036 G>A maps to NM_001369.2 N4151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:13864658 C>T maps to NM_001369.2 P1481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:13919425 C>T maps to NM_001369.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:13864741 G>A maps to NM_001369.2 R1454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr5:13865949 C>T maps to NM_001369.2 L1394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:13841920 C>T maps to NM_001369.2 W1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr5:13708284 G>A maps to NM_001369.2 R4429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:84745151 C>T maps to NM_001370.1 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:84785046 T>C maps to NM_001370.1 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr2:196837103 G>A maps to NM_018897.2 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:196718174 G>A maps to NM_018897.2 S2891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:196771408 G>A maps to NM_018897.2 R1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:196636410 C>T maps to NM_018897.2 S3802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:196825455 A>G maps to NM_018897.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr2:196636410 C>T maps to NM_018897.2 S3802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:196671553 T>C maps to NM_018897.2 E3362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:196825249 A>T maps to NM_018897.2 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:196750978 G>T maps to NM_018897.2 S1808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:196834719 T>A maps to NM_018897.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:196922785 G>A maps to NM_018897.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:196765041 G>A maps to NM_018897.2 A1504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:196723269 G>A maps to NM_018897.2 C2665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:196729214 C>T maps to NM_018897.2 A2388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:196673537 G>A maps to NM_018897.2 A3317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr2:196774919 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:196837115 G>A maps to NM_018897.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:196726634 T>C maps to NM_018897.2 S2514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:196722144 G>A maps to NM_018897.2 A2790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr6:38877484 C>T maps to ENST00000327475 D3223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr6:38906675 C>T maps to ENST00000327475 H3961H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:38781839 C>T maps to ENST00000327475 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:38840403 G>A maps to ENST00000327475 A2349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:38840415 C>T maps to ENST00000327475 C2353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:38781844 G>A maps to ENST00000327475 K1079K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:38863895 T>C maps to ENST00000327475 C2933C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:38905787 C>T maps to ENST00000327475 R3856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:38840745 C>T maps to ENST00000327475 S2422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:38840892 C>T maps to ENST00000327475 S2471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:38738193 C>T maps to ENST00000327475 C529C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:38813475 G>T maps to ENST00000327475 G1646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:38747810 C>T maps to ENST00000327475 Y691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr6:38840772 G>T maps to ENST00000327475 T2431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:38897348 A>G maps to ENST00000327475 R3715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:38759437 G>A maps to ENST00000327475 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:38994320 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr6:38905787 C>T maps to ENST00000327475 R3856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr6:38702322 G>A maps to ENST00000327475 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:38800180 C>T maps to ENST00000327475 D1412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:38843563 C>A maps to ENST00000327475 G2594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:38998044 T>C maps to ENST00000327475 C4655C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:38831682 T>C maps to ENST00000327475 D2103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:38790794 C>T maps to ENST00000327475 R1223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:38875808 T>C maps to ENST00000327475 P3130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:38828321 G>A maps to ENST00000327475 V2004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:38862577 C>T maps to ENST00000327475 C2883C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:38941549 T>G maps to ENST00000327475 T4201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr6:38899591 A>G maps to ENST00000327475 K3748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:38791450 T>C maps to ENST00000327475 L1266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:38840715 G>T maps to ENST00000327475 V2412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr6:38754673 A>C maps to ENST00000327475 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr6:38810489 C>G maps to ENST00000327475 L1540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:38810457 G>T maps to ENST00000327475 G1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:38997984 C>T maps to ENST00000327475 P4635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr6:38702361 C>T maps to ENST00000327475 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr17:11651039 G>A maps to NM_001372.3 E2189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:11520903 C>T maps to NM_001372.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr17:11687772 C>T maps to NM_001372.3 Q2660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:11520830 G>A maps to NM_001372.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:11660967 C>T maps to NM_001372.3 F2318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:11837234 C>T maps to NM_001372.3 I4112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:11840673 C>T maps to NM_001372.3 I4165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr17:11554621 T>G maps to NM_001372.3 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr17:11696839 G>A maps to NM_001372.3 V2694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr17:11711129 G>C maps to NM_001372.3 L2834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:11648121 C>T maps to NM_001372.3 Y2040Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr17:11696974 T>G maps to NM_001372.3 T2739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr17:11687793 C>T maps to NM_001372.3 L2667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:11872783 G>A maps to NM_001372.3 K4467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr17:11593497 C>T maps to NM_001372.3 P1453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:11833394 G>A maps to NM_001372.3 L4030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:11656222 C>T maps to NM_001372.3 G2228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:11554543 T>A maps to NM_001372.3 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:11511525 C>T maps to NM_001372.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:11572895 T>C maps to NM_001372.3 D1046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr17:11845741 G>C maps to NM_001372.3 R4261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:34500819 C>A maps to NM_012144.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:34500838 T>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:72278018 G>A maps to NM_023036.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:72301515 G>A maps to NM_023036.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:72308263 A>G maps to NM_023036.4 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:72301521 C>T maps to NM_023036.4 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:33034307 G>A maps to NM_001539.2 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:33036659 C>T maps to NM_001539.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr16:47005449 G>C maps to NM_005880.3 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:47001470 C>A maps to NM_005880.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:4491416 C>T maps to NM_005147.4 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr16:4492270 C>T maps to NM_005147.4 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:78566647 C>T maps to NM_018602.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:186290033 T>G maps to NM_016306.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:100844194 A>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:100824919 A>G maps to NM_001031723.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr4:100829970 A>T maps to NM_001031723.2 C178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:234652295 G>A maps to NM_001001394.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:234652343 C>T maps to NM_001001394.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:78478865 C>T maps to NM_007034.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr1:78481798 T>C maps to NM_007034.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:78470857 A>T maps to NM_007034.3 K22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:78478798 C>T maps to NM_007034.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:157177651 G>A maps to NM_058246.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr7:157155938 G>A maps to NM_058246.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:128181482 G>A maps to NM_153330.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr3:128181962 C>T maps to NM_153330.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:183622501 C>A maps to NM_018981.1 Y631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:183623584 G>A maps to NM_018981.1 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr1:6706031 C>T maps to NM_018198.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:6698425 T>C did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr1:6706038 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:6704673 G>A maps to NM_018198.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:6704703 G>A maps to NM_018198.3 Y337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:6712906 C>T maps to NM_018198.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:6714069 G>A maps to NM_018198.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:69583090 A>G maps to NM_021800.2 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:132199274 T>C maps to NM_015268.3 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:132193824 C>T maps to NM_015268.3 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:132196985 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:132172173 T>C maps to NM_015268.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr3:132172209 A>C maps to NM_015268.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:132213064 T>C maps to NM_015268.3 D1301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr3:132213067 T>C maps to NM_015268.3 A1302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:56221971 A>G maps to NM_032364.5 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:43652795 C>T maps to NM_013238.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:43597776 T>C maps to NM_013238.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr1:15886049 C>T maps to NM_015291.2 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:41068825 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:41066631 A>G maps to NM_018163.2 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:180703753 A>G maps to NM_145261.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:102982402 T>C maps to ENST00000426036 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:34954761 G>A maps to NM_194283.3 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr12:49743368 G>A maps to NM_024902.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr12:49743128 C>T maps to NM_024902.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr21:34861109 C>T maps to NM_001040192.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:34861339 C>A maps to NM_001040192.1 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:96443250 C>T maps to NM_006260.4 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr7:73097333 G>A maps to NM_032317.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:63999942 C>T maps to NM_005528.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:62560718 G>A maps to NM_025219.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:62560748 C>T maps to NM_025219.2 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr8:66989068 C>T maps to NM_033105.4 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr8:66989023 C>T maps to NM_033105.4 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:66989014 C>T maps to NM_033105.4 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:65878695 G>A maps to ENST00000371069 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:65855118 G>A maps to ENST00000371069 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:65830469 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:65858258 C>A maps to ENST00000371069 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:65858123 G>A maps to ENST00000371069 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:65860715 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:28527850 G>A maps to NM_014280.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:39175612 G>A maps to NM_005740.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:3707216 G>A maps to NM_005223.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:3706753 G>T maps to NM_005223.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:3707210 C>T maps to NM_005223.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:3707189 C>T maps to NM_005223.3 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:3707054 C>T maps to NM_005223.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:153631963 C>T did not map to a codon.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr23:153631878 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:153633398 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:153631130 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:58183579 C>T maps to NM_004944.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr3:58183573 C>T maps to NM_004944.2 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140052886 G>A maps to NM_194249.2 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:140052405 C>T maps to NM_194249.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:230312191 G>A maps to NM_139072.3 N442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:230253101 G>A maps to NM_139072.3 C578C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:230231599 G>A maps to NM_139072.3 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr2:230282863 G>C maps to NM_139072.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:230223362 C>A maps to NM_139072.3 G703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:230223321 G>A maps to NM_139072.3 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:230377496 A>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:6589804 A>G maps to NM_144666.2 P4220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:6588289 C>T maps to NM_144666.2 R3851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:6592277 C>T maps to NM_144666.2 G4512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:6540865 C>T maps to NM_144666.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:6591960 C>T maps to NM_144666.2 R4407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:6592034 C>T maps to NM_144666.2 G4431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:6524066 T>C maps to NM_144666.2 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr11:6532526 G>C maps to NM_144666.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:6520122 C>T maps to NM_144666.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:130984784 C>T maps to ENST00000372923 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:32893449 C>T maps to ENST00000381000 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:10893786 G>A maps to NM_001005361.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:10886517 G>A maps to NM_001005361.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:10908127 G>A maps to NM_001005361.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr19:10906868 C>T maps to NM_001005360.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr19:10934545 C>T maps to NM_001005361.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:10906071 C>T maps to NM_001005361.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:10934499 C>A maps to NM_001005361.2 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr19:10893682 A>T maps to NM_001005361.2 K246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:10935881 C>T maps to NM_001005361.2 H681H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:172357784 C>T maps to ENST00000359070 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr1:171810858 G>A maps to ENST00000359070 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:171958182 C>T maps to ENST00000359070 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:101728938 T>C maps to ENST00000342239 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr10:101715526 T>A maps to ENST00000342239 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:101715832 G>T maps to ENST00000342239 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:10250740 G>A maps to NM_001130823.1 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:10284548 T>C maps to NM_001130823.1 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr2:25497833 C>T maps to NM_175629.1 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:25523109 G>A maps to NM_175629.1 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:25464523 C>T maps to NM_175629.1 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:25468892 A>G maps to NM_175629.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:25523109 G>A maps to NM_175629.1 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:25462048 T>C maps to NM_175629.1 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr2:25505421 G>A maps to NM_175629.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:31375118 C>T maps to NM_006892.3 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:31386313 G>A maps to NM_006892.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr20:31388714 C>T maps to NM_006892.3 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:31368230 G>A maps to NM_006892.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr20:31387100 C>T maps to NM_006892.3 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:31380443 C>T maps to NM_006892.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:31376724 C>A maps to NM_006892.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr20:31394055 C>T maps to NM_006892.3 I781I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:31375118 C>T maps to NM_006892.3 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:31387078 C>T maps to NM_006892.3 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:31386361 G>A maps to NM_006892.3 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr21:45680689 G>A maps to NM_013369.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:45676038 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:220251034 C>T maps to NM_012100.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr2:220239642 C>T maps to NM_012100.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:98087279 C>T maps to NM_004088.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:98079059 G>A maps to NM_004088.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:98064271 G>A maps to NM_004088.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:94343391 C>T maps to NM_014597.4 A33A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-6452-01A-12D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:94338707 A>G maps to NM_014597.4 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6803-01A-11D-1882-08 chr10:128851028 G>T maps to ENST00000398025 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:128841407 T>C maps to ENST00000398025 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:128926003 C>A maps to ENST00000398025 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr10:129207377 A>T maps to ENST00000398025 P1445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:117722425 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:117773399 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:117722265 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:117677507 T>C did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr23:117748654 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:117695458 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:117742032 A>G did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:117810669 G>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:117788584 A>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:117817144 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:117805096 C>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:117788649 A>T did not map to a codon.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr23:117796672 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr23:117752691 G>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:117700535 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:117764370 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:117744265 A>T did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr23:117796707 G>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:117727301 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:117819757 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:169129409 G>A maps to NM_004946.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr5:169469087 G>A maps to NM_004946.2 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:169445979 C>T maps to NM_004946.2 C1083C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:169454949 A>G maps to NM_004946.2 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:169483738 C>T maps to NM_004946.2 R1449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:169141165 T>C maps to NM_004946.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:169435556 G>A maps to NM_004946.2 Q1043Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:169111315 C>T maps to NM_004946.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:169483705 C>T maps to NM_004946.2 Y1438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:169141081 T>G maps to NM_004946.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr5:169445985 C>T maps to NM_004946.2 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:169141078 T>G maps to NM_004946.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr5:169468061 C>G maps to NM_004946.2 Y1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:169081458 C>T maps to NM_004946.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr5:169474563 A>G maps to NM_004946.2 K1339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:51418569 C>T maps to NM_004947.4 S1891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:51273834 C>T maps to NM_004947.4 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:51376457 A>G maps to NM_004947.4 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:51393878 C>T maps to NM_004947.4 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:51392443 C>T maps to NM_004947.4 C1413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:51417639 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:51297727 C>T maps to NM_004947.4 R776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:51392351 C>T maps to NM_004947.4 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr3:51399382 C>T maps to NM_004947.4 D1700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:51393541 G>A maps to NM_004947.4 T1424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr3:51370660 C>T maps to NM_004947.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:111398723 G>A maps to ENST00000428084 R1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5716-01A-21D-1800-08 chr7:111381244 G>A maps to ENST00000428084 R1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:111386403 G>A maps to ENST00000428084 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:111379260 C>A maps to ENST00000428084 E1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:25246734 G>A maps to NM_024940.6 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:25246734 G>A maps to NM_024940.6 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:25253057 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:25258581 G>A maps to NM_024940.6 L1642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:11352749 G>A maps to ENST00000319867 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:11361639 C>T maps to ENST00000319867 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:11356355 C>T maps to ENST00000319867 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:11323940 G>A maps to ENST00000319867 R1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:63113776 C>T maps to ENST00000371140 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:62979472 G>A maps to ENST00000371140 Q1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:62979529 G>A maps to ENST00000371140 R1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:63008277 C>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:418149 G>T maps to NM_203447.3 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr9:332450 G>A maps to NM_203447.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr9:414889 C>T maps to NM_203447.3 A1213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr9:312042 T>C maps to NM_203447.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:311982 C>T maps to NM_203447.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr9:368029 T>C maps to NM_203447.3 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:99538085 C>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr13:99449685 G>A maps to ENST00000428223 R2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:99515770 C>T maps to ENST00000428223 E1106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:99520226 C>T maps to ENST00000428223 K1043K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:99532923 G>A maps to ENST00000428223 Y916Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:3496773 C>T maps to NM_001145165.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr5:176931352 G>A maps to NM_024872.2 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:57507618 C>T maps to NM_018110.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:53171480 C>T maps to NM_018431.3 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr20:53226971 C>T maps to NM_018431.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:53260109 C>T maps to NM_018431.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:67365808 G>A maps to NM_152721.5 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr18:67345089 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:67508531 C>T maps to NM_152721.5 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:3487305 G>A maps to ENST00000389653 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr9:131708025 G>A maps to NM_014908.3 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr9:131708694 G>A maps to NM_014908.3 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:131709461 G>A maps to NM_014908.3 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr21:34951682 G>A maps to NM_017613.2 C512C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr21:34958405 G>A maps to NM_017613.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:83848525 C>T maps to NM_015018.2 L1589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:83863282 T>C maps to NM_015018.2 V2061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:83838790 C>A maps to NM_015018.2 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:83818736 T>A maps to NM_015018.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:83863666 T>C maps to NM_015018.2 S2098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr6:83806788 C>T maps to NM_015018.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:83849799 T>A maps to NM_015018.2 C1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:83848665 A>G maps to NM_015018.2 T1635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:83848692 G>A maps to NM_015018.2 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:83830455 C>T maps to NM_015018.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:83872512 C>T maps to NM_015018.2 R2323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr21:37617397 C>T maps to NM_005128.2 C1040C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:37623581 G>A maps to NM_005128.2 K1707K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr21:37583891 T>C maps to NM_005128.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr21:37617518 C>T maps to NM_005128.2 R1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr21:37649358 G>A maps to NM_005128.2 P1891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr21:37653907 A>G maps to NM_005128.2 Q2053Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr21:37581039 G>A maps to NM_005128.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr21:37605195 C>A maps to NM_005128.2 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr21:37605202 C>T maps to NM_005128.2 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr21:37603427 G>T maps to NM_005128.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:2226521 T>C maps to ENST00000221482 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:2213581 C>T maps to ENST00000221482 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:2222098 C>T maps to ENST00000221482 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:2226314 C>T maps to ENST00000221482 S1265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr19:2217886 C>T maps to ENST00000221482 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:2193686 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:2217001 G>A maps to ENST00000221482 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:2199893 C>T maps to ENST00000221482 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr19:2226926 G>A maps to ENST00000221482 P1469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:118967731 G>A maps to NM_001382.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:118967887 A>G maps to NM_001382.3 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:30919762 G>A maps to NM_080870.3 T1174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr16:89702384 G>A maps to NM_004413.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:89703695 C>T maps to NM_004413.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr16:89696880 C>T maps to NM_004413.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:68025853 G>A maps to NM_022355.2 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:68026857 C>A maps to NM_022355.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:68014115 G>T maps to NM_022357.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr16:68011861 G>A maps to NM_022357.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr16:68014253 G>A maps to NM_022357.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr16:68014034 G>A maps to NM_022357.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:38704343 G>T maps to NM_001135155.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:38706785 G>A maps to NM_001135155.1 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:65113829 C>T maps to NM_006268.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:65108458 C>T maps to NM_006268.3 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:65109021 C>T maps to NM_006268.3 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:73137951 C>T maps to NM_012074.3 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:101458256 T>C maps to NM_015958.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:101456137 G>A maps to NM_015958.2 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:101456080 T>C maps to NM_015958.2 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:155112443 G>A maps to NM_018973.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:116497366 A>G maps to NM_020868.3 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:116534833 A>G maps to NM_020868.3 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr2:116503685 A>T maps to NM_020868.3 K293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr2:116538566 T>C maps to NM_020868.3 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:116101462 C>T maps to NM_020868.3 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:66262921 C>T maps to NM_005700.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:66262921 C>T maps to NM_005700.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:66260251 C>T maps to NM_005700.3 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:66262921 C>T maps to NM_005700.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:66260283 C>A maps to NM_005700.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:66276556 C>T maps to NM_005700.3 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:162929957 A>G maps to NM_001935.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:154645511 G>A maps to NM_130797.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:154561142 A>G maps to NM_130797.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:154681192 G>T maps to NM_130797.2 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:154684054 C>T maps to NM_130797.2 D821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr7:154237680 T>A maps to NM_130797.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr7:154667657 G>A maps to NM_130797.2 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr7:154595587 C>T maps to NM_130797.2 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr7:154172045 A>G maps to NM_130797.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:65771344 A>G maps to NM_197960.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:4703928 G>A maps to ENST00000357909 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:4683642 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:4690887 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:109028154 C>T maps to NM_138815.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:7867866 G>A maps to NM_199286.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:7867836 C>T maps to NM_199286.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:109049560 T>C maps to NM_018189.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:109052729 G>A maps to NM_018189.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:74063579 C>T maps to NM_001025290.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr6:74063726 G>A maps to NM_001025290.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:54139968 G>A maps to NM_001012728.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr7:35051047 A>G maps to NM_015283.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr12:64061912 A>G maps to NM_173812.4 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr12:64041118 T>A maps to NM_173812.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr12:64020293 C>G maps to NM_173812.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:63954354 G>A maps to NM_173812.4 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:95751976 G>A maps to NM_181787.2 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:95800257 T>G maps to NM_181787.2 L662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr8:95802136 G>A maps to NM_181787.2 *724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:95777452 G>T maps to NM_181787.2 G305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:98058818 G>A maps to NM_000110.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:97770821 T>A maps to NM_000110.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:97770838 G>A maps to NM_000110.3 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:97915674 C>T maps to NM_000110.3 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:97981498 T>C did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr8:105456578 C>T maps to NM_001385.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:105459575 C>T maps to NM_001385.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr8:105459626 G>A maps to NM_001385.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr8:105436538 T>G maps to NM_001385.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:105405031 G>A maps to NM_001385.2 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:26501483 G>A maps to NM_001197293.1 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:26505246 A>T maps to NM_001197293.1 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr8:26492330 C>T maps to NM_001197293.1 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:26510812 G>A maps to NM_001197293.1 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:26481758 T>C maps to NM_001197293.1 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:146788289 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:146792251 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:146788338 T>C maps to NM_001197294.1 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:146781176 C>T maps to NM_001197294.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr5:146781176 C>T maps to NM_001197294.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:134017366 C>T maps to NM_006426.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:134015484 G>A maps to NM_006426.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr10:134004330 C>A maps to NM_006426.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr10:134006209 C>T maps to NM_006426.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:27121504 C>T maps to NM_020134.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:27157456 C>T maps to NM_020134.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:27157485 G>A maps to NM_020134.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr2:27157485 G>A maps to NM_020134.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:27121529 G>T maps to NM_020134.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:74746198 G>T maps to NM_133637.2 C655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:74745581 G>T maps to NM_133637.2 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:74750266 G>A maps to NM_133637.2 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:74750441 G>A maps to NM_133637.2 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:74752200 G>A maps to NM_133637.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:102313939 T>C maps to NM_018370.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:111661435 A>G maps to NM_178454.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:111667450 T>C maps to NM_178454.4 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:174869223 G>A maps to NM_000794.3 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:113286313 A>G maps to ENST00000355319 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:113295139 C>T maps to ENST00000355319 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr11:113295232 G>T maps to ENST00000355319 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:113295136 G>A maps to ENST00000355319 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr3:113858529 G>T maps to NM_000796.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:113847733 G>A maps to NM_000796.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:113878639 T>C maps to NM_000796.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:113866313 C>T maps to NM_000796.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:113850001 C>T maps to NM_000796.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:639788 C>T maps to NM_000797.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr11:640542 C>T maps to NM_000797.3 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr4:9784831 C>T maps to NM_000798.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr4:9783745 G>A maps to NM_000798.4 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr4:9783985 G>A maps to NM_000798.4 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:9783754 G>A maps to NM_000798.4 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:31822636 T>C maps to NM_004147.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr22:31822648 C>T maps to NM_004147.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:18005285 C>T maps to NM_001388.3 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:18010552 A>G maps to NM_001388.3 *365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:18010523 T>C maps to NM_001388.3 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:100505441 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:100511131 C>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:100515564 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:100505456 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100515553 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:100505520 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:100515503 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:100494084 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:100513425 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:100492711 T>A did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:100490872 G>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:100505519 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:100496846 T>C did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr23:100492724 G>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:100496691 C>T did not map to a codon.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr18:28710575 T>A maps to NM_024421.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:28728575 G>T maps to NM_024421.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:28654829 G>A maps to ENST00000438199 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr18:28649081 G>A maps to ENST00000438199 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:28602466 A>G maps to NM_001941.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr18:28602424 C>T maps to NM_001941.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:41423885 C>T maps to NM_001389.3 T1728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr21:41423954 C>T maps to NM_001389.3 T1705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr21:42080476 A>C maps to NM_001389.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:41414400 G>A maps to NM_001389.3 S1861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr21:41496223 C>T maps to NM_001389.3 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:41516472 G>A maps to NM_001389.3 N1068N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr21:41385176 C>T maps to NM_001389.3 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr21:41516547 G>A maps to NM_001389.3 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:41457676 A>G maps to NM_001389.3 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:41416170 C>T maps to NM_001389.3 G1739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr21:42080530 G>A maps to NM_001389.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr21:41719669 G>A maps to NM_001389.3 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr21:41711214 C>T maps to NM_001389.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:41414451 C>T maps to NM_001389.3 S1844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr21:41711118 G>A maps to NM_001389.3 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr21:41450875 C>G maps to NM_001389.3 L1483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:117308797 G>A maps to NM_020693.2 G1475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:117376238 G>A maps to NM_020693.2 N724N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr11:117310021 A>G maps to NM_020693.2 T1428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr11:117332214 G>A maps to NM_020693.2 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:117374593 G>T maps to NM_020693.2 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:117389448 G>A maps to NM_020693.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:117307844 G>A maps to NM_020693.2 Y1631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr11:117352698 G>A maps to NM_020693.2 D906D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr11:117301567 G>A maps to NM_020693.2 A1912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:117389400 C>T maps to NM_020693.2 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr11:117389391 G>A maps to NM_020693.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr11:117335802 C>A maps to NM_020693.2 V1100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr11:117332256 G>A maps to NM_020693.2 A1167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr11:117299085 C>T maps to NM_020693.2 K2100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:117403211 G>A maps to NM_020693.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:117651376 G>A maps to NM_020693.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr11:117376175 G>A maps to NM_020693.2 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:117308779 C>T maps to NM_020693.2 S1481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:117374650 G>A maps to NM_020693.2 H816H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:120854137 G>A maps to NM_024094.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:39427041 A>T maps to NM_005867.2 C88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr21:38380462 G>A maps to NM_018962.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:116758027 A>G maps to NM_013352.2 Q799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr18:65180207 A>G maps to NM_032160.2 H556H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:65180564 T>C maps to NM_032160.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr18:65179388 C>T maps to NM_032160.2 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr18:65181635 T>C maps to NM_032160.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr18:65178782 T>C maps to NM_032160.2 G1031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr18:65180417 A>C maps to NM_032160.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:65180258 A>G maps to NM_032160.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:65181596 A>G maps to NM_032160.2 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:28914053 G>A maps to NM_001942.2 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr18:28913590 C>T maps to NM_001942.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr18:28914023 C>T maps to NM_001942.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr18:28913556 C>T maps to NM_001942.2 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr18:28906572 A>T maps to NM_001942.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:28934597 C>T maps to NM_001942.2 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:29125952 T>C maps to NM_001943.3 H868H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:29122691 C>T maps to NM_001943.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr18:29101198 T>C maps to NM_001943.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:29121195 C>T maps to NM_001943.3 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:29044084 T>C maps to NM_001944.2 Y337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr18:29038466 C>A maps to NM_001944.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr18:29038421 C>A maps to NM_001944.2 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr18:29044177 C>T maps to NM_001944.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:29038475 G>A maps to NM_001944.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:28986262 A>G maps to NM_001134453.1 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr18:28979458 A>T maps to NM_001134453.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr18:28991212 T>C maps to NM_001134453.1 Y738Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr18:28983412 T>C maps to NM_001134453.1 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:28986169 C>T maps to NM_001134453.1 C589C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr20:35399406 G>T maps to NM_001145315.1 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:7583314 T>C maps to NM_004415.2 D1940D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:7584583 C>T maps to NM_004415.2 H2363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:7584494 C>T maps to NM_004415.2 R2334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr6:7565710 C>T maps to NM_004415.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr6:7585999 C>G maps to NM_004415.2 S2835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:7565710 C>T maps to NM_004415.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:7578040 C>A maps to NM_004415.2 T969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:7585990 A>T maps to NM_004415.2 G2832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:7585228 C>T maps to NM_004415.2 S2578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:7575662 G>T maps to NM_004415.2 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:7585192 T>C maps to NM_004415.2 G2566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:7565701 C>T maps to NM_004415.2 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr6:7574925 C>A maps to NM_004415.2 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr6:7571731 G>A maps to NM_004415.2 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr6:7559467 G>A maps to NM_004415.2 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:88535298 T>C maps to NM_014208.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:88533279 G>A maps to NM_014208.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr4:88534063 C>T maps to NM_014208.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:56417103 C>A maps to ENST00000361203 E5285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:56382028 G>A maps to ENST00000361203 T5897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:56376117 G>A maps to ENST00000361203 S6008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:56483161 C>T maps to ENST00000281662 Q2454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:56485218 T>A maps to ENST00000281662 R1769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:56505004 A>C maps to ENST00000361203 L598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:56437712 A>G maps to ENST00000361203 S4251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr6:56362251 C>T maps to ENST00000361203 T6505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:56394278 A>T maps to ENST00000361203 T5643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:56400090 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:56505384 G>A maps to ENST00000361203 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:56325024 G>A maps to ENST00000361203 R7425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:56354332 G>A maps to ENST00000361203 I6733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:56499281 C>A maps to ENST00000361203 E947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:56485138 C>A maps to ENST00000281662 V1795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:56351909 A>C maps to ENST00000361203 S6802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:56358914 G>A maps to ENST00000361203 Q6552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr6:56504280 G>A maps to ENST00000361203 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:56391226 G>A maps to ENST00000361203 R5810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:56499276 C>T maps to ENST00000361203 A948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:56481979 A>C maps to ENST00000281662 T2659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr6:56458739 C>T maps to ENST00000361203 W3938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr6:56494186 C>A maps to ENST00000361203 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr6:56401711 G>C maps to ENST00000361203 P5334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:56483206 G>A maps to ENST00000281662 D2439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:17587776 G>T maps to NM_006870.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr20:17581447 C>T maps to NM_006870.3 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:205138543 A>G maps to NM_015375.2 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:205156905 A>G maps to NM_015375.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:205119922 C>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:18608855 T>C maps to NM_080820.4 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:212238292 A>G maps to NM_016448.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr18:32455315 C>T maps to NM_001390.4 D592D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:32346000 C>T maps to NM_001390.4 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:15627673 C>T maps to NM_032122.4 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:15523310 G>T maps to NM_032122.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:15524721 C>T maps to NM_183040.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr6:15663052 G>A maps to NM_032122.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:113496080 G>A maps to NM_004416.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:113534521 G>A maps to NM_004416.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:113532899 T>C maps to NM_004416.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:113534522 C>T maps to NM_004416.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:76109915 C>A maps to NM_020892.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr7:76112245 C>T maps to NM_020892.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:58001200 C>T maps to NM_178502.2 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:122289426 T>C maps to NM_138287.3 F687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:122287952 C>T maps to NM_138287.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:122284874 T>C maps to NM_138287.3 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr3:122288699 A>G maps to NM_138287.3 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr3:122288549 T>C maps to NM_138287.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:58949401 A>G maps to NM_015177.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr11:58962712 C>T maps to NM_015177.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:58949755 C>T maps to NM_015177.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:45445593 C>T maps to NM_175940.1 G1147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:45445635 C>T maps to NM_175940.1 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:45428766 C>T maps to NM_175940.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:45443387 C>T maps to NM_175940.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr15:45433196 C>T maps to NM_175940.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:45444514 C>T maps to NM_175940.1 I1075I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr15:45444703 C>T maps to NM_175940.1 I1138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:45440622 C>T maps to NM_175940.1 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:45431268 A>G maps to NM_175940.1 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:45444069 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:45453117 C>T maps to NM_175940.1 G1262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr15:45443389 G>T maps to NM_175940.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:45440628 G>A maps to NM_175940.1 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:45392025 T>C maps to NM_014080.4 S1083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:45399569 G>A maps to NM_014080.4 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:45404878 G>T maps to NM_014080.4 A66A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr15:45400357 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr15:45401048 G>A maps to NM_014080.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr15:45400421 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:45387775 C>T maps to NM_014080.4 P1366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:45399569 G>A maps to NM_014080.4 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:45410169 C>T maps to NM_144565.2 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:45408762 C>T maps to NM_207581.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr15:45408921 G>A maps to NM_207581.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:45408792 G>A maps to NM_207581.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr15:45408873 C>T maps to NM_207581.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr15:45408914 C>A maps to NM_207581.3 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:76818209 C>T maps to NM_001003892.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:76803594 C>T maps to NM_001003892.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr10:76803765 C>T maps to NM_001003892.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:80021383 G>A maps to NM_022156.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr16:68100495 C>A maps to NM_017803.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:68110606 G>A maps to NM_017803.3 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:68109392 T>C maps to NM_017803.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:68104049 C>T maps to NM_017803.3 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr19:5789319 G>A maps to NM_020175.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:5785222 C>T maps to NM_020175.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:5789526 C>T maps to NM_020175.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:172196763 G>A maps to NM_004417.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:172195818 C>T maps to NM_004417.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:172195767 G>T maps to NM_004417.3 C367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:221875831 C>T maps to NM_007207.3 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:221912435 G>T maps to NM_007207.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr1:221879716 G>A maps to NM_007207.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:221912918 C>T maps to NM_007207.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:76861701 G>A maps to ENST00000356369 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr20:30449247 G>A maps to NM_080611.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:30450408 G>A maps to NM_080611.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:12630759 C>T maps to NM_030640.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:12630317 G>A maps to NM_030640.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:12630723 T>C maps to NM_030640.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:12630350 G>A maps to NM_030640.2 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:96809600 C>T maps to NM_004418.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:96809591 C>T maps to NM_004418.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:44703682 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:44703422 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:44703931 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:44703613 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:44703613 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:44703614 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr6:311947 A>C maps to ENST00000457386 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr8:33449694 G>A maps to NM_024025.1 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:167097565 G>A maps to NM_001080426.1 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:167097442 G>A maps to NM_001080426.1 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:167095705 C>T maps to NM_001080426.1 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:167096068 C>T maps to NM_001080426.1 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:29195943 G>A maps to NM_001394.5 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:29195907 C>T maps to NM_001394.5 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:29194650 G>T maps to NM_001394.5 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr10:112257893 G>A maps to NM_004419.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:89744646 G>A maps to NM_001946.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr3:52090145 C>T maps to NM_001947.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:1578800 G>A maps to NM_004420.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:152915489 C>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:152915039 T>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:152914971 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:152915110 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:152915039 T>G did not map to a codon.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr23:152914820 G>A did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:152915609 G>C did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr23:152914820 G>A did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr19:57666680 C>T maps to NM_001012729.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:1275150 G>A maps to ENST00000378888 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:1277816 C>T maps to ENST00000378888 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:7130486 G>T maps to NM_004422.2 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr17:7133212 G>A maps to NM_004422.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:7132706 C>T maps to NM_004422.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:7133689 T>C maps to NM_004422.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr17:7132555 C>T maps to NM_004422.2 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:7129419 G>A maps to NM_004422.2 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:183884725 C>G maps to NM_004423.3 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:183883971 C>T maps to NM_004423.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:183884049 A>G maps to NM_004423.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr3:183885731 G>A maps to NM_004423.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:183888410 C>T maps to NM_004423.3 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:183888239 G>A maps to NM_004423.3 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:183888272 G>A maps to NM_004423.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:183885374 C>T maps to NM_004423.3 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:82122249 A>G maps to ENST00000372198 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:46956695 C>T maps to NM_017653.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:102453009 C>T maps to NM_001376.4 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:102471205 G>A maps to NM_001376.4 E1719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:102466417 G>A maps to NM_001376.4 K1299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:102461591 G>A maps to NM_001376.4 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:102471549 C>T maps to NM_001376.4 R1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:102515816 C>T maps to NM_001376.4 A4471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:102481479 G>A maps to NM_001376.4 A2351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr14:102507908 A>G did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr14:102510822 C>A maps to NM_001376.4 G4299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:102505979 G>A maps to NM_001376.4 A3867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:102446160 G>A maps to NM_001376.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:102505518 C>T maps to NM_001376.4 T3796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:102455090 C>T maps to NM_001376.4 Q924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr14:102516477 T>C maps to NM_001376.4 L4585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:102478747 C>T maps to NM_001376.4 L2319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr7:95709703 G>A maps to NM_004411.4 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:95499215 C>A maps to NM_004411.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:95726808 C>T maps to NM_004411.4 H614H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:172546718 G>T maps to NM_001378.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:172563833 C>T maps to NM_001378.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:172563872 C>T maps to NM_001378.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:172584864 G>C maps to NM_001378.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:32568308 C>T maps to NM_016141.3 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:66776563 C>T maps to NM_006141.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:103057189 C>T maps to NM_001080463.1 Q2285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:102987423 G>A maps to NM_001080463.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:103070065 C>A maps to NM_001080463.1 S2650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr11:103027274 G>A maps to NM_001080463.1 Q1301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:102988483 C>T maps to NM_001080463.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:103041694 T>C maps to NM_001080463.1 N1744N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:103178457 T>C maps to NM_001080463.1 N3804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:103068665 T>C maps to NM_001080463.1 S2571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr11:103306729 A>G maps to NM_001080463.1 R4149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:103048394 G>A maps to NM_001080463.1 A1995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr11:103086493 A>G maps to NM_001080463.1 E2913E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:103306684 G>A maps to NM_001080463.1 W4134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr11:103027242 C>T maps to NM_001080463.1 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:37701054 C>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:38884777 G>T maps to NM_001396.3 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:38845109 G>A maps to NM_001396.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr21:38862642 G>A maps to NM_001396.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:38862609 G>A maps to NM_001396.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr21:38858864 C>T maps to NM_001396.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:40319149 G>A maps to NM_004714.1 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:40317947 G>A maps to NM_004714.1 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:40319089 C>T maps to NM_004714.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:68052037 C>T maps to NM_006482.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:68050890 C>T maps to NM_006482.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:68050890 C>T maps to NM_006482.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:206821236 C>T maps to NM_003582.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:206821041 G>T maps to NM_003582.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:206821124 T>C maps to NM_003582.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:4722771 C>T maps to NM_003845.1 H472H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:71755437 C>T maps to NM_001130987.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:71743354 G>T maps to NM_001130987.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:71891478 C>T maps to NM_001130987.1 D1695D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:71901406 C>T maps to NM_001130987.1 F1955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:71762411 C>T maps to NM_001130987.1 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:71908138 G>T maps to NM_001130987.1 L2024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:71766359 G>T maps to NM_001130987.1 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:71788893 T>C maps to NM_001130987.1 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr2:71780316 C>T maps to NM_001130987.1 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr2:71825802 C>T maps to NM_001130987.1 I1228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:71740969 G>A maps to NM_001130987.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:71909698 C>A maps to NM_001130987.1 Y2071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:71839775 G>A maps to NM_001130987.1 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:71795420 G>A maps to NM_001130987.1 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:71891502 C>T maps to NM_001130987.1 V1703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:71730445 A>G maps to NM_001130987.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr2:207528028 C>A maps to NM_001093730.1 G411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:96239898 C>T maps to NM_198968.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:96242592 G>A maps to NM_198968.2 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr13:96237107 A>G maps to NM_198968.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr13:96237020 G>A maps to NM_198968.2 G831G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:96293995 C>T maps to NM_198968.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr3:137787138 C>T maps to NM_173543.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:137822591 G>T maps to NM_173543.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:137811251 G>A maps to NM_173543.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:137786532 C>T maps to NM_173543.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:108363341 G>A maps to NM_014648.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:108409686 C>T maps to NM_014648.3 H1190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:108380773 G>A maps to NM_014648.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:108405332 C>T maps to NM_014648.3 D1017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:108363260 G>A maps to NM_014648.3 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:32264962 G>T maps to NM_005225.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:23836470 T>C maps to NM_004091.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr1:23836398 G>A maps to NM_004091.3 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:20481644 C>T maps to NM_001949.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:20483130 C>T maps to NM_001949.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:20490486 G>A maps to NM_001949.3 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:20483076 G>A maps to NM_001949.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:20481644 C>T maps to NM_001949.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:20402540 C>T maps to NM_001949.3 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:20402546 C>A maps to NM_001949.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:86121435 T>C maps to ENST00000256117 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr8:86115406 A>G maps to ENST00000256117 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:11590209 G>A maps to NM_198256.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:77449853 T>C maps to NM_203394.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr12:77449853 T>C maps to NM_203394.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:77449891 G>A maps to NM_203394.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:77458397 T>C maps to NM_203394.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:77421846 G>A maps to NM_203394.2 D652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:19261659 G>A maps to NM_024680.2 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr11:19256428 T>A maps to NM_024680.2 K210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:19247353 C>A maps to NM_024680.2 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:19256570 G>A maps to NM_024680.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:2284178 G>A maps to NM_004424.3 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:2282575 G>A maps to NM_004424.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:2284965 G>A maps to NM_004424.3 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:2285459 C>T maps to NM_004424.3 Q748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:2285284 C>T maps to NM_004424.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr16:2283950 G>A maps to NM_004424.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr16:2282898 C>T maps to NM_004424.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:15477987 G>A maps to NM_033083.6 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:121554179 T>C maps to NM_018456.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:121573581 T>C maps to NM_018456.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr3:121554149 A>C maps to NM_018456.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:121591405 A>C maps to NM_018456.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:121591585 C>T maps to NM_018456.4 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:34985792 C>A did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr16:23546497 G>A maps to NM_001083614.1 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:23563614 G>A maps to NM_001083614.1 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr16:23546254 G>A maps to NM_001083614.1 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:110563097 A>G maps to ENST00000276658 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr8:110576742 G>T maps to ENST00000276658 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr5:158204507 G>T maps to NM_024007.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:158141122 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:158223391 C>T maps to NM_024007.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:158524020 G>A maps to NM_024007.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:158140002 G>A maps to NM_024007.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr5:158250211 C>T maps to NM_024007.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr5:158223439 C>T maps to NM_024007.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:25708131 G>A maps to NM_022659.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:25890599 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:25899685 C>T maps to NM_022659.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:25747346 G>T maps to NM_022659.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:25902264 G>A maps to NM_022659.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr8:25898455 G>A maps to NM_022659.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr10:131646718 G>A maps to ENST00000355311 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:131761906 G>T maps to ENST00000355311 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr10:131665477 G>A maps to ENST00000355311 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr10:131666102 G>A maps to ENST00000355311 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:131761750 C>T maps to ENST00000355311 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:131757222 G>A maps to ENST00000355311 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:131671782 G>A maps to ENST00000355311 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:131640509 G>A maps to ENST00000355311 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr10:131665477 G>A maps to ENST00000355311 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:73111663 T>C maps to NM_018029.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:43634635 G>A maps to NM_001159936.1 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48386693 A>G did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:48386664 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:48382273 A>G did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr10:74906051 G>C maps to NM_001135752.1 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:21599192 G>A maps to NM_001397.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:21563338 T>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:21599372 A>G maps to NM_001397.2 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:21551859 C>T maps to NM_001397.2 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:21562342 G>A maps to NM_001397.2 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:21554467 C>T maps to NM_001397.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr1:21573721 G>C maps to NM_001397.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:183976191 C>A maps to NM_032331.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:183976236 C>T maps to NM_032331.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr3:184008401 C>T maps to NM_014693.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:184009926 C>T maps to NM_014693.3 R851R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:184008628 G>A maps to NM_014693.3 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:184009926 C>T maps to NM_014693.3 R851R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr3:183994330 C>T maps to NM_001100120.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:233348872 C>T maps to NM_004826.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:233347856 C>T maps to NM_004826.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:233350721 G>A maps to NM_004826.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:233346257 G>A maps to NM_004826.2 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:233345161 C>T maps to NM_004826.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:39306273 G>A maps to NM_001398.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:53377250 G>A maps to ENST00000371522 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:11805347 G>A maps to NM_024693.4 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:150482171 C>T maps to ENST00000369049 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr1:150483400 G>A maps to ENST00000369049 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr1:150483496 G>A maps to ENST00000369049 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr1:150484237 G>A maps to ENST00000369049 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr9:95258656 G>C maps to NM_001393.3 Y680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:95277102 G>A maps to NM_001393.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:11617214 G>A maps to NM_016581.3 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:11624895 C>T maps to NM_016581.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:172473165 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:172525678 C>T maps to ENST00000392692 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:139186190 C>T maps to NM_001195037.2 C450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:139202170 C>T maps to NM_001195037.2 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:68836168 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:68836236 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:69243068 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:69243068 C>T did not map to a codon.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr23:69176913 C>T did not map to a codon.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr23:65835850 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:65822495 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:65824947 C>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:109524474 G>A maps to ENST00000376651 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr2:109513575 G>A maps to ENST00000376651 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr2:109522782 G>A maps to ENST00000376651 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr2:109545679 G>A maps to ENST00000376651 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:236557806 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:236645867 C>T maps to NM_145861.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:67916190 C>T maps to NM_014329.3 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr16:67917601 T>C maps to NM_014329.3 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:67915890 G>A maps to NM_014329.3 Q1013Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:67911504 C>T maps to NM_014329.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:67915311 G>A maps to NM_014329.3 K927K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:5244712 T>C maps to NM_014674.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:5255176 T>C maps to NM_014674.2 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:5243554 G>A maps to NM_014674.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:33722672 G>A maps to NM_018217.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:33703610 G>A maps to NM_018217.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr20:33722666 C>T maps to NM_018217.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:33703691 C>T maps to NM_018217.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:184692924 G>A maps to NM_025191.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:184688581 A>G maps to NM_025191.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:184677409 C>T maps to NM_025191.3 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:83476310 A>G maps to NM_005711.3 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:83239318 T>C maps to NM_005711.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:83680138 G>A maps to NM_005711.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr5:83476331 G>T maps to NM_005711.3 C78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr5:83433074 T>G maps to NM_005711.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:12296243 C>T maps to NM_001955.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr4:148463688 C>T maps to NM_001957.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:148461085 C>T maps to NM_001957.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr13:78477410 C>A maps to ENST00000377211 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:78472430 T>C maps to ENST00000377211 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:78475264 A>C maps to ENST00000377211 Y383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr13:78492237 G>A maps to ENST00000377211 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr13:78492699 C>T maps to ENST00000377211 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:93206753 A>G did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:93170682 G>A maps to NM_003566.3 A1350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr11:85988117 C>T maps to ENST00000351625 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:85979584 C>T maps to ENST00000351625 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:85979573 C>T maps to ENST00000351625 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:74228319 A>G maps to NM_001402.5 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:74229173 A>G maps to NM_001402.5 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr20:62126331 G>A maps to NM_001958.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:144662274 G>A maps to NM_032378.4 Y604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr8:144662229 C>T maps to NM_032378.4 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:62338496 G>A maps to ENST00000378019 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:62327790 T>C maps to ENST00000378019 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:62338496 G>A maps to ENST00000378019 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:3979946 G>A maps to NM_001961.3 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:3976710 G>A maps to NM_001961.3 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr19:3979371 G>A maps to NM_001961.3 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:3982368 G>T maps to NM_001961.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:22291578 T>C maps to NM_013302.3 C650C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:22237142 C>T maps to NM_013302.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr16:22268609 C>T maps to NM_013302.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:22274453 C>T maps to NM_013302.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr16:22268121 C>G maps to NM_013302.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:127965712 C>T maps to NM_021937.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:128127068 C>T maps to NM_021937.3 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:36194769 C>T maps to NM_030636.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:36194776 C>T maps to NM_030636.2 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:36338782 C>T maps to NM_030636.2 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:36194487 C>T maps to NM_030636.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:36336701 G>A maps to NM_030636.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:36194049 G>A maps to NM_030636.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:245245414 C>T maps to ENST00000421886 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:245246922 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:245245465 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr17:60464716 G>T maps to NM_001144933.1 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr11:831244 G>T maps to NM_173584.3 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:3788145 G>A maps to NM_001144958.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr17:28418901 C>G maps to NM_198529.3 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr22:44028035 G>T maps to NM_022785.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:43950973 T>G maps to NM_022785.3 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:43926829 C>T maps to NM_022785.3 A1416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:44031027 G>A maps to NM_022785.3 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr22:44022427 A>G maps to NM_022785.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:44067869 C>T maps to NM_022785.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:43926823 C>T maps to NM_022785.3 T1418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:44031066 G>A maps to NM_022785.3 D671D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:44112808 T>C maps to NM_022785.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr22:43976412 C>T maps to NM_022785.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:44063055 C>T maps to NM_022785.3 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:44028098 C>T maps to NM_022785.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr22:43933362 C>T maps to NM_022785.3 E1314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:64034138 C>T maps to NM_032437.2 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:56098193 G>A maps to NM_001039349.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:56108867 G>A maps to NM_001039349.1 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:56144863 G>A maps to NM_001039349.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:65637700 G>A maps to NM_016938.3 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr13:22113447 G>A maps to NM_152726.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:22095412 C>A maps to NM_152726.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:16884800 C>T maps to NM_181723.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:16921652 C>T maps to NM_181723.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:16884829 G>A maps to NM_181723.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:16884800 C>T maps to NM_181723.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:16921747 T>C did not map to a codon.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr3:19961393 G>A maps to NM_144715.3 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:19974822 T>G maps to NM_144715.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:19930050 A>G maps to NM_144715.3 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr6:52329712 C>T maps to NM_018100.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:52355111 G>A maps to NM_018100.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:52357069 A>G maps to NM_018100.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:44109671 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:44109679 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:44035572 A>C did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:233527520 T>C maps to NM_025202.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:1299832 G>A maps to NM_001405.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:155041453 C>T maps to NM_005227.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:106717054 G>A maps to NM_001962.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:106716987 G>A maps to NM_001962.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:68060285 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:68060179 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:68060448 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr23:68059542 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:68059550 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:107145576 T>C maps to NM_004093.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr13:107145777 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr13:107145762 G>A maps to NM_004093.2 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:7612611 T>C maps to NM_001406.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr17:7611545 G>T maps to NM_001406.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr17:7612770 C>T maps to NM_001406.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:133014886 G>A maps to NM_015137.3 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:132952815 T>C maps to NM_015137.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:132968152 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:132989339 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:132997308 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr8:133014025 C>A maps to NM_015137.3 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:23829152 C>T maps to NM_005864.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr14:23826719 C>T maps to NM_005864.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr15:82444607 A>G maps to NM_024580.5 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:82443815 A>G maps to NM_024580.5 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:82444039 C>A maps to NM_024580.5 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:82444244 A>G maps to NM_024580.5 G850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:82450184 G>A maps to NM_024580.5 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr15:82523296 G>A maps to NM_024580.5 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:82444712 T>C maps to NM_024580.5 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr17:42940214 G>A maps to NM_004247.3 H491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:42931921 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:42940175 C>T maps to NM_004247.3 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:42961082 C>T maps to NM_004247.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:110901128 T>C maps to NM_001963.4 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr4:110915913 G>A maps to NM_001963.4 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:110915958 T>C maps to NM_001963.4 C976C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:110902084 A>G maps to NM_001963.4 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:110862292 A>C maps to NM_001963.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:110901198 A>C maps to NM_001963.4 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr4:110915907 C>T maps to NM_001963.4 H959H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:110882029 T>C maps to NM_001963.4 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:13624571 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:13645221 A>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:38464057 G>A maps to ENST00000354891 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr5:38448448 C>A maps to ENST00000354891 Y845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:38350643 T>C maps to ENST00000354891 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:38352304 C>A maps to ENST00000354891 C139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:55224508 C>T maps to NM_005228.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:55214311 C>T maps to NM_005228.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:55220347 C>T maps to NM_005228.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:55221828 C>T maps to NM_005228.3 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:55233037 G>A maps to NM_005228.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr7:55232989 C>A maps to NM_005228.3 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:55270248 C>T maps to NM_005228.3 R1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:55229246 G>A maps to NM_005228.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:55229283 C>T maps to NM_005228.3 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:55240693 C>T maps to NM_005228.3 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:55224229 T>C maps to NM_005228.3 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:55087029 G>A maps to NM_005228.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:55238879 A>G maps to NM_005228.3 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:41306842 C>A maps to NM_053046.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr14:34400328 G>A maps to NM_022073.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:137802686 C>T maps to NM_001964.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:137803520 G>A maps to NM_001964.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:64575693 G>A maps to NM_001136178.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:64573059 G>A maps to NM_001136178.1 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:64573836 C>T maps to NM_001136178.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:64573059 G>A maps to NM_001136178.1 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:64573488 T>G maps to NM_001136178.1 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:22548120 C>T maps to NM_004430.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:22550361 C>T maps to NM_004430.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:22548027 C>T maps to NM_004430.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:22548120 C>T maps to NM_004430.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:73519505 G>A maps to NM_001965.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:73519604 C>T maps to NM_001965.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:73518650 C>T maps to NM_001965.3 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:73518761 G>A maps to NM_001965.3 H531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:73519751 C>T maps to NM_001965.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:63092085 T>C maps to NM_015252.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:63169986 T>C maps to NM_015252.3 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:63091875 T>C maps to NM_015252.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:63169882 C>T maps to NM_015252.3 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:65351052 T>C maps to NM_001099409.1 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:65350554 A>G maps to NM_001099409.1 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:65349627 C>T maps to NM_001099409.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:65357964 T>C maps to NM_001099409.1 G1395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:65347565 G>A maps to NM_001099409.1 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr11:64622308 G>A maps to NM_006795.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:64622104 G>A maps to NM_006795.2 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:64645588 C>T maps to NM_006795.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:48244184 G>A maps to NM_014601.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:48244373 C>T maps to NM_014601.3 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:48219934 C>T maps to NM_014601.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:31489098 G>T maps to NM_014600.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:31483571 C>T maps to NM_014600.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:31457552 T>C maps to NM_014600.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:31483571 C>T maps to NM_014600.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:42211659 G>A maps to NM_139265.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:42193247 C>T maps to NM_139265.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr15:42193247 C>T maps to NM_139265.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:34680475 T>C maps to NM_012153.4 *301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:34680176 C>T maps to NM_012153.4 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:34668229 C>T maps to NM_012153.4 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:34680176 C>T maps to NM_012153.4 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:34668229 C>T maps to NM_012153.4 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:184922381 G>T maps to NM_001966.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr3:184911201 C>T maps to NM_001966.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:184953083 G>A maps to NM_001966.3 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:140611141 G>A maps to NM_024757.4 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:140638448 C>T maps to NM_024757.4 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:140671152 C>T maps to NM_024757.4 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:140638439 C>T maps to NM_024757.4 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:140707882 C>T maps to NM_024757.4 N1027N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:140674137 A>G maps to NM_024757.4 Q748Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr9:140646787 C>T maps to NM_024757.4 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:140676800 C>T maps to NM_024757.4 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:140611396 G>A maps to NM_024757.4 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:140695336 C>T maps to NM_024757.4 D871D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:31852687 C>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:31857079 G>A maps to ENST00000395728 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr6:31855587 C>T maps to ENST00000395728 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:31855363 G>A maps to ENST00000395728 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:31856833 C>A maps to ENST00000395728 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr6:31864395 G>A maps to ENST00000395728 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:49170699 C>T maps to NM_014335.2 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:104697810 C>T maps to NM_001008394.1 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:104698566 G>A maps to NM_001008394.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:20153898 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:20153953 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:20153903 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr24:22741513 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:6066562 C>T maps to NM_014413.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr7:6094219 G>A maps to NM_014413.3 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr2:37364139 T>C maps to NM_001135651.1 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:37334429 G>A maps to NM_001135651.1 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:37349800 C>T maps to NM_001135651.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr2:88889964 G>A maps to NM_004836.5 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:88874528 A>G maps to NM_004836.5 T824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr2:88883032 G>A maps to NM_004836.5 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:88887533 A>G maps to NM_004836.5 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:40280267 C>T maps to NM_001013703.2 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:124106440 C>T maps to NM_001414.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr12:124107236 G>A maps to NM_001414.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:75471479 C>T maps to NM_014239.3 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:45407190 C>T maps to NM_020365.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:45345608 G>A maps to NM_020365.3 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:27591926 G>A maps to NM_172195.3 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr2:27587756 C>T maps to NM_172195.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:183858391 C>T maps to NM_003907.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:183856021 C>A maps to NM_003907.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:183860110 C>T maps to NM_003907.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr1:36359355 C>T maps to NM_012199.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:36367935 C>T maps to NM_012199.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:141570575 C>T maps to NM_012154.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:141542675 G>A maps to NM_012154.3 D770D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:141570557 G>A maps to NM_012154.3 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:141561442 C>T maps to NM_012154.3 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr8:141545599 G>A maps to NM_012154.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:141566003 G>A maps to NM_012154.3 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:141566042 G>A maps to NM_012154.3 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:141595330 G>A maps to NM_012154.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:141561436 G>A maps to NM_012154.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr8:141551454 C>T maps to NM_012154.3 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:141542205 G>A maps to NM_012154.3 H839H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:36509103 C>T maps to NM_024852.2 H743H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:36520602 A>G maps to NM_024852.2 A777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:36474378 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:36505945 C>T maps to NM_024852.2 C692C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr1:36520680 A>C maps to NM_024852.2 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:36306799 G>T maps to NM_017629.2 G587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:36306952 C>T maps to NM_017629.2 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:36291315 G>A maps to NM_017629.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr20:32677676 C>T maps to NM_003908.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:24089744 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:24086181 G>A did not map to a codon.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr23:24073776 C>A did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr23:24086194 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:120809333 G>A maps to NM_003750.2 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:120818858 A>G maps to NM_003750.2 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:120810114 C>T maps to NM_003750.2 Q797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr10:120802172 G>A maps to NM_003750.2 D953D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:120801863 C>T maps to NM_003750.2 E1056E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr10:120796690 G>A maps to NM_003750.2 R1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr10:120801842 A>G maps to NM_003750.2 A1063A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:2418870 C>T maps to ENST00000314800 R779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:2414229 G>A maps to ENST00000314800 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:2414217 C>T maps to ENST00000314800 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr7:2416709 G>A maps to ENST00000314800 K718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:36912575 G>A maps to NM_003753.3 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr8:109215228 G>A maps to NM_001568.2 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:8009135 T>C maps to ENST00000449102 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr11:8009015 C>T maps to ENST00000449102 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:10226485 G>A maps to NM_003755.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:117658815 A>G maps to ENST00000411422 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr8:117671100 A>G maps to ENST00000411422 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:117658743 C>T maps to ENST00000411422 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:32690020 G>A maps to NM_003757.2 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:39116702 C>T maps to NM_013234.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr22:38251634 T>A maps to ENST00000262832 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:7480011 T>C did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:53413752 T>C maps to ENST00000438209 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:99812386 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:176070735 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:233421203 G>A maps to NM_004846.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:71745672 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:71748796 A>G maps to NM_001134651.1 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:37914779 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:31884626 G>A maps to NM_019843.3 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:184040372 A>G maps to NM_001194947.1 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:184040474 T>C maps to NM_001194947.1 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:184044359 C>T maps to NM_001194947.1 R1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:184042122 T>C maps to NM_001194947.1 D876D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:184042670 G>A maps to NM_001194947.1 E882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr3:184041231 C>T maps to NM_001194947.1 R716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:184039598 G>A maps to NM_001194947.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:21167511 G>A maps to NM_001198801.1 Q1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:21205842 G>A maps to NM_001198801.1 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:21306911 C>G maps to NM_001198801.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:73609550 G>A maps to NM_022170.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:73604057 C>T maps to NM_022170.1 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:103803469 G>A maps to NM_183004.3 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr14:103806118 C>T maps to NM_183004.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:7214673 T>C maps to NM_001143760.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr10:81272563 C>T maps to NM_001099692.1 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:99977756 G>A maps to NM_015904.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:100010861 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:100006803 T>G maps to NM_015904.3 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:100009431 C>T maps to NM_015904.3 N917N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:99999374 A>G maps to NM_015904.3 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr2:99977639 C>G maps to NM_015904.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:99978089 G>A maps to NM_015904.3 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr17:12921102 G>C maps to NM_018127.6 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:852927 G>A maps to NM_001972.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:855751 C>T maps to NM_001972.2 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:855965 C>T maps to NM_001972.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:855592 C>T maps to NM_001972.2 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr19:8028579 G>A maps to ENST00000351593 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr9:23762097 G>C maps to ENST00000359598 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:23692860 G>A maps to ENST00000359598 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:23762151 T>G maps to ENST00000359598 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:11577546 G>A maps to NM_001420.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr19:11565550 G>A maps to NM_001420.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:11565637 G>A maps to NM_001420.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:11577462 G>A maps to NM_001420.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:11569309 G>A maps to NM_001420.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr19:11565631 C>T maps to NM_001420.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:11565616 C>T maps to NM_001420.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:50659453 G>A maps to NM_021952.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:50610681 C>T maps to NM_021952.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:41556142 A>G maps to NM_172373.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr13:41517137 C>T maps to NM_172373.3 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:139993140 A>G maps to ENST00000379550 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:201982111 C>T maps to NM_004433.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr23:129208702 C>G did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:129201299 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:129201410 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:129203501 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:129205113 C>T did not map to a codon.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr23:129206275 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:129205341 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:129200997 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:34527191 G>T maps to NM_198381.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr22:37769858 G>A maps to NM_052906.3 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:37770239 A>G maps to NM_052906.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:37771424 C>T maps to NM_052906.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:37771204 G>A maps to NM_052906.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:37771064 G>T maps to NM_052906.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr22:37769678 C>T maps to NM_052906.3 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:37769657 G>A maps to NM_052906.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:37769276 C>T maps to NM_052906.3 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr22:37769708 C>T maps to NM_052906.3 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:47500652 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:47497512 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:47497562 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:47498484 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47500809 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:47498578 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:47497296 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:96640800 G>A maps to NM_005230.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:96641160 C>T maps to NM_005230.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:96641142 C>T maps to NM_005230.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:96640866 C>T maps to NM_005230.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:96640800 G>A maps to NM_005230.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:96641214 C>T maps to NM_005230.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:96640851 G>A maps to NM_005230.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:18561503 C>T maps to NM_006532.3 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr19:18561437 C>T maps to NM_006532.3 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr19:18576689 C>T maps to NM_006532.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:18557205 C>T maps to NM_006532.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr19:18561590 C>A maps to NM_006532.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:18576360 G>A maps to NM_006532.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr5:95278748 A>T maps to NM_012081.5 L51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:95249472 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr5:95278737 G>A maps to NM_012081.5 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:95234462 G>A maps to NM_012081.5 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:44066517 T>C maps to NM_025165.2 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:44065394 A>G maps to NM_025165.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:37052933 T>C maps to NM_014800.9 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:36934619 T>C maps to NM_014800.9 V480V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-6852-01A-11D-1882-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr7:37298853 C>T maps to NM_014800.9 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:37272711 C>T maps to NM_014800.9 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:36917660 T>C maps to NM_014800.9 E592E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:44996114 G>A maps to ENST00000439931 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr20:45003172 A>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:45017706 G>T maps to ENST00000439931 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:45002175 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:67234672 C>T maps to NM_024712.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:67236872 G>A maps to NM_024712.3 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:67237065 C>T maps to NM_024712.3 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:67233096 C>T maps to NM_024712.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:107518219 T>G maps to NM_018712.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr11:107535877 G>A maps to NM_018712.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:107518325 C>T maps to NM_018712.3 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:107535877 G>A maps to NM_018712.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:85604482 A>G maps to NM_001135023.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:85598686 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:73474270 T>C maps to ENST00000358929 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:73477987 C>T maps to ENST00000358929 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:73462848 A>G maps to ENST00000358929 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:73462020 C>A maps to ENST00000358929 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:73457317 T>C maps to ENST00000358929 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:73470664 C>T maps to ENST00000358929 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:73456947 C>T maps to ENST00000358929 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:11664599 G>A maps to NM_032377.3 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:11664578 G>A maps to NM_032377.3 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:43831047 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:10990046 C>T maps to NM_017770.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr6:10989962 G>A maps to NM_017770.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:80629159 G>A maps to NM_022726.3 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:80656945 C>T maps to NM_022726.3 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:110972635 C>T maps to NM_024090.2 W219*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8680-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:60067918 A>G maps to NM_024930.2 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr18:33726215 C>T maps to ENST00000442325 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:33744529 G>A maps to ENST00000442325 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr18:33725917 C>T maps to ENST00000442325 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:33713226 T>C maps to ENST00000442325 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:33721157 T>C maps to ENST00000442325 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:33750063 T>C maps to ENST00000442325 C770C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr18:33718381 T>C maps to ENST00000442325 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:33713214 T>C maps to ENST00000442325 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:33744529 G>A maps to ENST00000442325 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:28013467 A>G maps to NM_018091.5 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:27995409 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:31625327 C>A maps to ENST00000395934 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:31653828 T>C maps to ENST00000395934 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:31625346 C>T maps to ENST00000395934 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:79412004 G>A maps to NM_022159.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:79358835 A>C maps to NM_022159.3 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:79383339 T>C maps to NM_022159.3 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:79392575 G>A maps to NM_022159.3 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:79386011 C>T maps to NM_022159.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr1:79387375 G>T maps to NM_022159.3 Y393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr1:79357355 G>A maps to NM_022159.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr1:79383336 T>C maps to NM_022159.3 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:49695731 G>A maps to NM_198449.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr4:101338290 T>C maps to NM_016242.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr4:101342535 T>G did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:153609453 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:153609113 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:1824334 C>T maps to NM_001010865.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:1823423 C>T maps to NM_001010865.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:1825688 C>T maps to NM_001010865.1 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:1825584 C>T maps to NM_001010865.1 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr22:29654827 G>A maps to NM_133455.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:29621173 G>A maps to NM_133455.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:101187337 C>T maps to ENST00000397927 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:27305167 G>A maps to NM_007046.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:27305041 A>G maps to NM_007046.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:27306220 C>T maps to NM_007046.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:27306196 C>T maps to NM_007046.3 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:27303753 C>T maps to NM_007046.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:2891624 T>C maps to NM_032048.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr18:2892083 G>A maps to NM_032048.2 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr20:39991416 G>T maps to NM_052846.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:100380550 C>T maps to NM_001008707.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:100317245 G>T maps to NM_001008707.1 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr14:100405582 G>T maps to NM_001008707.1 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr14:100377909 G>T maps to NM_001008707.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:100380562 C>T maps to NM_001008707.1 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:46136130 G>A maps to NM_001193268.1 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:46128025 G>A maps to NM_001193268.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:46133283 A>G maps to NM_001193268.1 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr19:46113007 C>T maps to NM_001193268.1 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:46137613 G>A maps to NM_001193268.1 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr19:46124854 G>A maps to NM_001193268.1 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr11:62370361 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:62370278 G>A maps to ENST00000278845 D814D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:89124529 C>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:89163260 T>C maps to ENST00000380664 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:89123817 A>G maps to ENST00000380664 N1302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:89206879 G>A maps to ENST00000380664 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr14:89168804 G>C maps to ENST00000380664 Y741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:89181529 C>T maps to ENST00000380664 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:89087176 C>A maps to ENST00000380664 E1766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr14:89130843 A>G maps to ENST00000380664 D1134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr14:89088956 G>A maps to ENST00000380664 C1668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr14:89123847 T>C did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:10626815 G>A maps to NM_001424.4 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:6924822 C>T maps to ENST00000381407 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:6921818 T>C maps to ENST00000381407 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:14857719 G>A maps to NM_013447.2 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:14863293 G>A maps to NM_013447.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:14877173 G>A maps to NM_013447.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:14883283 C>A maps to NM_013447.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr19:14887535 A>G did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:14736375 G>A maps to NM_032571.3 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr19:14730284 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr19:14749083 C>T maps to NM_032571.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr2:73161037 G>A maps to NM_004097.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:119305239 G>A maps to NM_004098.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:119303109 C>A maps to NM_004098.3 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:119604371 C>T maps to NM_001426.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:225702534 T>C maps to ENST00000284563 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:225755070 A>G maps to ENST00000284563 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:71509089 C>T maps to NM_031889.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:71508726 A>G maps to NM_031889.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:73931956 T>C maps to NM_003633.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:73932217 G>A maps to NM_003633.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr5:73931383 C>T maps to NM_003633.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:73931914 G>A maps to NM_003633.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:73932232 G>T maps to NM_003633.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:94862577 C>T maps to NM_015036.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr11:94861548 C>T maps to NM_015036.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr9:130586618 G>A maps to NM_001114753.1 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr17:77082220 G>A maps to NM_001042573.1 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:77080691 G>A maps to NM_001042573.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr17:77082044 C>T maps to NM_001042573.1 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:34521675 G>T maps to NM_198573.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:34521555 T>C maps to NM_198573.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:25273738 C>T maps to NM_145010.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr10:25273692 T>A maps to NM_145010.2 K246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:8922983 G>A maps to NM_001428.2 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:4858518 C>A maps to NM_053013.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:4860185 T>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:4856097 C>T maps to NM_053013.3 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:4856580 G>A maps to NM_053013.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:4858822 G>A maps to NM_053013.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr18:683257 G>A maps to ENST00000319815 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:677833 C>T maps to ENST00000319815 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:674306 A>G maps to ENST00000319815 *454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr13:43986136 G>A maps to NM_001127615.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:43872522 G>A maps to NM_001127615.1 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr13:43896598 G>A maps to NM_001127615.1 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr13:43930091 C>T maps to NM_001127615.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:43896585 C>A maps to NM_001127615.1 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:43900599 C>T maps to NM_001127615.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:43930085 G>A maps to NM_001127615.1 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:43900655 G>A maps to NM_001127615.1 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:43934137 G>A maps to NM_001127615.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:43918854 C>T maps to NM_001127615.1 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:129771266 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:129804044 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:129801657 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:111470986 A>T maps to NM_001977.3 K816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:111474509 T>G maps to NM_001977.3 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:111398196 G>T maps to NM_001977.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr4:111397884 C>T maps to NM_001977.3 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:111434596 A>G maps to NM_001977.3 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:111397806 G>A maps to NM_001977.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr4:111397947 C>T maps to NM_001977.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:111397843 C>T maps to NM_001977.3 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:132190496 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:120583060 G>A maps to NM_006209.3 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:120608104 C>T maps to NM_006209.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:120581580 C>A maps to NM_006209.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:120612962 C>T maps to NM_006209.3 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:132014639 C>T maps to NM_005021.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:132014758 T>C maps to NM_005021.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:132014690 C>T maps to NM_005021.3 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:46111217 C>T maps to NM_014936.4 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:46107817 T>C maps to NM_014936.4 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:46111163 T>C maps to NM_014936.4 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:46129476 A>T maps to NM_021572.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:46135504 A>G maps to NM_021572.4 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:185012491 G>A maps to NM_153343.3 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:185033920 G>A maps to NM_153343.3 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:185138759 C>T maps to NM_153343.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr4:185038989 G>A maps to NM_153343.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:77705065 C>T maps to NM_178543.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr17:77709071 G>A maps to NM_178543.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:77707393 C>T maps to NM_178543.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:77709290 C>T maps to NM_178543.3 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:77709044 G>A maps to NM_178543.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:77709290 C>T maps to NM_178543.3 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:77708984 G>A maps to NM_178543.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:150599822 G>A maps to NM_207168.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:97599482 A>G maps to NM_001098175.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:97605163 C>A maps to NM_001098175.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr9:139946038 C>T maps to NM_203468.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr9:139946008 C>T maps to NM_203468.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr9:139945371 C>A maps to NM_203468.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:40456332 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:23294524 G>A maps to NM_004901.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr8:23305222 G>A maps to NM_004901.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:23291936 C>T maps to NM_004901.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:23290495 G>C maps to NM_004901.3 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:23291936 C>T maps to NM_004901.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:140330593 A>G maps to NM_001033113.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:140332629 G>T maps to NM_001033113.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:140330620 C>T maps to NM_001033113.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:140329373 G>A maps to NM_001033113.1 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:27758599 T>C maps to ENST00000449599 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr3:27760139 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr22:41573804 A>G maps to NM_001429.3 Q2030Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr22:41527638 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr22:41556644 G>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:41545049 C>T maps to NM_001429.3 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:41543949 G>A maps to NM_001429.3 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:41574434 A>G maps to NM_001429.3 G2240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:41513539 G>A maps to NM_001429.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr22:41568500 A>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:132490714 G>A maps to ENST00000333577 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:132529373 C>T maps to ENST00000333577 D2256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:132446240 G>A maps to ENST00000333577 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:132504626 C>T maps to ENST00000333577 P1473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:132502082 T>C maps to ENST00000333577 T1345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:132505627 A>G maps to ENST00000333577 A1520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:132546815 C>T maps to ENST00000333577 N2718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:132547128 G>A maps to ENST00000333577 Q2775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:132547128 G>A maps to ENST00000333577 Q2775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:132528816 G>A maps to ENST00000333577 A2218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:132539740 T>C maps to ENST00000333577 P2660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:132547134 G>A maps to ENST00000333577 Q2777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:132508376 C>T maps to ENST00000333577 R1618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:132510284 G>A maps to ENST00000333577 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr12:132479415 C>T maps to ENST00000333577 D950D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr12:132464273 C>A maps to ENST00000333577 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr12:132446432 G>A maps to ENST00000333577 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:132511985 C>T maps to ENST00000333577 G1709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:132547101 G>A maps to ENST00000333577 Q2766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:132547131 G>A maps to ENST00000333577 Q2776Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:132479501 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:132510234 C>T maps to ENST00000333577 R1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:132508397 G>A maps to ENST00000333577 P1625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:132551913 C>A maps to ENST00000333577 T2955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:132537748 C>T maps to ENST00000333577 R2521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:132445397 C>T maps to ENST00000333577 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:46611726 C>T maps to NM_001430.4 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:29379778 C>T maps to NM_001166005.1 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:29391661 G>T maps to NM_001166005.1 G726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:34773104 G>A maps to NM_012156.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr20:34778616 C>T maps to NM_012156.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr20:34766562 C>T maps to NM_012156.2 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:34763504 G>A maps to NM_012156.2 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:34773146 T>C maps to NM_012156.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:34797801 G>A maps to NM_012156.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:131247749 G>A maps to NM_001431.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:131277430 C>T maps to NM_001431.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr6:131225627 A>C maps to NM_001431.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr18:5398076 C>T maps to NM_012307.2 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:5415927 G>A maps to NM_012307.2 Y652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr18:5398037 A>C maps to NM_012307.2 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr18:5406838 G>A maps to NM_012307.2 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:5489032 G>A maps to NM_012307.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:5415966 G>T maps to NM_012307.2 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr18:5397407 C>T maps to NM_012307.2 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr18:5398076 C>T maps to NM_012307.2 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr18:5398075 G>A maps to NM_012307.2 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:5397137 G>A maps to NM_012307.2 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:5428377 G>T maps to NM_012307.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr18:5415870 C>T maps to NM_012307.2 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr18:5397320 C>T maps to NM_012307.2 E859E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr18:5489080 C>T maps to NM_012307.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr18:5416251 C>T maps to NM_012307.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:5397121 G>A maps to NM_012307.2 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:111576501 G>A maps to NM_022140.3 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:111600663 A>C maps to NM_022140.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:111506044 G>A maps to NM_022140.3 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr5:111754700 G>T maps to NM_022140.3 Y12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr5:111601942 C>T maps to NM_022140.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr9:111947779 T>A maps to NM_019114.3 K803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:111956583 G>A maps to NM_019114.3 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr9:111947795 G>T maps to NM_019114.3 C797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:111970202 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:112017945 C>T maps to NM_019114.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:111938871 C>T maps to NM_019114.3 Q864Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:112017873 G>A maps to NM_019114.3 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:120844813 C>T maps to NM_020909.3 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:120885422 T>C maps to NM_020909.3 Y499Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:43500865 G>A maps to NM_000119.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:43500967 G>A maps to NM_000119.2 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:43495431 G>A maps to NM_000119.2 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:43508550 C>T maps to NM_000119.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:21938931 G>A maps to ENST00000265800 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:21931344 C>A maps to ENST00000265800 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:32560681 T>C maps to NM_025209.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr10:32560981 G>A maps to NM_025209.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:32581986 G>A maps to NM_025209.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr2:149526717 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:37988639 A>G maps to NM_017549.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:37988555 T>C maps to NM_017549.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr7:37989871 C>A maps to NM_017549.3 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr7:37960771 G>A maps to NM_017549.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:37960369 C>T maps to NM_017549.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:143096873 C>T maps to NM_005232.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:143095473 C>T maps to NM_005232.4 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:143096039 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:143096756 G>A maps to NM_005232.4 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:38227344 G>A maps to NM_001099439.1 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:38227119 G>A maps to NM_001099439.1 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:38186493 G>A maps to NM_001099439.1 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:38227512 G>A maps to NM_001099439.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:38227452 G>A maps to NM_001099439.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:38197251 A>G maps to NM_001099439.1 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:16461627 G>A maps to NM_004431.3 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:16459801 C>T maps to NM_004431.3 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:16464531 G>A maps to NM_004431.3 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:16458606 G>A maps to NM_004431.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:16464555 C>T maps to NM_004431.3 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:89259599 C>T maps to NM_005233.5 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:89498433 G>A maps to NM_005233.5 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr3:89176407 T>C maps to NM_005233.5 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:89498523 T>C maps to NM_005233.5 D832D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr3:89468409 T>C maps to NM_005233.5 I648I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr3:89499324 A>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:89521670 A>G maps to NM_005233.5 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:89259308 T>C maps to NM_005233.5 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr3:89456458 C>T maps to NM_005233.5 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:222301232 A>G maps to NM_004438.3 H744H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:222308272 G>A maps to NM_004438.3 R610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:222433472 C>A maps to NM_004438.3 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:222429020 G>A maps to NM_004438.3 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:222298981 C>T maps to NM_004438.3 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr2:222429002 G>A maps to NM_004438.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:222433478 G>A maps to NM_004438.3 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:66280008 G>A maps to NM_004439.5 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr4:66356148 A>G maps to NM_004439.5 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr4:66467569 G>A maps to NM_004439.5 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:66286257 T>C maps to NM_004439.5 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr4:66356299 G>A maps to NM_004439.5 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:66467569 G>A maps to NM_004439.5 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:66233107 C>A maps to NM_004439.5 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr4:66197824 T>C maps to NM_004439.5 E958E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr4:66509143 C>A maps to NM_004439.5 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr4:66356239 G>A maps to NM_004439.5 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:66467464 G>A maps to NM_004439.5 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr4:66356377 G>T maps to NM_004439.5 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:96945106 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr3:96706400 A>C maps to NM_001080448.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:93982021 G>A maps to NM_004440.3 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:94120756 A>T maps to NM_004440.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:93982013 A>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:22902837 C>T maps to NM_020526.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:22925426 C>T maps to NM_020526.3 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:22927278 C>T maps to NM_020526.3 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:22903023 C>T maps to NM_020526.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:22902825 C>T maps to NM_020526.3 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr1:22913045 C>T maps to NM_020526.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:22923859 C>T maps to NM_020526.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr1:22925446 C>T maps to NM_020526.3 N765N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:22915422 G>T maps to NM_020526.3 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:134873003 C>G maps to NM_004441.4 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr3:134851682 C>T maps to NM_004441.4 C363C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:134898741 C>T maps to NM_004441.4 Y600Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr3:134851754 G>A maps to NM_004441.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr3:134670562 A>T maps to NM_004441.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:134884864 G>A maps to NM_004441.4 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:23111525 C>T maps to ENST00000400191 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:23191487 C>T maps to ENST00000400191 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:23111411 G>A maps to ENST00000400191 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:23234597 G>A maps to ENST00000400191 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:23233320 C>T maps to ENST00000400191 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:23191442 C>T maps to ENST00000400191 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr1:23236927 G>T maps to ENST00000400191 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:23111123 G>A maps to ENST00000400191 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr1:23234546 C>T maps to ENST00000400191 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:23240029 G>A maps to ENST00000400191 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:23237053 G>A maps to ENST00000400191 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:184290698 C>T maps to NM_004443.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:184297349 C>T maps to NM_004443.3 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:184299145 C>T maps to NM_004443.3 F946F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:184290962 C>T maps to NM_004443.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr3:184298950 T>C maps to NM_004443.3 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:100421409 C>T maps to NM_004444.4 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:100414921 G>A maps to NM_004444.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:100416266 C>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:100417380 T>C maps to NM_004444.4 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:100403277 C>T maps to NM_004444.4 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:100417392 G>A maps to NM_004444.4 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:100404107 G>A maps to NM_004444.4 Y806Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:100410616 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:142562205 G>A maps to NM_004445.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:142561974 C>T maps to NM_004445.3 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:142566347 C>T maps to NM_004445.3 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr7:142567598 C>T maps to NM_004445.3 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr7:142562154 G>A maps to NM_004445.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:226032197 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:226027727 T>C maps to NM_001136018.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:226030176 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:15342830 G>A maps to NM_001142886.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:15342857 G>A maps to NM_001142886.1 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr1:92508452 G>T maps to NM_173567.4 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:37034532 G>A maps to NM_014805.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:56203247 C>T maps to NM_001130071.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:56196847 G>A maps to NM_001130071.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:56197003 C>T maps to NM_001130071.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:19186548 G>A maps to NM_014964.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:19232060 G>A maps to NM_014964.4 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:19186554 C>T maps to NM_014964.4 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr17:19235244 C>T maps to NM_014964.4 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr17:48618641 C>A maps to NM_017957.2 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:144945090 C>T maps to NM_031308.1 T777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:144941616 G>A maps to NM_031308.1 A1935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:144945174 G>A maps to NM_031308.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:144942444 C>T maps to NM_031308.1 Q1659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:144940620 C>T maps to NM_031308.1 A2267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:144946749 C>T maps to NM_031308.1 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:144942152 G>A maps to NM_031308.1 L1757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:144940341 G>A maps to NM_031308.1 D2360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:144941901 C>T maps to NM_031308.1 T1840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:144940818 T>C maps to NM_031308.1 E2201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr8:144941838 G>A maps to NM_031308.1 N1861N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:144945126 C>T maps to NM_031308.1 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:144941538 G>A maps to NM_031308.1 N1961N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:144945810 G>A maps to NM_031308.1 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:144945717 T>C maps to NM_031308.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:144944067 A>G maps to NM_031308.1 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr8:144946344 G>A maps to NM_031308.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:144945477 A>G maps to NM_031308.1 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:144946806 C>T maps to NM_031308.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr8:144940956 C>T maps to NM_031308.1 A2155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr8:144945513 C>A maps to NM_031308.1 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr8:144941153 G>T maps to NM_031308.1 R2090R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:220162057 C>T maps to NM_004446.2 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:220193340 T>C maps to NM_004446.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:220170681 G>T maps to NM_004446.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:220208264 T>C maps to NM_004446.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:220191832 G>A maps to NM_004446.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:220146716 A>C maps to NM_004446.2 V1369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:220152062 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:51938528 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:51826914 A>G maps to NM_001981.2 C824C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:16535965 C>T maps to ENST00000455140 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:16515476 G>A maps to ENST00000455140 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:16536013 G>A maps to ENST00000455140 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:16524606 T>G maps to ENST00000455140 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:15811493 T>C maps to NM_004447.5 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:15793746 G>A maps to NM_004447.5 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr12:15823801 T>C maps to NM_004447.5 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:55597334 A>G maps to NM_133180.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr19:55597229 A>G maps to NM_133180.2 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:55597493 C>A maps to NM_133180.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:55591185 C>T maps to NM_133180.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:723323 A>G maps to NM_022772.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:724756 C>T maps to NM_022772.3 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:720210 C>T maps to NM_022772.3 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr11:709559 C>T maps to NM_022772.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:110301239 C>A maps to NM_139053.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:110300587 C>T maps to NM_139053.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr13:43543242 C>T maps to NM_001002264.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:56276416 G>A maps to NM_000502.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:56272518 C>A maps to NM_000502.4 C263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:56274427 C>T maps to NM_000502.4 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr17:56270779 G>C maps to NM_000502.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr17:56270827 C>T maps to NM_000502.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:56280559 T>C maps to NM_000502.4 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:91358018 G>A maps to NM_004950.4 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr12:91371991 A>G maps to NM_004950.4 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr12:91371909 G>A maps to NM_004950.4 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:91371988 T>C maps to NM_004950.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:96139410 C>T maps to NM_016442.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr5:96127838 G>A maps to NM_016442.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:96116879 C>A maps to NM_016442.3 G824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:96232521 C>T maps to NM_001130140.1 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:96244663 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:96235868 G>A maps to NM_001130140.1 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:48687627 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:48687743 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:48687742 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:37864635 G>A maps to NM_004448.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:37866591 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:65340098 T>C maps to ENST00000506030 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr5:65288677 T>C maps to ENST00000506030 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr5:65349644 T>C maps to ENST00000506030 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr5:65288671 T>C maps to ENST00000506030 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:65344493 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:65321329 G>A maps to ENST00000506030 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:56477655 G>A maps to NM_001982.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:56482559 C>T maps to NM_001982.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:212293209 T>A did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr2:212286785 C>T maps to NM_005235.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr2:212251752 A>G maps to NM_005235.2 F1102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:212251788 T>C maps to NM_005235.2 E1090E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr2:212483973 A>G maps to NM_005235.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:1137464 T>A maps to NM_178040.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:1137660 C>T maps to NM_178040.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:55733483 G>A maps to ENST00000460849 Y923Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:55733492 A>G maps to ENST00000460849 H920H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr3:56468564 C>A maps to ENST00000460849 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr3:56468845 G>A maps to ENST00000460849 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:56468489 A>G maps to ENST00000460849 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr3:56044586 G>A maps to ENST00000460849 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:45923661 G>A maps to NM_202001.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:45855904 C>T maps to NM_000400.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:45873414 C>T maps to NM_000400.3 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr2:128051202 C>A maps to NM_000122.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:128050326 T>C maps to NM_000122.1 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:128028933 C>T maps to NM_000122.1 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:128030524 G>A maps to NM_000122.1 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:128038145 C>T maps to NM_000122.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr2:128051229 C>T maps to NM_000122.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:14029334 C>T maps to NM_005236.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:103514377 A>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr10:50686482 G>A maps to NM_000124.2 R735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:50678711 A>G maps to NM_000124.2 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:50736484 G>A maps to ENST00000515869 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr10:50732317 G>A maps to ENST00000515869 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:50682249 G>A maps to NM_000124.2 N807N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:50686477 A>G maps to NM_000124.2 D736D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr10:50681582 G>C maps to NM_000124.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:50691466 G>A maps to NM_000124.2 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:50680489 G>A maps to NM_000124.2 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:50682093 C>T maps to NM_000124.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:71425357 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:71425827 T>A did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:71427425 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:71428341 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:71425718 A>T did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:71425289 G>A did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:71426112 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:71425174 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:71428265 A>G did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:71427961 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:71428007 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:60195511 T>C maps to NM_000082.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr4:75246851 C>T maps to NM_001432.2 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:42753168 C>T maps to NM_006494.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr19:42753351 G>A maps to NM_006494.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr19:42753282 G>A maps to NM_006494.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:42754649 C>T maps to NM_006494.2 W30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:39755693 T>C maps to NM_001136154.1 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:39755780 G>A maps to NM_001136154.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr21:39795449 G>A maps to NM_001136154.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:39755648 G>A maps to NM_001136154.1 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr21:39755333 A>C maps to NM_001136154.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr21:39755498 G>A maps to NM_001136154.1 H429H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:172315746 G>A maps to NM_001031711.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr5:172377767 C>T maps to NM_001031711.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:29524559 G>A maps to NM_016570.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:29523048 A>C maps to NM_016570.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:8869246 G>A maps to NM_153332.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:8865586 G>A maps to NM_153332.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:8865586 G>A maps to NM_153332.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:44687310 G>A maps to NM_024066.1 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr1:44785404 C>T maps to NM_024066.1 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:44804977 T>C maps to NM_024066.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:44774043 G>T maps to NM_024066.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:642607 A>G maps to NM_207332.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:624005 T>A maps to NM_207332.1 K116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:623802 A>G maps to NM_207332.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:54041677 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr10:101914622 T>C maps to NM_001100626.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:101945290 G>A maps to NM_001100626.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr8:37611482 T>A maps to NM_007175.6 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:37597885 C>T maps to NM_007175.6 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:37611431 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:37607996 G>A maps to NM_007175.6 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:158182016 T>C maps to NM_001009959.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:5787566 G>A maps to NM_024896.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr9:5805110 G>A maps to NM_024896.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:62141445 C>T maps to NM_001433.3 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:62144206 G>A maps to NM_001433.3 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr17:62122823 C>A maps to NM_001433.3 E850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:62149395 C>T maps to NM_001433.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:62144206 G>A maps to NM_001433.3 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:23713785 G>A maps to NM_033266.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:23713537 G>A maps to NM_033266.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:23703619 G>A maps to NM_033266.3 C759C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:236389789 T>C maps to NM_019891.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr1:236399098 C>T maps to NM_019891.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:236406752 A>G maps to NM_019891.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:15073928 G>A maps to NM_152321.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:102778629 G>A maps to NM_015051.1 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:102782968 C>T maps to NM_015051.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr1:8073677 C>T maps to NM_018948.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:64452894 C>T maps to NM_001007253.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:64453023 T>C maps to NM_001007253.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr6:11105534 C>T maps to NM_207582.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:124624153 G>A maps to NM_138961.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr11:124626485 T>C maps to NM_138961.2 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:27650264 T>C maps to NM_001017420.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr8:27660906 C>G maps to NM_001017420.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr8:27634041 C>T maps to NM_001017420.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:27634064 G>A maps to NM_001017420.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:13763471 G>A maps to NM_016649.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:54281198 G>A maps to NM_007036.4 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:53683933 C>T maps to NM_012291.4 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:53681904 A>T maps to NM_012291.4 P1442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:53680215 G>A maps to NM_012291.4 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:53668728 A>G maps to NM_012291.4 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:53685586 A>G maps to NM_012291.4 G1878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:53680077 C>T maps to NM_012291.4 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:53687095 C>T maps to NM_012291.4 R2067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:53677868 C>T maps to NM_012291.4 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr12:53663424 G>A maps to NM_012291.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:53677232 C>T maps to NM_012291.4 C996C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:53679948 A>G maps to NM_012291.4 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:53666522 T>A maps to NM_012291.4 L463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:6520164 C>T maps to NM_031475.2 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:6488422 C>T maps to NM_031475.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:6504599 G>A maps to NM_031475.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:239039950 C>T maps to NM_194312.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:239039977 C>A maps to NM_194312.2 R875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:239010706 G>A maps to NM_194312.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:239040288 C>T maps to NM_194312.2 N978N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:152201883 C>T maps to NM_001122741.1 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:152415578 C>T maps to NM_001122741.1 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:152129400 G>A maps to NM_001122741.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr6:152419947 C>T maps to NM_001122741.1 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr14:64699875 G>A maps to NM_001437.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:64727248 G>A maps to NM_001437.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:64694262 C>T maps to NM_001040276.1 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:64694322 C>T maps to NM_001040276.1 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:68265114 G>A maps to NM_024939.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:68266192 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr14:76928918 C>T maps to NM_004452.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr14:76964734 C>T maps to NM_004452.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:76905755 G>A maps to NM_004452.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr14:76905764 G>A maps to NM_004452.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr1:216692752 C>T maps to NM_001438.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:216680462 G>A maps to NM_001438.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:216850739 C>T maps to NM_001438.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:103495261 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:103499106 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:103495265 C>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:103495303 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:103495215 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:56530568 G>A maps to NM_001184796.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr12:56525561 C>T maps to NM_001184796.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:56536103 A>G maps to NM_001184796.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:56527632 C>T maps to NM_001184796.1 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr12:56526117 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:56531348 C>T maps to NM_001184796.1 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:56526317 C>A maps to NM_001184796.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:158526906 C>T maps to NM_020728.2 A891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:158536258 C>T maps to NM_020728.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:158557480 C>A maps to NM_020728.2 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:158534290 C>T maps to NM_020728.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:158529776 G>A maps to NM_020728.2 H814H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr3:138191675 C>T maps to NM_031913.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:138187555 G>A maps to NM_031913.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:67630572 G>A maps to NM_019002.3 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr5:137844017 T>C maps to NM_004730.2 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:51857745 A>G maps to NM_001014763.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:51848575 G>T maps to NM_001014763.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr1:204110560 T>C maps to NM_018208.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:128354757 G>A maps to NM_001143820.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:40194776 C>T maps to NM_005239.4 H458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr21:40186200 C>T maps to NM_005239.4 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:40194677 C>T maps to NM_005239.4 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:13971340 G>T maps to NM_004956.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:13946201 T>G maps to NM_004956.4 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:13971289 G>C maps to NM_004956.4 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:36134635 C>T maps to ENST00000222279 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr1:157069033 G>A maps to NM_001004341.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:157069093 G>A maps to NM_001004341.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:41610240 G>T maps to NM_001079675.1 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr12:12022502 C>G maps to NM_001987.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:36339254 G>A maps to NM_016135.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:5803720 C>T maps to NM_153717.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:5733276 C>T maps to NM_153717.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr4:5733297 C>T maps to NM_153717.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr4:5803747 G>A maps to NM_153717.2 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:5803720 C>T maps to NM_153717.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr4:5749975 G>A maps to NM_153717.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:5800368 G>T maps to NM_153717.2 R718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:5731071 C>T maps to NM_153717.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:5785416 C>T maps to NM_153717.2 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:5664925 A>G maps to NM_147127.4 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr4:5620290 G>A maps to NM_147127.4 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:5687114 G>T maps to NM_147127.4 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr4:5624325 G>A maps to NM_147127.4 D813D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:5578093 G>A maps to NM_147127.4 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:5620261 C>T maps to NM_147127.4 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr4:5617238 C>T maps to NM_147127.4 K913K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:5630344 C>T maps to NM_147127.4 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr4:5567009 G>A maps to NM_147127.4 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:5620257 G>A maps to NM_147127.4 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:5624400 G>A maps to NM_147127.4 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:5570349 C>T maps to NM_147127.4 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:29645464 C>T maps to NM_001003927.2 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr17:29631446 G>T maps to NM_006495.3 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr17:29632468 C>T maps to NM_006495.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr17:29632561 C>T maps to NM_006495.3 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:93029201 A>G maps to NM_005665.4 H705H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:93202118 C>T maps to NM_005665.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:7914149 G>A maps to NM_001159944.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:7913811 G>A maps to NM_001159944.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:7925500 C>T maps to NM_001159944.1 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:7911451 C>T maps to NM_001159944.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:7928437 C>T maps to NM_001159944.1 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:100603982 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:74004368 C>T maps to NM_001988.2 S1639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:74018091 G>A maps to NM_001988.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:74003903 A>G maps to NM_001988.2 S1794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:74005244 C>T maps to NM_001988.2 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr17:74003288 G>A maps to NM_001988.2 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:74017835 G>A maps to NM_001988.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:74018607 G>A maps to NM_001988.2 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:74005309 G>A maps to NM_001988.2 L1326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:74004929 C>T maps to NM_001988.2 R1452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:74003198 C>T maps to NM_001988.2 P2029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:74004806 G>A maps to NM_001988.2 T1493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:74018595 G>A maps to NM_001988.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:74015719 G>A maps to NM_001988.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:18284811 G>A maps to NM_001145127.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:18286167 G>A maps to NM_001145127.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr17:18284925 G>A maps to NM_001145127.1 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr7:27282960 C>T maps to NM_001989.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:27285698 C>A maps to NM_001989.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:176945560 C>T maps to NM_001080458.1 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:176945392 G>A maps to NM_001080458.1 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr2:176947088 G>A maps to NM_001080458.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr2:176945404 G>A maps to NM_001080458.1 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr2:176945350 C>T maps to NM_001080458.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:29696150 G>T maps to NM_013986.3 *662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:41509323 G>A maps to NM_152596.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr9:140242606 C>A maps to NM_017820.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:242020785 T>C did not map to a codon.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr1:242016725 A>G maps to NM_006027.4 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:242015656 C>T maps to NM_006027.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr1:242021852 C>T maps to NM_006027.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:242035406 T>C maps to NM_006027.4 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr1:242020684 C>T maps to NM_006027.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:242035394 G>A maps to NM_006027.4 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:56730484 G>A maps to NM_018261.3 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr4:56736992 G>A maps to NM_018261.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:637805 G>A maps to NM_018303.4 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:532475 A>T maps to NM_018303.4 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:598084 C>A maps to NM_018303.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr6:564036 C>T maps to NM_018303.4 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:619530 C>T maps to NM_018303.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:465329 C>T maps to ENST00000315013 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:67221486 C>T maps to NM_178516.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:67219059 G>A maps to NM_178516.3 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr16:67220249 G>A maps to NM_178516.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr19:45728122 C>T maps to NM_138568.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:45731455 G>A maps to NM_138568.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:133580443 C>T maps to NM_021807.3 C609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr7:132990650 G>A maps to NM_021807.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:133502135 C>T maps to NM_021807.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:133164812 G>A maps to NM_021807.3 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:133749274 C>T maps to NM_021807.3 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:57675500 T>C maps to ENST00000340918 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:57698339 G>T maps to ENST00000340918 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:94733808 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:94688100 C>T maps to NM_019053.4 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:94818015 T>C maps to NM_019053.4 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr10:94816715 T>G maps to NM_019053.4 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr2:72958338 T>C maps to NM_015189.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:72742234 C>T maps to NM_015189.1 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:72968531 G>A maps to NM_015189.1 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:73052952 G>A maps to NM_015189.1 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:74097458 T>C did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr17:74093927 G>A maps to NM_001145297.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr17:74081410 G>A maps to NM_001145297.2 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:74080648 C>T maps to NM_001145297.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:231471823 G>A maps to NM_175876.3 H556H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:38565786 T>C maps to NM_005107.3 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:38565615 C>T maps to NM_005107.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:11137672 C>T maps to NM_001001998.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:11141136 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:37784756 G>A maps to NM_016042.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:41892594 C>T maps to NM_020158.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:122737548 T>C maps to NM_001034194.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:108383614 C>T maps to NM_015065.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:108388962 T>C maps to NM_015065.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:108385273 C>T maps to NM_015065.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:108382342 T>C maps to NM_015065.2 K1297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr11:108385483 G>A maps to NM_015065.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:108383971 G>A maps to NM_015065.2 N754N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:108412487 A>G maps to NM_015065.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:118817059 A>G maps to NM_000127.2 C652C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:118830742 C>T maps to NM_000127.2 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:118819538 A>G maps to NM_000127.2 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:44135752 C>T maps to NM_000401.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:44255774 G>A maps to NM_000401.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:44129624 T>C maps to NM_000401.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:44219524 A>G maps to NM_000401.3 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:26360245 G>A maps to NM_004455.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:26361732 C>T maps to NM_004455.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:28575030 G>A maps to NM_001440.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr8:28574838 C>G maps to NM_001440.2 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:28575030 G>A maps to NM_001440.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:28574160 G>A maps to NM_001440.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr8:72123447 T>C maps to NM_000503.4 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:72229847 G>A maps to NM_000503.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:72211324 C>T maps to NM_000503.4 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:72127928 C>A maps to NM_000503.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:72127877 G>A maps to NM_000503.4 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr8:72184107 G>T maps to NM_000503.4 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:72111655 C>T did not map to a codon.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr8:72128978 G>A maps to NM_000503.4 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:45702897 G>A maps to ENST00000360649 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:45618723 T>C maps to ENST00000360649 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:133844196 T>C maps to ENST00000452339 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:133834177 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:133846243 C>T maps to NM_172105.3 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:133802625 C>A maps to ENST00000452339 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:133783598 C>A maps to ENST00000452339 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr6:133802607 C>T maps to ENST00000452339 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr6:133777748 G>T maps to ENST00000452339 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr6:133789786 G>A maps to ENST00000452339 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:66054020 C>T maps to ENST00000370616 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:66115114 A>G maps to ENST00000370616 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr6:66200565 T>C maps to ENST00000370616 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:66204601 A>G maps to ENST00000370616 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:66205063 C>T maps to ENST00000370616 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:66204802 C>G maps to ENST00000370616 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:66204764 G>T maps to ENST00000370616 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:40879700 T>C maps to ENST00000264646 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:40864369 A>G maps to ENST00000264646 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:148525901 G>A maps to NM_004456.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:159191889 G>A maps to NM_001111077.1 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:159188493 C>A maps to NM_001111077.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr13:113783898 C>T maps to NM_000504.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:113793677 C>T maps to NM_000504.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr13:113795329 C>A maps to NM_000504.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:113795260 C>T maps to NM_000504.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:113803659 C>T maps to NM_000504.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:113783886 C>T maps to NM_000504.3 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:187192763 A>G maps to NM_000128.3 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:160970514 G>A maps to NM_016946.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:160969678 C>T maps to NM_016946.4 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:176830303 G>T maps to NM_000505.3 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:176831588 G>A maps to NM_000505.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:6167837 C>T maps to NM_000129.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:6167822 G>A maps to NM_000129.3 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr6:6266872 A>G maps to NM_000129.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:6266818 C>T maps to NM_000129.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:197009700 G>A maps to NM_001994.2 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr1:197021788 C>A maps to NM_001994.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:197009743 A>C maps to NM_001994.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:46747670 C>T maps to NM_000506.3 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:46748105 C>T maps to NM_000506.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:46740827 C>T maps to NM_000506.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:76029168 C>T maps to NM_001992.3 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:76129239 C>T maps to NM_005242.4 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:75913672 G>T maps to NM_004101.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:17001149 C>T maps to NM_003950.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:17001116 G>A maps to NM_003950.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:94998734 T>G maps to NM_001993.4 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:95001575 A>C maps to NM_001993.4 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:169515678 C>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:169510763 T>C maps to ENST00000367796 P1193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:169529840 G>A maps to ENST00000367796 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:169511873 T>C maps to ENST00000367796 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:113768257 C>T maps to NM_000131.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr13:113771896 G>A maps to NM_000131.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:113772766 C>T maps to NM_000131.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:154159119 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:154130416 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:154158735 T>G did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:154176145 G>T did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:154159498 A>C did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:154225315 A>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:154091410 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:154133271 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:154185407 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:154194943 A>G did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:154225312 T>G did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:154194355 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:154158280 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:154128210 T>C did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:154194365 T>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:154130393 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:154158194 T>C did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:154088773 T>G did not map to a codon.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr23:154197691 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr23:154158079 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:154157610 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:154159623 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:154157810 A>C did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:154159895 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:154133115 T>G did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:154159297 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:154157016 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:154115594 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:154115731 A>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:138644000 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:138644003 A>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:138633257 T>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:138644208 G>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:138642957 G>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:138630578 A>G did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:138630606 G>C did not map to a codon.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr23:138633423 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:138643009 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:138643969 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr23:138633257 T>G did not map to a codon.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr16:74750314 C>A maps to NM_024306.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr16:74750395 T>C maps to NM_024306.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:74750314 C>T maps to NM_024306.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:46876499 A>G maps to NM_001441.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:46874198 G>A maps to NM_001441.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:57337163 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:57474978 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:57367812 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:57318992 C>A did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:57473428 C>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:57367775 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:57313395 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:88425859 C>T maps to NM_001443.1 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr2:88425811 G>A maps to NM_001443.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:31845852 G>A maps to NM_004102.3 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:82195628 C>T maps to NM_001444.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:159659201 C>T maps to NM_001040442.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:159665629 C>T maps to NM_001040442.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:82373716 A>G maps to NM_001080526.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr8:82371456 G>A maps to NM_001080526.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:61624929 G>C maps to NM_004265.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:61596029 C>G maps to NM_004265.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:61646250 G>A maps to NM_021727.3 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:50941255 G>A maps to NM_007051.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:51323598 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:175919215 G>A maps to NM_014613.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr5:175916029 T>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:175933770 A>G maps to NM_014613.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr15:80450430 C>T maps to NM_000137.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:1877454 C>T maps to NM_001018104.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:96072862 C>T maps to NM_016044.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:96072706 G>A maps to NM_016044.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:97751466 G>A maps to NM_199336.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:97751577 G>A maps to NM_199336.1 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:50291300 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr12:50295006 C>T maps to NM_012306.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:207085271 C>T maps to NM_005449.4 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:130707134 G>A maps to NM_001035254.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:130710443 C>T maps to NM_001035254.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:130707095 G>A maps to NM_001035254.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:130710443 C>T maps to NM_001035254.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr9:130707125 C>A maps to NM_001035254.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:109143274 A>G maps to NM_001010883.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr23:55172585 G>A did not map to a codon.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr23:55172536 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr23:55185631 C>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:14602335 A>C maps to NM_019018.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr3:58555473 C>T maps to ENST00000474531 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:14816290 G>A maps to NM_031453.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:1880892 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:1881328 G>A maps to NM_031213.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr12:111801240 C>T maps to NM_001177996.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:111801243 G>A maps to NM_001177996.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:111801078 G>A maps to NM_001177996.1 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:42473683 C>T maps to NM_001002034.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr8:59059520 G>T maps to NM_147189.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:59059292 G>A maps to NM_147189.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:59058956 C>T maps to NM_147189.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr8:59059175 G>A maps to NM_147189.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:58920783 C>A maps to NM_198847.2 S548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:58920617 C>T maps to NM_198847.2 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:58893586 C>T maps to NM_198947.3 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:58891821 G>A maps to NM_198947.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr12:47629391 G>T maps to NM_138371.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:38910295 G>A maps to NM_138389.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:38916594 G>A maps to NM_138389.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:153406048 C>A maps to ENST00000442256 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:153406875 C>A maps to ENST00000442256 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr5:153406810 C>A maps to ENST00000442256 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:143573263 G>A maps to NM_014719.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:143573695 C>T maps to NM_014719.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:143573677 G>A maps to NM_014719.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:57649397 G>A maps to NM_152678.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr22:50754804 C>A maps to NM_001001794.3 E185*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-4363-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:203622054 C>T maps to NM_173511.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:45728580 G>A maps to NM_017911.2 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:45726599 C>T maps to NM_017911.2 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:45726515 C>T maps to NM_017911.2 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:45723844 C>T maps to NM_017911.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:126124234 C>T maps to NM_024556.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:208478020 C>A maps to ENST00000272839 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:58174221 C>A maps to NM_015433.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:58174182 C>T maps to NM_015433.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:58174092 C>T maps to NM_015433.2 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:96312894 G>A maps to ENST00000333936 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:96278449 G>A maps to ENST00000333936 P439P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-4306-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:96214613 G>A maps to ENST00000333936 L139L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-4449-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:96261169 T>C did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:96278467 C>T maps to ENST00000333936 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:96291729 G>A maps to ENST00000333936 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:96261127 G>A maps to ENST00000333936 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr9:96259787 C>T maps to ENST00000333936 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:96278437 G>A maps to ENST00000333936 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:96320185 G>A maps to ENST00000333936 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:170632309 A>G maps to NM_032448.1 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:170657407 C>T maps to NM_032448.1 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:170632249 C>A maps to NM_032448.1 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:54208984 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:54107838 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:54162022 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:54209256 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:54209085 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:54209091 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:54114279 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:54159185 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:54117832 C>T did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:54161997 C>T did not map to a codon.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr23:54107881 T>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:54161465 A>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:54209077 C>A did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:71395739 C>T maps to NM_138333.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:133988191 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:133941655 T>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:25745589 G>A maps to NM_152704.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:25745238 C>T maps to NM_152704.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:25745358 G>A maps to NM_152704.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr13:25745637 C>T maps to NM_152704.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr13:25743819 G>A maps to NM_152704.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:63411826 C>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:63410309 G>T did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:63410102 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:63411067 G>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:63411524 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:63412010 C>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:63411092 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:63411776 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:63413025 G>A did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:63409831 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:63411808 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr23:63411780 T>C did not map to a codon.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr23:63412938 T>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:63410055 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:63412442 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:63412261 T>C did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:63413008 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:63412544 C>T did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:131520538 C>T maps to NM_001105195.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:131521510 G>A maps to NM_001105195.1 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:131521708 C>T maps to NM_001105195.1 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:131520178 G>A maps to NM_001105195.1 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:51855295 C>T maps to NM_145019.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:51855295 C>T maps to NM_145019.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:51854974 G>T maps to NM_145019.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr13:51825625 G>A maps to NM_145019.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:225266119 C>T maps to NM_001122779.1 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:225265912 C>T maps to NM_001122779.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17534351 G>A maps to NM_138401.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:129157977 T>C maps to NM_001011703.1 *222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:201846040 C>T maps to NM_173822.3 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:201862259 A>G maps to NM_173822.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:134166472 G>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:134166474 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:134166473 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:134166504 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:134186057 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:134156175 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:134156234 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:184777282 C>T maps to NM_052966.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:184764989 T>C maps to NM_052966.2 K636K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:184764590 G>A maps to NM_052966.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:184764287 G>A maps to NM_052966.2 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:130279402 C>T maps to NM_022833.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:130272445 G>A maps to NM_022833.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr9:130271313 G>A maps to NM_022833.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr9:130272484 C>T maps to NM_022833.2 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:17641675 C>T maps to ENST00000335393 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:17644499 T>A maps to ENST00000335393 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr19:17654223 C>T maps to ENST00000335393 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:17643095 C>T maps to ENST00000335393 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:17641669 C>A maps to ENST00000335393 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17651297 G>A maps to ENST00000335393 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:184062388 C>A maps to NM_144635.4 C244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:184062580 G>A maps to NM_144635.4 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:184062580 G>A maps to NM_144635.4 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:184062595 C>A maps to NM_144635.4 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:184062664 G>A maps to NM_144635.4 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr1:1177987 G>A maps to NM_001014980.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:92964510 A>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:92964421 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:92964586 G>A did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:92965164 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:92965079 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:92964437 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr23:92965162 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:71186927 T>C maps to NM_001162529.1 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:71238144 C>T maps to NM_001162529.1 H1255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:71235708 A>G maps to NM_001162529.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:139153504 C>T maps to NM_015912.3 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:139180135 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:139277999 T>C maps to NM_015912.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr8:139163506 A>G maps to NM_015912.3 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:139164494 G>A maps to NM_015912.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:139164494 G>A maps to NM_015912.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:139163660 G>A maps to NM_015912.3 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:139380190 T>C maps to NM_015912.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:139164317 A>G maps to NM_015912.3 D800D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:139153504 C>T maps to NM_015912.3 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:139153549 G>A maps to NM_015912.3 V1227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:139164839 C>T maps to NM_015912.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:139164308 G>A maps to NM_015912.3 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:139164395 G>A maps to NM_015912.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr8:139255225 A>G maps to NM_015912.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:89668865 C>T maps to NM_014883.2 K766K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:89653283 G>A maps to NM_014883.2 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:89859379 C>T maps to NM_014883.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr4:89772202 T>C maps to NM_014883.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:89658706 C>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:137278576 G>A maps to NM_016603.2 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:61043189 C>T maps to ENST00000442566 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:61011368 C>A maps to ENST00000442566 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr10:61029743 G>T maps to ENST00000442566 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr10:61112134 G>A maps to ENST00000442566 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:61062599 C>T maps to ENST00000442566 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr4:187074825 C>T maps to ENST00000356371 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:187075711 G>A maps to ENST00000356371 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:55075117 C>T maps to NM_176782.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:55075224 G>A maps to NM_176782.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr1:55075099 G>T maps to NM_176782.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:79837533 C>T maps to NM_205548.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr5:175526046 C>T maps to NM_001079529.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:18928403 G>A maps to NM_153707.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:18928991 C>T maps to NM_153707.2 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:82564030 T>C maps to NM_001008226.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr13:108518596 G>A maps to NM_001080396.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr13:108518521 G>A maps to NM_001080396.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr13:108518656 C>G maps to NM_001080396.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr13:107822997 T>C maps to NM_001080396.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr13:108518530 G>A maps to NM_001080396.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr13:107822919 C>G maps to NM_001080396.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:108518650 C>T maps to NM_001080396.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:68749652 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:68748852 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:68725894 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:68725962 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:68749750 G>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:68725855 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:68749673 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:24610159 T>G maps to NM_016049.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr14:24610339 G>A maps to NM_016049.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:53122576 C>T maps to NM_001042693.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:6239209 G>A maps to NM_032127.3 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:116595303 G>A maps to NM_020940.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:116608483 C>T maps to NM_020940.3 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:116605174 C>T maps to NM_020940.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:116602748 T>C maps to NM_020940.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:116603549 T>C maps to NM_020940.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:21958381 C>T maps to NM_022749.5 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:21959323 C>T maps to NM_022749.5 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:21960330 C>T maps to NM_022749.5 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:21959238 C>T maps to NM_022749.5 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:62067453 G>A maps to ENST00000404929 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr2:62066568 C>A maps to ENST00000404929 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr2:62067291 G>A maps to ENST00000404929 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:74401051 A>G maps to NM_152445.1 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:74404366 C>A maps to NM_152445.1 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:74404378 C>A maps to NM_152445.1 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:79629710 C>T maps to NM_016010.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:79601499 T>C maps to NM_016010.2 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:75537987 C>T maps to NM_024643.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:75537317 C>T maps to NM_024643.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:140139907 G>A maps to NM_001001710.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:140140190 G>A maps to NM_001001710.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:140139863 G>A maps to NM_001001710.1 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:140139779 G>A maps to NM_001001710.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:35563009 A>G maps to NM_001164310.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:35563289 C>T maps to NM_001164310.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:11301680 C>T maps to NM_053279.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:11301554 C>T maps to NM_053279.2 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr8:11282088 G>A maps to NM_053279.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:32713240 C>T maps to NM_032648.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:32713255 C>T maps to NM_032648.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr11:73120595 G>A maps to ENST00000064778 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:73131003 A>T maps to ENST00000064778 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:131810508 C>T maps to NM_001009993.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:118969896 T>C maps to ENST00000420106 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:118970279 G>A maps to ENST00000420106 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:118969757 G>A maps to ENST00000420106 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:15256308 G>A maps to NM_001010924.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:15255459 G>A maps to NM_001010924.1 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:15255000 G>A maps to NM_001010924.1 D862D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:15256158 G>A maps to NM_001010924.1 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:187605048 G>A maps to NM_177454.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:187559046 G>A maps to NM_177454.3 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:187605147 C>T maps to NM_177454.3 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:187605099 C>A maps to NM_177454.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:93217342 C>A maps to NM_032042.5 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr5:99871537 G>T maps to NM_198507.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:99871434 C>T maps to NM_198507.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr5:99871317 G>T maps to NM_198507.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:99897773 C>T maps to NM_198507.1 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:84384688 G>A maps to NM_139076.2 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:84406226 C>T did not map to a codon.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr10:126517345 C>T maps to NM_032182.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:75720678 G>A maps to NM_032181.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:75720568 G>A maps to NM_032181.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:75720460 G>A maps to NM_032181.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:36788572 G>A maps to NM_018166.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr14:35546405 T>G maps to NM_173607.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:222922879 C>T maps to NM_207468.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:102684470 A>G maps to NM_001136123.1 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:102676414 G>A maps to NM_001136123.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr10:102684320 C>T maps to NM_001136123.1 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:102683945 G>A maps to NM_001136123.1 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr2:97559779 C>T maps to ENST00000417561 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr2:29246050 T>C maps to NM_199280.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:29240817 C>A maps to NM_199280.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:29240781 C>T maps to NM_199280.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:45432442 T>G maps to ENST00000361462 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr14:45433300 A>G maps to ENST00000361462 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:45432815 T>C maps to ENST00000361462 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:45433586 G>T maps to ENST00000361462 G655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr14:45432034 T>C maps to ENST00000361462 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:45542709 T>C maps to ENST00000361462 H1756H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr14:45431743 C>T maps to ENST00000361462 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:45432457 C>T maps to ENST00000361462 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr14:45432406 C>G maps to ENST00000361462 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:45475362 G>T maps to ENST00000361462 G933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:135419013 G>A maps to NM_205855.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:94394714 C>T maps to NM_138344.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:94395002 G>A maps to NM_138344.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:94394711 G>A maps to NM_138344.3 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:94395122 C>A maps to NM_138344.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr11:82444663 G>A maps to NM_175885.3 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr1:43621983 G>T maps to NM_001101376.2 *135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:119301422 C>T maps to NM_024581.4 Q727Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr12:49993475 A>G maps to NM_032130.2 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:35719207 T>G maps to NM_152481.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:35719445 G>T maps to NM_152481.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:15885238 C>T maps to NM_024948.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:15875659 T>C maps to NM_024948.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:15883458 A>G maps to NM_024948.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:30821829 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:30931598 C>T maps to NM_032222.2 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:155221666 T>C maps to ENST00000368370 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:18707467 T>C maps to NM_016078.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:91230340 T>G maps to NM_001145065.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:86273258 G>T maps to ENST00000372088 G794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr10:86131566 T>A maps to ENST00000372088 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:86133489 C>T maps to ENST00000372088 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:57207745 A>G maps to NM_024946.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:2673876 T>A maps to ENST00000324666 C412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:2695385 G>A maps to ENST00000324666 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:2641565 C>T maps to ENST00000324666 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:2701951 G>A maps to ENST00000324666 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr4:2641517 G>C maps to ENST00000324666 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr4:2701990 G>A maps to ENST00000324666 Q1073Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:2661727 A>G maps to ENST00000324666 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:176965989 G>A maps to ENST00000442143 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:150421355 G>A maps to NM_152394.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:150398594 G>A maps to NM_152394.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:128973735 T>C maps to NM_001039762.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:128973965 G>T maps to NM_001039762.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:128952171 C>T maps to NM_001039762.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:128973810 C>T maps to NM_001039762.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:128974386 G>A maps to NM_001039762.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:159091969 C>T maps to NM_001128424.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:103434328 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:103434327 C>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:103431171 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:103432818 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:103432970 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:103430849 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:113264890 C>T maps to NM_001004440.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:68782294 A>G maps to NM_182522.3 *141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:49103571 T>C maps to ENST00000336769 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:49103655 G>A maps to ENST00000336769 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:66551754 G>A maps to NM_017565.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:66533688 G>A maps to NM_017565.3 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr17:66539846 C>T maps to NM_017565.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr1:179033213 C>T maps to NM_014864.3 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:179019497 C>T maps to NM_014864.3 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:195592 C>T maps to NM_020223.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:195727 C>T maps to NM_020223.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:195604 C>T maps to NM_020223.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:46248153 G>A maps to ENST00000399588 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr10:88988554 C>T maps to NM_001099338.1 H306H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr10:89120862 G>A maps to ENST00000330762 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr10:89118031 G>A maps to ENST00000330762 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:97082561 G>A maps to NM_017561.1 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr9:97082644 G>A maps to NM_017561.1 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:99697696 G>A maps to NM_001170741.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr9:99701031 T>C maps to NM_001170741.1 H609H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:99694442 C>A maps to NM_001170741.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:124671215 C>T maps to NM_001029888.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr10:124672298 T>G maps to NM_001029888.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:124608898 C>T maps to NM_152644.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:116879010 C>A maps to ENST00000368596 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:116836935 C>T maps to NM_153711.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:245006390 T>C maps to ENST00000366528 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:10696473 G>A maps to NM_022068.2 S2184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:10696407 G>A maps to NM_022068.2 F2206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:10671646 T>G maps to NM_022068.2 T2712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:10671565 T>C maps to NM_022068.2 S2739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:10696428 C>A maps to NM_022068.2 V2199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:10671625 C>T maps to NM_022068.2 E2719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr18:10681656 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153741209 C>T did not map to a codon.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr21:42710318 A>C maps to ENST00000398652 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr21:42718973 T>C maps to ENST00000398652 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:121019009 A>G maps to NM_014888.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr7:121012193 C>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:121002999 T>A maps to NM_014888.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:58631237 G>A maps to NM_138805.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:58620026 G>A maps to NM_138805.2 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:110581320 G>A maps to NM_033088.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:110587675 C>T maps to NM_033088.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr1:110586376 G>A maps to NM_033088.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:110593030 G>A maps to NM_033088.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:129098163 C>T maps to ENST00000450266 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:129102881 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:129096401 G>A maps to ENST00000450266 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:129096459 C>T maps to ENST00000450266 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:20879813 G>A maps to NM_207334.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:20879492 C>T maps to NM_207334.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:82460080 A>G maps to ENST00000369756 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:82459684 A>G maps to ENST00000369756 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:27332692 G>A maps to NM_052943.3 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:27332833 C>A maps to NM_052943.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:79698309 T>A did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:79698242 A>C did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr23:79698242 A>G did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:79698242 A>C did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:79698242 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:79698239 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:34149284 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:34148407 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:34148796 C>A did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:34148535 A>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:34148103 A>C did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:34149531 G>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:34149432 C>T did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:34149498 C>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:34149739 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:34148466 C>A did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:34148982 G>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:34148535 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:34149083 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:34148722 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:34150285 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:34148625 G>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:34150215 G>A did not map to a codon.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr23:34148842 C>T did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:34148893 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:34148075 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:34148202 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:34149548 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:34961413 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:34962858 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:34961162 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:34961838 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:34962796 A>G did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:34962028 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:34961019 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:34961044 C>T did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:34962852 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:34961383 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:34961420 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:34961699 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:34962107 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:34961350 C>A did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:34961130 C>A did not map to a codon.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr23:34962139 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:34960963 C>T did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr23:34961579 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:34962517 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:34962699 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:37028324 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:37028756 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:37027010 G>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:37028446 G>A did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:37028373 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:37026822 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:37027560 G>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:37028338 G>A did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr23:37028306 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:37027113 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:37027774 C>T did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:37028748 G>C did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr23:37029348 C>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:37028755 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:37026601 T>C did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:37026508 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:37027954 C>A did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:37027956 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:37026662 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:37027783 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:37028707 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:37029393 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:37028318 G>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:37027833 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr23:37026573 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:37029015 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:37027001 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr23:37027567 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:37618212 A>G did not map to a codon.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr13:37622736 C>T did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:16736389 T>C maps to NM_030797.3 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:16746919 G>T maps to NM_030797.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:16746918 G>A maps to NM_030797.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:130863079 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153678622 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153674213 G>A did not map to a codon.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr6:3850758 C>T maps to NM_012135.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:3850779 G>A maps to NM_012135.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:1656775 G>T maps to NM_001174070.1 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:126370547 G>T maps to NM_014661.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:137682482 C>A maps to NM_001135647.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:137681157 C>T maps to NM_001135647.1 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:136560839 A>T maps to NM_138419.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr11:114393748 A>C maps to ENST00000424269 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:101525941 G>A maps to NM_145037.2 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:101520159 C>T maps to NM_145037.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:101504475 C>T maps to NM_145037.2 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:114453245 G>A maps to NM_001077639.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr11:114453677 G>A maps to NM_001077639.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:114453605 T>C maps to NM_001077639.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:114453197 T>C maps to NM_001077639.1 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:114453401 C>T maps to NM_001077639.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:644551 G>A maps to NM_024792.1 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:152860095 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:152860095 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:152861627 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:152858039 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:29867431 G>A maps to ENST00000269209 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr18:29867374 G>A maps to ENST00000269209 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:29867406 G>A maps to ENST00000269209 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:29972945 G>A maps to ENST00000269209 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:29848391 G>A maps to ENST00000269209 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:177199053 G>A maps to NM_021165.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:177245457 C>T maps to NM_021165.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:177245496 C>T maps to NM_021165.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr1:177245463 C>A maps to NM_021165.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:177199155 C>T maps to NM_021165.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:177226396 C>T maps to NM_021165.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:177245415 T>C maps to NM_021165.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr1:177245563 G>T maps to NM_021165.2 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:190067861 C>T maps to NM_199051.1 W529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:190067600 G>A maps to NM_199051.1 N616N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:190129802 T>C maps to NM_199051.1 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr1:190067603 C>T maps to NM_199051.1 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:190068095 T>C maps to NM_199051.1 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:190129951 A>G maps to NM_199051.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:190067834 C>T maps to NM_199051.1 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:190067639 T>C maps to NM_199051.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr1:190067204 C>T maps to NM_199051.1 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:190068209 G>A maps to NM_199051.1 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr1:190068068 G>A maps to NM_199051.1 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr1:190067963 G>A maps to NM_199051.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:150973066 G>A maps to NM_001163258.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:150971952 C>T maps to NM_001163258.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr1:150974703 G>A maps to NM_001163258.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:59144133 T>A maps to NM_001040450.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:59080106 G>A maps to NM_001040450.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr15:59146715 A>G maps to NM_001040450.1 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr15:59063681 C>T maps to NM_001040450.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:67576356 T>C maps to NM_001193523.1 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:67576572 T>C maps to NM_001193523.1 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:24850863 T>C maps to NM_014722.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:24848383 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:49225218 A>G maps to NM_080829.2 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:49225478 G>A maps to NM_080829.2 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:49218794 G>A maps to NM_080829.2 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:49247291 T>C maps to NM_080829.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:49214160 G>A maps to NM_080829.2 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:93309347 G>A maps to NM_001006605.3 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:139617652 G>A maps to NM_152421.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:139617493 G>A maps to NM_152421.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:139617799 C>T maps to NM_152421.3 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:139612105 C>T maps to NM_152421.3 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:119419029 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:119419024 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:119438314 G>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:119445131 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:119394854 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:119410900 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:119394877 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr13:114514860 C>T maps to NM_182614.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:212798362 C>T maps to NM_153606.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:212799664 G>T maps to NM_153606.3 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:212798998 C>T maps to NM_153606.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:212799661 G>A maps to NM_153606.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr5:156592828 T>C maps to NM_130899.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr12:100042167 C>G maps to NM_153364.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:100042080 A>T maps to NM_153364.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:67669863 C>T maps to NM_173526.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:50979588 T>C maps to ENST00000391816 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:50971040 G>A maps to ENST00000391816 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:128356949 G>A maps to NM_032599.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:128320140 G>A maps to NM_001012454.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:78325056 C>T maps to NM_198549.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:40702861 A>G maps to NM_001083124.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr9:40704211 G>A maps to NM_001083124.1 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:43630569 G>T maps to NM_001145196.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr9:43627225 G>T maps to NM_001145196.1 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr9:43628662 C>T maps to NM_001145196.1 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr9:43627078 A>G maps to NM_001145196.1 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:90535640 G>A maps to NM_001145124.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:90535892 C>T maps to NM_001145124.1 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:90535682 T>C maps to NM_001145124.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:90535706 G>A maps to NM_001145124.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:90535406 C>A maps to NM_001145124.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:95512121 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:95516361 C>A maps to NM_144664.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr11:95520841 G>A maps to NM_144664.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr9:134136310 C>T maps to NM_033387.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr9:134151257 G>A maps to NM_033387.3 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:59752284 T>C maps to NM_152450.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:94772529 A>G maps to NM_152548.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr5:94764399 C>T maps to NM_152548.2 P250P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-4465-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:94772541 T>C maps to NM_152548.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:38178435 C>T maps to NM_144713.3 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:87487046 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:124204040 A>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:54805454 C>T maps to NM_001010872.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:54805206 C>T maps to NM_001010872.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr6:54806757 C>T maps to NM_001010872.1 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:33876761 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:33874634 A>G maps to NM_178468.4 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr20:37581153 C>T maps to NM_030919.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr20:37580586 G>A maps to NM_030919.2 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:37580193 G>A maps to NM_030919.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:37580193 G>A maps to NM_030919.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:40417464 T>G maps to NM_138435.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr22:40417953 T>C maps to NM_138435.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr22:40417653 G>A maps to NM_138435.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:18874740 G>A maps to NM_001039999.2 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:18881505 G>A maps to NM_001039999.2 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr17:18907188 G>A maps to NM_001039999.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:18881934 C>T maps to NM_001039999.2 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:18881427 G>T maps to NM_001039999.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr8:144812560 C>T maps to NM_198488.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:144810853 C>T maps to NM_198488.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:144810850 G>A maps to NM_198488.3 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:144811445 G>A maps to NM_198488.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:144811165 G>A maps to NM_198488.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:5141893 G>A maps to NM_201400.2 H81H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:5139162 G>A maps to NM_201400.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:12285238 C>T maps to NM_001137610.1 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr8:12283472 C>T maps to NM_001137610.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr8:12283472 C>T maps to NM_001137610.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr8:12286291 G>A maps to NM_001137610.1 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:71502819 G>A maps to NM_001099653.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:17601000 C>T maps to NM_016255.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:17602851 C>T maps to NM_016255.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr12:8375359 C>T maps to NM_018088.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:8375188 G>A maps to NM_018088.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr12:8375059 G>C maps to NM_018088.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:124812009 A>G did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:124798812 G>A maps to NM_144963.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr16:85143909 G>A maps to ENST00000393246 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:85143873 G>A maps to ENST00000393246 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr15:64373350 C>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:33810304 G>A maps to ENST00000395190 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:33813509 G>A maps to ENST00000395190 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr2:33817165 C>T maps to ENST00000395190 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr2:33810019 A>G maps to ENST00000395190 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:33812388 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:33810139 G>A maps to ENST00000395190 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:38895638 A>C maps to NM_174905.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr19:38899404 C>T maps to NM_174905.3 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:38899422 C>G maps to NM_174905.3 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:8767014 T>C did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr23:8761696 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:8766402 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:8763145 T>G did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr23:8768143 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr23:8998321 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:8995917 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:13058874 A>G did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr16:89869664 A>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:14876020 C>T did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:14862734 G>C did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr23:14883233 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:14871244 A>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:14883326 A>G did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:14863286 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:14868778 A>C did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:14883087 A>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:97933361 G>A maps to NM_000136.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr9:97864002 G>A maps to NM_000136.2 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr3:10088404 T>C maps to NM_033084.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:10074519 C>T maps to NM_033084.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:10114935 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:10138153 C>T maps to NM_033084.3 Q1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr3:10094103 C>T maps to NM_033084.3 Q527*. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:35423661 C>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:22646318 G>T maps to NM_022725.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:35077351 A>G maps to NM_004629.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:35074152 G>T maps to NM_004629.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:89828431 C>T maps to NM_001113378.1 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:45606350 T>C maps to NM_020937.2 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:163031452 T>C maps to NM_004460.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:163057080 G>T maps to NM_004460.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr2:163057098 G>A maps to NM_004460.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:13732383 G>A maps to NM_032228.5 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:13749176 C>T maps to NM_032228.5 Y444Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:13716474 C>T maps to NM_032228.5 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:29423429 G>A maps to NM_018099.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:29474808 G>A maps to NM_018099.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr12:29423405 T>G maps to NM_018099.3 Y8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:29469772 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:29474808 G>A maps to NM_018099.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:99047704 A>G maps to NM_005766.2 K463K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr13:99092252 C>A maps to NM_005766.2 C824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:99061769 C>T maps to NM_005766.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr13:99100537 C>T maps to NM_005766.2 H1035H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:242432734 C>T maps to NM_014808.2 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr6:5771526 G>A maps to NM_006567.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:223478635 A>G maps to NM_005687.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:223499244 A>G maps to NM_005687.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:223488428 A>C maps to NM_005687.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:223507643 A>G maps to NM_005687.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:90774041 G>A maps to NM_000043.3 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:172635149 G>A maps to NM_000639.1 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr1:172635149 G>A maps to NM_000639.1 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:172628523 A>G maps to NM_000639.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:172628409 G>A maps to NM_000639.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:80037253 G>A maps to NM_004104.4 G2459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:80048925 G>A maps to NM_004104.4 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:80044983 C>A maps to NM_004104.4 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:80038667 C>T maps to NM_004104.4 R2242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:80041486 C>T maps to NM_004104.4 A1749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:80049206 G>A maps to NM_004104.4 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr17:80039960 C>A maps to NM_004104.4 A2029A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:80046752 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:80046320 G>A maps to NM_004104.4 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:80047251 C>A maps to NM_004104.4 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:80046329 G>A maps to NM_004104.4 D843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:150774415 C>T maps to NM_006712.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:170413694 A>G did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:170417152 G>A maps to NM_024622.3 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:207651570 T>A maps to NM_014929.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr2:207655331 T>C maps to NM_014929.3 C645C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:207655403 G>A maps to NM_014929.3 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:207652862 A>G maps to NM_014929.3 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:7867446 T>C maps to NM_024091.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:7866894 G>A maps to NM_024091.3 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr5:7866834 T>A maps to NM_024091.3 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:7866770 G>A maps to NM_024091.3 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:3128083 G>A maps to NM_021826.4 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:3128086 A>G maps to NM_021826.4 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr20:3127666 G>A maps to NM_021826.4 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:3129629 T>C maps to NM_021826.4 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:3129640 G>A maps to NM_021826.4 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:187628542 G>A maps to ENST00000260147 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:187540077 A>C maps to ENST00000260147 L2557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:187549800 A>G maps to ENST00000260147 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:187627795 G>A maps to ENST00000260147 D1062D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:187557822 C>T maps to ENST00000260147 E1296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:187522470 C>T maps to ENST00000260147 T3867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:187630438 G>A maps to ENST00000260147 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:187541628 C>T maps to ENST00000260147 T2040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr4:187554957 G>A maps to ENST00000260147 H1401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr4:187557879 G>A maps to ENST00000260147 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:187557245 G>T maps to ENST00000260147 P1372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:187527364 A>T maps to ENST00000260147 I3406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:187530972 A>G maps to ENST00000260147 L3353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:187549305 A>G maps to ENST00000260147 G1604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:187628365 G>A maps to ENST00000260147 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr4:187628513 A>T maps to ENST00000260147 L823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:187524834 G>A maps to ENST00000260147 S3618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:187519256 G>T maps to ENST00000260147 A4045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr4:187541091 G>T maps to ENST00000260147 Y2219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:187539003 G>A maps to ENST00000260147 N2915N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:187630012 A>G maps to ENST00000260147 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr4:187527352 C>T maps to ENST00000260147 T3410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:187540839 C>T maps to ENST00000260147 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:150930357 A>G maps to NM_001447.2 V1457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:150932867 C>T maps to NM_001447.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:150946761 C>T maps to NM_001447.2 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:150946644 G>A maps to NM_001447.2 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:150924750 C>T maps to NM_001447.2 E1979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:150924501 A>G maps to NM_001447.2 D2062D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr5:150934213 C>A maps to NM_001447.2 G1218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr5:150922740 C>A maps to NM_001447.2 L2649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr5:150925274 A>G maps to NM_001447.2 L1805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:150914045 G>A maps to NM_001447.2 H3117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr5:150947106 G>T maps to NM_001447.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:150924237 C>T maps to NM_001447.2 T2150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr5:150932810 C>T maps to NM_001447.2 T1361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr5:150945698 G>A maps to NM_001447.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr5:150889711 G>A maps to NM_001447.2 Q3977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:150885605 G>A maps to NM_001447.2 R4190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:150947570 G>T maps to NM_001447.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:92533873 A>G maps to ENST00000298047 E2565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:92543081 C>T maps to ENST00000298047 D3107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr11:92533858 G>T maps to ENST00000298047 R2560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:92531573 C>A maps to ENST00000298047 R1799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:92623906 G>T maps to ENST00000298047 L4466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:92257896 C>A maps to ENST00000298047 S1130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:92590422 G>A maps to ENST00000298047 P3803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:92088049 T>G maps to ENST00000298047 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr11:92086976 C>T maps to ENST00000298047 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr11:92532763 C>T maps to ENST00000298047 V2195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:92086519 T>C maps to ENST00000298047 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr11:92258061 C>A maps to ENST00000298047 Y1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr11:92533456 T>C maps to ENST00000298047 F2426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr11:92086576 G>A maps to ENST00000298047 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:92495038 T>C maps to ENST00000298047 G1229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:92531032 G>A maps to ENST00000298047 P1618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr11:92086453 T>C maps to ENST00000298047 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:92539640 T>C maps to ENST00000298047 Y3069Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr11:92087017 A>G maps to ENST00000298047 K580K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:92543234 C>T maps to ENST00000298047 P3158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:92600058 C>T maps to ENST00000298047 Y3937Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:92577839 G>A maps to ENST00000298047 T3769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr11:92088478 T>C maps to ENST00000298047 A1067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr11:92616095 C>T maps to ENST00000298047 I4158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr11:92087431 T>C maps to ENST00000298047 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:92531143 A>G maps to ENST00000298047 A1655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:92087536 C>T maps to ENST00000298047 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:92258013 G>A maps to ENST00000298047 Q1169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:92086840 T>C maps to ENST00000298047 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:92600034 G>A maps to ENST00000298047 T3929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr11:92568066 T>A maps to ENST00000298047 Y3301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr11:92531035 C>A maps to ENST00000298047 V1619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:92616431 G>A maps to ENST00000298047 S4270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:92531125 G>A maps to ENST00000298047 P1649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:92531785 C>T maps to ENST00000298047 V1869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr11:92534446 C>T maps to ENST00000298047 F2756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr11:92532649 C>T maps to ENST00000298047 T2157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:126411788 C>T maps to NM_024582.4 T4604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr4:126372619 T>G maps to NM_024582.4 V3483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr4:126370558 T>G maps to NM_024582.4 T2796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:126238231 G>A maps to NM_024582.4 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:126370099 C>T maps to NM_024582.4 D2643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr4:126411218 G>A maps to NM_024582.4 L4414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr4:126370492 T>C maps to NM_024582.4 S2774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:126371860 G>A maps to NM_024582.4 A3230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:126389937 A>T maps to NM_024582.4 G4057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr4:126412391 C>A maps to NM_024582.4 I4805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:126242389 T>C maps to NM_024582.4 P1608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:126336507 T>A maps to NM_024582.4 G2130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr4:126412148 T>A maps to NM_024582.4 P4724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:126336825 C>T maps to NM_024582.4 S2236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr4:126412592 A>G maps to NM_024582.4 Q4872Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:126239986 G>A maps to NM_024582.4 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:126372052 T>C maps to NM_024582.4 Y3294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:126400928 C>T maps to NM_024582.4 S4169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr4:126238414 G>A maps to NM_024582.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr4:126412364 C>T maps to NM_024582.4 N4796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:126238439 G>T maps to NM_024582.4 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:126370813 C>T maps to NM_024582.4 C2881C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr4:126237929 C>T maps to NM_024582.4 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr4:126411764 T>C maps to NM_024582.4 T4596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:126336234 T>C maps to NM_024582.4 I2039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:126389697 T>C maps to NM_024582.4 S3977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:126398438 A>G maps to NM_024582.4 G4141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:126400952 T>C maps to NM_024582.4 C4177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr4:126411350 G>A maps to NM_024582.4 T4458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr4:126411254 T>C maps to NM_024582.4 P4426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:126238849 C>T maps to NM_024582.4 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr4:126411251 C>T maps to NM_024582.4 V4425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr4:126239458 C>T maps to NM_024582.4 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr4:126398336 T>A maps to NM_024582.4 V4107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:126241558 T>C maps to NM_024582.4 G1331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:126239734 T>G maps to NM_024582.4 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr4:126237907 G>A maps to NM_024582.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:126241906 T>C maps to NM_024582.4 P1447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr4:126240496 C>T maps to NM_024582.4 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:126370870 T>C maps to NM_024582.4 D2900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr4:126241855 T>C maps to NM_024582.4 V1430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:126336783 C>A maps to NM_024582.4 T2222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:126337623 C>T maps to NM_024582.4 R2289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:126373057 C>T maps to NM_024582.4 P3629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:126412418 T>C maps to NM_024582.4 S4814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:150891226 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:150885863 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr23:150889934 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:73922937 C>A maps to ENST00000389570 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:40331272 T>A maps to NM_001436.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:40331066 C>T maps to NM_001436.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:16095084 A>G maps to NM_017556.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr1:16091543 C>T maps to NM_017556.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:16095093 G>A maps to NM_017556.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:45938086 C>T maps to ENST00000348697 C373C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:45959040 C>T maps to ENST00000402984 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr22:45937241 G>A maps to ENST00000348697 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:45939287 C>T maps to ENST00000348697 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:45970456 C>T maps to NM_006486.2 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr3:13649664 C>T maps to NM_001165035.1 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:13661293 C>T maps to NM_001165035.1 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:13672307 C>A maps to NM_001165035.1 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:13659598 C>T maps to NM_001165035.1 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:92406951 G>A maps to ENST00000267620 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:92353636 G>A maps to ENST00000267620 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:92347754 G>A maps to ENST00000267620 N387N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8381-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr2:112940368 C>T maps to NM_153214.2 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr2:112940380 T>C maps to NM_153214.2 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:48829958 G>A maps to NM_000138.4 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:48936858 T>C maps to NM_000138.4 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:48936888 G>A maps to NM_000138.4 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:48936959 G>A maps to NM_000138.4 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:48829943 G>A maps to NM_000138.4 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:48703476 G>A maps to NM_000138.4 R2776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:48776090 G>A maps to NM_000138.4 C1254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr15:48766497 G>A maps to NM_000138.4 R1388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:48780613 G>A maps to NM_000138.4 C1053C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:48707827 A>G maps to NM_000138.4 C2652C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr15:48782210 G>A maps to NM_000138.4 G973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:48888507 G>A maps to NM_000138.4 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr5:127681047 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:127685072 G>A maps to NM_001999.3 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:127686695 G>A maps to NM_001999.3 D892D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr5:127855062 T>G did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:127671201 G>C maps to NM_001999.3 Y1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:127624226 G>A maps to NM_001999.3 G2220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:127873116 C>T maps to NM_001999.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:127595416 G>A maps to NM_001999.3 P2823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:127648404 G>A maps to NM_001999.3 G1600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:127782260 C>A maps to NM_001999.3 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:127599208 C>T maps to NM_001999.3 S2700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:127647034 G>A maps to NM_001999.3 C1677C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:127800498 G>A maps to NM_001999.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr5:127873077 G>A maps to NM_001999.3 R73R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D7-A6EY-01A-21D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:127681103 G>A maps to NM_001999.3 R1054R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:127664436 G>A maps to NM_001999.3 C1474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:127623048 G>A maps to NM_001999.3 C2277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:127681172 C>T maps to NM_001999.3 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr5:127681250 C>T maps to NM_001999.3 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:127595437 C>T maps to NM_001999.3 E2816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:8190893 G>A maps to NM_032447.3 N871N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:8136979 G>A maps to NM_032447.3 G2680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:8176640 G>A maps to NM_032447.3 C1325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:8137978 G>A maps to NM_032447.3 G2635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:8175762 G>A maps to NM_032447.3 G1433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:8171109 G>A maps to NM_032447.3 D1565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr19:8176640 G>A maps to NM_032447.3 C1325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:8196633 G>A maps to NM_032447.3 C598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr19:8155086 G>T maps to NM_032447.3 S2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:8201335 C>T maps to NM_032447.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:8138041 G>A maps to NM_032447.3 C2614C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:8194244 G>A maps to NM_032447.3 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:8203326 C>T maps to NM_032447.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:8171031 T>C maps to NM_032447.3 P1591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:8201149 G>A maps to NM_032447.3 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:8186193 G>A maps to NM_032447.3 C1053C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:97382706 G>A maps to NM_001127628.1 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr9:97369108 C>T maps to NM_001127628.1 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr9:97333767 G>A maps to NM_003837.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr9:97321299 G>A maps to NM_003837.2 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:9922249 G>A maps to NM_017703.1 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:9921712 A>G maps to NM_017703.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:102518011 G>A maps to NM_145032.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr7:102572362 G>A maps to NM_145032.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:102566737 C>T maps to NM_145032.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:102517973 A>G maps to NM_145032.3 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr12:1675939 T>G maps to NM_152441.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr16:747114 C>T maps to NM_153350.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:745551 G>A maps to NM_153350.3 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:107216830 G>A maps to NM_001163315.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr5:107216862 G>A maps to NM_001163315.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr7:5521540 C>T maps to NM_024963.4 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:5545126 G>A maps to ENST00000312577 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr7:5521432 G>A maps to NM_024963.4 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr7:5521432 G>A maps to NM_024963.4 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:37455301 C>T maps to NM_032875.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:37420565 C>T maps to NM_032875.2 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:37455284 A>T maps to NM_032875.2 L96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:77592809 C>T maps to NM_012158.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:77581882 T>C maps to NM_012158.2 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:77592812 T>C maps to NM_012158.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:77592809 C>T maps to NM_012158.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:15642490 A>G maps to NM_012161.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:145580724 A>G maps to NM_012162.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:145579641 T>C maps to NM_012162.1 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:15937246 C>T maps to NM_012304.3 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:15936703 G>A maps to NM_012304.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr5:15936808 C>T maps to NM_012304.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:15936713 C>T maps to NM_012304.3 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr5:15928113 C>T maps to NM_012304.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:15936820 C>T maps to NM_012304.3 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:15928281 C>T maps to NM_012304.3 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:15937210 C>T maps to NM_012304.3 C464C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr5:15936910 C>T maps to NM_012304.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr5:15936832 C>T maps to NM_012304.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:15937066 C>T maps to NM_012304.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:15928474 C>T maps to NM_012304.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:37521835 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:37531989 G>A maps to NM_012166.2 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr9:37518121 T>C maps to NM_012166.2 K838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:37532016 C>T maps to NM_012166.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:37541441 A>G maps to NM_012166.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:48049366 A>G maps to NM_001190274.1 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:48066831 T>C maps to NM_001190274.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:48046159 C>A maps to NM_001190274.1 G619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr10:5956182 G>A maps to NM_032807.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr10:5978465 C>T maps to NM_032807.3 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:117593746 G>A maps to NM_033624.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:401416 C>T maps to NM_183421.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:400033 C>T maps to NM_183421.1 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:413101 C>T maps to NM_183421.1 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:418722 A>G maps to NM_183421.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:39516155 G>A maps to NM_178820.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:224302028 G>A maps to NM_015176.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:33772170 C>T maps to NM_012175.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr11:33772190 C>A maps to NM_012175.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:33780073 A>G maps to NM_012175.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:146126253 A>G maps to NM_032145.4 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:146126323 T>G maps to NM_032145.4 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:146125876 G>A maps to NM_032145.4 C555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:146126056 C>T maps to NM_032145.4 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:87376515 C>T maps to NM_024735.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:87368984 A>G maps to NM_024735.3 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:87364947 C>T maps to NM_024735.3 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr16:87364950 C>T maps to NM_024735.3 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:87377317 G>A maps to NM_024735.3 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:124518694 G>A maps to NM_058229.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:39870865 G>A maps to NM_203301.3 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:39900889 G>A maps to NM_203301.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:55818440 C>T maps to NM_152231.1 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:230861561 T>C maps to NM_174899.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:230861640 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:147813208 A>G maps to NM_205836.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr5:147803680 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:147807424 C>T maps to NM_205836.1 D856D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:147793714 G>A maps to NM_205836.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:147793697 G>T did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:147807088 G>A maps to NM_205836.1 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:147781950 G>A maps to NM_205836.1 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:147807058 C>T maps to NM_205836.1 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:6684071 C>T maps to NM_153230.2 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:41927176 T>C maps to NM_012176.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:41927194 T>C maps to NM_012176.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr3:121345654 T>G maps to NM_016298.3 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:121345700 C>T maps to NM_016298.3 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:73493773 C>T maps to ENST00000295133 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:16577503 C>T maps to NM_018994.1 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:101153422 A>G maps to NM_001029860.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:101154025 A>G maps to NM_001029860.3 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr1:11715957 C>T maps to ENST00000376768 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr1:11716011 C>A maps to ENST00000376768 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:196311018 C>T maps to NM_001105573.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:46216102 C>T maps to NM_001080469.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:46215277 C>T maps to NM_001080469.1 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:46215952 G>A maps to NM_001080469.1 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr19:46215502 G>A maps to NM_001080469.1 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:46215640 C>T maps to NM_001080469.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:46215858 G>T maps to NM_001080469.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:46215460 C>T maps to NM_001080469.1 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:46216375 G>A maps to NM_001080469.1 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:46215157 C>T maps to NM_001080469.1 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr19:46215448 G>A maps to NM_001080469.1 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:46215694 C>T maps to NM_001080469.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:153296040 C>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:11728892 C>T maps to NM_018438.5 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:11728892 C>T maps to NM_018438.5 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr22:32894360 G>A maps to NM_012179.3 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:32894315 T>C maps to NM_012179.3 Y456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:18654314 T>C maps to ENST00000395665 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:18668093 C>T maps to ENST00000395665 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:18673377 C>T maps to ENST00000395665 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:18651269 C>T maps to ENST00000395665 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:18670081 C>A maps to ENST00000395665 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:171337639 C>T maps to NM_012300.2 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr5:171305022 A>C maps to NM_012300.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:48423257 G>T maps to NM_207102.2 G352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:48436036 T>C maps to NM_207102.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr9:123527049 G>A maps to NM_012164.3 N384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:103371116 A>G maps to ENST00000331272 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:103436162 C>T maps to ENST00000331272 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr9:139835749 G>A maps to NM_018998.2 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:153271191 A>G did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr4:153247166 A>C maps to NM_033632.2 Y545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:153258982 G>A maps to NM_033632.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr4:153251933 G>A maps to NM_033632.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:153245513 A>G maps to NM_033632.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr4:153253816 G>A maps to NM_033632.2 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr4:153245338 G>A maps to NM_033632.2 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:117365829 T>C maps to NM_153348.2 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:117365933 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:12800035 C>T maps to ENST00000380339 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:55401039 G>A maps to NM_002000.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr19:55396776 G>A maps to NM_002000.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:159277557 C>T maps to ENST00000368115 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:40368705 G>A maps to NM_003890.2 C4214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:40382379 G>A maps to NM_003890.2 G3502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:40364394 A>G maps to NM_003890.2 G4749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr19:40389650 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:40399802 C>T maps to NM_003890.2 P1964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:40398081 G>A maps to NM_003890.2 D2295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr19:40366307 G>A maps to NM_003890.2 C4642C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr19:40370212 G>A maps to NM_003890.2 D4151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr19:40370470 G>A maps to NM_003890.2 G4065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:40433050 C>T maps to NM_003890.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr19:40370470 G>A maps to NM_003890.2 G4065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:40421346 G>T maps to NM_003890.2 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:40434016 G>A maps to NM_003890.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:40421157 G>A maps to NM_003890.2 R921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr19:40366184 G>A maps to NM_003890.2 G4683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:40398288 G>A maps to NM_003890.2 G2226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:40398354 C>T maps to NM_003890.2 A2204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr19:40370257 G>A maps to NM_003890.2 V4136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr19:40368552 C>T maps to NM_003890.2 T4265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40362796 G>A maps to NM_003890.2 C5091C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40362835 G>A maps to NM_003890.2 Y5078Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40398321 G>A maps to NM_003890.2 N2215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40433092 C>T maps to NM_003890.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:161480729 G>A maps to NM_001136219.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:161642903 G>A maps to NM_004001.4 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:17893891 C>T maps to NM_015122.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:17883345 G>T maps to NM_015122.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr19:17886790 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:72313085 T>C maps to NM_138782.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:141029027 C>T maps to ENST00000354789 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr5:141026259 G>A maps to ENST00000354789 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:141028997 A>G maps to ENST00000354789 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr11:72695248 G>T maps to ENST00000409314 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:72600986 G>A maps to ENST00000409314 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr11:72554208 G>A maps to ENST00000409314 N588N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr9:137805454 G>A maps to NM_002003.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr9:137804876 G>A maps to NM_002003.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:137806228 A>G did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr9:137806260 G>A maps to NM_002003.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr9:137775148 A>G maps to NM_004108.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:137775199 C>T maps to NM_004108.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr9:137778357 C>T maps to NM_004108.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:27695731 G>A maps to NM_003665.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:157765954 G>T maps to NM_052938.4 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:157771759 C>T maps to NM_052938.4 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr1:157771299 A>C maps to NM_052938.4 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:157738405 T>C maps to NM_030764.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr1:157738348 G>T maps to NM_030764.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:157719464 C>A maps to NM_030764.3 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:157666066 G>A maps to NM_052939.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:157668420 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:157660198 G>A maps to NM_052939.3 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr1:157667485 A>G maps to NM_052939.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:157667002 A>C maps to NM_052939.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:157667008 T>C maps to NM_052939.3 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:157548309 C>T maps to NM_031282.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:157557084 C>T maps to NM_031282.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:157557324 T>C maps to NM_031282.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:157494243 T>C maps to NM_031281.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:157497671 G>A maps to NM_031281.2 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr1:157508894 C>T maps to NM_031281.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:157494243 T>C maps to NM_031281.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr1:159779402 G>A maps to NM_001004310.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:159779225 C>T maps to NM_001004310.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:159785384 G>A maps to NM_001004310.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr1:161682977 G>A maps to NM_001184866.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr1:161681754 A>G maps to NM_001184866.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:161681811 G>A maps to NM_001184866.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:161681776 G>T maps to NM_001184866.1 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:161695836 C>T maps to NM_001002901.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:161697259 G>A maps to NM_001002901.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:161693277 C>T maps to NM_001002901.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:161695677 C>T maps to NM_001002901.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:161697328 C>T maps to NM_001002901.2 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:161697064 C>T maps to NM_001002901.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:161693397 C>A maps to NM_001002901.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:11667359 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:155282161 G>A maps to NM_001135821.1 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:155290372 G>A maps to NM_001135821.1 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:10421566 A>G maps to NM_001031734.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:111747698 G>A maps to ENST00000428306 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:111747641 C>T maps to ENST00000428306 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:111746443 G>A maps to NM_138378.1 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr11:111749798 G>A maps to ENST00000428306 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:72861879 G>A maps to ENST00000442102 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:72862565 A>G did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:72862959 A>T maps to ENST00000442102 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:55238723 C>T maps to NM_001012515.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr18:55247366 G>T maps to NM_001012515.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:55238741 T>C maps to NM_001012515.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:4792750 A>G maps to NM_018708.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:4792618 T>G maps to NM_018708.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:4792760 G>T maps to NM_018708.2 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:68582358 G>A maps to NM_015322.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:114860031 T>C maps to NM_020177.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:61562937 C>A maps to NM_004111.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:108290575 T>C maps to NM_005246.2 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr5:108134019 T>A maps to NM_005246.2 L46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:108523206 A>G maps to NM_005246.2 K800K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:108203634 G>T maps to NM_005246.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:108168617 C>T maps to NM_005246.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:108294934 C>T maps to NM_005246.2 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:125015461 T>C maps to NM_001039112.2 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:125113579 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:125074166 T>C maps to NM_001039112.2 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:125131153 C>T maps to NM_001039112.2 R1787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:125015416 A>G maps to NM_001039112.2 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:125078739 C>T maps to NM_001039112.2 N1209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:125083871 G>A maps to NM_001039112.2 A1364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:125035714 G>A maps to NM_001039112.2 W722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:124989712 C>A maps to NM_001039112.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:19184631 G>A maps to NM_152898.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:6075584 C>G did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr20:6088220 G>C maps to NM_017671.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:6096553 G>A maps to NM_017671.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:53331515 G>T maps to NM_001134999.1 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:53386021 A>G maps to NM_001134999.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:53325163 T>C maps to NM_001134999.1 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:53331479 C>T maps to NM_001134999.1 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:63978891 A>C maps to NM_178443.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:91428313 C>T maps to NM_002005.3 H13H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91430450 G>A maps to NM_002005.3 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91436380 C>T maps to NM_002005.3 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91436955 A>T maps to NM_002005.3 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:91432866 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr15:91433450 C>T maps to NM_002005.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:91430229 C>T maps to NM_002005.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:91437187 C>T maps to NM_002005.3 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:91434324 G>A maps to NM_002005.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr15:91433163 G>T maps to NM_002005.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:186364089 T>C maps to NM_014375.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:186362567 C>T maps to NM_014375.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:186358296 C>T maps to NM_014375.2 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr2:219846751 A>G maps to NM_017521.2 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:125359541 G>A maps to NM_005103.4 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:125324073 C>T maps to NM_005103.4 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr11:125359439 G>A maps to NM_005103.4 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:62355880 G>A maps to NM_018008.3 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:62355817 G>A maps to NM_018008.3 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:62358210 G>A maps to NM_018008.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:62358228 T>G maps to NM_018008.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:62358180 G>A maps to NM_018008.3 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr3:62356907 T>C maps to NM_018008.3 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr19:35842693 C>T maps to NM_005303.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr19:35941122 C>T maps to NM_005306.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr19:35940918 G>A maps to NM_005306.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:35850475 G>A maps to NM_005304.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr19:35850475 G>A maps to NM_005304.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr19:35850656 G>T maps to NM_005304.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr19:35850556 G>A maps to NM_005304.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr4:155507815 C>T maps to NM_000508.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr4:155507658 G>A maps to NM_000508.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr4:155506852 A>C maps to NM_000508.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:155507086 G>A maps to NM_000508.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr4:155507125 G>A maps to NM_000508.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr4:155508743 T>A maps to NM_000508.3 K144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr4:155508043 A>C maps to NM_000508.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:54496508 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:54491891 T>C did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:54472780 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:54482796 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:54482982 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:54473853 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:54496844 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:54496802 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr23:54497833 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:54521706 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:54475617 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:54492002 T>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:54497787 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:54472655 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:54491963 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:54496699 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:54482959 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:54492146 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:36982425 C>A maps to NM_173558.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:36993650 C>T maps to NM_173558.3 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:95796863 C>T maps to NM_033086.2 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr9:95772661 G>A maps to NM_033086.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:95768398 A>G maps to NM_033086.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:95738813 C>T maps to NM_033086.2 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:32778592 T>C maps to NM_139241.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:32777362 C>T maps to NM_139241.2 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr12:32772669 C>T maps to NM_139241.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:14960289 C>A maps to NM_152536.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:14964572 G>A maps to NM_152536.3 S1276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:14861612 C>T maps to NM_152536.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:14861888 C>T maps to NM_152536.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr3:14862659 A>G maps to NM_152536.3 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:14862389 C>T maps to NM_152536.3 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:95603553 A>G maps to NM_018351.3 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:95478316 A>G maps to NM_018351.3 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:95610998 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:95488365 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:95546739 A>G maps to NM_018351.3 V872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr5:44388472 C>T maps to NM_004465.1 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:44388463 C>T maps to NM_004465.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:192125844 G>A maps to NM_021032.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr3:192053208 G>A maps to NM_021032.4 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr3:191888295 T>C maps to NM_021032.4 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:192125937 C>T maps to NM_021032.4 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:137717646 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:137793062 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:137715070 G>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:137939796 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:137793156 C>T did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr23:137717618 T>C did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:138286219 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:137717758 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:137717661 T>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:137717718 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr23:137717628 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:137939774 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr23:137717658 T>G did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr13:102521140 A>C maps to NM_175929.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr13:102568923 C>A maps to NM_004115.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr13:102379051 A>G maps to NM_175929.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:102375252 C>T maps to NM_175929.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:21905675 C>T maps to NM_003867.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:21903770 C>A maps to NM_003867.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:21905618 C>T maps to NM_003867.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:170883625 C>T maps to NM_003862.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:170883544 C>A maps to NM_003862.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:170883661 G>A maps to NM_003862.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr5:170863107 C>G maps to NM_003862.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr11:69518052 G>A maps to NM_005117.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr19:49260234 C>A maps to NM_019113.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:643534 G>C maps to NM_020637.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr12:4479724 G>A maps to NM_020638.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:4479889 G>A maps to NM_020638.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr11:69625120 G>A maps to NM_005247.2 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:81196159 T>C maps to NM_004464.3 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr12:4554415 G>A maps to NM_020996.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr12:4554595 C>T maps to NM_020996.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:103531217 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:22275427 C>A maps to NM_002010.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:22275387 G>A maps to NM_002010.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr13:22275427 C>T maps to NM_002010.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:15964673 C>A maps to NM_031950.3 G27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:15964407 G>A maps to NM_031950.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:38271462 G>A maps to NM_001174067.1 D786D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr8:38275475 G>A maps to NM_001174067.1 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:38279324 G>A maps to NM_001174067.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:38273507 G>T maps to NM_001174067.1 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:38271764 G>A maps to NM_001174067.1 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:27113509 T>C maps to NM_015633.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:123244910 T>C maps to ENST00000351936 E751E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:123279675 C>T maps to ENST00000351936 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr10:123244997 C>T maps to ENST00000351936 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:123279675 C>T maps to ENST00000351936 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr4:1807567 C>T maps to NM_000142.4 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:1803601 G>A maps to NM_000142.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:1801005 G>A maps to NM_000142.4 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:176524325 G>A maps to NM_213647.1 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:176524577 C>T maps to NM_213647.1 D770D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr4:1016195 C>T maps to NM_021923.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:1018156 C>T maps to NM_021923.3 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:1018876 G>A maps to NM_021923.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:1018192 C>T maps to NM_021923.3 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:59811946 G>A maps to NM_001113411.1 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:60106989 G>A maps to NM_001113411.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:60125949 A>G maps to NM_001113411.1 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:17739682 G>A maps to NM_201552.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:76825712 G>A maps to NM_006682.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr7:76828645 A>G maps to NM_006682.2 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:27949551 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:27939439 G>A maps to NM_005248.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:241672067 A>G maps to NM_000143.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:153896632 T>C maps to NM_033393.2 D730D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:153895834 C>T maps to NM_033393.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:153896473 A>C maps to NM_033393.2 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:153896827 C>T maps to NM_033393.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:153897217 G>T maps to NM_033393.2 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:153897211 A>G maps to NM_033393.2 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr3:60522602 C>A maps to NM_002012.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:59999864 G>A maps to NM_002012.2 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:135290002 C>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:135292048 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:135291439 A>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:135290660 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:135288661 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:135290722 A>C did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr6:97052642 C>T maps to NM_020482.4 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:97052726 C>T maps to NM_020482.4 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr6:97058455 T>G maps to NM_020482.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:67271644 C>T maps to NM_013241.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:67271632 C>T maps to NM_013241.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:67271560 G>A maps to NM_013241.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr18:34156415 T>C maps to NM_025135.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr18:34205505 C>T maps to NM_025135.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:34310606 A>C did not map to a codon.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr18:34340741 C>T maps to NM_025135.2 R1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:133805406 G>A maps to NM_001145106.1 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:27016105 C>T maps to NM_203371.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:65652090 G>A maps to NM_198897.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:65651888 C>T maps to NM_198897.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:108912564 A>G maps to NM_007076.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:108912783 C>T maps to NM_007076.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:108912981 C>T maps to NM_007076.2 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:108910877 G>A maps to NM_007076.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:108913185 G>A maps to NM_007076.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:110048402 C>T maps to NM_014845.5 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr6:110048333 C>G maps to NM_014845.5 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr23:15402055 A>T did not map to a codon.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr23:15381402 C>A did not map to a codon.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr23:15365303 A>G did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:15402023 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:164467531 C>T maps to NM_018086.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:164467864 T>C maps to NM_018086.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:164467696 A>G maps to NM_018086.2 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:164466808 C>T maps to NM_018086.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:164466843 C>A maps to NM_018086.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:50514361 A>G maps to NM_022116.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:50513107 A>G maps to NM_022116.3 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:50513893 T>A maps to NM_022116.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:50513344 C>T maps to NM_022116.3 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr7:50514331 T>C maps to NM_022116.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:50514211 C>T maps to NM_022116.3 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:50514187 A>G maps to NM_022116.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:76023156 A>G maps to NM_015687.2 D797D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:76022148 C>T maps to NM_015687.2 P1133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:76018592 G>T maps to NM_015687.2 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr6:76063346 G>T maps to NM_015687.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:76022913 G>A maps to NM_015687.2 N878N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:76024860 A>G maps to NM_015687.2 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:76024841 G>A maps to NM_015687.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:76024479 C>T maps to NM_015687.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:99567351 A>G maps to NM_001042459.1 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:99568035 A>G maps to NM_001042459.1 Y828Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:99569706 A>G maps to NM_001042459.1 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:99569757 G>T maps to NM_001042459.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr3:99568538 G>A maps to NM_001042459.1 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr3:99569564 G>A maps to NM_001042459.1 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr3:99569911 A>T maps to NM_001042459.1 L203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:99569424 G>A maps to NM_001042459.1 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:54324829 C>T maps to NM_030917.3 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:54325483 C>T maps to NM_030917.3 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:54245410 G>A maps to NM_030917.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:54244046 C>T maps to NM_030917.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:54324898 C>T maps to NM_030917.3 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr14:24601698 C>T maps to NM_203402.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr14:24601500 G>A maps to NM_203402.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr20:42935515 G>A maps to NM_001080472.1 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:56104136 C>G maps to NM_032836.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:56104133 G>A maps to NM_032836.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:35640852 G>A maps to NM_014344.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:35641110 C>A maps to NM_014344.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:39974509 C>T maps to NM_021939.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:39977934 C>T maps to NM_021939.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:49318419 T>C maps to NM_016594.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:115945144 A>G maps to ENST00000446284 Y630Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:115959247 C>T maps to ENST00000446284 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:115931874 T>C maps to ENST00000446284 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:115936845 T>C maps to ENST00000446284 K772K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr9:115959232 C>A maps to ENST00000446284 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:115948582 G>A maps to ENST00000446284 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:24285953 G>A maps to NM_004116.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:24285968 C>A maps to NM_004116.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:45599092 A>G maps to NM_002013.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:2907921 C>T maps to NM_002014.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:35547911 C>T maps to NM_001145775.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:18652560 G>A maps to NM_012181.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr19:18650399 C>T maps to NM_012181.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:18652693 C>T maps to NM_012181.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:33042306 T>C maps to NM_007270.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr7:33014947 C>T maps to NM_007270.3 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:33014896 G>A maps to NM_007270.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:32097116 G>A maps to NM_022110.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr9:108358938 G>A did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr17:17127307 G>T maps to NM_144997.5 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:17127262 G>A maps to NM_144997.5 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:17117129 G>A maps to NM_144997.5 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:17117097 G>A maps to NM_144997.5 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr17:17119727 C>T maps to NM_144997.5 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:17122404 G>T maps to NM_144997.5 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:17129579 G>T maps to NM_144997.5 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:152283155 T>C maps to NM_002016.1 S1402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:152283083 G>A maps to NM_002016.1 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:152282225 T>C maps to NM_002016.1 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:152285765 G>A maps to NM_002016.1 H532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:152284169 C>T maps to NM_002016.1 W1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:152283878 A>G maps to NM_002016.1 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:152276315 G>A maps to NM_002016.1 H3682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:152282030 G>A maps to NM_002016.1 S1777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr1:152285860 G>A maps to NM_002016.1 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:152281388 C>T maps to NM_002016.1 A1991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:152285027 G>A maps to NM_002016.1 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:152285860 G>A maps to NM_002016.1 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:152278661 A>G maps to NM_002016.1 H2900H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:152278748 T>C maps to NM_002016.1 S2871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:152280491 G>A maps to NM_002016.1 A2290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:152280572 C>A maps to NM_002016.1 A2263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:152280596 A>G maps to NM_002016.1 D2255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:152283116 T>C maps to NM_002016.1 Q1415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152276354 T>C maps to NM_002016.1 G3669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152279150 A>C maps to NM_002016.1 S2737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152285753 T>C maps to NM_002016.1 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152286131 G>A maps to NM_002016.1 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr1:152278832 A>G maps to NM_002016.1 N2843N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:152282657 G>A maps to NM_002016.1 A1568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr1:152276816 G>A maps to NM_002016.1 S3515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr1:152284142 A>G maps to NM_002016.1 D1073D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr1:152277421 T>A maps to NM_002016.1 R3314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr1:152282996 G>A maps to NM_002016.1 H1455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:152287064 G>A maps to NM_002016.1 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:152276339 T>C maps to NM_002016.1 S3674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:152279958 G>C maps to NM_002016.1 S2468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:152283236 G>A maps to NM_002016.1 H1375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:152282728 T>G maps to NM_002016.1 R1545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:152280890 C>T maps to NM_002016.1 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr1:152277359 C>A maps to NM_002016.1 G3334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:152283659 C>T maps to NM_002016.1 G1234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr1:152277296 C>A maps to NM_002016.1 V3355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:152280935 C>T maps to NM_002016.1 P2142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:152279183 G>A maps to NM_002016.1 G2726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:152286866 T>C maps to NM_002016.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:152279698 C>A maps to NM_002016.1 E2555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:152277474 G>T maps to NM_002016.1 S3296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:152284760 T>C maps to NM_002016.1 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr1:152284616 T>C maps to NM_002016.1 E915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:152286566 G>T maps to NM_002016.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr1:152325464 G>A maps to NM_001014342.2 Y1599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:152326949 T>C maps to NM_001014342.2 Q1104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:152323457 T>G maps to NM_001014342.2 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:152325464 G>A maps to NM_001014342.2 Y1599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr1:152327387 G>T maps to NM_001014342.2 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr1:152327122 G>A maps to NM_001014342.2 Q1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr1:152329103 T>G maps to NM_001014342.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:152328722 T>C maps to NM_001014342.2 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:152325455 G>A maps to NM_001014342.2 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr1:152329418 A>C maps to NM_001014342.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:152331354 G>A maps to NM_001014342.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:152328119 T>A maps to NM_001014342.2 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:128638141 C>T maps to NM_002017.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr11:128680435 G>T maps to NM_002017.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr11:128679073 G>T maps to NM_002017.3 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:128680621 C>T maps to NM_002017.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:128680441 C>T maps to NM_002017.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:128628086 C>T maps to NM_002017.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:18154277 G>A maps to NM_002018.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:18148505 G>A maps to NM_002018.2 H1252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:18148974 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:21542395 G>A maps to NM_018071.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr14:21543326 C>T maps to NM_018071.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:21542131 G>A maps to NM_018071.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr14:21543172 C>T maps to NM_018071.3 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:21547084 C>T maps to NM_018071.3 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:142517186 G>A maps to NM_207414.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:84607322 C>T maps to NM_001001670.2 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:84609581 T>G maps to NM_001001670.2 T1399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:84608051 C>A maps to NM_001001670.2 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr9:84606104 C>A maps to NM_001001670.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:84608291 T>C maps to NM_001001670.2 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:84607679 C>T maps to NM_001001670.2 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr9:84608946 A>C maps to NM_001001670.2 R1188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr9:84606816 G>T maps to NM_001001670.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr9:84609974 T>G maps to NM_001001670.2 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:84607907 C>A maps to NM_001001670.2 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:153592919 C>A did not map to a codon.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr23:153593614 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:153585837 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:153577240 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153579954 G>A did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr23:153594680 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:153596211 G>A did not map to a codon.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr23:153587983 C>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:153588106 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153581381 A>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:153593585 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:153599570 C>T did not map to a codon.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr23:153586886 G>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:153592918 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153581804 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153595184 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:153587360 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153593796 C>T did not map to a codon.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr23:153594995 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:153592412 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:153596064 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:153596064 C>T did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:153580565 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:153583312 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153578114 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153588877 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153593011 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153594736 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:153591074 G>A did not map to a codon.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr23:153579999 A>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:153585943 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr23:153591143 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:153588684 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:153594461 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:153578053 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:153590102 G>T did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:153592920 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153581468 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:58129200 A>T maps to NM_001164317.1 G1793G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:58155347 C>T maps to NM_001164317.1 N2514N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:58104627 T>C maps to NM_001164317.1 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:58121815 C>T maps to NM_001164317.1 Y1625Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr3:58109298 C>G maps to NM_001164317.1 Y1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:58080593 G>A maps to NM_001164317.1 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:58131772 G>T maps to NM_001164317.1 E1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr3:58134045 C>T maps to NM_001164317.1 R1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:58094187 C>T maps to NM_001164317.1 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:58131753 C>T maps to NM_001164317.1 I1875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:58121815 C>T maps to NM_001164317.1 Y1625Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr3:58064474 G>A maps to NM_001164317.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:58112361 T>C maps to NM_001164317.1 V1365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr3:58111471 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:128483510 C>T maps to NM_001458.4 A897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:128470735 C>T maps to NM_001458.4 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:128470876 C>T maps to NM_001458.4 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:128486418 C>T maps to NM_001458.4 G1343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:128495310 G>T maps to NM_001458.4 V2398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:128497220 C>A maps to NM_001458.4 A2537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:128488743 C>T maps to NM_001458.4 G1570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:128486948 G>A maps to NM_001458.4 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:128498534 C>T maps to NM_001458.4 D2712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:128496835 C>T maps to NM_001458.4 G2474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:128494554 C>T maps to NM_001458.4 S2272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr7:128487898 G>C maps to NM_001458.4 V1479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:128482406 C>T maps to NM_001458.4 N748N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:128470735 C>T maps to NM_001458.4 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr7:128492693 C>T maps to NM_001458.4 D1964D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:128482428 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:27207774 G>A maps to ENST00000394906 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:27208829 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:63884683 C>T maps to NM_013280.4 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:63884887 G>A maps to NM_013280.4 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:63884233 C>T maps to NM_013280.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:63884461 C>T maps to NM_013280.4 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:63885481 C>T maps to NM_013280.4 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:86089441 C>T maps to NM_013231.4 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr14:86087926 C>A maps to NM_013231.4 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr14:86088580 G>A maps to NM_013231.4 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:86088133 G>A maps to NM_013231.4 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:86089273 C>T maps to NM_013231.4 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:14306568 A>C maps to NM_198391.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr20:14306205 T>G maps to NM_198391.2 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:14307225 G>A maps to NM_198391.2 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:14306859 T>C maps to NM_198391.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr20:14306394 G>A maps to NM_198391.2 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr13:29001982 G>A maps to NM_002019.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:29001438 G>A maps to NM_002019.4 Y431Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr13:29008006 A>G maps to NM_002019.4 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr13:28903857 G>T maps to NM_002019.4 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr13:29012429 G>A maps to NM_002019.4 H147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr13:28877423 G>A maps to NM_002019.4 H1299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr13:28877303 C>T maps to NM_002019.4 *1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:28880897 G>A maps to NM_002019.4 G1244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr13:28895659 A>T maps to NM_002019.4 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:28885866 A>G maps to NM_002019.4 D1165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:28877423 G>A maps to NM_002019.4 H1299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:28608270 T>C maps to NM_004119.2 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:28626755 G>A maps to NM_004119.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:28611390 C>A maps to NM_004119.2 G414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr13:28636173 C>T maps to NM_004119.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:28608282 G>A maps to NM_004119.2 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:49983618 G>A maps to NM_001459.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:180048189 G>A maps to NM_182925.4 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr5:180030233 G>T maps to NM_182925.4 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:180048229 C>T maps to NM_182925.4 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr5:180045908 G>T maps to NM_182925.4 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:180047710 G>A maps to NM_182925.4 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr5:180057789 G>A maps to NM_182925.4 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr5:180057714 C>A maps to NM_182925.4 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:180047182 C>T maps to NM_182925.4 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr5:180039517 G>A maps to NM_182925.4 G1175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:180050991 G>A maps to NM_182925.4 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:180039543 C>A maps to NM_182925.4 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:213032159 C>T maps to NM_014053.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr15:33358801 C>T maps to NM_001103184.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:33359554 A>C maps to NM_001103184.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr15:33360042 C>A maps to NM_001103184.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:33359422 G>A maps to NM_001103184.2 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:33359152 C>T maps to NM_001103184.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:240256746 G>A maps to ENST00000406993 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:240497203 T>C maps to ENST00000406993 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr1:240256758 C>A maps to ENST00000406993 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr1:240555823 A>G maps to ENST00000406993 Q1767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:240255579 C>T maps to ENST00000406993 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:240371912 G>A maps to ENST00000406993 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:240256611 C>T maps to ENST00000406993 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:240370964 G>A maps to ENST00000406993 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr1:240256749 G>A maps to ENST00000406993 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:240370991 C>T maps to ENST00000406993 P1103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr1:240371483 A>T maps to ENST00000406993 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:240256068 G>A maps to ENST00000406993 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:240371408 G>A maps to ENST00000406993 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:240255951 G>T maps to ENST00000406993 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:240371492 G>A maps to ENST00000406993 A1270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:43317919 G>A maps to NM_005892.3 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr17:43314721 C>A maps to NM_005892.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:43318566 C>T maps to NM_005892.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:43318960 T>C maps to NM_005892.3 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:43322381 C>T maps to NM_005892.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr17:43323027 C>T maps to NM_005892.3 F974F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr17:43320549 C>A maps to NM_005892.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:153475529 A>C maps to NM_052905.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:153488587 G>T maps to NM_052905.3 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:153483214 T>C maps to NM_052905.3 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:50041554 G>A maps to NM_175736.4 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:50050606 T>G maps to NM_175736.4 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr12:50052241 C>T maps to NM_175736.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr12:50043300 C>T maps to NM_175736.4 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr1:171251384 C>T maps to NM_002021.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr1:171154908 G>A maps to NM_001460.2 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:171076862 C>T maps to NM_006894.5 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:171300893 T>G maps to NM_002022.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:171300851 C>T maps to NM_002022.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:171303825 C>T maps to NM_002022.1 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr1:146684984 C>T maps to NM_001461.2 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:146683978 A>G maps to NM_001461.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:203317278 A>G maps to NM_002023.3 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:147027083 G>A did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:147024688 T>C did not map to a codon.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr23:147007064 C>G did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:147026474 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:147009865 G>A did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr23:147011747 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr23:147013988 A>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:147010199 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:147019097 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:147011718 T>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:147030285 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:147010205 T>C did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:147009863 G>C did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:147088342 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:147106455 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:147106429 G>T did not map to a codon.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr23:147084749 C>A did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:147088343 T>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:216269110 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:216273120 G>A maps to NM_212482.1 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:216236931 C>A maps to NM_212482.1 G2138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:216249628 A>G maps to NM_212482.1 A1561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:216299476 C>T maps to NM_212482.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:216272918 C>T maps to NM_212482.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:216288949 G>A maps to NM_212482.1 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:216269190 A>G maps to NM_212482.1 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:216273075 A>T maps to NM_212482.1 Y791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:216245648 A>G maps to NM_212482.1 G1773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:216288118 T>C maps to NM_212482.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr2:216232682 G>A maps to NM_212482.1 A2307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:216272843 C>T maps to NM_212482.1 Q835Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:216293029 G>T maps to NM_212482.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:216274340 C>T maps to NM_212482.1 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:216226781 G>A maps to NM_212482.1 C2424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:216229622 G>A maps to NM_212482.1 C2410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:216248174 G>A maps to NM_212482.1 T1642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:216226285 G>A maps to NM_212482.1 R2476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:216288949 G>A maps to NM_212482.1 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:216271856 T>C maps to NM_212482.1 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:216246971 G>A maps to NM_212482.1 S1709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:216300402 G>A maps to NM_212482.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr2:216259305 A>C maps to NM_212482.1 V1247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:80684411 C>A maps to NM_024619.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:80680763 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:94001887 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:47744590 A>T maps to NM_015308.2 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:47765531 G>A maps to NM_015308.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:47744587 T>A maps to NM_015308.2 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:47754207 G>A maps to NM_015308.2 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:47744608 T>A maps to NM_015308.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:47776157 G>A maps to NM_015308.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:47776214 G>A maps to NM_015308.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:47776172 A>G maps to NM_015308.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:49705292 T>C maps to NM_001079673.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:49772302 C>A maps to NM_001079673.1 I892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr13:49772647 T>G maps to NM_001079673.1 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:172065072 A>G maps to NM_022763.3 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:172013304 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:131008483 C>T maps to NM_133372.2 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:131042174 A>G maps to NM_133372.2 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:131055059 G>A maps to NM_133372.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:159789545 A>G maps to ENST00000379346 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr4:159790448 T>C maps to ENST00000379346 I910I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr4:159756588 G>T maps to ENST00000379346 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:159790070 G>A maps to ENST00000379346 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:42939921 T>C maps to NM_002027.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:42939924 T>C maps to NM_002027.2 H306H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr14:65521394 C>T maps to ENST00000448390 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr14:65507580 C>T maps to ENST00000448390 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:65520040 G>A maps to ENST00000448390 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:65494204 G>T maps to ENST00000448390 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:65520028 C>T maps to ENST00000448390 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-5721-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr11:49170269 T>G maps to NM_004476.1 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:49229937 G>A maps to NM_004476.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr11:89421770 G>T maps to NM_153696.2 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:89424666 C>T maps to NM_153696.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:71906953 C>T maps to NM_016729.2 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:71850829 G>A maps to ENST00000442948 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:71850032 C>T maps to ENST00000442948 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:94040767 C>T maps to NM_001080486.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:45976209 C>T maps to NM_006732.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:28627026 C>T maps to NM_005253.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:28631708 G>T maps to NM_005253.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr14:38061193 G>T maps to NM_004496.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:38061520 G>A maps to NM_004496.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:22563594 G>A maps to NM_021784.4 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr20:22564867 C>A maps to NM_021784.4 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:46375538 C>T maps to NM_004497.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr19:46375694 C>G maps to NM_004497.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr15:60297452 C>T maps to NM_012182.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:60297515 G>A maps to NM_012182.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:60297959 G>A maps to NM_012182.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:60297941 C>A maps to NM_012182.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:79635850 G>A maps to NM_001013735.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:79634779 C>A maps to NM_001013735.1 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr9:79634959 C>T maps to NM_001013735.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:79635082 G>A maps to NM_001013735.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:79635622 G>A maps to NM_001013735.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:79635217 G>A maps to NM_001013735.1 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:79635343 G>T maps to NM_001013735.1 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:79635349 G>C maps to NM_001013735.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:79634611 G>A maps to NM_001013735.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:79634950 G>A maps to NM_001013735.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:86601057 C>T maps to NM_005251.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr16:86601966 C>T maps to NM_005251.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:86601222 C>T maps to NM_005251.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:86602287 C>T maps to NM_005251.2 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr16:86601238 C>T maps to NM_005251.2 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:47905015 C>T maps to NM_004474.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:63789967 G>A maps to NM_012183.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:63789163 G>A maps to NM_012183.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:63790036 G>A maps to NM_012183.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:117618 G>A maps to NM_207305.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:117534 C>T maps to NM_207305.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:116988 G>A maps to NM_207305.3 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:116841 C>T maps to NM_207305.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:114257504 C>T maps to NM_012184.4 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:114257060 C>T maps to NM_012184.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:70919006 C>T maps to NM_199135.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:70177146 G>A maps to NM_001126334.1 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:70177104 C>T maps to NM_001126334.1 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr9:100616579 G>A maps to NM_004473.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:100617251 C>T maps to NM_004473.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100616669 G>T maps to NM_004473.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:47882313 C>T maps to NM_012186.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:86544747 C>T maps to NM_001451.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:86544714 G>A maps to NM_001451.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr6:1390808 C>T maps to NM_001452.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr14:29237756 G>A maps to NM_005249.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr14:29237783 C>A maps to NM_005249.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr14:29237468 C>T maps to NM_005249.3 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:29237390 C>T maps to NM_005249.3 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:29237591 C>T maps to NM_005249.3 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr14:29237639 C>T maps to NM_005249.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr14:29237813 G>A maps to NM_005249.3 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:169533488 G>A maps to NM_012188.4 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:169533116 C>T maps to NM_012188.4 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:129536817 C>T maps to NM_207426.2 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:129536845 C>T maps to NM_207426.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:74134075 G>A maps to NM_001454.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr17:74134138 G>A maps to NM_001454.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:74136101 C>T maps to NM_001454.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:8200529 T>C maps to NM_018416.2 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr12:8203211 C>T maps to NM_018416.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:42776749 T>A maps to NM_001198850.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:42693607 C>T maps to NM_001198850.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:42657106 T>C maps to NM_001198850.1 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:4796711 C>T maps to ENST00000450194 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr7:4800737 G>A maps to ENST00000450194 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:4800719 G>A maps to ENST00000450194 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr7:4796711 C>T maps to ENST00000450194 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:80521331 C>T maps to NM_004514.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:80543921 C>T maps to NM_004514.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr17:80559218 C>T maps to NM_004514.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:80477946 G>A maps to NM_004514.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:86612373 G>A maps to NM_005250.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:86612388 G>A maps to NM_005250.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:86613222 G>T maps to NM_005250.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:86612469 G>A maps to NM_005250.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:138665126 G>C maps to NM_023067.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:2983599 C>T maps to NM_202002.1 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:2983278 C>T maps to NM_202002.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr12:2968019 A>T maps to NM_202002.1 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:2981272 G>A maps to NM_202002.1 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr17:26851591 A>C maps to NM_003593.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:26851945 G>A maps to NM_003593.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:26851810 C>T maps to NM_003593.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:48602419 A>G maps to NM_002158.3 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:48602512 A>G maps to NM_002158.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:48602441 C>T maps to NM_002158.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:48602242 C>T maps to NM_002158.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:48589833 C>T maps to NM_002158.3 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:89878418 G>A maps to NM_001085471.1 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr14:89878583 C>T maps to NM_001085471.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr12:109719323 C>A maps to NM_213596.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:109719236 C>T maps to NM_213596.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr12:109719350 G>A maps to NM_213596.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:41134253 C>T maps to NM_002015.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr13:41134247 T>C maps to NM_002015.3 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:41134253 C>T maps to NM_002015.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr13:41134409 C>T maps to NM_002015.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:41134523 G>A maps to NM_002015.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr6:108985298 G>A maps to NM_001455.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr6:108985241 G>A maps to NM_001455.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:70320654 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:70316713 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:70320818 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:70321312 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:70320702 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:70320594 C>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:70321550 A>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:70321309 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:71247409 C>T maps to NM_032682.4 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:71247445 G>A maps to NM_032682.4 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:71015108 G>A maps to NM_032682.4 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:71247403 G>A maps to NM_032682.4 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:71015108 G>A maps to NM_032682.4 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:71247445 G>A maps to NM_032682.4 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr7:114269984 A>G maps to NM_148898.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr7:114210929 A>T maps to NM_148898.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr7:114298185 T>G maps to NM_148898.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:114298149 G>A maps to NM_148898.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr7:114299724 G>A maps to NM_148898.3 W573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:114304350 A>G maps to NM_148898.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:114269963 G>A maps to NM_148898.3 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr7:114282670 C>T maps to NM_148898.3 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:114298279 C>T maps to NM_148898.3 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:49110449 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:49107880 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:41566655 G>A maps to NM_001012426.1 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:41533593 C>T maps to NM_001012426.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:41533641 G>A maps to NM_001012426.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:41562612 C>T maps to NM_001012426.1 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:41553173 G>A maps to NM_001012426.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr6:1313595 C>T maps to NM_033260.3 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:118851385 C>T maps to NM_181721.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118851223 G>A maps to NM_181721.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:55650538 C>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:55650329 G>A did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:55650730 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:55650414 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:126146976 G>A maps to NM_017547.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:126145766 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:126147470 C>T maps to NM_017547.3 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:36897390 G>A maps to NM_001102371.1 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr22:36892206 C>G maps to NM_001102371.1 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:30433126 G>A maps to NM_004118.3 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:130572386 T>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:130571112 C>T maps to NM_004957.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr9:130566590 C>T maps to NM_004957.4 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr1:74664040 A>C maps to NM_001112808.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:74670753 T>C maps to NM_003838.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:52250103 G>A maps to NM_002029.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:52249509 G>A maps to NM_002029.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr19:52272261 T>G maps to NM_001005738.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:52272774 C>T maps to NM_001005738.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:52328044 G>A maps to NM_002030.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:52327576 C>T maps to NM_002030.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:52327282 C>A maps to NM_002030.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr10:95441292 G>C maps to NM_145246.4 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:95445099 T>C maps to NM_145246.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:95447190 G>A maps to NM_145246.4 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:95458055 A>G did not map to a codon.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr10:95441347 C>A maps to NM_145246.4 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr4:79229314 G>T maps to NM_025074.6 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:79420975 C>T maps to NM_025074.6 Q3073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr4:79293924 C>T maps to NM_025074.6 Q975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:99093645 G>T maps to NM_012083.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:14775837 G>A maps to ENST00000380880 G1605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:14842569 G>A maps to ENST00000380880 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:14784440 G>A maps to ENST00000380880 Q1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:14842485 C>T maps to ENST00000380880 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:14813041 C>T maps to ENST00000380880 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:14748530 A>G maps to ENST00000380880 G1891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr9:14748593 G>A maps to ENST00000380880 S1870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr9:14859322 A>C maps to ENST00000380880 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:14859190 G>A maps to ENST00000380880 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:14737552 G>A maps to ENST00000380880 I2130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr13:39262146 C>T maps to NM_207361.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:39265722 C>T maps to NM_207361.4 I1414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr13:39343782 C>T maps to NM_207361.4 Q1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:39432106 C>T maps to NM_207361.4 D2384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr13:39262882 T>C maps to NM_207361.4 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr13:39264486 G>A maps to NM_207361.4 E1002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:39435610 G>A maps to NM_207361.4 P2521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:39448721 C>T maps to NM_207361.4 P2760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr13:39448643 C>T maps to NM_207361.4 R2734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr13:39262882 T>C maps to NM_207361.4 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:39262101 C>T maps to NM_207361.4 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:39262269 C>T maps to NM_207361.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr13:39438622 C>T maps to NM_207361.4 S2621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr13:39262113 C>T maps to NM_207361.4 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr13:39425245 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:39425964 C>T maps to NM_207361.4 G2295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:39261552 G>A maps to NM_207361.4 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:39420859 G>A did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr6:168465673 G>A maps to NM_024919.3 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:168457998 C>A maps to NM_024919.3 G476G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-6452-01A-12D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr9:86004623 C>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:85964664 T>C maps to NM_174938.4 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr9:86153104 G>A maps to NM_174938.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:13824972 A>G maps to NM_018027.3 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr10:13701381 G>A maps to NM_018027.3 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:69246142 G>A maps to NM_015123.1 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:69299229 G>A maps to NM_015123.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:69435089 G>A maps to NM_015123.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:44198147 C>T maps to NM_032892.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr14:52187079 C>T maps to ENST00000344768 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:52186866 G>A maps to ENST00000344768 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:52178271 G>A maps to ENST00000344768 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr14:52174909 C>T maps to ENST00000344768 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:52174909 C>T maps to ENST00000344768 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr23:131212785 T>C did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:131220026 T>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:131216452 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:131211939 T>A did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr23:131212238 A>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:131214289 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:131212882 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:65178713 C>T maps to NM_031904.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:65161803 C>T maps to NM_031904.3 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:37744581 A>G maps to NM_014907.2 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr9:37740285 C>T maps to NM_014907.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr9:37745802 A>G maps to NM_014907.2 E1258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:37745883 T>C maps to NM_014907.2 S1285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr9:37746717 C>A maps to NM_014907.2 A1563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:49420095 G>A maps to NM_001018071.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:49446166 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:49450201 A>G did not map to a codon.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr10:49482598 T>C maps to NM_001018071.3 L4L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4G9-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:49459732 G>A maps to NM_001018071.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:49457096 T>C maps to NM_001018071.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:12712492 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:12736507 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:12722593 C>T did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr23:12736051 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:12734368 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:12736058 A>G did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:12735633 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:12701696 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:12728601 A>G did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:12736164 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:12627881 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:12734821 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:12736156 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:12735697 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:12736294 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:12734917 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:100195231 G>A maps to NM_001013660.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:69968695 T>C maps to NM_006654.3 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:69968090 C>T maps to NM_006654.3 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:41739172 C>T maps to NM_006653.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:41739085 C>T maps to NM_006653.3 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:41738914 C>T maps to NM_006653.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:32821626 C>T maps to NM_023037.2 F2332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:32792900 C>A maps to NM_023037.2 I1566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:32808831 A>G maps to NM_023037.2 A1883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:32841345 G>A maps to NM_023037.2 S2662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:32783062 G>A maps to NM_023037.2 L1364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:32721439 C>T maps to NM_023037.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:32776593 C>T maps to NM_023037.2 S1316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:32821605 G>A maps to NM_023037.2 G2325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr13:32868605 C>T maps to NM_023037.2 S2894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:32653053 C>T maps to NM_023037.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr13:32776518 C>A maps to NM_023037.2 Y1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr13:32811573 G>T maps to NM_023037.2 G1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:32808877 G>T maps to NM_023037.2 E1899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr13:32711036 C>G maps to NM_023037.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:32811639 C>T maps to NM_023037.2 Q1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr13:32705856 G>A maps to NM_023037.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr13:32868620 G>A maps to NM_023037.2 T2899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:32749687 C>T maps to NM_023037.2 D780D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr13:32729635 C>T maps to NM_023037.2 N496N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:48591778 C>T maps to NM_015030.1 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr4:48592823 G>A maps to NM_015030.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:48572886 G>A maps to NM_015030.1 R985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr4:48564916 G>A maps to NM_015030.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:183731238 G>A maps to NM_001463.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:183731001 C>T maps to NM_001463.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:183730944 G>A maps to NM_001463.3 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:183731028 C>T maps to NM_001463.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:44976166 A>G maps to NM_032135.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:44976055 G>T maps to NM_032135.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr14:44975245 T>C maps to NM_032135.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:44975347 C>T maps to NM_032135.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr14:44974297 G>A maps to NM_032135.3 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:5643548 C>T maps to ENST00000340250 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:5644942 G>A maps to ENST00000340250 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:5632671 G>A maps to ENST00000340250 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:5633136 C>T maps to ENST00000340250 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:79495835 G>A maps to NM_001077182.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:127235918 T>C maps to NM_020369.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr7:127235722 C>T maps to NM_020369.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:127239579 C>T maps to NM_020369.2 C422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:4318364 G>A maps to NM_024333.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:4318415 C>T maps to NM_024333.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:4323384 G>A maps to NM_024333.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:4323028 C>T maps to NM_024333.2 Y362Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:83451612 A>G maps to NM_001007122.2 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:83456127 C>T maps to NM_001007122.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:83451558 C>A maps to NM_001007122.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:83451732 G>A maps to NM_001007122.2 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:83433915 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr15:83434003 G>A maps to NM_001007122.2 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:49189949 G>A maps to NM_000145.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:49190888 T>C maps to NM_000145.3 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr2:49216183 T>C maps to NM_000145.3 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:40005644 C>T maps to NM_152597.4 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:39910002 A>G maps to NM_152597.4 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:40057944 C>A maps to NM_152597.4 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:40018787 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:40034090 A>G maps to NM_152597.4 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr2:186671019 C>T maps to NM_173651.2 Q5752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:186671180 T>C maps to NM_173651.2 N5805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:186678387 T>C maps to NM_173651.2 I6737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:186670649 T>A maps to NM_173651.2 V5628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:186673679 A>G maps to NM_173651.2 Q6638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr2:186678561 G>T maps to NM_173651.2 T6795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:186670734 A>C maps to NM_173651.2 R5657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:186670613 T>A maps to NM_173651.2 I5616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:186689208 T>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:186669821 T>C maps to NM_173651.2 G5352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:132560965 G>A maps to NM_015082.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:132560965 G>A maps to NM_015082.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr5:132545909 G>A maps to NM_015082.1 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:132561500 G>A maps to NM_015082.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:163032430 G>A maps to NM_020116.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:162307354 A>T maps to NM_020116.3 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr4:162508613 T>C maps to NM_020116.3 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr4:162508605 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:163032430 G>A maps to NM_020116.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:162459393 A>G maps to NM_020116.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:162307294 T>C maps to NM_020116.3 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr4:162307120 C>A maps to NM_020116.3 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:162307518 A>G maps to NM_020116.3 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr4:162307021 A>G maps to NM_020116.3 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr21:47574135 C>T maps to ENST00000397748 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr21:47574135 C>T maps to ENST00000397748 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr21:47571483 G>A maps to ENST00000397748 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:31089730 T>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:31090061 G>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr19:49469091 C>G maps to NM_000146.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:121187846 C>T maps to NM_177478.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:121188032 C>T maps to NM_177478.1 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr16:53913790 C>T maps to NM_001080432.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:54145699 T>A maps to NM_001080432.2 L464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48337070 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48339901 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48340053 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:48337472 G>A did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:61898449 G>A maps to NM_017647.3 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:61897299 T>A maps to NM_017647.3 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:61902761 A>G maps to NM_017647.3 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:61902274 A>G maps to NM_017647.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr17:61897523 T>G maps to NM_017647.3 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:61897226 T>G maps to NM_017647.3 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:61902523 C>A did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr16:71319388 T>C maps to NM_018348.5 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr16:71317996 A>G maps to NM_018348.5 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:37403506 A>G maps to NM_015050.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:37418079 T>C maps to NM_015050.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr6:37430703 C>T maps to NM_015050.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:78425902 A>T maps to ENST00000436586 Y535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:78429942 C>T maps to ENST00000436586 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:78430611 C>T maps to ENST00000436586 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:78429830 G>A maps to ENST00000436586 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:133511485 G>A maps to NM_003934.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:133501833 C>T maps to NM_003934.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:143823102 G>A maps to NM_032020.4 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:70503176 C>T maps to NM_145059.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:70503128 C>G maps to NM_145059.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:70497628 C>T maps to NM_145059.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:70497628 C>T maps to NM_145059.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:154279962 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:154255309 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:154280048 T>C did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:154261742 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:154255298 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:154282920 G>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:91424193 C>T maps to NM_002569.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:91424618 C>T maps to NM_002569.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:91422154 G>A maps to NM_002569.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr16:31195218 G>C maps to NM_004960.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:31196401 T>C maps to NM_004960.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:31202335 C>T maps to NM_004960.3 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:31196422 T>C maps to NM_004960.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:49254355 C>T maps to NM_000148.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:49254454 A>G maps to NM_000148.3 H28H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:49254322 C>T maps to NM_000148.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:49253764 G>A maps to NM_000148.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:49253485 G>A maps to NM_000148.3 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr19:49253836 A>G maps to NM_000148.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr19:49254118 C>T maps to NM_000148.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:33246846 A>G maps to ENST00000380081 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr8:33246605 G>A maps to ENST00000380081 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:33247215 A>G maps to ENST00000380081 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:33310938 C>T maps to ENST00000380081 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:33310842 C>T maps to ENST00000380081 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:75532693 G>A maps to NM_173540.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:49206866 C>T maps to NM_001097638.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:49206416 A>G maps to NM_001097638.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:5844583 G>A maps to NM_001097641.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:94278117 A>G maps to NM_002033.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:94278207 C>T maps to NM_002033.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:94278033 G>C maps to NM_002033.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr11:94278699 C>A maps to NM_002033.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:5867619 G>A maps to NM_002034.2 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr19:5831738 G>A maps to NM_001040701.1 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:5832131 G>A maps to NM_001040701.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr9:139925608 C>T maps to NM_004479.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:66082938 G>A maps to NM_178155.1 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:96651600 C>T maps to NM_006581.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:50314649 G>A maps to NM_025129.4 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:50314682 C>T maps to NM_025129.4 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:50315900 C>A maps to NM_025129.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:180680861 T>C maps to NM_005087.3 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:180666220 A>G maps to NM_005087.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:180666157 T>A maps to NM_005087.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr3:180666229 A>G maps to NM_005087.3 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:35630988 G>A maps to NM_005031.3 A2A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:35648364 G>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:39203056 C>T maps to ENST00000263405 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:39202426 G>A maps to ENST00000263405 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:39202747 C>T maps to ENST00000263405 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:46008704 G>A maps to NM_024513.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:46008020 G>A maps to NM_024513.2 D935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:46011205 G>T maps to NM_024513.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:46014623 C>T maps to NM_024513.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:46008704 G>A maps to NM_024513.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr3:46008077 G>A maps to NM_024513.2 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr6:112035641 C>T maps to NM_153047.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr6:112029213 A>G maps to NM_153047.1 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:112020733 G>A maps to NM_153047.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:90895499 G>A maps to NM_003505.1 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:90894470 G>T maps to NM_003505.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:90894773 C>A maps to NM_003505.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:90896030 C>T maps to NM_003505.1 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:90895673 G>A maps to NM_003505.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr7:90895694 T>C maps to NM_003505.1 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:90894914 C>T maps to NM_003505.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:130647639 T>C maps to NM_007197.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:130648122 G>A maps to NM_007197.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:130647984 G>A maps to NM_007197.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:130648779 C>T maps to NM_007197.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr12:130647612 C>T maps to NM_007197.3 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:130648560 C>A maps to NM_007197.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:42635523 C>T maps to NM_001466.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:42635442 T>C maps to NM_001466.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr17:42636498 C>T maps to NM_001466.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr17:42636453 C>T maps to NM_001466.3 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:42636576 G>A maps to NM_001466.3 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr17:42635637 G>A maps to NM_001466.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr17:42636252 C>T maps to NM_001466.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr17:42636387 C>A maps to NM_001466.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:42636660 G>A maps to NM_001466.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:28385114 G>T maps to NM_017412.3 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:28385353 C>T maps to NM_017412.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:28413393 C>T maps to NM_017412.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr8:28385011 C>T maps to NM_017412.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:28360586 T>C maps to NM_017412.3 H19H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:86663068 G>A maps to NM_012193.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:86665895 G>A maps to NM_012193.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:86662732 G>A maps to NM_012193.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr11:86663041 C>T maps to NM_012193.2 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:208632317 G>A maps to NM_003468.3 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:208633250 C>T maps to NM_003468.3 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:208633258 G>A maps to NM_003468.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:104340602 C>T maps to NM_003506.3 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:104312356 T>C maps to NM_003506.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:104342149 C>T maps to NM_003506.3 D603D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:104341960 A>G maps to NM_003506.3 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:202900524 G>A maps to NM_003507.1 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:202900701 C>T maps to NM_003507.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:202900155 G>A maps to NM_003507.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:202900332 C>T maps to NM_003507.1 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr2:202900836 C>A maps to NM_003507.1 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:202899723 G>A maps to NM_003507.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:35929385 C>T maps to NM_031866.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:35929472 G>A maps to NM_031866.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:35928905 G>A maps to NM_031866.2 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:35929175 C>T maps to NM_031866.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:35929019 C>T maps to NM_031866.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:35929103 C>T maps to NM_031866.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:72849398 C>T maps to NM_003508.2 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:72849434 C>T maps to NM_003508.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:72849455 C>A maps to NM_003508.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:3527033 C>G maps to NM_001136198.1 Y148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr19:3533299 G>T maps to NM_001136198.1 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:31050311 A>G maps to NM_017769.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:31062797 C>T maps to NM_017769.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:151179535 T>C maps to NM_198395.1 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr5:151183480 C>T maps to NM_198395.1 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:76570766 T>C maps to NM_203505.2 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:41056040 C>A maps to NM_000151.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:41063034 A>T maps to NM_000151.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr17:41063340 C>A maps to NM_000151.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr2:169761039 C>T maps to NM_021176.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:153762670 C>T did not map to a codon.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr23:153763394 C>A did not map to a codon.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr23:153760799 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:153762273 T>C did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:153762283 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:153761217 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153760975 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:78090850 C>T maps to NM_001079804.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:78091484 G>A maps to NM_001079804.1 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:78081639 G>A maps to NM_001079804.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:78078702 C>T maps to NM_001079804.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:78081651 C>T maps to NM_001079804.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:144387374 T>C maps to NM_207123.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:144380562 A>G maps to NM_207123.2 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:144390299 A>G maps to NM_207123.2 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:77936162 G>A maps to NM_080491.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:77934560 T>C maps to NM_080491.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr11:77961261 G>A maps to NM_080491.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:77933206 G>A maps to NM_080491.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153940894 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153941520 A>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153944590 C>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:153940728 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153944424 G>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:153925469 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153906490 T>C did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:153944503 C>T did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:153924212 G>A did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr23:153941630 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:17449186 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr22:17444668 C>T maps to NM_001037814.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr22:17472780 T>G maps to NM_001037814.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:17444638 C>T maps to NM_001037814.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr22:17488992 C>T maps to NM_001037814.1 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:17473060 C>T maps to NM_001037814.1 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:10374384 G>A did not map to a codon.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr12:10373114 C>T maps to NM_031412.2 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr16:75602020 G>A maps to NM_007285.6 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr16:75611221 A>C maps to NM_007285.6 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:29589895 G>A maps to NM_001470.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:29574228 A>G maps to NM_001470.2 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr6:29591186 C>T maps to NM_001470.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:29599374 A>G maps to NM_001470.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:29599308 C>G maps to NM_001470.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:29581263 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:29595418 C>T maps to NM_001470.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:101340345 G>A maps to NM_005458.7 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:101304193 G>A maps to NM_005458.7 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:101151209 G>T maps to NM_005458.7 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr9:101148038 C>T maps to NM_005458.7 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:101258739 G>A maps to NM_005458.7 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr9:101304172 G>A maps to NM_005458.7 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:101125068 G>A maps to NM_005458.7 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:101304160 G>A maps to NM_005458.7 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr9:101065693 C>G maps to NM_005458.7 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr9:101235571 G>A maps to NM_005458.7 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr21:27136925 C>T maps to NM_002040.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:27136557 A>G maps to NM_002040.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:151076044 C>T maps to NM_144618.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:151063024 G>A maps to NM_144618.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr5:161300184 A>C maps to NM_001127648.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:161309606 G>A maps to NM_001127648.1 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:161292757 C>T maps to NM_001127648.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:161318036 A>G maps to NM_001127648.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:161322837 T>G maps to NM_001127648.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr5:161302599 G>T maps to NM_001127648.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr5:161324160 C>T maps to NM_001127648.1 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:161318018 G>A maps to NM_001127648.1 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr5:161324160 C>A maps to NM_001127648.1 Y368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:46334630 C>T did not map to a codon.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr4:46264077 A>G maps to ENST00000507069 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:46334688 A>G maps to ENST00000507069 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:46263975 C>T maps to ENST00000507069 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:151358340 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:151376567 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:151366165 G>A did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:151336799 C>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:151532938 T>C did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:151424323 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:151358314 C>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:151358275 C>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:151336737 G>A did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr23:151424319 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:151366115 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:151393245 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:151366134 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr23:151514086 G>A did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr4:46967136 A>C maps to NM_000809.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:46930535 A>C maps to NM_000809.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr4:46967013 T>C maps to NM_000809.2 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr4:46930535 A>C maps to NM_000809.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:46995417 G>A maps to NM_000809.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:46930667 A>C maps to NM_000809.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr4:46979470 C>T maps to NM_000809.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr4:46930376 A>C maps to NM_000809.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr4:46995387 G>A maps to NM_000809.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:27160003 G>A maps to NM_000810.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:27114457 C>A maps to NM_000810.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:27188485 G>A maps to NM_000810.3 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr15:27185159 C>T maps to NM_000810.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:161113334 G>A maps to NM_000811.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr4:47033960 G>A maps to NM_000812.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:47427857 C>T maps to NM_000812.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr4:47405586 C>T maps to NM_000812.3 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr4:47405724 C>T maps to NM_000812.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:26793062 T>C maps to NM_021912.4 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:26812788 C>T maps to NM_021912.4 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:26806129 T>C maps to NM_021912.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:26866630 G>A maps to NM_021912.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr15:27018862 G>A maps to NM_021912.4 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:26825567 G>A maps to NM_021912.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:1961101 C>T maps to NM_000815.4 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:151138712 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:151123858 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:151138814 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:151129821 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:151123877 T>G did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:151128319 T>C did not map to a codon.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr23:151124294 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:46053587 A>C maps to NM_173536.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr4:46053587 A>C maps to NM_173536.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:46099284 T>G maps to NM_173536.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr4:46067469 T>C maps to NM_173536.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:161520893 C>A maps to NM_198903.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr5:161530998 A>C maps to NM_198903.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:170232765 C>T maps to NM_014211.2 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:151821084 C>T did not map to a codon.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr23:151808924 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:151821313 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:151820164 C>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:151817719 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:151820032 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:151821215 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:151821167 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:151806729 A>G did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:151820192 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:151815582 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:151820207 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:151806714 T>G did not map to a codon.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr6:89907860 G>A maps to NM_002042.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:171700572 A>G maps to NM_000817.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:171716256 T>C maps to NM_000817.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr2:171713631 C>T maps to NM_000817.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:26505770 C>T maps to NM_001134366.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr10:26506780 C>T maps to NM_001134366.1 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:26506864 G>A maps to NM_001134366.1 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:26505752 C>T maps to NM_001134366.1 G5G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GU-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:49369668 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:49161404 A>T did not map to a codon.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr23:49161380 C>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:49179706 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:876505 G>A maps to NM_005255.2 N502N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr4:906521 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:30951568 G>A maps to NM_004861.1 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:30951875 G>A maps to NM_004861.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:30951161 G>A maps to NM_004861.1 H350H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr22:30951854 G>A maps to NM_004861.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:30951415 G>A maps to NM_004861.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:30952061 C>T maps to NM_004861.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr2:242741297 C>T maps to NM_022134.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:242741375 G>A maps to NM_022134.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:242742902 G>A maps to NM_022134.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:242742941 C>T maps to NM_022134.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:65810682 G>A maps to NM_033036.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:65810643 G>A maps to NM_033036.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:65810616 G>A maps to NM_033036.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:99757826 C>T maps to NM_024637.4 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:24125134 G>A maps to NM_001008216.1 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:24124304 G>A maps to NM_001008216.1 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:73754609 C>T maps to ENST00000437911 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:38903118 G>T maps to NM_138801.2 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:88901651 G>A maps to NM_000512.4 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:33263469 G>A maps to NM_020474.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:153792468 G>A maps to NM_198321.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:153789219 C>T maps to NM_198321.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:153674464 C>T maps to NM_198321.3 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:153795428 C>T maps to NM_198321.3 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:151818746 G>A maps to NM_022087.2 W604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:151800310 G>A maps to NM_022087.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:151791455 C>T maps to NM_022087.2 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr7:151805279 C>T maps to NM_022087.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:151791542 C>T maps to NM_022087.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:151805282 C>T maps to NM_022087.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:151797925 C>T maps to NM_022087.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:101602363 T>G maps to NM_024642.3 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr9:101589067 G>A maps to NM_024642.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:155102399 T>C maps to NM_052917.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:155157974 T>C maps to NM_052917.2 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr2:155115620 G>A maps to NM_052917.2 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr2:155115554 C>A maps to NM_052917.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:155102336 C>T maps to NM_052917.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr2:155102466 A>C maps to NM_052917.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:155295133 C>T maps to NM_052917.2 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr2:31165142 G>A maps to NM_024572.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:31215789 G>A maps to NM_024572.2 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:230379076 G>T maps to NM_004481.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:230372167 T>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:230372443 C>T maps to NM_004481.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:166605291 T>C maps to NM_004482.3 *634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:166611516 T>C maps to NM_004482.3 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:89917609 C>T maps to NM_003774.4 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:158115853 G>A maps to NM_014568.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:158114722 G>T maps to NM_014568.1 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:158152253 A>G maps to NM_014568.1 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:51773151 C>T maps to NM_007210.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr4:174089994 G>A maps to NM_017423.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr4:174169234 A>G maps to NM_017423.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:174219376 T>C maps to NM_017423.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:4835983 G>A maps to NM_017417.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:4848406 T>C maps to NM_017417.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:69795263 G>A maps to NM_020692.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:69795197 C>T maps to NM_020692.2 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr14:69787486 G>A maps to NM_020692.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:69798191 C>T maps to NM_020692.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:69818885 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:69806297 T>C maps to NM_020692.2 Y383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:69806333 C>A maps to NM_020692.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:16254149 C>A maps to NM_054110.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:16261499 C>T maps to NM_054110.4 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr3:16217179 C>T maps to NM_054110.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:16260986 T>C maps to NM_054110.4 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:11470433 G>T maps to NM_198516.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr11:11394148 A>G maps to NM_198516.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:11354261 G>A maps to NM_198516.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr4:173942661 C>T maps to NM_001034845.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:172735856 C>T maps to NM_001034845.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr18:74980855 T>C maps to NM_001480.3 *350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:74962968 C>T maps to NM_001480.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr18:74962767 C>T maps to NM_001480.3 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr22:38221182 C>T maps to NM_003614.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:34648865 T>C maps to NM_000155.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr19:1397405 G>A maps to NM_000156.4 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr16:81399029 G>A maps to NM_022041.3 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:81410859 C>T maps to NM_022041.3 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:81398966 G>A maps to NM_022041.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:62406582 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:62400958 G>A maps to NM_198335.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:62394110 G>A maps to NM_198335.2 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:62402471 C>T maps to NM_198335.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr11:62394518 C>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:36033283 C>T maps to NM_014364.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:36027832 C>T maps to NM_014364.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:36024440 C>T maps to NM_014364.4 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr19:36029511 C>T maps to NM_014364.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:128061328 T>C maps to NM_015635.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:110739134 T>C maps to NM_018983.3 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:110745140 G>T maps to NM_018983.3 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:130075747 C>T maps to NM_032293.4 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:130111297 C>T maps to NM_032293.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:130097539 T>C maps to NM_032293.4 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:130111246 C>T maps to NM_032293.4 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:130149473 G>A maps to NM_032293.4 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr9:130073919 A>T maps to NM_032293.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:130155472 C>T maps to NM_032293.4 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:30671953 C>T maps to NM_002047.2 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:30656803 T>C maps to NM_002047.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr21:34882225 A>G maps to NM_001136006.1 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr21:34876431 C>A maps to NM_001136006.1 *1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr21:34889349 C>A maps to NM_001136006.1 G685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr21:34907048 C>T maps to NM_001136006.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:89561022 G>A maps to NM_002048.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:89560863 G>A maps to NM_002048.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr11:22833441 C>T maps to NM_005256.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:22707286 T>C maps to NM_005256.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr11:22770785 A>G maps to NM_005256.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr11:22759299 C>T maps to NM_005256.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr22:29708171 G>T maps to NM_152236.1 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr22:29708282 C>T maps to NM_152236.1 H614H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:34072895 G>T maps to NM_139285.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:34073120 G>A maps to NM_139285.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr17:34072127 G>A maps to NM_139285.2 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:34074066 C>T maps to NM_139285.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:34072286 G>T maps to NM_139285.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:34073270 C>T maps to NM_139285.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:101005887 T>C maps to NM_174942.1 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:101017692 T>C maps to NM_174942.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:101017767 G>A maps to NM_174942.1 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr12:100995420 A>T maps to NM_174942.1 K65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:114526404 G>A maps to ENST00000357389 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:114535358 G>A maps to ENST00000357389 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:114525102 G>A maps to ENST00000357389 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:114538549 G>A maps to ENST00000357389 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr13:114535424 G>A maps to ENST00000357389 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:10101596 G>A maps to NM_201433.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:9850222 G>A maps to NM_201433.1 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr16:90106767 C>T maps to NM_001481.2 Q358*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-A4G8-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:48649664 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:48649620 C>A did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:48652489 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:48651641 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:128200152 C>T maps to NM_032638.4 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:8100469 G>A maps to NM_001002295.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr10:8100562 C>T maps to NM_001002295.1 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr10:8106092 C>T maps to NM_001002295.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:8106091 G>A maps to NM_001002295.1 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:8097848 G>A maps to NM_001002295.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr10:8115987 G>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:11615980 G>A maps to NM_002052.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr8:11614477 C>T maps to NM_002052.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:11614471 C>T maps to NM_002052.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr20:61040938 C>T maps to NM_080473.4 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:19762728 A>G maps to NM_005257.3 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:19761505 C>T maps to NM_005257.3 C465C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:19609409 C>T maps to ENST00000404158 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:19606901 G>A maps to ENST00000404158 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:19609526 A>G maps to ENST00000404158 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:19576259 T>C maps to ENST00000404158 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:19613276 C>T maps to ENST00000404158 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:19613207 A>G maps to ENST00000404158 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:153800616 G>A maps to NM_020699.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:153785763 G>A maps to NM_020699.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:45661662 A>G maps to ENST00000432007 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:45668933 T>G maps to ENST00000432007 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:99821642 G>A maps to NM_178831.6 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:30681647 G>A maps to ENST00000434291 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:155207191 G>A maps to NM_001005742.2 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:35737771 G>A maps to NM_020944.2 Y826Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:35737836 G>A maps to NM_020944.2 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:35737836 G>A maps to NM_020944.2 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:35738602 A>G maps to NM_020944.2 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr3:81640312 G>A maps to ENST00000264326 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr3:81754640 T>C maps to ENST00000264326 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:104119941 C>T maps to NM_004193.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:104140950 C>T maps to NM_004193.2 G1746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr10:104136716 C>T maps to NM_004193.2 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:104117860 G>A maps to NM_004193.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:104129984 C>T maps to NM_004193.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:104128077 C>T maps to NM_004193.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:104128501 C>T maps to NM_004193.2 C961C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:104128513 C>T maps to NM_004193.2 S965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:136031292 C>T maps to NM_021996.4 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:136030622 G>A maps to NM_021996.4 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:136031316 C>T maps to NM_021996.4 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:89523756 T>C maps to NM_002053.2 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:89528740 A>T maps to NM_002053.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:89525079 G>A maps to NM_002053.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:89523768 G>T maps to NM_002053.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr1:89525061 C>T maps to NM_002053.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:89480279 G>A maps to NM_018284.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:89479831 A>G maps to NM_018284.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr1:89657070 A>G maps to NM_052941.4 H263H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:89661003 G>A maps to NM_052941.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:89735133 C>T maps to NM_052942.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:89726431 G>A maps to NM_052942.3 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:89849838 G>A maps to NM_198460.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:89849284 C>T maps to NM_198460.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:89630431 G>A maps to NM_207398.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:89618394 G>A maps to NM_207398.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:89616126 G>A maps to NM_207398.2 R253*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4361-01A-01D-1158-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-6566-01A-11D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:237076275 G>A maps to ENST00000415226 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:237075033 G>A maps to NM_001485.2 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:237075078 G>A maps to NM_001485.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:237074892 G>A maps to NM_001485.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:237074907 C>T maps to NM_001485.2 P232P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:237076119 G>A maps to ENST00000415226 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:72634050 C>A maps to ENST00000504199 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:72649717 T>C maps to ENST00000504199 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:72618267 G>A maps to ENST00000504199 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:72623794 G>T maps to ENST00000504199 C284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:38211679 G>A maps to NM_001171690.1 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:127222277 G>A maps to NM_024523.5 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:109088539 C>T maps to NM_181453.3 R919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:109088196 T>C maps to NM_181453.3 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:109111807 G>A maps to NM_181453.3 P1503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:109116110 T>C maps to NM_181453.3 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:109086172 G>T maps to NM_181453.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:109088539 C>T maps to NM_181453.3 R919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:109088058 G>A maps to NM_181453.3 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr19:13004402 C>T maps to NM_000159.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:34117159 T>C maps to NM_016631.3 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:34134491 A>G maps to NM_016631.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:163002047 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:44190668 G>A maps to NM_000162.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:44186117 G>A maps to NM_000162.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:44189377 G>A maps to NM_000162.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr7:44193049 G>A maps to NM_000162.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:53363724 G>A maps to NM_001498.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr6:52993581 C>A maps to NM_003643.3 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:52993438 G>A maps to NM_003643.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr6:10876692 G>A maps to NM_004752.3 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:10874820 G>A maps to NM_004752.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:10874461 G>T maps to NM_004752.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:10874820 G>A maps to NM_004752.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:10874776 A>G maps to NM_004752.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:120591160 C>T maps to NM_006836.1 A1306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:120569132 G>A maps to NM_006836.1 D2473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:120597680 G>A maps to NM_006836.1 N899N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr12:120613606 C>T maps to NM_006836.1 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:120583064 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:120567100 C>T maps to NM_006836.1 R2623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr12:120575733 C>A maps to NM_006836.1 E2122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:120575042 G>A maps to NM_006836.1 G2248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr12:120621398 C>T maps to NM_006836.1 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr12:120565738 G>A maps to NM_006836.1 L2644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:120569802 G>A maps to NM_006836.1 A2447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:79118406 G>A maps to NM_001097636.1 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:10586429 C>T maps to NM_145655.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:10586362 T>C maps to NM_145655.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:10530034 C>T maps to NM_145649.4 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:10529644 C>T maps to NM_145649.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:59911534 G>A maps to NM_004751.2 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:74324700 G>A maps to NM_016591.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:57929927 T>C maps to NM_001018090.3 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:57918077 C>A maps to NM_001018090.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr15:57925902 C>T maps to NM_001018090.3 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr16:81121263 C>T maps to NM_004483.4 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:74842915 C>T maps to ENST00000238018 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:74817549 A>G maps to ENST00000238018 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr9:74840637 T>C maps to ENST00000238018 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:75272474 T>C maps to NM_018972.2 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr8:75262743 G>A maps to NM_018972.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr8:75263616 G>T maps to NM_018972.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:118461255 T>C maps to NM_017686.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:48429171 G>A maps to NM_004962.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:48438587 G>A maps to NM_004962.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr10:48438518 G>A maps to NM_004962.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:48428829 C>T maps to NM_004962.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:48429417 G>A maps to NM_004962.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:48438578 G>A maps to NM_004962.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:48438500 G>A maps to NM_004962.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:48429189 C>A maps to NM_004962.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:48429495 C>T maps to NM_004962.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:18499231 A>C maps to NM_004864.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr19:18499105 A>G maps to NM_004864.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:18499615 C>T maps to NM_004864.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:18499096 G>A maps to NM_004864.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr19:18499303 G>A maps to NM_004864.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:48414240 G>A maps to NM_016204.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:48413793 G>A maps to NM_016204.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr10:48416402 C>T maps to NM_016204.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:48414099 G>A maps to NM_016204.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:48413793 G>A maps to NM_016204.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:48413907 G>A maps to NM_016204.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:7848093 G>A maps to NM_020634.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:7843256 G>A maps to NM_020634.1 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:7842722 G>A maps to NM_020634.1 I282I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B7-5816-01A-21D-1600-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-6452-01A-12D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:34022039 T>C maps to ENST00000374375 G28G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8591-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr20:34021880 C>T maps to NM_000557.2 T444T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-4306-01A-01D-1158-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-F1-6177-01A-11D-1800-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FP-7829-01A-11D-2053-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:97157036 C>T maps to NM_001001557.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:97156922 G>A maps to NM_001001557.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:97157633 C>T maps to NM_001001557.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr8:97172647 G>A maps to NM_001001557.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:97172740 C>T maps to NM_001001557.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:20871148 C>T maps to NM_182828.2 Y439Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr2:20871022 C>T maps to NM_182828.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr2:20871058 G>A maps to NM_182828.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:20870890 G>A maps to NM_182828.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:20870995 G>A maps to NM_182828.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:20870629 G>A maps to NM_182828.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr5:132198129 G>A maps to NM_005260.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:132197385 T>C maps to NM_005260.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153669508 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:153670029 G>C did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:153670510 T>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:153668346 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:153666939 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:153667453 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153670472 T>C did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:5808593 G>A maps to NM_001494.3 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr5:37834835 C>T maps to NM_001190468.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:37815866 T>C maps to NM_001190468.1 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:57351091 T>A maps to NM_182569.3 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:57344491 C>T maps to NM_182569.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:57344478 C>A maps to NM_182569.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:57311889 T>C maps to NM_182569.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:69647040 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:69647034 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:69649836 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:69652203 A>G did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:69646219 G>C did not map to a codon.
Alternatively spliced codon TCGA-D7-A4YV-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:30124113 G>A maps to NM_024307.2 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr11:76956373 G>A maps to ENST00000376217 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:76982268 C>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:75146601 G>A maps to NM_030792.6 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:75146620 G>A maps to NM_030792.6 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:58008141 C>T maps to NM_001111270.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:58005682 G>A maps to NM_182947.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:58005682 G>A maps to NM_182947.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:58006731 C>A maps to NM_001111270.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:58007884 C>T maps to NM_001111270.1 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:95272704 G>T maps to NM_181702.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:95272653 A>G maps to NM_181702.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:95262719 G>A maps to NM_181702.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:650202 C>T maps to NM_015721.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6803-01A-11D-1882-08 chr17:648915 T>C maps to NM_015721.2 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:650619 G>A maps to NM_015721.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr17:649623 G>A maps to NM_015721.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:649965 G>T maps to NM_015721.2 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:154284998 T>C maps to NM_015465.3 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:154299618 C>A maps to NM_015465.3 G503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:154304026 A>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:45593470 C>A maps to NM_024707.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:45593575 C>T maps to NM_024707.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:14027110 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:14038455 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:14038455 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:14027268 A>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:14027101 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:42987608 G>A maps to NM_001131019.1 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:42992512 G>A maps to NM_002055.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr17:42987518 C>T maps to NM_001131019.1 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr17:42992740 G>A maps to NM_002055.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:42992566 C>T maps to NM_002055.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:92948990 C>T maps to NM_005263.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr1:92944271 G>A maps to NM_005263.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:92946568 G>A maps to NM_005263.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:135865238 C>T maps to NM_004188.4 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:135862759 G>A maps to NM_004188.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:135862798 G>A maps to NM_004188.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:135863632 C>T maps to NM_004188.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:135864464 C>T maps to NM_004188.4 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:135863632 C>T maps to NM_004188.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:158366883 T>A maps to ENST00000264263 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:158369950 G>A maps to ENST00000264263 E271E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8591-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:158402329 C>T maps to ENST00000264263 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:158383229 A>G maps to ENST00000264263 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:158363452 G>A maps to ENST00000264263 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N0-01A-12D-A364-08 chr3:158383241 A>G maps to ENST00000264263 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:74026117 G>A maps to NM_032380.3 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:74047273 G>A maps to NM_032380.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:74026202 C>A maps to NM_032380.3 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:74054701 G>A maps to NM_032380.3 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr6:13365510 G>A maps to NM_018988.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:13365583 G>A maps to NM_018988.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:67709347 C>A maps to NM_030819.3 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:67709885 C>T maps to NM_030819.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:69555474 C>T maps to ENST00000357308 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:179745955 G>A maps to NM_005110.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr5:179729481 G>A maps to NM_005110.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:179731780 C>T maps to NM_005110.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:179743814 G>A maps to NM_005110.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr5:179763494 G>A maps to NM_005110.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:179734304 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:179762942 G>A maps to NM_005110.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr5:179751273 C>T maps to NM_005110.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr5:179729554 G>A maps to NM_005110.2 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:118030415 G>A maps to NM_005264.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:118030601 G>A maps to NM_005264.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:117884985 C>T maps to NM_005264.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:117849371 T>C maps to NM_005264.4 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:21608380 A>G maps to NM_001495.4 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:137593530 G>A maps to NM_001496.3 H194H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:137593488 G>A maps to NM_001496.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:137599950 A>G maps to NM_001496.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:137600130 G>T maps to NM_001496.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:137593395 G>A maps to NM_001496.3 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:137593557 C>T maps to NM_001496.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:137600036 G>A maps to NM_001496.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:137589530 G>T maps to NM_001496.3 C316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr6:55266590 T>G maps to NM_207410.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:55264053 A>T maps to NM_207410.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:38021855 C>T maps to ENST00000381756 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:38016859 C>A maps to ENST00000381756 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr22:38027047 C>T maps to ENST00000381756 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:38027011 C>T maps to ENST00000381756 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:38021903 T>G maps to ENST00000381756 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:38021957 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:23499986 T>C maps to NM_015044.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr17:73235958 G>A maps to NM_138619.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr7:30544314 G>T maps to NM_024051.3 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:85779651 G>A maps to NM_000821.4 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr2:85777203 A>T maps to NM_000821.4 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:85782689 C>T maps to NM_000821.4 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:38876200 G>A maps to NM_152657.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:38877099 G>A maps to NM_152657.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:38877091 G>A maps to NM_152657.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr19:38877508 G>A maps to NM_152657.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:38876359 G>A maps to NM_152657.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr19:38876923 G>A maps to NM_152657.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:38877382 C>T maps to NM_152657.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:38876167 G>A maps to NM_152657.3 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:34935803 G>A maps to NM_024835.3 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:34941791 T>C maps to NM_024835.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:34934410 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:34935675 C>T maps to NM_024835.3 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:25019834 C>T maps to NM_005265.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:25024356 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:25010757 C>T maps to NM_005265.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:25024063 G>A maps to NM_005265.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr22:25019155 G>A maps to NM_005265.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr22:25007110 C>A maps to NM_005265.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:24628049 G>A maps to NM_001099781.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:4462880 G>C maps to ENST00000414312 Y105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr20:33437809 G>A maps to NM_178026.2 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:33450618 G>A maps to NM_178026.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr20:23967071 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:23966582 C>T maps to NM_178311.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:22989735 G>A maps to ENST00000215938 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:61995388 T>C maps to NM_000515.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:61957643 G>A maps to NM_022558.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:61958091 G>A maps to NM_022557.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr17:61958859 G>A maps to NM_002059.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr17:61957794 G>A maps to NM_002059.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:61958242 G>A maps to NM_002059.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:40344953 T>C maps to NM_032484.4 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:40344469 G>A maps to NM_032484.4 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:40343228 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:85903820 C>A maps to ENST00000436406 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:42719405 T>C maps to NM_000163.2 H599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr5:42719132 G>A maps to NM_000163.2 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:35882610 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:31014630 A>G maps to NM_000823.3 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr7:31011682 C>T maps to NM_000823.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:31014104 G>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:10328490 G>A maps to NM_016362.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:172166023 G>A maps to NM_198407.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:172165335 A>G maps to NM_004122.2 *290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:172165750 G>A maps to NM_198407.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr3:172166107 G>A maps to NM_198407.2 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:172165645 G>A maps to NM_198407.2 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr3:172166086 G>A maps to NM_198407.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:59611433 C>T maps to NM_005142.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:59599166 T>C maps to NM_005142.2 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:59609976 G>A maps to NM_005142.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:100285024 G>A maps to NM_022574.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:100281680 C>T maps to NM_022574.4 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:100279975 C>T maps to NM_022574.4 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:100281713 C>T maps to NM_022574.4 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:100283826 G>T maps to NM_022574.4 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:100283672 C>T maps to NM_022574.4 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr7:100283657 G>A maps to NM_022574.4 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:233655445 C>T maps to ENST00000373566 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:233671201 T>C maps to ENST00000373566 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:233620986 G>T maps to ENST00000373566 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:233652023 C>T maps to ENST00000373566 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:233684581 C>T maps to ENST00000373566 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:233715061 C>T maps to ENST00000373566 Q1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:233655450 T>C maps to ENST00000373566 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:233681682 C>T maps to ENST00000373566 R793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:233721520 C>A maps to ENST00000373566 S1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:150417151 T>C maps to NM_130759.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:150390072 T>C maps to NM_015660.2 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:150269274 C>T maps to ENST00000430830 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:150325007 G>A maps to ENST00000438845 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:150325346 G>A maps to ENST00000438845 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:150324880 G>A maps to ENST00000438845 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr7:150325355 G>A maps to ENST00000438845 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:150171328 G>A maps to NM_175571.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:150174378 C>T maps to NM_175571.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:150164043 C>T maps to NM_175571.2 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:102444276 G>A maps to NM_017676.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:25405923 T>C maps to NM_021067.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr20:25398807 C>T maps to NM_021067.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:41399515 C>T maps to NM_032336.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:41397443 G>A maps to NM_032336.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:47039153 C>T maps to NM_004123.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr19:14589278 G>A maps to NM_202470.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr19:14591449 G>A maps to NM_202470.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr19:3589486 G>A maps to NM_133261.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:46180361 C>A maps to NM_000164.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:46173990 A>C maps to NM_000164.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr19:46174615 G>A maps to NM_000164.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:27905344 G>A maps to NM_001085454.1 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr17:27903634 G>A maps to NM_001085454.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:110370842 G>A maps to NM_057169.3 Y740Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:110427529 A>G maps to NM_057169.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:110427529 A>G maps to NM_057169.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:110371862 G>A maps to NM_057169.3 H677H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:121768697 C>T maps to NM_000165.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:121768434 C>T maps to NM_000165.3 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:121768937 A>G maps to NM_000165.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:121768886 C>T maps to NM_000165.3 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr6:121768766 A>G maps to NM_000165.3 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:20716875 C>T maps to NM_021954.3 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:20716950 G>A maps to NM_021954.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:35259867 G>A maps to NM_002060.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:147231340 G>A maps to NM_005266.5 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:147231085 C>T maps to NM_005266.5 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:147230448 G>A maps to NM_005266.5 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:147230280 G>A maps to NM_005266.5 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr1:147381266 G>T maps to NM_005267.4 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:147380699 C>T maps to NM_005267.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr1:147381080 C>T maps to NM_005267.4 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr1:147380210 C>T maps to NM_005267.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:147380279 C>T maps to NM_005267.4 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:147380981 C>T maps to NM_005267.4 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:39341488 G>A maps to NM_030772.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:39341335 A>G maps to NM_030772.4 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:39341359 A>G maps to NM_030772.4 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:70444364 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr23:70443565 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:20763534 G>A maps to NM_004004.5 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:35250435 C>T maps to NM_001005752.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:35250845 G>T maps to NM_001005752.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:35227148 C>T maps to NM_153212.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:35226974 G>T maps to NM_153212.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr13:20797121 C>G maps to NM_001110221.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr13:20797604 C>T maps to NM_001110221.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr6:87993986 A>T maps to NM_198568.2 L215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:42882357 A>G maps to NM_001080383.1 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:228345674 G>A maps to NM_020435.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:228346214 C>T maps to NM_020435.2 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:228345731 G>A maps to NM_020435.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:228346016 C>T maps to NM_020435.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr1:228346652 C>G maps to NM_020435.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:228346346 C>T maps to NM_020435.2 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:228346745 C>T maps to NM_020435.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:99526643 A>C maps to NM_181538.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr15:35045437 G>A maps to NM_020660.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr15:35044978 G>A maps to NM_020660.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr15:35045226 G>A maps to NM_020660.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:35045230 G>T maps to NM_020660.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr15:35045223 C>A maps to NM_020660.1 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr15:35045155 C>T maps to NM_020660.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr15:35045038 T>C maps to NM_020660.1 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:30686190 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:30686199 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:30737591 T>G did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:30686200 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:30745649 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:30739079 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:80329114 A>G maps to NM_033214.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:69174389 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:69177311 G>T maps to NM_182536.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:100656665 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:100653080 T>C did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:100653411 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:100653513 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:100653777 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:100656739 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr3:33055718 G>A maps to NM_000404.2 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:134212845 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:134212846 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:134147249 C>T maps to NM_001080407.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:8062114 A>G maps to NM_138426.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:8125840 G>A maps to NM_138426.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr7:8126035 G>A maps to NM_138426.2 T504T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:69560893 G>T maps to NM_015554.1 G389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:6605271 A>G maps to NM_000170.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:6553432 C>A maps to NM_000170.2 G798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:6553496 G>A maps to NM_000170.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:6645244 C>T maps to NM_000170.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:6554673 G>A maps to NM_000170.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:51634198 C>T maps to NM_181789.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:51689757 C>T maps to NM_181789.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:51634171 C>T maps to NM_181789.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:51696680 C>T maps to NM_181789.2 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr15:51687171 C>T maps to NM_181789.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:51696611 G>A maps to NM_181789.2 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:51689790 C>T maps to NM_181789.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:131271264 G>A maps to NM_001003722.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:74537580 G>A maps to NM_012201.5 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:74519763 G>A maps to NM_012201.5 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:57859039 T>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:57865759 G>C maps to NM_005269.2 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:57864328 G>A maps to NM_005269.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:121747437 C>T maps to NM_005270.4 H1316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr2:121746630 G>A maps to NM_005270.4 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr2:121712926 G>A maps to NM_005270.4 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:121746624 C>T maps to NM_005270.4 D1045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:121744182 G>A maps to NM_005270.4 P762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:121684991 C>T maps to NM_005270.4 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:121728139 C>T maps to NM_005270.4 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:121684973 A>G maps to NM_005270.4 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:121732660 C>T maps to NM_005270.4 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:121747788 G>A maps to NM_005270.4 P1433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr2:121736089 C>A maps to NM_005270.4 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:121728103 G>A maps to NM_005270.4 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:121712923 C>T maps to NM_005270.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:121743882 G>A maps to NM_005270.4 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:121743999 C>A maps to NM_005270.4 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:121745997 C>T maps to NM_005270.4 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:121747851 C>T maps to NM_005270.4 Y1454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:121747866 C>T maps to NM_005270.4 G1459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr7:42005934 G>A maps to NM_000168.5 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:42005250 G>T maps to NM_000168.5 G1140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:42005484 C>T maps to NM_000168.5 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:42005568 C>T maps to NM_000168.5 A1034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:42007443 C>T maps to NM_000168.5 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:42005904 C>T maps to NM_000168.5 T922T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr7:42004615 G>T maps to NM_000168.5 S1352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr7:42006102 C>T maps to NM_000168.5 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr7:42005604 C>T maps to NM_000168.5 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr7:42085088 C>T maps to NM_000168.5 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:42018274 G>A maps to NM_000168.5 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:42005616 C>A maps to NM_000168.5 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:42005619 G>A maps to NM_000168.5 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:42004152 G>A maps to NM_000168.5 F1506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:42004713 T>C maps to NM_000168.5 G1319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:42018305 G>A maps to NM_000168.5 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:42005217 G>A maps to NM_000168.5 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:42005544 G>A maps to NM_000168.5 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:42005508 G>A maps to NM_000168.5 G1054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:42005763 G>T maps to NM_000168.5 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:42005280 G>A maps to NM_000168.5 D1130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:42004863 G>A maps to NM_000168.5 D1269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr7:42005997 C>T maps to NM_000168.5 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr7:42011985 T>A maps to NM_000168.5 K685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:42063102 G>A maps to NM_000168.5 C487C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:42005484 C>T maps to NM_000168.5 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:42006000 G>A maps to NM_000168.5 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:42003926 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:144358658 C>T maps to NM_138465.3 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:144358415 T>C maps to NM_138465.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:75737645 T>G maps to ENST00000378695 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr12:75816695 G>A maps to ENST00000378692 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:36148588 G>A maps to NM_022343.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:36162401 C>T maps to NM_022343.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr9:36162425 C>T maps to NM_022343.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr1:53980407 G>A maps to NM_147193.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:53974835 C>T maps to NM_147193.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:4384869 C>T maps to NM_032575.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:4383519 G>A maps to NM_032575.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:4382337 G>A maps to NM_032575.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr16:4384893 C>T maps to NM_032575.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:3898790 G>A maps to NM_001042413.1 C676C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:4117944 G>A maps to NM_001042413.1 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:4117860 G>A maps to NM_001042413.1 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:4118079 C>T maps to NM_001042413.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr9:4286251 G>A maps to NM_001042413.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:4118133 C>T maps to NM_001042413.1 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:4118412 G>A maps to NM_001042413.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:4118511 C>T maps to NM_001042413.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:4118616 C>T maps to NM_001042413.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:38650638 A>G maps to NM_006708.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:685453 T>C maps to ENST00000397393 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:48629415 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:48631800 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:39046913 C>A maps to NM_002062.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr6:39048490 A>C maps to NM_002062.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:39041465 C>T maps to NM_002062.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:9739793 T>C did not map to a codon.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr17:9745872 C>T maps to NM_004246.1 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:9792952 C>T maps to NM_004246.1 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr17:9739736 T>G maps to NM_004246.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:14592653 C>A did not map to a codon.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr23:14708968 G>T did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr23:14625360 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:14748343 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:175598419 G>A maps to NM_006529.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:175603982 A>G maps to NM_006529.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:102979003 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:102962290 C>T did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:102978849 A>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:102979113 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:102962422 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr23:102979871 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:193066845 G>T maps to NM_016066.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:131958296 T>A maps to NM_006541.4 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:131943556 G>T maps to NM_006541.4 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:191819481 T>C maps to NM_014905.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:191819387 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:191819481 T>C maps to NM_014905.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:56866477 G>A maps to NM_013267.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:56872955 G>A maps to NM_013267.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr12:56874167 A>G maps to NM_013267.2 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr12:56868375 G>C maps to NM_013267.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr12:129442112 A>G maps to ENST00000442111 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr12:129467524 G>T maps to ENST00000442111 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:17678315 G>A maps to NM_024656.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:183938580 G>A maps to NM_015101.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:183933049 G>A maps to NM_015101.2 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:183909827 G>A maps to NM_015101.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:183909737 T>C maps to NM_015101.2 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:183908026 C>A maps to NM_015101.2 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:184006290 C>T maps to NM_015101.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr9:138516451 G>A maps to NM_182974.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:138516491 C>T maps to NM_182974.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:138516206 C>T maps to NM_182974.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:52729485 G>A maps to NM_018446.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:52729495 C>T maps to NM_018446.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr3:52730256 A>T maps to NM_018446.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:104388144 C>T maps to NM_031302.3 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:1262941 C>A maps to NM_001029885.1 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:1262394 C>T maps to NM_001029885.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:48184028 C>T maps to NM_015711.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:48183377 C>T maps to NM_015711.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:48201923 C>T maps to NM_015711.3 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr19:48185351 A>T maps to NM_015711.3 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:48254216 C>T maps to NM_015710.4 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr19:48248917 G>A maps to NM_015710.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:88822562 A>G maps to NM_005271.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:88820770 T>C maps to NM_005271.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:120181965 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:120181687 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:120181789 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:120182574 A>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:120182521 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:120181649 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:120182453 G>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:120182311 A>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:120182192 G>A did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:120181759 C>T did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:120183117 A>C did not map to a codon.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr23:120182258 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:120182816 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:120183164 A>G did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:120182119 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:120181763 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:182353563 A>G maps to NM_002065.5 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:182353566 G>A maps to NM_002065.5 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr11:58477535 C>T maps to NM_201648.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:58722274 C>T maps to NM_080661.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:58711065 G>A maps to NM_080661.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr11:58711066 C>T maps to NM_080661.2 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:58722656 G>T maps to NM_080661.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr3:52327138 G>A maps to NM_145262.3 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:52326883 G>A maps to NM_145262.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:1624442 G>A maps to NM_001500.2 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:1726688 G>A maps to NM_001500.2 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:1726672 T>A maps to NM_001500.2 K322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:62221651 G>A maps to NM_012384.3 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:62250678 G>A maps to NM_012384.3 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr20:62234353 C>T maps to NM_012384.3 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:62226975 G>A maps to NM_012384.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:39819711 G>A maps to NM_004877.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:19745392 G>A maps to NM_016573.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:19744833 G>A maps to NM_016573.2 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr8:143921918 C>T maps to NM_002066.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:143927871 T>C maps to NM_002066.2 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:24784680 G>T maps to NM_015895.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:220366624 C>T maps to ENST00000373917 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:220366241 T>C maps to ENST00000373917 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:220368860 C>T maps to ENST00000373917 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:220364855 A>G maps to ENST00000373917 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:49760112 G>A maps to NM_013334.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:49760139 C>T maps to NM_013334.2 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:16274704 C>A maps to NM_006877.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:16295239 C>A maps to NM_006877.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:24705333 G>A maps to ENST00000348719 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:24707912 G>T maps to ENST00000348719 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:155633941 T>C maps to NM_003875.2 H391H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:155652815 T>C maps to NM_003875.2 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:3110204 C>T maps to NM_002067.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:63052590 C>A maps to NM_006572.4 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:80046286 G>T maps to NM_004297.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:80262589 C>A maps to NM_004297.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr9:80043932 G>A maps to NM_004297.3 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:3155823 C>T maps to NM_002068.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:3151731 C>T maps to NM_002068.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:3148613 C>T maps to NM_002068.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:3157793 C>A maps to NM_002068.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:79828641 T>C maps to NM_002069.5 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr3:50294235 C>T maps to NM_002070.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr3:50289849 C>T maps to NM_002070.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:110134704 C>T maps to NM_006496.2 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:110128868 C>T maps to NM_006496.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:11753645 C>T maps to NM_182978.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:11876644 C>A maps to NM_182978.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:11868560 C>T maps to NM_182978.2 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr16:56362637 C>T maps to NM_020988.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr16:56385345 G>A maps to NM_020988.2 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:80336239 T>C maps to NM_002072.3 *360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:80430565 G>A maps to NM_002072.3 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr20:57429489 C>T maps to NM_080425.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:57485416 C>T maps to NM_080425.2 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:57429084 C>T maps to NM_080425.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr20:57428502 C>T maps to NM_080425.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr20:57466873 G>A maps to NM_001077488.1 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr20:57428721 C>T maps to NM_080425.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr20:57429165 C>A maps to NM_080425.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:50231006 G>A maps to NM_000172.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr3:50231584 C>T maps to NM_000172.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:50231209 G>A maps to NM_000172.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:50231087 G>A maps to NM_000172.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:110146143 C>T maps to NM_005272.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:23438055 C>T maps to NM_002073.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:23438484 C>T maps to NM_002073.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:23438115 C>T maps to NM_002073.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:23438407 C>T maps to NM_002073.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:1721995 C>T maps to NM_002074.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:1735885 G>A maps to NM_002074.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr22:19808156 C>T maps to NM_053004.2 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:100276169 G>A maps to NM_005273.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:100276157 G>A maps to NM_005273.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr12:6954784 G>A maps to NM_002075.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:179132742 G>A maps to NM_021629.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:36246456 G>A maps to NM_001128227.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:36233982 G>A maps to NM_001128227.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr7:93555471 G>T maps to NM_004126.3 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr1:68171253 C>T maps to NM_018841.5 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:68171241 C>T maps to NM_018841.5 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr7:93540227 T>C maps to NM_021955.3 *75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr7:93536130 G>T maps to NM_021955.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:93540133 C>T maps to NM_021955.3 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:47284706 T>C maps to NM_001198754.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:47284190 G>A maps to NM_001198754.1 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:38033288 C>T maps to NM_013285.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr3:52725621 T>G maps to NM_014366.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:54584944 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:54559015 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:54577457 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:54578084 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:54578109 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:54585016 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr23:54578095 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:54578158 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:54578116 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:231401889 T>G maps to NM_014236.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr1:231386759 T>C maps to NM_014236.3 H44H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:141384601 G>A maps to NM_005471.4 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:102158447 T>C maps to NM_024312.4 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:102164270 C>T maps to NM_024312.4 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:102161839 G>A maps to NM_024312.4 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:102155451 G>A maps to NM_024312.4 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:102158612 T>C maps to NM_024312.4 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:102158267 G>A maps to NM_024312.4 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:1412834 G>T maps to NM_032520.4 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:1412310 C>T maps to NM_032520.4 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr16:1412688 G>A maps to NM_032520.4 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:25280720 A>G maps to NM_001083111.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:3025349 C>T maps to NM_001501.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr4:68610325 G>T maps to NM_000406.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:127650642 G>A maps to NM_002077.3 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:127652730 C>A maps to NM_002077.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:127643509 T>C maps to NM_002077.3 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr9:127662754 G>T maps to NM_002077.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:131022374 G>A maps to NM_004486.4 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:131020066 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:133385135 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:133350861 C>T maps to NM_005895.3 T1396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:133350798 C>T maps to NM_005895.3 P1417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:133351738 G>A maps to NM_005895.3 G1377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:133360752 G>A maps to NM_005895.3 D1088D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:133353593 G>A maps to NM_005895.3 Q1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr12:133353342 C>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:133362987 C>T maps to NM_005895.3 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr12:133349747 G>A maps to NM_005895.3 R1480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:37340399 T>G maps to NM_001172713.1 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:37368530 T>C maps to NM_001172713.1 Y1740Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:37368395 T>C maps to NM_001172713.1 H1695H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr3:37379167 A>G maps to NM_001172713.1 A2128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:37368263 T>C maps to NM_001172713.1 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:37292887 G>A maps to NM_001172713.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:37366802 C>T maps to NM_001172713.1 D1164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr14:93264324 C>T maps to NM_005113.2 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:93263964 G>A maps to NM_005113.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:93275768 C>A maps to NM_005113.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:72956778 G>A maps to NM_018652.4 E476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:75558554 G>A maps to NM_001164404.1 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:75562506 C>T maps to NM_001164404.1 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:75581814 C>T maps to NM_001145224.1 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:99623790 C>T maps to NM_001010917.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr15:34673665 G>A maps to NM_181077.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:34678851 G>A maps to NM_181077.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:34673719 G>A maps to NM_181077.3 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:121395742 G>A maps to ENST00000393667 S3058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:121415484 A>G maps to ENST00000393667 S1295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:121416179 C>A maps to ENST00000393667 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:121417442 C>A maps to ENST00000393667 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:121415619 G>A maps to ENST00000393667 D1250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr3:121415805 G>C maps to ENST00000393667 A1188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:121395737 A>G did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:167750556 A>G maps to NM_014498.3 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:167750633 G>A maps to NM_014498.3 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:167759194 C>T maps to NM_014498.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:88650319 G>A maps to ENST00000376023 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:88650484 C>T maps to ENST00000376023 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:88655668 G>A maps to ENST00000376023 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:21665286 C>T maps to NM_016072.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:155722379 T>C maps to ENST00000368331 A1948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:155736193 G>A maps to ENST00000368331 R1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:155726823 C>T maps to ENST00000368331 E1814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:155790394 A>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:155791288 A>G maps to ENST00000368331 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:155735155 C>A maps to ENST00000368331 E1370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:155736365 T>C maps to ENST00000368331 E966E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:155735825 A>C maps to ENST00000368331 T1146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:155726823 C>T maps to ENST00000368331 E1814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:117884446 C>T maps to NM_020399.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:117923424 T>C maps to NM_020399.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:117890791 G>A maps to NM_020399.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:117923400 G>A maps to NM_020399.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:170508633 C>A maps to NM_152281.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:39139894 C>T maps to NM_031899.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:171811193 C>T maps to NM_015530.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:171822462 C>T maps to NM_015530.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:171822430 C>T maps to NM_015530.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:101157411 C>T maps to NM_002079.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:101163224 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:101180554 G>A maps to NM_002079.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:101163326 G>T maps to NM_002079.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:37792609 G>A maps to NM_152413.2 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr8:37791993 C>T maps to NM_152413.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:37796361 G>A maps to NM_152413.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr16:58752442 C>T maps to NM_002080.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:58756074 G>A maps to NM_002080.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:20335201 G>A maps to NM_001007240.1 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:20325982 A>G maps to NM_001007240.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:20329676 C>T maps to NM_001007240.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:194118477 C>T maps to NM_004488.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:194118378 C>T maps to NM_004488.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:194117601 C>T maps to NM_004488.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:194118297 G>A maps to NM_004488.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:55539168 G>A maps to NM_001083899.1 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr19:55525821 G>A maps to NM_001083899.1 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr19:55526286 G>A maps to NM_001083899.1 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:55525818 G>T maps to NM_001083899.1 C498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:128780906 C>T maps to NM_000174.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr3:128780695 C>T maps to NM_000174.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:167024301 A>G maps to NM_005814.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr1:167042756 G>A maps to NM_005814.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:167024307 G>A maps to NM_005814.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:145139998 C>T maps to NM_003801.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:145139148 C>T maps to NM_003801.3 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:145139351 C>T maps to NM_003801.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:113913351 G>A maps to NM_020918.4 R815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:113918097 C>T maps to NM_020918.4 Q652Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr10:113933595 C>A maps to NM_020918.4 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:113917102 C>T maps to NM_020918.4 Q675Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:96690196 G>T maps to NM_207328.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:96698080 G>A maps to NM_207328.2 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:33602673 C>T maps to NM_018025.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:33621033 A>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:33608732 C>T maps to NM_018025.2 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:33585161 C>T maps to NM_018025.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr19:33579068 C>T maps to NM_018025.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr1:217793303 G>A maps to NM_018040.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:217793648 C>T maps to NM_018040.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr1:217622645 C>T maps to NM_018040.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:217793654 C>T maps to NM_018040.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:27218930 G>T maps to NM_022078.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:27224205 G>T maps to NM_022078.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr1:27223866 A>G maps to NM_022078.2 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:27223979 G>T maps to NM_022078.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:156565166 G>A maps to NM_015590.3 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:42476723 G>A maps to NM_001002909.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:42478562 T>C maps to NM_001002909.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:42477191 T>C maps to NM_001002909.2 Q751Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:42477059 G>A maps to NM_001002909.2 C795C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:42476192 G>A maps to NM_001002909.2 D1084D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:42476611 G>A maps to NM_001002909.2 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:42477896 G>T maps to NM_001002909.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:42474961 G>A maps to NM_001002909.2 Q1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr17:42476440 T>A maps to NM_001002909.2 R1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr17:42478328 T>C maps to NM_001002909.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:56531794 G>A maps to NM_001127236.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:56509989 T>C maps to NM_001127236.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:56527096 C>T maps to NM_001127236.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:56546782 T>C maps to NM_001127236.2 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:56526979 A>G maps to NM_001127236.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:99774669 G>A maps to NM_152742.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:99768092 G>A maps to NM_152742.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr7:99771476 A>G maps to NM_152742.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:132887714 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:132888178 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:132887948 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:132888058 A>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:132887800 T>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:132445390 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:132438840 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:132439827 G>A did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:132548986 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:132439844 G>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:132439864 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:92345909 G>A maps to NM_004466.4 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:93518631 G>A maps to NM_004466.4 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr13:92560226 C>A maps to NM_004466.4 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:92408614 T>C maps to NM_004466.4 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:92345483 T>C maps to NM_004466.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:92051398 T>C maps to NM_004466.4 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:92051381 C>T maps to NM_004466.4 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr13:92051455 G>A maps to NM_004466.4 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr13:92345468 A>T maps to NM_004466.4 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:94938666 G>A maps to NM_005708.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr13:95034747 C>T maps to NM_005708.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:5564948 G>A maps to NM_019593.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr20:5579447 A>T maps to NM_019593.3 C23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:50498450 G>T maps to NM_005276.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr12:50501570 G>A maps to NM_005276.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr12:50499446 C>T maps to NM_005276.2 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:32181856 C>T maps to NM_015141.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:32200522 C>T maps to NM_015141.3 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:157407126 C>T maps to NM_000408.4 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:157369850 G>A maps to NM_000408.4 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:157370006 C>T maps to NM_000408.4 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:157425875 T>C maps to NM_000408.4 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:157407126 C>T maps to NM_000408.4 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:157407126 C>T maps to NM_000408.4 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:1131744 C>T maps to NM_001505.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr7:1131744 C>T maps to NM_001505.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:67646302 T>C maps to NM_020806.4 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:67576951 C>T maps to NM_020806.4 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:34857701 C>T maps to NM_000175.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:34890895 G>A maps to NM_000175.3 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr8:144297359 C>T maps to NM_178172.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:144296963 C>T maps to NM_178172.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48970831 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48972253 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:48973466 A>G did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:48972593 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:48974061 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:48973475 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:48979944 G>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:24445780 A>G maps to NM_001503.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:24436911 C>T maps to NM_001503.2 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:176573101 G>A maps to NM_005277.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr4:176594962 G>T maps to NM_005277.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:176594944 C>T maps to NM_005277.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:13803831 C>T did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:13795512 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:13803812 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:13801528 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr23:13803802 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:27865300 C>T maps to NM_007266.3 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:27210733 A>G maps to NM_018066.3 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:110897616 G>A maps to NM_001164373.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:110902983 T>C maps to NM_001164373.1 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:23306136 A>G maps to ENST00000435486 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:23300168 C>G maps to ENST00000435486 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:23309690 G>C maps to ENST00000435486 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr7:23292998 T>G maps to ENST00000435486 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:23293878 C>T maps to ENST00000435486 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:136113193 C>T did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr23:136113610 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:136112977 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:136112733 A>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:136113043 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:136113695 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:136112820 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:136113349 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:136113076 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr23:136113306 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:136113786 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:136113510 A>C did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:136113447 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:132866787 C>T maps to NM_001136557.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr19:6735917 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:6732166 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:123187302 C>T maps to NM_177551.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr12:123186810 G>A maps to NM_177551.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:123187047 C>T maps to NM_177551.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:123201179 C>T maps to NM_006018.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:123200618 C>T maps to NM_006018.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:47649995 C>A maps to NM_153839.6 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:47649716 A>G maps to NM_153839.6 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:47647922 T>C maps to NM_153839.6 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:135431522 C>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:135405356 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:135494506 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135405391 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135427955 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135429099 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135430772 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135482126 T>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:135390961 A>C did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr23:135445659 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:135429445 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:135405371 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:135428616 A>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:135431469 A>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:135430009 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:135429335 C>A did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:135430801 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:135430502 T>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:135488094 T>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:135431509 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:135431649 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:135432562 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:135443642 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:135426977 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:135428782 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:135429584 C>A did not map to a codon.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr23:135496391 G>T did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:135427961 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:135494506 C>T did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:135427614 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:135426783 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:135427927 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:135431439 C>G did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:135431279 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr23:135430103 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:135494467 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:135427816 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:135485416 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr23:135428767 C>G did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:135482191 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:135430073 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:57601917 G>A maps to ENST00000349457 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:57609002 C>T maps to ENST00000349457 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr16:57601782 C>A maps to ENST00000349457 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr16:57608777 C>T maps to ENST00000349457 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:57597821 C>T maps to ENST00000349457 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:47675982 T>C maps to NM_153838.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr6:47675061 G>A maps to NM_153838.3 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:47682297 T>C maps to NM_153838.3 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:47681946 A>G maps to NM_153838.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:46828547 A>G maps to NM_015234.4 H761H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:46849829 G>A maps to NM_015234.4 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:129518464 C>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:129518495 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:129518541 C>A did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:129518528 T>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:129518616 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:129519386 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:27333370 G>A maps to NM_005288.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:27332974 C>T maps to NM_005288.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:27332960 T>C maps to NM_005288.3 *335W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr13:27333451 C>A maps to NM_005288.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr13:27333355 C>T maps to NM_005288.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:95347048 C>T maps to NM_181745.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr10:134942948 G>A maps to ENST00000368577 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:134942135 C>T maps to ENST00000368577 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:134941862 C>T maps to ENST00000368577 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:134942525 C>T maps to ENST00000368577 H938H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:37689007 C>T maps to NM_032777.9 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr8:37691339 C>T maps to NM_032777.9 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:37672411 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:22422523 C>T maps to NM_145290.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:22463403 A>G maps to NM_145290.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:22422538 A>G maps to NM_145290.2 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:22422643 G>A maps to NM_145290.2 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:22389933 C>T maps to NM_145290.2 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:22425957 A>G maps to NM_145290.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:22425930 A>G maps to NM_145290.2 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:22389705 C>T maps to NM_145290.2 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:142758631 G>A maps to NM_198569.2 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:142741056 G>A maps to NM_198569.2 V1045V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:142688973 G>A maps to NM_198569.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:142691310 C>T maps to NM_198569.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr6:142721725 C>A maps to NM_198569.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:100413712 G>A maps to NM_032787.2 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:100348463 C>T maps to NM_032787.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr3:100373804 C>T maps to NM_032787.2 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:105517540 G>T maps to NM_013345.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr14:105517585 C>T maps to NM_013345.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr14:105517675 G>A maps to NM_013345.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:105518035 G>A maps to NM_013345.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:131593288 C>T maps to NM_198827.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:131488737 C>T maps to NM_198827.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:131593315 T>C maps to NM_198827.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr12:131590403 G>A maps to NM_198827.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:59931389 G>A maps to NM_022571.5 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:59930993 G>A maps to NM_022571.5 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:59931428 C>T maps to NM_022571.5 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr14:59930837 G>A maps to NM_022571.5 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:64054478 C>T maps to NM_001170726.1 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr11:64055813 G>A maps to NM_001170726.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:236371376 A>G maps to NM_003272.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:20043575 G>A maps to NM_001002911.2 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr16:20043131 C>T maps to NM_001002911.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:20084881 G>A maps to NM_001002911.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:20084899 C>T maps to NM_001002911.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr7:37780619 C>T maps to NM_181791.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr7:37780084 C>T maps to NM_181791.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:72368330 C>T maps to ENST00000440684 G1290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:72366672 A>G maps to ENST00000440684 R1087R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr23:9693808 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:9693831 T>C did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:9693828 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:9716641 C>T did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr7:1097510 C>A maps to NM_138445.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:1097240 G>A maps to NM_138445.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:131487356 G>A maps to NM_207364.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:131487110 C>T maps to NM_207364.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:131487569 G>T maps to NM_207364.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:154146891 G>T maps to NM_001038705.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr3:154146456 C>T maps to NM_001038705.1 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr3:154139262 G>A maps to NM_001038705.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:98251362 C>T maps to NM_005290.1 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:98251068 C>T maps to NM_005290.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:94956653 G>A maps to NM_199243.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:145895103 T>C maps to NM_194251.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:145895250 G>A maps to NM_194251.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:145895163 C>T maps to NM_194251.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:145894833 C>T maps to NM_194251.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:67218800 C>T maps to NM_206997.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:67218800 C>T maps to NM_206997.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr11:67219256 G>A maps to NM_206997.1 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:6313840 C>T maps to NM_207370.2 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:6311497 C>A maps to NM_207370.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:6314056 G>A maps to NM_207370.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr1:6314866 G>A maps to NM_207370.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr1:6314737 G>A maps to NM_207370.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:6311551 C>T maps to NM_207370.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr2:175335231 G>A maps to NM_152529.5 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6803-01A-11D-1882-08 chr2:175304636 G>C maps to NM_152529.5 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr2:175301065 G>A maps to NM_152529.5 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:175318564 G>A maps to NM_152529.5 C592C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr3:119886799 G>A maps to NM_153002.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:9165733 C>T maps to NM_024980.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr10:25887233 C>T maps to NM_020752.2 H893H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:25464597 C>A maps to NM_020752.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr10:25684865 C>T maps to NM_020752.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr10:25861697 T>G maps to NM_020752.2 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr10:25886813 C>A maps to NM_020752.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr10:25886792 G>A maps to NM_020752.2 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:25464702 G>A maps to NM_020752.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:169801906 C>T maps to NM_014373.2 N49N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:168059835 C>T maps to NM_153832.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr1:168074013 G>T maps to NM_153832.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:128408488 C>T maps to NM_005291.2 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:128408875 C>A maps to NM_005291.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:128409082 C>T maps to NM_005291.2 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:150916402 G>A maps to NM_013308.3 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:145583652 G>T maps to NM_024531.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145582976 T>C maps to NM_024531.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:145583307 T>C maps to NM_024531.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr8:145584500 C>T maps to NM_024531.3 Y388Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:4936398 C>T maps to NM_017986.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:4936376 A>G maps to NM_017986.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:53106172 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:53106196 G>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:53106154 A>G did not map to a codon.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr23:53106024 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:53106764 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:53106173 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:53106554 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:53105839 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:53106225 G>A did not map to a codon.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr23:78426684 T>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:78426930 C>A did not map to a codon.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr23:78426761 T>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:40094112 A>G maps to NM_007223.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:36485248 A>G maps to ENST00000398597 D1402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:36484564 G>A maps to ENST00000398597 I1630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:36485202 C>A maps to ENST00000398597 E1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr17:36495311 G>A maps to ENST00000398597 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:36482647 G>A maps to ENST00000398597 P2269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:36486852 T>A maps to ENST00000398597 K868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr17:36486358 C>T maps to ENST00000398597 R1032R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr17:36483370 G>T maps to ENST00000398597 I2028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:36484762 G>A maps to ENST00000398597 C1564C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr17:36499027 C>G maps to ENST00000398597 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr13:99907712 G>A maps to NM_005292.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:57389028 G>T maps to NM_007264.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:57389283 C>T maps to NM_007264.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:99948201 G>A maps to NM_004951.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:12815319 C>T maps to NM_006143.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:142367699 C>T maps to NM_005293.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:142367315 G>A maps to NM_005293.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr9:125797423 G>A maps to NM_005294.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr9:125796919 C>T maps to NM_005294.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:125797168 A>G maps to NM_005294.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:107115657 C>T maps to NM_005295.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:200843190 C>T maps to NM_005298.2 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:200843107 C>T maps to NM_005298.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:200842740 C>T maps to NM_005298.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr10:125434363 G>A maps to NM_153442.3 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:125426516 G>T maps to NM_153442.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr10:125425979 G>A maps to NM_153442.3 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:71804102 C>T maps to NM_018971.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:27721177 C>T maps to NM_005281.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr1:27720841 C>T maps to NM_005281.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:27721003 G>A maps to NM_005281.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:51273871 G>A maps to NM_001506.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:51274804 C>T maps to NM_001506.1 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:51274381 G>A maps to NM_001506.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:41554897 T>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:241569452 C>T maps to NM_001195381.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr2:241569890 G>A maps to NM_001195381.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:124404742 C>T maps to NM_005302.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:124387073 A>G maps to NM_005302.2 C449C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:124404241 C>T maps to NM_005302.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:124387106 G>A maps to NM_005302.2 Y438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:202092195 C>T maps to NM_004767.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:202092387 G>A maps to NM_004767.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:133403127 G>A maps to NM_001508.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:133174992 G>A maps to NM_001508.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr2:133175220 C>T maps to NM_001508.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:46094725 G>A maps to NM_005282.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:46094296 G>A maps to NM_005282.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:46095109 C>T maps to NM_005282.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:46094646 G>A maps to NM_005282.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:60620601 C>T maps to NM_004778.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:105858893 C>T maps to NM_007227.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr2:105859310 C>T maps to NM_007227.3 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:105859046 G>A maps to NM_007227.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr2:105858362 G>A maps to NM_007227.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:150348462 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:150348462 C>T did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:150349051 C>T did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:150349065 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:150348871 A>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:150348781 T>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:150345309 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:150349305 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:150349151 G>A did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:150349597 C>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:150348664 G>A did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr23:150348895 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:150349106 G>A did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:150348957 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:150348482 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:150349385 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:174417413 T>C maps to NM_005684.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:174418037 C>T maps to NM_005684.4 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:231775248 G>A maps to NM_005683.3 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:231775008 G>T maps to NM_005683.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:57689864 G>A maps to NM_005682.5 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:57694770 C>T maps to NM_005682.5 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:57684225 G>A maps to NM_005682.5 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr16:57697362 G>A did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr16:57695839 C>T maps to NM_005682.5 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:110300638 C>T maps to ENST00000414000 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:110300629 G>A maps to ENST00000414000 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:110085826 C>T maps to NM_031936.4 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:110086192 C>A maps to NM_031936.4 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:110086504 G>T maps to NM_031936.4 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:51990270 C>T maps to NM_080865.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:97247001 A>G maps to NM_030784.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr6:97246869 A>G maps to NM_030784.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:19031841 G>A did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:19045345 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:19031991 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:19031935 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:19041546 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:19045370 T>C did not map to a codon.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr23:19024131 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:19020961 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:19031983 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:19041549 T>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:19013014 A>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:19049102 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:19028803 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:19028749 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:91701202 C>T maps to ENST00000238699 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr14:91700983 C>T maps to ENST00000238699 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:54080671 G>A maps to NM_006794.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:54080408 G>A maps to NM_006794.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr19:47844985 C>T maps to NM_018485.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:8589020 G>A maps to NM_080819.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr4:8583110 G>A maps to NM_080819.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:123214586 G>A maps to NM_032554.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:123214130 G>A maps to NM_032554.3 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:123213847 A>G maps to NM_032554.3 *347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:41586601 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:41587117 A>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:41586423 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:41587062 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:41586780 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:94113476 C>T maps to NM_016540.3 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr11:94134338 G>A maps to NM_016540.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:112724293 G>A maps to NM_018970.6 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr7:112724142 G>A maps to NM_018970.6 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:151012733 A>G maps to NM_023915.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:151012787 G>A maps to NM_023915.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:151012130 G>A maps to NM_023915.3 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:145769446 G>A maps to NM_001097612.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:57719833 G>A maps to NM_170776.4 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr16:57707258 A>C maps to NM_170776.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr5:90074405 C>T maps to NM_032119.3 R4277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:89979548 T>C maps to NM_032119.3 P1937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:89923353 T>C maps to NM_032119.3 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:90052420 G>T maps to NM_032119.3 G3911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr5:89981639 G>A maps to NM_032119.3 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:89949698 C>A maps to NM_032119.3 I1436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:89986684 C>T maps to NM_032119.3 R2260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr5:89923173 T>C maps to NM_032119.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:89939633 C>G maps to NM_032119.3 Y856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:89948235 C>T maps to NM_032119.3 Q1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr5:89971102 C>T maps to NM_032119.3 D1718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr5:90086865 A>T maps to NM_032119.3 G4740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:90087049 C>T maps to NM_032119.3 R4802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:101910392 T>G did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:101911868 G>A did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr23:101911300 G>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:101911910 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:101912463 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:101909849 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:101911430 T>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:101911262 G>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:101909664 C>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:101912900 G>A did not map to a codon.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr23:101908901 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr23:101912115 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:101912463 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:101912158 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:101910108 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr23:101912052 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:101910952 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:101912595 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:101912760 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr23:101909789 T>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:101969871 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:101970122 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:101969891 T>C did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:101970602 G>C did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:101971715 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:101970069 A>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:101971336 T>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:101969938 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:101971621 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:101970626 A>G did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr12:13061830 G>A maps to NM_003979.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:13065433 C>T maps to NM_003979.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr12:13061935 C>T maps to NM_003979.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr16:19883642 G>A maps to NM_016235.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:19884071 G>A maps to NM_016235.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:19873221 G>A maps to NM_016235.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr17:72428203 A>G maps to NM_022036.2 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:72428191 C>T maps to NM_022036.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:13095227 T>C maps to NM_018654.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:117113343 T>C maps to NM_148963.2 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr6:117127958 A>G maps to NM_148963.2 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:176023871 G>A maps to NM_052899.2 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:176025083 C>T maps to NM_052899.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:176024900 T>C maps to NM_052899.2 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:176024846 T>C maps to NM_052899.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:176025083 C>T maps to NM_052899.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:176025263 C>T maps to NM_052899.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr10:46999167 C>A maps to NM_014696.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:46999284 T>G maps to NM_014696.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:47000004 G>A maps to NM_014696.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:46999540 C>T maps to NM_014696.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:46999908 G>A maps to NM_014696.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:47000061 C>T maps to NM_014696.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:90170133 C>T maps to NM_198281.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:90170220 G>A maps to NM_198281.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:80011877 C>T maps to NM_212492.1 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:80014951 G>A maps to NM_212492.1 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr17:7217634 C>A maps to NM_004489.4 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:139243179 C>T maps to NM_001145638.1 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:109440140 G>A maps to NM_013296.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:109445746 G>T did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr1:109444441 A>G maps to NM_013296.4 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:145730438 T>C maps to NM_005309.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:145729842 G>A maps to NM_005309.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:46943744 G>A maps to NM_133443.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr16:46960946 C>T maps to NM_133443.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:46958311 G>A maps to NM_133443.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr6:28501817 T>C maps to NM_001509.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:35514415 C>T maps to NM_020895.3 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:35501005 C>T maps to NM_020895.3 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:35500085 G>A maps to NM_020895.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:35504471 C>T maps to NM_020895.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:35504570 A>C maps to NM_020895.3 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:123479433 C>T maps to ENST00000456860 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:123464791 G>A maps to ENST00000456860 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr11:123481038 C>T maps to ENST00000456860 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:123481016 C>A maps to ENST00000456860 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr3:113652377 G>A maps to NM_017577.4 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:113652476 T>G maps to NM_017577.4 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:113658738 G>A maps to NM_017577.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr15:72455725 C>T maps to NM_001012642.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:125821456 T>C maps to NM_023927.2 Y350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:125813385 C>A maps to NM_023927.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:47054102 G>A maps to NM_015124.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:47022779 G>A maps to NM_015124.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr22:40366976 C>T maps to NM_004810.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:40351854 G>A maps to NM_004810.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:52404700 C>A maps to NM_181711.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:50771542 C>T maps to NM_005311.4 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:50742166 G>A maps to NM_005311.4 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr7:50737430 G>A maps to NM_005311.4 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:50660792 G>A maps to NM_005311.4 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:165364962 A>G did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr2:165365251 C>T maps to NM_004490.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:165378576 C>T maps to NM_004490.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr2:165381561 A>C maps to NM_004490.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:165353778 T>C maps to NM_004490.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:37898827 A>T maps to ENST00000445327 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:37900453 C>A maps to ENST00000445327 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:37898610 A>G maps to ENST00000445327 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:11750918 G>A maps to NM_014668.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:11765301 G>A maps to NM_014668.3 W1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr2:11750963 G>A maps to NM_014668.3 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:11702637 G>A maps to NM_014668.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:11774325 C>T maps to NM_014668.3 D1687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:11777870 G>A maps to NM_014668.3 P1792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:11750855 C>T maps to NM_014668.3 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:11759032 C>T maps to NM_014668.3 S1344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr2:11770189 T>C maps to NM_014668.3 P1522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr2:11755255 C>G maps to NM_014668.3 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:11733022 G>A maps to NM_014668.3 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:11727562 G>A maps to NM_148903.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr2:11780552 C>G maps to NM_014668.3 L1941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr2:11758783 G>A maps to NM_014668.3 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr2:11761032 C>T maps to NM_014668.3 I1349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:11751000 C>T maps to NM_014668.3 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr2:11774337 C>T maps to NM_014668.3 Y1691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr2:11729004 C>T maps to NM_014668.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:11780549 G>A maps to NM_014668.3 P1940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:240656298 G>A maps to NM_022469.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:240656286 G>A maps to NM_022469.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr1:240656337 G>C maps to NM_022469.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr1:240656342 G>A maps to NM_022469.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:10130831 G>A maps to NM_198182.2 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:10130873 A>G maps to NM_198182.2 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:10095049 G>C maps to NM_198182.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:10105452 C>T maps to NM_198182.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:102589721 G>A maps to NM_024915.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:102571012 C>T maps to NM_024915.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr8:102570940 C>T maps to NM_024915.3 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:102570820 G>T maps to NM_024915.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:24669457 G>A maps to NM_021180.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:24663061 A>G maps to NM_021180.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:24669403 G>A maps to NM_021180.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:37428511 C>T maps to ENST00000377824 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:37424907 G>A maps to ENST00000377824 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:153029893 A>G maps to NM_001114183.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:153149894 A>G maps to NM_001114183.1 K730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr5:153085358 A>T maps to NM_001114183.1 K519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr5:153056675 T>C maps to NM_001114183.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:153078485 C>T maps to NM_001114183.1 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr5:153144131 G>A maps to NM_001114183.1 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr4:158254089 A>G maps to NM_000826.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:158257879 G>T maps to NM_000826.3 G609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:158262571 T>G maps to NM_000826.3 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:158224770 C>A maps to NM_000826.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:158254506 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:158233829 G>T did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr4:158254030 A>C maps to NM_000826.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr4:158282687 A>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:122537362 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:122616764 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:122319736 G>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:122537341 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:122538695 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:122319769 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:122537367 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:122616701 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:122599636 A>G did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:122551611 A>C did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:122319753 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:122599621 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:122599627 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:122387363 A>C did not map to a codon.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr23:122551302 A>C did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr11:105795339 A>C maps to NM_000829.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:105845044 G>A maps to NM_000829.3 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:105836773 G>T maps to NM_001077243.2 G799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr11:105850357 G>C maps to NM_000829.3 V867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:105781165 T>C maps to NM_000829.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:105483046 C>T maps to NM_000829.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:87406988 G>A maps to NM_017551.2 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr10:87966202 G>A maps to NM_017551.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:87482809 T>C maps to NM_017551.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:87615783 A>G did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:87487638 G>A maps to NM_017551.2 N502N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:87484277 G>A maps to NM_017551.2 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr10:87484322 G>A maps to NM_017551.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr10:87615902 G>A maps to NM_017551.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:94690471 C>T maps to NM_001510.2 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr4:94344118 G>A maps to NM_001510.2 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:94411865 C>A maps to NM_001510.2 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:94690429 G>A maps to NM_001510.2 Q810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr4:94138007 T>C maps to NM_001510.2 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr21:30949412 C>T maps to ENST00000327783 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr21:31062213 G>A maps to ENST00000327783 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:30925893 G>T maps to NM_000830.3 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr21:31015232 C>T maps to ENST00000327783 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:102074495 G>C maps to NM_021956.4 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr6:102074312 A>G maps to NM_021956.4 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr6:102307262 C>A maps to NM_021956.4 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr6:102247635 C>T maps to NM_021956.4 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr6:102483397 C>T maps to NM_021956.4 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:102074489 G>A maps to NM_021956.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:102337739 T>C maps to ENST00000436862 *183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:102134228 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:102483232 G>A maps to NM_021956.4 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:37337827 G>A maps to NM_000831.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr1:37271723 G>A maps to NM_000831.3 Y765Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr1:37346292 G>A maps to NM_000831.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:37319218 C>T maps to NM_000831.3 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:37307336 G>A maps to NM_000831.3 H510H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:120702711 C>A maps to NM_014619.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:120702612 G>A maps to NM_014619.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr11:120811159 C>T maps to NM_014619.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr11:120702684 C>T maps to NM_014619.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:120833349 C>T maps to NM_014619.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:120837913 C>T maps to NM_014619.2 F759F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:120673450 C>T maps to NM_014619.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:120744854 C>T maps to NM_014619.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:42507555 G>A maps to NM_002088.3 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr19:42546811 G>A maps to NM_002088.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:140058118 C>T maps to ENST00000371546 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:140051348 C>T maps to ENST00000371546 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr16:9862887 G>A maps to NM_000833.3 N805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:9857425 G>A maps to NM_000833.3 Y1325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr16:9857286 T>G maps to NM_000833.3 R1372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr16:9923492 A>C maps to NM_000833.3 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr16:9934864 G>A maps to NM_000833.3 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:9858349 G>A maps to NM_000833.3 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr16:9892257 G>A maps to NM_000833.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:9858091 G>T maps to NM_000833.3 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr16:10274133 G>A maps to NM_000833.3 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr16:9857895 G>T maps to NM_000833.3 R1169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:9857692 G>A maps to NM_000833.3 C1236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:9858517 G>A maps to NM_000833.3 N961N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr12:13716420 G>A maps to NM_000834.3 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:13716214 C>T maps to NM_000834.3 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:13716526 G>A maps to NM_000834.3 C1215C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:13715914 C>T maps to NM_000834.3 P1419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:13715770 G>A maps to NM_000834.3 G1467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:13716250 G>A maps to NM_000834.3 F1307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr12:13716622 C>T maps to NM_000834.3 T1183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:13716607 G>A maps to NM_000834.3 G1188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:13717417 C>T maps to NM_000834.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:14018806 G>A maps to NM_000834.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:13715899 A>G maps to NM_000834.3 L1424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:13906603 C>T maps to NM_000834.3 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:72846359 G>A maps to NM_000835.3 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr17:72846371 G>A maps to NM_000835.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:72846401 C>T maps to NM_000835.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:48919410 C>T maps to NM_000836.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:48908190 G>A maps to NM_000836.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr19:48946587 C>T maps to NM_000836.2 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr19:48908091 C>T maps to NM_000836.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:48918246 C>T maps to NM_000836.2 H513H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr9:104499893 C>T maps to NM_133445.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N4-01A-21D-A364-08 chr9:104449191 G>A maps to NM_133445.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:1003295 C>T maps to NM_138690.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr15:58001340 G>A maps to NM_015532.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:14538014 G>A maps to ENST00000507975 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:14545129 C>A maps to ENST00000507975 E973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:14555173 C>T maps to ENST00000507975 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:14549156 G>A maps to ENST00000507975 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:14561746 G>A maps to ENST00000507975 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:14552949 G>A maps to ENST00000507975 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:14564547 C>T maps to ENST00000507975 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:14554309 G>A maps to ENST00000507975 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr3:14545115 G>A maps to ENST00000507975 D977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:14564511 G>A maps to ENST00000507975 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:48832465 C>T did not map to a codon.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr23:48837685 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48837852 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48839423 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:48839704 G>A did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr23:48847496 T>C did not map to a codon.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr23:48839838 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:3037112 T>C maps to NM_182982.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:3006043 C>A maps to NM_182982.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr4:3015510 C>T maps to NM_182982.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr4:3006016 G>C maps to NM_182982.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:3030967 C>T maps to NM_182982.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:121212265 C>T maps to NM_005308.2 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:176868758 G>A maps to NM_002082.3 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr5:176867834 C>T maps to NM_002082.3 N513N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:176863242 C>T maps to NM_002082.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:176859780 C>T maps to NM_002082.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:141497440 G>A maps to NM_139209.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:141499583 C>T maps to NM_139209.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:141499526 T>C maps to NM_139209.2 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:47422066 G>A maps to NM_004491.4 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:47425364 C>T maps to NM_004491.4 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:47492889 C>T maps to NM_004491.4 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:47492912 C>T maps to NM_004491.4 I1339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:47421988 G>T maps to NM_004491.4 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:47423228 C>T maps to NM_004491.4 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr19:47422057 C>T maps to NM_004491.4 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:146350907 G>A maps to NM_000838.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:146351043 C>A maps to NM_000838.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:146351240 T>G maps to NM_000838.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:146351336 T>C maps to NM_000838.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr6:146351240 T>G maps to NM_000838.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:146755716 C>T maps to NM_000838.3 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr6:146350943 C>A maps to NM_000838.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr6:146720604 C>A maps to NM_000838.3 Y810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:146720019 A>G maps to NM_000838.3 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr6:146351156 C>T maps to NM_000838.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr6:146755496 G>A maps to NM_000838.3 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr6:146720425 C>T maps to NM_000838.3 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:146720721 C>A maps to NM_000838.3 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:146351102 C>A maps to NM_000838.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr6:146720481 C>A maps to NM_000838.3 Y769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr6:146720676 G>A maps to NM_000838.3 K834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr6:146350922 C>T maps to NM_000838.3 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:51752121 G>A maps to NM_000839.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:51752115 G>A maps to NM_000839.3 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:51743098 C>T maps to NM_000839.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:51743226 G>A maps to NM_000839.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:51749474 C>A maps to NM_000839.3 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr3:51749519 C>T maps to NM_000839.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:51743397 C>T maps to NM_000839.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:86416343 T>C maps to NM_000840.2 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:86468222 C>T maps to NM_000840.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:86468839 C>T maps to NM_000840.2 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr7:86415968 C>T maps to NM_000840.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:86416292 C>T maps to NM_000840.2 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:86416106 C>T maps to NM_000840.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:86468222 C>T maps to NM_000840.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr7:86416410 T>C maps to NM_000840.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr7:86416410 T>C maps to NM_000840.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr7:86416010 C>T maps to NM_000840.2 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:86469091 C>T maps to NM_000840.2 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr7:86415917 C>T maps to NM_000840.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:34008490 C>T maps to NM_000841.1 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr6:34029746 G>A maps to NM_000841.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:34059858 G>A maps to NM_000841.1 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr6:34101105 C>T maps to NM_000841.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:34003600 C>T maps to NM_000841.1 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:34029713 C>T maps to NM_000841.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:33996038 C>T maps to NM_000841.1 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:34008451 G>A maps to NM_000841.1 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:34101000 G>A maps to NM_000841.1 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr6:34004260 G>A maps to NM_000841.1 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:34026813 G>A maps to NM_000841.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:88242506 G>A maps to NM_001143831.2 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr11:88300436 G>T maps to NM_001143831.2 S805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr11:88780944 C>T maps to NM_001143831.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:88781001 T>C maps to NM_001143831.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:88780734 C>T maps to NM_001143831.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:88241900 C>T maps to NM_001143831.2 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr11:88781017 G>C maps to NM_001143831.2 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:88300671 G>A maps to NM_001143831.2 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr5:178416041 G>A maps to NM_000843.3 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:178413949 G>A maps to NM_000843.3 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:178413721 G>A maps to NM_000843.3 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:178413853 C>T maps to NM_000843.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:178408746 G>A maps to NM_000843.3 Q849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr5:178413682 C>T maps to NM_000843.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:178413487 C>T maps to NM_000843.3 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:178416050 G>A maps to NM_000843.3 H413H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:6903440 C>T maps to NM_181874.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:6903380 C>T maps to NM_181874.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:7620323 G>A maps to NM_181874.2 Q577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:7620161 C>T maps to NM_181874.2 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:6903449 G>A maps to NM_181874.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:7721812 G>A maps to NM_181874.2 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr3:6903437 T>C maps to NM_181874.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr3:7494337 A>T maps to NM_181874.2 K407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr3:7456776 C>A maps to NM_181874.2 Y367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr3:6903380 C>T maps to NM_181874.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:6903440 C>T maps to NM_181874.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:126883249 G>A maps to NM_001127323.1 C3C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:126173161 G>A maps to NM_001127323.1 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:126746610 A>C maps to NM_001127323.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr7:126542633 G>C maps to NM_001127323.1 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:126409970 A>G maps to NM_001127323.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr7:126882943 C>T maps to NM_001127323.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr7:126086135 A>C maps to NM_001127323.1 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr7:126746637 C>A maps to NM_001127323.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:42430030 C>T maps to NM_002087.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:42430078 C>T maps to NM_002087.2 C565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:42427919 C>T maps to NM_002087.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:16170759 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:16168542 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:16142437 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:16170714 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:16170749 T>C did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr23:16142389 G>T did not map to a codon.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr23:16168545 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:16142168 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:113978838 G>A maps to NM_024719.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr19:48956278 C>A maps to NM_031485.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:48954442 C>T maps to NM_031485.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:48954304 C>T maps to NM_031485.3 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:48956119 C>T maps to NM_031485.3 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr4:43032467 C>T maps to NM_001080476.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr4:42895342 C>T maps to NM_001080476.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr5:145246081 G>A maps to NM_001080516.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:145252432 C>T maps to NM_001080516.1 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:95234923 C>A maps to NM_173849.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:38068678 C>A maps to NM_001165958.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:38066177 C>T did not map to a codon.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr8:130763791 C>T maps to NM_031415.2 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:130760755 A>G maps to NM_031415.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr8:130789617 G>A maps to NM_031415.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:144643942 G>A maps to NM_024736.6 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:144643936 C>T maps to NM_024736.6 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr12:13241738 G>A maps to ENST00000405543 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:27818853 G>A maps to NM_001109763.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:3629364 C>T maps to NM_031965.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:3628866 C>T maps to NM_031965.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:3628051 C>T maps to NM_031965.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:3629190 C>T maps to NM_031965.2 N654N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:42736813 C>T maps to NM_019884.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr19:42736835 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:42736795 G>A maps to NM_019884.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:42738767 G>A maps to NM_019884.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:119631657 C>G did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:119642240 C>T maps to NM_002093.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:119634949 T>C maps to NM_002093.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:119582416 T>C maps to NM_002093.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:124064371 C>T maps to NM_000177.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:124081158 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:124072990 C>T maps to NM_000177.4 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:124089584 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:51488077 C>T did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:51487717 T>C did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:51487268 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:51487353 A>C did not map to a codon.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr23:51487600 T>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:51488293 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:51487095 A>T did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:51487184 G>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:51487890 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr23:51487819 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:30541659 G>A maps to NM_000637.3 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:33530760 C>T maps to NM_000178.2 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:52657736 G>T maps to NM_145740.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr6:52622670 T>A maps to NM_000846.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr6:52701077 G>C maps to NM_153699.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:106639055 C>T maps to NM_001031720.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:106755631 T>C maps to NM_001031720.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:106640590 C>A maps to NM_001031720.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:106744428 T>A maps to NM_001031720.2 C466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:106640590 C>T maps to NM_001031720.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:142962277 G>A maps to NM_001143679.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr1:110211093 C>T maps to ENST00000369830 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:110280340 T>C maps to NM_000849.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:110280141 A>G maps to NM_000849.4 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:110201635 T>C maps to NM_000850.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr10:106019438 C>T maps to NM_004832.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:106059033 C>T maps to NM_183239.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:67352166 G>A maps to NM_000852.3 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr22:24300606 C>T maps to NM_000854.3 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:28367781 C>T maps to NM_145657.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:28367832 G>A maps to NM_145657.1 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:54967833 A>G maps to NM_133267.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:54966567 G>A maps to NM_133267.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:54966537 G>A maps to NM_133267.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:144903179 C>T maps to NM_001164629.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:144765059 G>A maps to NM_001164629.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:144899477 G>T maps to NM_001164629.2 Y164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr2:144728241 T>A maps to NM_001164629.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:81659126 A>G maps to NM_015859.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:48873847 T>C maps to NM_172311.2 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:48873956 C>T maps to NM_172311.2 Q956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr2:48848412 A>T maps to NM_172311.2 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:89323036 A>G maps to NM_001514.5 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:89325945 G>A maps to NM_001514.5 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:120500127 A>G maps to NM_005513.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:120469476 T>G maps to NM_005513.2 Y26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:30436554 C>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:30511087 C>A maps to NM_002095.4 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:6387560 G>A maps to NM_002096.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:6380350 G>A maps to NM_002096.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:6389624 G>A maps to NM_002096.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:68875668 T>C maps to NM_001042490.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:124139505 T>C maps to NM_001516.3 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:30879000 G>T maps to NM_001517.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:30881129 G>A maps to NM_001517.4 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:158613098 C>T maps to NM_207118.2 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr7:74113411 C>T maps to NM_032999.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr7:73927296 C>T maps to NM_016328.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:73935628 T>C did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:73932541 C>T maps to NM_016328.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:73933978 C>T maps to NM_016328.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr7:73922529 C>A maps to NM_016328.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:73960132 C>T maps to NM_016328.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:74211874 G>T maps to NM_173537.2 S659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr7:74211858 C>T maps to NM_173537.2 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:74211660 G>A maps to NM_173537.2 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:74212017 C>T maps to NM_173537.2 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:74564094 A>G maps to NM_001003795.2 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:74565058 T>C maps to NM_001003795.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:74539000 G>A maps to NM_001003795.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr7:74538989 C>T maps to NM_001003795.2 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:74564013 G>A maps to NM_001003795.2 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:74564634 G>A maps to NM_001003795.2 W794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:27539960 G>A maps to NM_001520.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:27481631 G>A maps to NM_001520.3 D1537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:27499692 G>A maps to NM_001520.3 S1185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:27481580 G>A maps to NM_001520.3 N1554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:27519889 G>A maps to NM_001520.3 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr16:27480771 C>T maps to NM_001520.3 A1638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:27499731 G>A maps to NM_001520.3 N1172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:27514178 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:27503680 G>A maps to NM_001520.3 C1043C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:27503680 G>A maps to NM_001520.3 C1043C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:27475893 G>A maps to NM_001520.3 T1873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:27500444 G>A maps to NM_001520.3 A1116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:27544695 G>A maps to NM_001520.3 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:27565051 C>T maps to NM_001521.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:27566373 G>A maps to NM_001521.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:27558810 T>A maps to NM_001521.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:27560868 G>A maps to NM_001521.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr2:197639880 G>C maps to NM_012086.2 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr2:197657760 T>C maps to NM_012086.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:197662542 G>T maps to NM_012086.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:197629313 C>T maps to NM_012086.2 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:197657703 A>G maps to NM_012086.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:197631287 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:135553704 C>T maps to NM_012204.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr9:135554538 A>G maps to NM_012204.2 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:135553404 C>T maps to NM_012204.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr9:135546199 G>A maps to NM_012204.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr9:135553704 C>T maps to NM_012204.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:135931463 C>T maps to NM_001122823.1 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:135919142 G>A maps to NM_001122823.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr9:135932245 G>A maps to NM_001122823.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:135919229 G>A maps to NM_001122823.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr9:135932233 C>T maps to NM_001122823.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:111288881 T>C maps to NM_138408.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr22:39112920 C>T maps to NM_004286.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr22:39122318 C>T maps to NM_004286.4 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:90014458 T>C maps to NM_033107.3 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:43593575 G>A maps to NM_019096.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr10:1055494 A>G maps to NM_012341.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr10:1058413 G>T maps to NM_012341.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr10:1053032 C>T maps to NM_012341.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr20:60776090 G>A maps to NM_015666.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr20:60768649 G>A maps to NM_015666.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:60772932 G>A maps to NM_015666.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr20:60770904 C>T maps to NM_015666.3 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:60775761 C>T maps to NM_015666.3 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:112709896 T>G maps to NM_014170.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:46712230 C>T maps to NM_016426.6 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:46712214 T>C maps to NM_016426.6 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:46704359 C>T maps to NM_016426.6 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:46704464 T>A maps to NM_016426.6 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr22:46725337 C>T maps to NM_016426.6 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:46708147 G>A maps to NM_016426.6 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:42355288 G>A maps to NM_176791.3 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:42146990 C>A maps to NM_000409.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr6:42146127 C>T maps to NM_000409.3 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:108634980 G>A maps to NM_005459.3 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:108639351 C>T maps to NM_005459.3 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:108672543 C>T maps to NM_005459.3 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:106810869 A>G maps to ENST00000282249 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr11:106647284 G>T maps to ENST00000282249 Y572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr11:106810752 A>G maps to ENST00000282249 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:106888514 C>T maps to ENST00000282249 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr11:106558375 T>G maps to ENST00000282249 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr4:156632252 A>G maps to NM_001130684.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:156632138 G>A maps to NM_001130684.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr4:156632318 G>T maps to NM_001130684.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:156721175 G>A maps to ENST00000502959 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:156725804 C>T maps to ENST00000502959 R561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr4:156717662 G>T did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr4:156716575 T>C maps to ENST00000502959 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr4:156721188 T>C maps to ENST00000502959 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:156723544 G>A maps to ENST00000502959 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:156717620 C>A maps to ENST00000502959 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:14822719 A>G maps to NM_004963.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:14849241 A>G maps to NM_004963.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:14796577 G>A maps to NM_004963.3 C620C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:14825884 G>A maps to NM_004963.3 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:14834326 A>G maps to NM_004963.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:7907206 C>T maps to NM_000180.3 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:7910803 C>T maps to NM_000180.3 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:108631746 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:108691392 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:108719094 T>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:108718958 C>A did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:108684662 T>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:108708391 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:108635325 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:108708381 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:108636251 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:108638568 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:108638640 G>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:108635292 T>C did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:108631759 T>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:108638687 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr23:108708370 T>C did not map to a codon.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr23:108619316 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:108718608 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:108641868 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:44699433 C>T maps to NM_021927.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:44691983 T>C maps to NM_021927.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:228334591 C>T maps to ENST00000366720 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr1:228335193 C>T maps to ENST00000366720 T179T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IN-A6RO-01A-12D-A33T-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr2:189406026 A>T maps to NM_016315.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:65439576 G>A maps to NM_000181.3 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:65441106 G>A maps to NM_000181.3 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:65444730 G>T maps to NM_000181.3 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:65444871 C>T maps to NM_000181.3 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:65444795 G>A maps to NM_000181.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:65441043 C>T maps to NM_000181.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:42499687 C>A maps to NM_173601.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:42512918 A>G maps to NM_173601.1 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:42512846 G>A maps to NM_173601.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:72971425 A>G maps to NM_001080393.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr3:73024222 A>G maps to NM_001080393.1 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:73016807 C>T maps to NM_001080393.1 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:148714686 T>C maps to NM_004130.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:148741947 C>T maps to NM_004130.3 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:2795349 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:2773048 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:2772035 G>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:2799209 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:2795325 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:45947885 G>A maps to NM_152312.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:45948970 C>A maps to NM_152312.3 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr4:144801594 G>T maps to NM_198682.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr19:49489175 G>A maps to NM_002103.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:49494705 C>T maps to NM_002103.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:49472667 C>T maps to NM_002103.4 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:21712081 G>A maps to NM_021957.3 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:21693394 C>T maps to NM_021957.3 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:21728966 C>A maps to NM_021957.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:21721850 C>T maps to NM_021957.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:21695511 C>T maps to NM_021957.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr20:23350828 T>C maps to NM_022482.3 Y629Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:23345799 T>C maps to NM_022482.3 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:23346228 C>T maps to NM_022482.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:23345919 A>G maps to NM_022482.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr20:23350248 C>T maps to NM_022482.3 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:23346138 C>T maps to NM_022482.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:23350332 C>T maps to NM_022482.3 C580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:23350275 C>A maps to NM_022482.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:54404083 C>T maps to NM_006144.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr5:54405922 C>T maps to NM_006144.3 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr14:25101616 C>T maps to ENST00000382542 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr14:25078786 A>C maps to NM_033423.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:25076613 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:25077549 G>A maps to NM_033423.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:25077607 G>A maps to NM_033423.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:54327391 C>T maps to NM_002104.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:54327394 C>T maps to NM_002104.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:549784 G>A maps to NM_005317.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:549628 G>T did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr22:38202069 C>T maps to NM_005318.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr22:38201676 C>T maps to NM_005318.3 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:48723394 G>A maps to NM_181788.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:48723421 C>T maps to NM_181788.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:129034478 G>A maps to NM_006026.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:154113535 C>T did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr23:154113539 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:154113527 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:44882917 G>A maps to ENST00000421098 A66A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8295-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr5:134679098 C>A maps to ENST00000432382 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:134686546 C>T maps to NM_138609.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:134724630 G>A maps to NM_138610.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:71849834 C>T maps to NM_018649.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:71860045 C>T maps to NM_018649.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:71871426 C>T maps to NM_018649.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr10:71871327 C>T maps to NM_018649.2 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:71868957 C>T maps to NM_018649.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:103267880 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:103267749 A>G did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:103268175 C>T did not map to a codon.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr23:103267817 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:103267316 A>G did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:103267792 G>A did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:103267816 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:103268023 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:226253371 G>A maps to NM_002107.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:31944761 G>A maps to NM_001013699.2 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:9324909 C>T maps to NM_004285.3 Y786Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:9322284 A>C maps to NM_004285.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:9305526 T>C maps to NM_004285.3 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:9305382 C>T maps to NM_004285.3 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:9305621 T>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:9305487 C>T maps to NM_004285.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:9324703 C>T maps to NM_004285.3 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:43015740 C>T maps to NM_012205.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:115338384 G>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:115336939 C>T maps to NM_004132.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr10:115341701 A>T maps to NM_004132.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:99220763 C>A maps to NM_014282.2 Y151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr9:99227648 G>A maps to NM_014282.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:99252310 G>A maps to NM_014282.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:105243554 C>T maps to NM_020771.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:15604966 T>C maps to NM_012260.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:15610024 T>C maps to NM_012260.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr3:15613245 G>A maps to NM_012260.2 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:15604924 G>A maps to NM_012260.2 D548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:108935648 C>T maps to ENST00000351726 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:108940768 C>T maps to ENST00000351726 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:26414235 G>A maps to NM_000182.4 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:26437358 G>A maps to NM_000182.4 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:26437358 G>A maps to NM_000182.4 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:1866932 G>T maps to NM_005326.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:1866932 G>A maps to NM_005326.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:1866995 C>A did not map to a codon.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr12:96377754 C>T maps to NM_002108.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr12:96387250 G>A maps to NM_002108.2 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:96389535 C>T maps to NM_002108.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:96384169 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:153857061 C>T maps to NM_004821.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:7866430 A>G maps to NM_017545.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr20:7920961 A>G maps to NM_017545.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr20:7915152 G>A maps to NM_017545.2 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:7894827 T>C maps to NM_017545.2 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr20:7895046 C>T maps to NM_017545.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:119925648 C>T maps to ENST00000361035 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:119927487 C>T maps to ENST00000361035 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:119934794 C>T maps to ENST00000361035 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:119927487 C>T maps to ENST00000361035 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:39888481 C>T maps to ENST00000310778 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:39890670 C>T maps to ENST00000310778 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr17:39890670 C>T maps to ENST00000310778 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:39888481 C>T maps to ENST00000310778 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:39890670 C>T maps to ENST00000310778 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:82940460 G>A maps to NM_001884.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:156594420 C>T maps to NM_021817.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:156593353 C>A maps to NM_021817.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:156593629 C>T maps to NM_021817.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:156593863 C>T maps to NM_021817.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr15:89424846 C>A maps to NM_178232.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:89424612 G>A maps to NM_178232.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:19371750 G>A maps to NM_023002.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:19371868 G>A maps to NM_023002.2 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr19:19371982 C>T maps to NM_023002.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:19371880 G>A maps to NM_023002.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr11:46637421 T>C maps to NM_173811.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:46625303 C>A maps to NM_173811.3 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:140053862 G>T maps to NM_002109.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr5:140054667 A>G maps to NM_002109.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140054287 G>A maps to NM_002109.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:52216916 G>A maps to NM_001523.2 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr19:52222533 C>A maps to NM_001523.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:52216787 C>A maps to NM_001523.2 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:52222460 G>A maps to NM_001523.2 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:122641064 C>T maps to NM_005328.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:122627010 G>A maps to NM_005328.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr8:122626531 C>G maps to NM_005328.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr8:122627196 G>A maps to NM_005328.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:122641433 A>G maps to NM_005328.2 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:122641064 C>T maps to NM_005328.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr8:122641301 T>C maps to NM_005328.2 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:122641121 G>A maps to NM_005328.2 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:69148718 C>T maps to NM_005329.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:69143687 C>A maps to NM_005329.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:69143441 C>T maps to NM_005329.2 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:69143819 G>A maps to NM_005329.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:69143669 C>T maps to NM_005329.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:43698273 G>A maps to NM_138443.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr4:2240725 G>A maps to NM_024511.5 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:2240517 G>A maps to NM_024511.5 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:2242354 G>A maps to NM_024511.5 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:36109908 A>G maps to NM_015302.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:36105981 C>T maps to NM_015302.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:36106175 C>T maps to NM_015302.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:36113614 G>A maps to NM_015302.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:19083041 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:19082942 A>G maps to NM_017645.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:19093207 T>G maps to NM_017645.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:152722662 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:152721807 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:152721107 T>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:152721026 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17166749 G>A maps to NM_033417.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:156479582 C>T maps to NM_001173393.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:156514217 A>G maps to NM_032782.3 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr5:156514151 T>C maps to NM_032782.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:223270 G>A maps to NM_000517.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr11:5289716 C>G maps to NM_005330.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr11:5290788 A>C maps to NM_005330.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr11:5269718 T>A did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr11:5275626 A>C maps to ENST00000399563 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:5274527 G>C maps to ENST00000399563 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr11:5275584 G>C maps to ENST00000399563 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:106820373 T>C maps to NM_012257.3 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:106827053 G>A maps to NM_012257.3 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:135318742 C>T maps to NM_006620.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:135300362 G>A maps to NM_006620.3 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:135317928 G>A maps to NM_006620.3 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:135360708 A>G did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr6:135317943 G>A maps to NM_006620.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:110944144 T>C maps to NM_006402.2 *174W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:110946653 G>A maps to NM_006402.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:11133051 T>C did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:11136636 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:11133047 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:11139094 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr23:11135396 C>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:153219665 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153222822 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:153219883 G>A did not map to a codon.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr23:153225352 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:153225828 A>G did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:153228858 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:153228707 C>T did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr23:153219977 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153220366 G>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153229697 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:153220507 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153228873 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153219632 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153227747 G>A did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:153220023 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:153221774 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:153228737 T>C did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:153220896 G>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:153225597 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153225268 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:153218044 G>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:153215717 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:153220075 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:153227067 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:153219913 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:153220522 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:153219889 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:153223660 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:104480793 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:104487252 G>A maps to NM_013320.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:30681808 G>T maps to NM_002110.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr20:30671800 C>T maps to NM_002110.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr20:30674563 G>A maps to NM_002110.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:30686918 C>T maps to NM_002110.3 Y453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:30671778 C>T maps to NM_002110.3 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr20:30671832 G>A maps to NM_002110.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:30671799 C>T maps to NM_002110.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:30689271 C>T maps to NM_002110.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr20:30659530 C>T maps to NM_002110.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:121351278 G>A maps to NM_005335.4 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:121354597 C>T maps to NM_005335.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:121363691 G>A maps to NM_005335.4 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr5:45262135 G>A maps to NM_021072.2 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:45267275 C>T maps to NM_021072.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:45262406 C>T maps to NM_021072.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:45396641 G>A maps to NM_021072.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr5:45262334 G>A maps to NM_021072.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr5:45262220 C>T maps to NM_021072.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:45262883 C>T maps to NM_021072.2 K604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr5:45695942 C>A maps to NM_021072.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr5:45396782 G>T maps to NM_021072.2 Y347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr5:45303800 T>C maps to NM_021072.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:45262135 G>A maps to NM_021072.2 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:45262442 C>T maps to NM_021072.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr5:45695889 C>A maps to NM_021072.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:45695922 G>A maps to NM_021072.2 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:605188 G>A maps to NM_001194.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:610371 C>T maps to NM_001194.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:608109 C>T maps to NM_001194.3 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:613948 G>A maps to NM_001194.3 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr19:615919 G>T maps to NM_001194.3 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:155257626 T>C maps to NM_020897.1 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:155255657 C>T maps to NM_020897.1 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:155247629 C>A maps to NM_020897.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr15:73617683 G>A maps to NM_005477.2 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr15:73615925 C>T maps to NM_005477.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:73617458 C>T maps to NM_005477.2 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:73617773 C>A maps to NM_005477.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:40336522 T>C maps to NM_001524.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:32086580 G>A maps to NM_001525.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:32086454 G>A maps to NM_001525.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr6:55145213 G>A maps to NM_001526.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:55145213 G>A maps to NM_001526.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:55039525 C>T maps to NM_001526.3 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr1:32797378 C>T maps to NM_004964.2 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:32794716 C>T maps to NM_004964.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:32793259 A>G maps to NM_004964.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr1:32798643 G>T maps to NM_004964.2 *483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:50686205 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:13542246 C>T maps to NM_024827.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:114264667 G>A maps to ENST00000398283 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:141008156 G>A maps to NM_003883.3 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:141004854 G>A maps to NM_003883.3 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:240055965 C>T maps to NM_006037.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:239976530 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:240036771 C>A maps to NM_006037.3 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr2:240033330 G>A maps to NM_006037.3 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr2:240003863 G>A maps to NM_006037.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr17:42158247 G>A maps to NM_001015053.1 D871D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:42162479 G>A maps to NM_001015053.1 C699C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:48673823 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:48681195 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:48674552 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:48678588 C>T did not map to a codon.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr23:48666707 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:48661557 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:48666715 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:48674584 A>G did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr23:48678617 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:48673430 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:48681770 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:48673387 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:48188644 G>A maps to NM_015401.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:48192417 C>T maps to NM_015401.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:48189158 G>A maps to NM_015401.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:71681926 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:71787752 C>T did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:71549910 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:71788640 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:18875106 C>T maps to NM_178425.2 N828N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:18687587 G>T maps to NM_178425.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:18975447 G>A maps to NM_178425.2 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr7:18630089 C>A maps to NM_178425.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr7:18705930 C>T maps to NM_178425.2 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr7:18625091 C>T maps to NM_178425.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr7:18688165 T>C maps to NM_178425.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr7:18669054 G>A maps to NM_178425.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:18767280 G>T maps to NM_178425.2 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:19015513 C>T maps to NM_178425.2 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:50534933 C>T maps to NM_002112.3 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:50535354 C>T maps to NM_002112.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:50534777 C>T maps to NM_002112.3 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:125619867 G>A maps to NM_016063.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:156714904 G>A maps to NM_001126050.1 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr6:22570001 C>T maps to NM_138574.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:6995383 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:6968350 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:6995273 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:44641700 T>C maps to NM_032124.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:44662729 G>A maps to NM_032124.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:44639387 C>T maps to NM_032124.4 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:116136220 G>A maps to NM_031219.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:116136583 C>T maps to NM_031219.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:116136523 C>T maps to NM_031219.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:242179356 G>A maps to NM_005336.3 R784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:242170271 G>A maps to NM_005336.3 Q1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:242203991 G>A maps to NM_005336.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr2:242178203 T>A did not map to a codon.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr2:242179014 A>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:83724398 T>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:83616609 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:83724525 C>G did not map to a codon.
Sequencing variant TCGA-BR-6710-01A-11D-1882-08 chr23:83723682 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:83724231 G>T did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:83576952 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:83723661 T>C did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:83599418 T>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:83724101 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:236751265 C>T maps to NM_018072.5 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:236766614 C>T maps to NM_018072.5 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:236744678 G>A maps to NM_018072.5 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:236746033 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:236749197 G>A maps to NM_018072.5 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr1:236723046 C>T maps to NM_018072.5 A1579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:236719130 G>A maps to NM_018072.5 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:236760180 G>A maps to NM_018072.5 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:236749679 T>C maps to NM_018072.5 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr1:236718880 G>A maps to NM_018072.5 S1908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:236715408 T>C did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr1:236730095 C>G maps to NM_018072.5 A1386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:236749212 C>T maps to NM_018072.5 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr1:236735823 T>C maps to NM_018072.5 E1198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:50112910 C>T maps to NM_182922.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr16:50106620 A>G maps to NM_182922.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:50112650 G>C did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:50100170 G>C maps to NM_182922.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:73989271 A>G maps to ENST00000334988 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr14:73989211 G>T maps to ENST00000334988 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr14:73973209 G>T maps to ENST00000334988 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:73945319 A>G maps to ENST00000334988 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr14:73959793 A>G maps to ENST00000334988 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:31856443 A>T maps to ENST00000389961 C351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:31785041 T>C maps to ENST00000389961 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:31856541 G>A maps to ENST00000389961 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr14:31819923 C>A did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:37293012 G>A maps to NM_019024.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:37255303 T>C maps to NM_019024.1 A1205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:37255955 G>A maps to NM_019024.1 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:37297375 C>T maps to NM_019024.1 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:37284573 A>G maps to NM_019024.1 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:37267562 C>T maps to NM_019024.1 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:37310521 T>C maps to NM_019024.1 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:58121400 G>T maps to NM_022070.4 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:58147143 C>T maps to NM_022070.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:58121370 G>A maps to NM_022070.4 Y1033Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:58137346 G>A maps to NM_022070.4 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:145235328 G>A maps to NM_032450.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:145278099 C>T maps to NM_032450.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:145267943 C>T maps to NM_001099281.1 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:40998234 C>T maps to ENST00000296803 P1560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:41018857 C>A maps to ENST00000296803 G871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:41065463 C>T maps to ENST00000296803 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:41018875 G>A maps to ENST00000296803 R865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr5:41065469 G>A maps to ENST00000296803 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr6:138734046 G>A maps to NM_014320.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:139495645 C>T maps to NM_016217.2 Y479Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:139488111 C>T maps to NM_016217.2 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:139488243 C>T maps to NM_016217.2 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:31604295 A>G maps to NM_015382.2 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:31581679 G>A maps to NM_015382.2 L2074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:31641111 T>C maps to NM_015382.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:31598571 T>C maps to NM_015382.2 A1335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr14:31598601 G>A maps to NM_015382.2 G1325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:31614148 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr14:31647240 G>A maps to NM_015382.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr14:31582499 G>C maps to NM_015382.2 S2016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:93242785 T>C maps to ENST00000446394 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:93185147 T>C maps to ENST00000446394 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:93221958 C>T maps to NM_173497.2 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr1:45475898 T>C maps to NM_024602.5 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:43485062 C>T maps to NM_015052.3 N764N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:43546740 C>T maps to NM_015052.3 Q1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:43594296 C>T maps to NM_015052.3 S1539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr7:43477735 C>T maps to NM_015052.3 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:43484720 G>A maps to NM_015052.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:43508575 C>T maps to NM_015052.3 R991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr7:43483815 G>T did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr7:43503376 G>T maps to NM_015052.3 E924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:43503274 C>T maps to NM_015052.3 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:43351402 G>A maps to NM_015052.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:43484840 G>A maps to NM_015052.3 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr7:43477643 G>T maps to NM_015052.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:43508670 G>A maps to NM_015052.3 R1022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:43351513 C>T maps to NM_015052.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:43351498 C>T maps to NM_015052.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:43484039 G>A maps to NM_015052.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr7:43548588 G>A maps to NM_015052.3 S1296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:197080602 G>A maps to NM_020760.1 I1531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:197080626 G>A maps to NM_020760.1 F1523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr2:197183522 C>T maps to NM_020760.1 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr2:197172768 G>A maps to NM_020760.1 Y825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:197183521 G>A maps to NM_020760.1 Q698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:197185164 T>G did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:124732091 G>A maps to NM_020733.1 D777D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:124716536 G>A maps to NM_020733.1 C1216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:124739857 G>A maps to NM_020733.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:66703904 T>C maps to NM_033647.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:66704384 T>C maps to NM_033647.2 C559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr12:66704240 G>A maps to NM_033647.2 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:96350526 A>G maps to NM_018063.3 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr10:96347999 C>T maps to NM_018063.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr10:96341222 A>G maps to NM_018063.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:185941700 G>A maps to NM_001029887.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:185940638 G>A maps to NM_001029887.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:185940959 A>G maps to NM_001029887.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:185940638 G>A maps to NM_001029887.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:65199437 G>T maps to NM_014877.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:65184690 A>C maps to NM_014877.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:100692643 C>A maps to NM_018437.3 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:50608705 C>T maps to NM_016173.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:50608615 C>T maps to NM_016173.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:50609605 G>A maps to NM_016173.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:50615292 C>T maps to NM_016173.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:124794858 C>T maps to NM_152722.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:124794735 G>A maps to NM_152722.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr11:124794666 G>A maps to NM_152722.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr7:92826555 G>T maps to ENST00000453812 S423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:92844978 C>T maps to ENST00000453812 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:65415011 G>T did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:65476118 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:65486429 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:65423337 T>C did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:65392441 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:65428057 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr23:65393488 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:65412068 T>C did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:65417540 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:65413404 C>T did not map to a codon.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr23:65476000 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:65420423 T>C did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr23:65474919 C>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:65479957 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr23:65476077 G>C did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:65483490 T>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:65427136 C>T did not map to a codon.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr23:65392219 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:65409534 G>A did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:93808526 C>T maps to NM_001098672.1 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:93822026 C>T maps to NM_001098672.1 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:93800818 C>T maps to NM_001098672.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr11:93844119 C>T maps to NM_001098672.1 Q1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:93808352 A>C maps to NM_001098672.1 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:93754617 G>A maps to NM_001098672.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:63943554 C>T maps to ENST00000261887 L3481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:63952004 G>A maps to ENST00000261887 S3118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:63937701 C>T maps to ENST00000261887 K3686K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:64067599 G>A maps to ENST00000261887 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:63953189 G>A maps to ENST00000261887 Q3069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:63950762 C>T maps to ENST00000261887 A3193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr15:64020011 G>A maps to ENST00000261887 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:63970207 C>T maps to ENST00000261887 E2302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:63901306 G>A maps to ENST00000261887 N4854N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:63990924 A>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:64026997 T>C maps to ENST00000261887 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:63944641 T>C maps to ENST00000261887 S3463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr15:63970194 G>A maps to ENST00000261887 L2307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:63904726 C>T maps to ENST00000261887 W4709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:63958254 C>T maps to ENST00000261887 S2806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:63966684 G>A maps to ENST00000261887 R2568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr15:64067603 A>G maps to ENST00000261887 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:63937788 C>T maps to ENST00000261887 S3657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:63966684 G>A maps to ENST00000261887 R2568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:28447610 C>T maps to NM_004667.4 S2454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:28538034 T>C maps to NM_004667.4 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:28413567 C>T maps to NM_004667.4 W3466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:28447490 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:28511076 G>A maps to NM_004667.4 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:28419592 G>A maps to NM_004667.4 H3335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:28473544 C>T maps to NM_004667.4 P1761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:28510806 C>T maps to NM_004667.4 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:28422650 G>A maps to NM_004667.4 G3056G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:28441713 A>G maps to NM_004667.4 A2671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr15:28459816 G>A maps to NM_004667.4 D2114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr15:28441686 A>G maps to NM_004667.4 I2680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:28361853 C>T maps to NM_004667.4 P4522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:28422218 A>G maps to NM_004667.4 D3103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:28427564 G>A maps to NM_004667.4 G2973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:28467260 C>T maps to NM_004667.4 Q1855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:28474909 C>T maps to NM_004667.4 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:28377828 G>A maps to NM_004667.4 S4126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr15:28473508 T>C maps to NM_004667.4 S1773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:28389352 G>A maps to NM_004667.4 C3723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:28501286 C>T maps to NM_004667.4 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr15:28443795 C>T maps to NM_004667.4 Q2612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:28482136 C>T maps to NM_004667.4 P1325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:28482214 A>G maps to NM_004667.4 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:28473457 G>A maps to NM_004667.4 L1790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:28446622 T>C maps to NM_004667.4 V2565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:28463701 G>A maps to NM_004667.4 S1987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:28447384 G>T maps to NM_004667.4 A2497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:28359774 C>T maps to NM_004667.4 R4632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:28478842 A>G maps to NM_004667.4 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:28447514 G>A maps to NM_004667.4 S2486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:28493821 A>G maps to NM_004667.4 C1037C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:28366497 G>A maps to NM_004667.4 R4422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:28377924 G>A maps to NM_004667.4 V4094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:28419604 C>T maps to NM_004667.4 T3331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:28369269 G>A maps to NM_004667.4 F4367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:28474422 G>A maps to NM_004667.4 V1730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr15:28443584 A>G maps to NM_004667.4 S2650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:28389843 G>A maps to NM_004667.4 T3705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr10:69682804 G>A maps to NM_022079.2 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:89388314 G>A maps to NM_016323.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:89384764 A>G maps to NM_016323.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:89390311 C>A maps to NM_016323.2 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr4:89391824 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:89425505 C>T maps to NM_016323.2 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr4:89383349 C>A maps to NM_016323.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:89408221 C>T maps to NM_016323.2 D618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:89326075 C>T maps to NM_017912.3 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:89356987 C>T maps to NM_017912.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:56974001 T>C maps to NM_014685.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr3:57233802 G>A maps to NM_003865.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr5:74001087 A>T maps to NM_000521.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:80400467 A>G maps to NM_173620.2 *586W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:80393720 C>T maps to NM_173620.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr17:80391604 C>T maps to NM_173620.2 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:43227535 C>T maps to NM_006460.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:43227396 G>A maps to NM_006460.2 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:43246698 C>T maps to NM_144608.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:43246698 C>T maps to NM_144608.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr8:80677767 G>A maps to NM_001040708.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:80677869 C>T maps to NM_001040708.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr6:126080848 G>A maps to NM_012259.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr6:126080779 C>T maps to NM_012259.2 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr6:126080737 C>T maps to NM_012259.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:126080752 G>A maps to NM_012259.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr6:126080830 G>A maps to NM_012259.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:40105267 G>A maps to NM_014571.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:40092676 C>T maps to NM_014571.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr1:40092769 C>A maps to NM_014571.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:145415498 G>A maps to NM_213653.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:145415690 C>T maps to NM_213653.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:145415459 C>T maps to NM_213653.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:91779568 C>T maps to NM_001017975.3 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:91816379 A>G maps to NM_001017975.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:91784847 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:91728051 C>A maps to NM_001017975.3 G1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:91843979 G>A maps to NM_001017975.3 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr1:91816301 A>G maps to NM_001017975.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:91817107 G>A maps to NM_001017975.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:120369652 G>A maps to NM_000187.3 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:120393818 G>A maps to NM_000187.3 C35C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-4362-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:81381565 C>T maps to NM_000601.4 S165S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CD-5800-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr7:81381460 G>T maps to NM_000601.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr7:81381519 G>A maps to NM_000601.4 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:81372787 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:81388060 G>T maps to NM_000601.4 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6803-01A-11D-1882-08 chr4:3447796 G>T maps to ENST00000511533 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:3449320 C>A maps to ENST00000511533 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr4:3446392 G>A maps to ENST00000511533 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr4:3446110 C>T maps to ENST00000511533 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:3446080 C>T maps to ENST00000511533 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr4:3449700 C>T maps to ENST00000511533 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:79667726 C>T maps to NM_004712.4 N673N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr17:79663722 G>A maps to NM_004712.4 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:79667551 G>A maps to NM_004712.4 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr17:79662907 G>A maps to NM_004712.4 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:43048913 C>A maps to ENST00000458501 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:43013830 C>A maps to ENST00000458501 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:210686511 A>G maps to NM_001170580.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:210761244 T>G maps to NM_001170580.1 Y349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:210577854 G>A maps to NM_001170580.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:210522328 C>T maps to NM_001170580.1 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr3:42735276 G>A maps to NM_020707.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:42735291 A>G maps to NM_020707.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:94452212 C>T maps to NM_002729.4 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:145636547 C>T maps to NM_022475.1 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:145629317 A>G did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr4:145568030 G>T maps to NM_022475.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:145629370 C>T maps to NM_022475.1 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr4:145655991 G>A maps to NM_022475.1 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:145640025 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:145568051 G>A maps to NM_022475.1 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:100119153 C>T maps to NM_001127258.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:222717210 G>A maps to NM_024746.3 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:222696077 T>C maps to NM_024746.3 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:222716948 C>A maps to NM_024746.3 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr1:222717243 G>A maps to NM_024746.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:108076863 C>T maps to NM_007072.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:108072322 C>T maps to NM_007072.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:100533729 G>A maps to NM_033055.2 W228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:100547719 G>A maps to NM_033055.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:100534099 G>A maps to NM_033055.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:97203360 C>T maps to NM_032558.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:27669049 C>A maps to NM_152740.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:27570864 G>A maps to NM_152740.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr2:191069953 T>C maps to NM_014362.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr2:191161619 C>T maps to NM_014362.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:1961288 G>A maps to NM_001098202.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:1961159 G>A maps to NM_001098202.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:1959995 G>A maps to NM_001098202.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr17:1961552 G>A maps to NM_001098202.1 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr22:21800713 C>T maps to NM_015094.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:21799828 C>T maps to NM_015094.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:21799283 C>T maps to NM_015094.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:21799657 G>C maps to NM_015094.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:21799519 C>T maps to NM_015094.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr22:21800635 C>T maps to NM_015094.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:62207346 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:62188500 T>C maps to ENST00000394997 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:62187240 G>A maps to ENST00000394997 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr10:102305758 C>T maps to ENST00000442724 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:46815456 C>A maps to NM_152795.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr19:46823750 C>T maps to NM_152795.2 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:42926631 C>T maps to NM_016438.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr11:119002252 C>T maps to NM_198971.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr11:118997699 C>T maps to NM_198971.1 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:75186990 C>T maps to NM_005338.4 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:75183784 G>A maps to NM_005338.4 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:75182749 A>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:75176317 G>A maps to NM_005338.4 C826C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:123339494 C>T maps to NM_003959.1 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:123333392 C>T maps to NM_003959.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr12:123342782 T>C maps to NM_003959.1 C650C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:114499898 G>A maps to ENST00000426820 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:114483979 T>C maps to ENST00000426820 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:114516065 C>T maps to ENST00000426820 R1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr1:114483280 G>T maps to ENST00000426820 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:114483031 G>A maps to ENST00000426820 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:139416404 G>A maps to NM_022740.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:139285326 G>A maps to NM_022740.4 H757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:139416623 G>T maps to NM_022740.4 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:139416653 C>T maps to NM_022740.4 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:139416428 G>A maps to NM_022740.4 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:139268716 G>A maps to NM_022740.4 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:33350148 G>A maps to NM_005734.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:33308271 G>A maps to NM_005734.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:33370343 C>A maps to NM_005734.3 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr11:33360382 A>T maps to NM_005734.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:40886654 G>A maps to NM_144685.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:19346866 C>T maps to NM_003325.3 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:19341011 G>A maps to NM_003325.3 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr22:19398266 G>A maps to NM_003325.3 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr22:19363239 T>C maps to NM_003325.3 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:19365411 G>A maps to NM_003325.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:19373205 G>A maps to NM_003325.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:30004973 C>T maps to NM_003609.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:26017924 A>G maps to NM_005325.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr6:27834673 T>A maps to NM_005322.2 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr6:27834887 C>T maps to NM_005322.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:27835085 G>A maps to NM_005322.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:27835295 G>A maps to NM_005322.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:26056482 A>T maps to NM_005319.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr6:26156641 G>T maps to NM_005321.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:26107823 G>A maps to NM_005323.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:26108174 G>A maps to NM_005323.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:25726409 G>A maps to NM_170745.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:25726368 T>C maps to NM_170745.3 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:25726455 G>A maps to NM_170745.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:25726614 G>A maps to NM_170745.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr6:25726539 G>A maps to NM_170745.3 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr6:26199398 G>A maps to NM_021065.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:26199227 G>A maps to NM_021065.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr6:26199141 G>A maps to NM_021065.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:26217402 T>A maps to NM_021052.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr6:26217504 G>C maps to NM_021052.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr6:27101072 A>T maps to NM_021064.4 K75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:27100888 T>A maps to NM_021064.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr6:27100903 C>G maps to NM_021064.4 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:27114939 T>C maps to NM_080596.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:27115218 G>A maps to NM_080596.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:27114951 C>T maps to NM_080596.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:27833263 C>T maps to NM_003511.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr6:27833332 G>T maps to NM_003511.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr6:27833305 C>T maps to NM_003511.2 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:27860699 C>T maps to NM_003514.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr6:27860702 T>C maps to NM_003514.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr6:27860771 C>A maps to NM_003514.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:26043726 G>A maps to NM_021062.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:26123955 G>T maps to NM_003526.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:26123772 G>A maps to NM_003526.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr6:26123997 C>A maps to NM_003526.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:26123916 C>T maps to NM_003526.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr6:26184286 G>C maps to NM_003523.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr6:26200064 G>A maps to NM_003522.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:26252013 C>T maps to NM_003524.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr6:26252141 G>C maps to NM_003524.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:27100150 A>G maps to NM_021058.3 *127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr6:27100277 G>A maps to NM_021058.3 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:27100412 G>A maps to NM_021058.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:27782979 C>T maps to NM_003521.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:27783153 C>T maps to NM_003521.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr6:27806582 G>A maps to NM_003520.3 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:27861579 G>T maps to NM_003527.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:27861422 C>T maps to NM_003527.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr6:26045664 C>G maps to NM_003531.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:26225714 C>T maps to NM_003532.2 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:26225387 G>A maps to NM_003532.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:26225780 G>A maps to NM_003532.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr6:26271498 T>C maps to NM_003534.2 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:26271324 G>T maps to NM_003534.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:26271321 G>A maps to NM_003534.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:27839988 G>A maps to NM_003533.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:27858480 A>C maps to NM_003535.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:26027234 G>A maps to NM_003544.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:26027195 T>C maps to NM_003544.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr6:26104228 C>T maps to NM_003542.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:26189067 G>A maps to NM_003539.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:26240922 G>A maps to NM_003540.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr6:26240796 G>T maps to NM_003540.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:27107158 C>T maps to NM_003495.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:27799299 A>G maps to NM_003541.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr1:149858826 C>T maps to NM_003517.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:149858892 C>T maps to NM_003517.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:149857995 G>T maps to NM_003528.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:149398888 C>T maps to NM_001024599.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:149785230 G>C maps to NM_001123375.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:228646132 G>A maps to NM_175055.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:228646201 C>T maps to NM_175055.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:228612738 C>T maps to NM_003493.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr6:12120525 T>C maps to NM_002114.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:12125502 T>C maps to NM_002114.2 N1825N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:12122643 C>T maps to NM_002114.2 G872G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:12125940 C>T maps to NM_002114.2 S1971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr6:12123036 C>T maps to NM_002114.2 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:12131030 C>T maps to NM_002114.2 R2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:12121956 C>T maps to NM_002114.2 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:12164141 C>T maps to NM_002114.2 P2535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:12122679 C>T maps to NM_002114.2 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr6:12122175 G>A maps to NM_002114.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:143092793 G>A maps to NM_006734.3 R1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:143093400 G>A maps to NM_006734.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:143091477 G>A maps to NM_006734.3 Y1466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr6:143095785 T>C maps to NM_006734.3 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:143091557 G>A maps to NM_006734.3 R1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:143094968 G>A maps to NM_006734.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:143093048 G>A maps to NM_006734.3 R943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:143091557 G>A maps to NM_006734.3 R1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr6:143074615 C>T maps to NM_006734.3 E2323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:143092524 G>A maps to NM_006734.3 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr6:143081658 G>A maps to NM_006734.3 D1922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr6:143095263 C>T maps to NM_006734.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr6:143093769 G>A maps to NM_006734.3 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:143091582 G>A maps to NM_006734.3 S1431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:143093292 C>T maps to NM_006734.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:143091171 T>C maps to NM_006734.3 E1568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:143091177 T>C maps to NM_006734.3 S1566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:143074741 C>T maps to NM_006734.3 Q2281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:143093267 G>A maps to NM_006734.3 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:143094153 G>A maps to NM_006734.3 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:41990483 G>A maps to NM_024503.3 L1769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:42046232 T>C maps to NM_024503.3 S1412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:42046987 C>A maps to NM_024503.3 E1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:42049391 C>T maps to NM_024503.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr1:42047174 G>A maps to NM_024503.3 P1098P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:42047177 T>A maps to NM_024503.3 G1097G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:42045428 G>A maps to NM_024503.3 S1680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:41978717 G>T maps to NM_024503.3 T2058T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:41976127 G>A maps to NM_024503.3 N2405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:42049802 G>A maps to NM_024503.3 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:42046169 T>C maps to NM_024503.3 S1433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:42046925 A>G maps to NM_024503.3 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:42041237 C>T maps to NM_024503.3 A1728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr1:42048614 C>T maps to NM_024503.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:42048425 T>C maps to NM_024503.3 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:42045767 A>C maps to NM_024503.3 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:234750288 C>T maps to NM_018410.3 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:71128990 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:71152040 T>C maps to ENST00000439900 Y767Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:71144667 C>T maps to ENST00000439900 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:71139812 G>A maps to ENST00000439900 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:71048516 G>A maps to ENST00000439900 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:71124645 C>T maps to ENST00000439900 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr2:75061722 C>T maps to NM_000189.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:75112658 T>G maps to NM_000189.4 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:176314231 G>A maps to NM_002115.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:176317897 C>T maps to NM_002115.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:176310831 C>T maps to NM_002115.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:176309123 G>A maps to NM_002115.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:176308304 C>T maps to NM_002115.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:176311090 G>A maps to NM_002115.2 C634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:176314249 G>A maps to NM_002115.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr5:176314264 G>A maps to NM_002115.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:71008476 C>T maps to NM_025130.3 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:71010408 G>T did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr10:71008284 C>T maps to NM_025130.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr10:71003046 C>T maps to NM_025130.3 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:37854118 C>T maps to NM_181786.2 C474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:37854404 A>C maps to NM_181786.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:37853629 G>A maps to NM_181786.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr6:29911226 G>T maps to ENST00000376806 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:29911959 C>A maps to ENST00000376806 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:31323091 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:31323370 T>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:31323265 C>T maps to ENST00000428231 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:31322882 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:31323307 G>T maps to ENST00000428231 C297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:31239467 C>T maps to ENST00000383329 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr6:31238152 C>T maps to ENST00000383329 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr6:31238915 C>A maps to ENST00000383329 E185*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-7703-01A-11D-2053-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr6:32974921 G>A maps to NM_002119.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:32975163 G>A maps to NM_002119.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr6:32975991 G>A maps to NM_002119.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:32713799 C>T maps to NM_020056.4 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr6:32714122 C>A maps to NM_020056.4 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:32713170 C>T maps to NM_020056.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:32712972 G>A maps to NM_020056.4 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:32410333 G>A maps to NM_019111.4 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:32411067 G>A maps to NM_019111.4 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:30459055 C>T maps to NM_005516.5 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:30458188 T>C maps to NM_005516.5 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:30459323 C>T maps to NM_005516.5 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:29691260 C>G maps to NM_001098479.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr6:29693081 G>A maps to NM_001098479.1 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:29797195 C>T maps to ENST00000376828 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr6:29795656 G>A maps to ENST00000376828 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr6:29795656 G>A maps to ENST00000376828 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr6:29795914 G>A maps to ENST00000376828 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr21:38308844 G>T maps to NM_000411.5 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr21:38128940 G>T maps to NM_000411.5 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr21:38309375 C>T maps to NM_000411.5 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:53392615 A>G maps to NM_002126.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:53342892 G>A maps to NM_002126.4 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:148789133 G>A maps to NM_003071.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:148786025 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:221053525 G>A maps to NM_021958.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:221053382 G>T maps to NM_021958.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:221053222 C>A maps to NM_021958.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:28876277 C>T maps to ENST00000444075 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:28908611 C>A maps to ENST00000444075 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:118963178 C>T maps to NM_000190.3 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:186097322 C>T maps to NM_031935.2 D4268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:186147695 C>T maps to NM_031935.2 G5364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:185964205 G>A maps to NM_031935.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:185931758 C>T maps to NM_031935.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr1:185959497 A>G maps to NM_031935.2 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:185958729 C>G maps to NM_031935.2 A1053A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:186106002 G>T maps to NM_031935.2 E4506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:185970778 C>A maps to NM_031935.2 L1418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:186147638 A>G maps to NM_031935.2 Q5345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:186056428 G>T maps to NM_031935.2 E3043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:186122925 C>T maps to NM_031935.2 Y5021Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:185892597 T>C maps to NM_031935.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:185950198 G>T maps to NM_031935.2 G886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:186063434 C>T maps to NM_031935.2 V3408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:186151324 T>C maps to NM_031935.2 D5440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:186158952 C>A maps to NM_031935.2 T5617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr1:186099204 A>T maps to NM_031935.2 K4338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr1:186081952 C>T maps to NM_031935.2 R3667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:185959419 G>A maps to NM_031935.2 V1074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:185969175 G>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:186056778 T>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:185962439 T>C maps to NM_031935.2 H1168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:186114658 G>T maps to NM_031935.2 G4797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:186037086 G>A maps to NM_031935.2 W2609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:186072685 T>G maps to NM_031935.2 A3552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr1:186060047 C>T maps to NM_031935.2 R3296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:186092098 C>T maps to NM_031935.2 S4082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr1:186057322 G>A maps to NM_031935.2 T3164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:186008081 C>T maps to NM_031935.2 C1991C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:185834898 T>C maps to NM_031935.2 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:186026531 A>G maps to NM_031935.2 S2437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:186088389 G>A maps to NM_031935.2 A3972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:186055507 C>T maps to NM_031935.2 I3005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:185970772 G>A maps to NM_031935.2 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:186114580 G>A maps to NM_031935.2 R4771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:186147633 G>T maps to NM_031935.2 G5344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr1:186043952 C>T maps to NM_031935.2 T2740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr1:186084056 C>T maps to NM_031935.2 R3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:186014934 C>T maps to NM_031935.2 D2140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:186083983 T>C maps to NM_031935.2 I3770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:186097423 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:66308837 G>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:150156289 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:150154641 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:24140702 C>T maps to NM_000191.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:24140705 C>T maps to NM_000191.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr6:55381356 T>C maps to NM_019036.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr6:55360219 A>T maps to NM_019036.2 L294L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4H8-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:74647030 A>G maps to NM_000859.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:74655257 T>C maps to NM_000859.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr5:43298854 A>G maps to NM_002130.6 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr5:43298982 G>A maps to NM_002130.6 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:120301891 G>A maps to NM_005518.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:120298075 G>A maps to NM_005518.3 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr1:120301825 C>T maps to NM_005518.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:35661160 A>G maps to NM_001003681.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:1074127 C>T maps to NM_012292.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr19:1079751 G>T maps to NM_012292.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:1085683 G>A maps to NM_012292.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:1074617 C>T maps to NM_012292.2 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:1080042 C>T maps to NM_012292.2 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:1085953 C>T maps to NM_012292.2 G1120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:1083157 C>T maps to NM_012292.2 Q921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr19:1073508 C>T maps to NM_012292.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:35783001 C>T maps to NM_002133.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:35782985 C>A maps to NM_002133.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:4555533 G>A maps to NM_001127205.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:173534315 G>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr5:173473784 C>T maps to NM_015980.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:61621686 C>T maps to NM_001123366.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:124909353 C>T maps to NM_005519.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr10:124909458 G>T maps to NM_005519.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:124896862 G>A maps to NM_001105574.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:124896766 G>A maps to NM_001105574.1 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:121438865 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:121434122 C>T maps to NM_000545.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:121438946 C>T maps to NM_000545.5 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:36099530 C>T maps to NM_000458.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:36059099 G>A maps to NM_000458.2 N545N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:36099530 C>T maps to NM_000458.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:36065014 C>T maps to NM_000458.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:43034815 C>T maps to ENST00000338692 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:43057108 C>T maps to ENST00000338692 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:76471264 A>G maps to NM_004133.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:138762704 C>T maps to NM_006895.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr5:137089635 C>T maps to NM_006805.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr5:137088876 G>A maps to NM_006805.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:53216743 G>A maps to NM_001011725.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:53217088 C>T maps to NM_001011725.1 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:26232143 G>A maps to NM_031243.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:26233315 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:178081473 C>A maps to NM_194247.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:177637253 C>T maps to NM_031266.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:177636437 T>A maps to NM_031266.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:12907860 G>A maps to NM_001013631.1 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:12908010 C>T maps to NM_001013631.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:12908037 C>T maps to NM_001013631.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr1:12907827 G>A maps to NM_001013631.1 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:43882123 G>A maps to NM_001098204.1 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr10:43882561 G>A maps to NM_001098204.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:43882891 G>A maps to NM_001098204.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:179045187 C>A maps to NM_005520.2 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:100667789 T>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:100667239 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:100667960 G>A did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:100667849 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:100667762 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:100667061 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:100667423 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:8533718 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:8553713 C>T maps to NM_005968.3 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:23637093 A>G maps to ENST00000414299 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:23650159 G>A maps to ENST00000414299 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:245021315 A>G maps to NM_031844.2 C497C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:245017772 A>G maps to NM_031844.2 H819H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:245019224 A>G maps to NM_031844.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:41811717 G>A maps to NM_007040.3 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr19:41808847 C>T maps to NM_007040.3 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:62483024 G>A maps to NM_001079559.1 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:62483394 G>T maps to NM_001079559.1 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:62490152 G>A maps to NM_001079559.1 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:62482998 T>C maps to NM_001079559.1 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr11:62482773 C>A maps to NM_001079559.1 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:62483057 G>A maps to NM_001079559.1 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr11:62491802 G>A maps to NM_001079559.1 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:83350540 A>G maps to NM_031372.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:83349474 C>A maps to NM_031372.2 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:78697765 G>A maps to NM_004272.3 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:78734855 C>T maps to NM_004272.3 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:83518520 A>G maps to NM_199330.1 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:19049617 C>T maps to NM_004838.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:23745053 C>T maps to NM_020834.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:23746063 G>A maps to NM_020834.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:23745098 G>A maps to NM_020834.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:60299105 T>C maps to NM_015888.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:12882019 C>T maps to NM_013312.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:12883717 C>T maps to NM_013312.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:12875860 T>G maps to NM_013312.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:42828457 C>T maps to NM_032410.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:42812259 C>T maps to NM_032410.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:42761365 G>A maps to NM_032410.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:42828541 C>T maps to NM_032410.3 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr8:42823233 A>G maps to NM_032410.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:42865515 C>T maps to NM_032410.3 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr4:57522175 G>A maps to NM_032495.5 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:27135153 G>A maps to NM_005522.4 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr7:27224673 G>A maps to NM_005523.5 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:27140674 G>A maps to NM_006735.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:27141055 G>A maps to NM_006735.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:27141759 T>G maps to NM_006735.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:27140533 A>C maps to NM_006735.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:27140827 G>A maps to NM_006735.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:27147923 C>T maps to NM_153631.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:27150220 G>A maps to NM_153631.2 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:27149899 C>T maps to NM_153631.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr7:27147986 C>T maps to NM_153631.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:27149772 G>A maps to NM_153631.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr7:27147974 G>A maps to NM_153631.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr7:27183091 G>A maps to NM_019102.2 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:27186999 G>A maps to NM_024014.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr7:27186927 C>T maps to NM_024014.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr7:27185318 C>T maps to NM_024014.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:27185489 C>T maps to NM_024014.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:27195864 G>T maps to NM_006896.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:27195918 G>A maps to NM_006896.3 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:27194722 C>T maps to NM_006896.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:27196038 C>T maps to NM_006896.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr7:27204563 G>A maps to NM_152739.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:27204710 C>T maps to NM_152739.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:46608176 G>T maps to NM_002144.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:46805652 G>T maps to NM_006361.5 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:46804340 C>T maps to NM_006361.5 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:46621964 G>A maps to NM_002145.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:46629791 G>A maps to NM_002146.4 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:46628517 A>G maps to NM_002146.4 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:46628523 G>A maps to NM_002146.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:46629515 G>A maps to NM_002146.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:46628526 G>A maps to NM_002146.4 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:46628217 G>C maps to NM_002146.4 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:46629701 G>A maps to NM_002146.4 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:46628307 G>A maps to NM_002146.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:46628526 G>A maps to NM_002146.4 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:46629613 T>G maps to NM_002146.4 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:46628478 A>G maps to NM_002146.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:46654329 C>T maps to NM_024015.4 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr17:46655264 G>A maps to NM_024015.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr17:46655324 C>T maps to NM_024015.4 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:46669801 G>A maps to NM_002147.3 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr17:46670651 G>A maps to NM_002147.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:46670642 G>A maps to NM_002147.3 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:46670720 G>A maps to NM_002147.3 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:46685442 G>A maps to NM_004502.3 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:46691691 G>A maps to NM_024016.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr17:46703514 C>T maps to NM_024017.4 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:54379096 G>A maps to NM_017409.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr12:54367429 C>T maps to NM_014212.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:54367108 C>T maps to NM_014212.3 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:54348880 G>A maps to NM_173860.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:54350166 G>A maps to NM_173860.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:54348982 C>T maps to NM_173860.1 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:54338838 C>T maps to NM_017410.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:54333265 G>A maps to NM_017410.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr12:54447816 C>T maps to NM_153633.2 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:54448770 C>T maps to NM_153633.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:54428170 C>T maps to NM_018953.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:54428191 T>C maps to NM_018953.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:54423568 G>A maps to NM_004503.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr12:54423484 G>A maps to NM_004503.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:54423565 C>T maps to NM_004503.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:54403385 G>A maps to NM_022658.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:54403112 C>T maps to NM_022658.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:54403220 C>T maps to NM_022658.3 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr12:54394040 C>T maps to NM_006897.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:54396439 C>T maps to NM_006897.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:177053567 C>T maps to ENST00000331462 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:177053882 G>A maps to ENST00000331462 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:176982112 C>T maps to NM_002148.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:176983955 T>G maps to NM_002148.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr2:176981725 G>A maps to NM_002148.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:176982040 C>T maps to NM_002148.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr2:176982145 G>A maps to NM_002148.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:176973734 G>A maps to NM_021192.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:176965451 C>T maps to NM_021193.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:176965304 G>A maps to NM_021193.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr2:176964777 C>T maps to NM_021193.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:176965307 G>A maps to NM_021193.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:176964612 C>T maps to NM_021193.3 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:176965451 C>T maps to NM_021193.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr2:176965101 C>T maps to NM_021193.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:176964837 C>T maps to NM_021193.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:176957800 A>G maps to NM_000523.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:176957878 G>A maps to NM_000523.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:176958154 G>A maps to NM_000523.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:176958220 G>A maps to NM_000523.3 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:176959238 C>T maps to NM_000523.3 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:176957896 C>T maps to NM_000523.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:176959214 G>A maps to NM_000523.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:177036881 G>A maps to NM_006898.4 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:177034213 G>A maps to NM_006898.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:177036779 C>T maps to NM_006898.4 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:177036308 G>A maps to NM_006898.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:177036785 C>T maps to NM_006898.4 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:177036641 C>T maps to NM_006898.4 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:177036653 G>A maps to NM_006898.4 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr2:177034088 G>T maps to NM_006898.4 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:177016723 G>A maps to NM_014621.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:176995510 C>T maps to NM_019558.3 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:176987684 C>T maps to NM_014213.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:176987558 C>T maps to NM_014213.3 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:176988302 A>G maps to NM_014213.3 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:21097458 T>C maps to NM_016287.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:21083670 C>A maps to NM_016287.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr1:21071397 T>C maps to NM_016287.3 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:33354831 C>T maps to NM_002143.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:10560002 C>T maps to NM_002149.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:10560032 G>A maps to NM_002149.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:10566919 C>T maps to NM_002149.2 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:10559957 C>T maps to NM_002149.2 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:40149755 G>A maps to NM_016257.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:40149647 G>A maps to NM_016257.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr1:40150245 G>A maps to NM_016257.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:40149644 C>T maps to NM_016257.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:122294531 C>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:45793584 C>T maps to NM_032756.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:45793665 T>C maps to NM_032756.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr4:175416734 T>C maps to NM_000860.4 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:175413245 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:95220653 G>A maps to NM_014485.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:35556187 C>T maps to NM_182983.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:35556773 C>T maps to NM_182983.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:35550828 G>A maps to NM_182983.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:35556773 C>T maps to NM_182983.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:72110826 C>T maps to ENST00000228226 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr10:100179891 C>T maps to NM_000195.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:100185360 G>A maps to NM_000195.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:148880505 T>A maps to NM_032383.3 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:148872965 G>A maps to NM_032383.3 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr3:148881672 C>T maps to NM_032383.3 H842H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:148859111 C>G maps to NM_032383.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:26861509 T>C maps to NM_022081.4 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:26860584 C>T maps to NM_022081.4 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:26859914 G>A maps to NM_022081.4 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:26860140 C>T maps to NM_022081.4 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr22:26849267 C>T maps to NM_022081.4 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:26861446 G>A maps to NM_022081.4 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:18320517 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:18330491 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:18309205 G>A maps to NM_181507.1 R865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:103826833 C>T maps to NM_024747.4 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:103826898 A>G maps to NM_024747.4 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:103826085 C>T maps to NM_024747.4 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:103826052 C>A maps to NM_024747.4 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr4:84227445 T>C maps to NM_006665.5 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:100481538 G>A maps to NM_021828.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:6452539 A>G maps to NM_000613.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:21980011 G>A maps to NM_005144.4 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:21978589 C>T maps to NM_005144.4 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:21983111 G>A maps to NM_005144.4 H513H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:21976567 T>G maps to NM_005144.4 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:21976796 C>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:21973914 G>A maps to NM_005144.4 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:21978589 C>T maps to NM_005144.4 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:63256438 A>G maps to NM_054108.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:49657747 A>G maps to NM_002152.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:49657747 A>G maps to NM_002152.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:49657744 A>G maps to NM_002152.2 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:49656859 C>T maps to NM_002152.2 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:49657888 T>C maps to NM_002152.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:49658083 G>A maps to NM_002152.2 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:49657831 A>G maps to NM_002152.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:186395125 T>C maps to NM_000412.2 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:11302081 C>T maps to NM_001098211.1 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr5:175111231 C>A maps to NM_001131055.1 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:22048785 G>A maps to NM_021624.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:152188548 G>A maps to NM_001009931.1 S1852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:152187975 A>G maps to NM_001009931.1 G2043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr1:152185611 A>G maps to NM_001009931.1 F2831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr1:152193510 C>G maps to NM_001009931.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:152185617 G>C maps to NM_001009931.1 L2829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:152192964 C>T maps to NM_001009931.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:152190972 G>A maps to NM_001009931.1 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr1:152187978 G>A maps to NM_001009931.1 H2042H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:152191476 G>A maps to NM_001009931.1 H876H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:152188392 T>C maps to NM_001009931.1 S1904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr1:152192826 G>A maps to NM_001009931.1 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152185823 G>A maps to NM_001009931.1 R2761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152187699 T>C maps to NM_001009931.1 Q2135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152188413 G>A maps to NM_001009931.1 Y1897Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr1:152190834 G>A maps to NM_001009931.1 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:152185590 A>G maps to NM_001009931.1 Y2838Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr1:152193480 G>A maps to NM_001009931.1 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:152193810 C>T maps to NM_001009931.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:152188011 T>C maps to NM_001009931.1 Q2031Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:152190999 T>G maps to NM_001009931.1 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr1:152192588 G>A maps to NM_001009931.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:152191656 A>G maps to NM_001009931.1 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:152191749 T>C maps to NM_001009931.1 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:152191460 G>A maps to NM_001009931.1 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:20818782 G>A maps to NM_022460.3 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:87538642 C>T maps to NM_012262.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:87563549 C>T maps to NM_012262.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:11401089 G>A maps to NM_005114.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:11401251 C>T maps to NM_005114.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:11400897 C>T maps to NM_005114.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:11400912 C>T maps to NM_005114.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:11400810 C>T maps to NM_005114.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr4:11401182 C>T maps to NM_005114.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:22826338 A>G maps to NM_006043.1 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:22926717 C>T maps to NM_006043.1 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:22926591 C>T maps to NM_006043.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:22826227 C>T maps to NM_006043.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr16:22926777 T>C maps to NM_006043.1 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:22926591 C>T maps to NM_006043.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:22926459 C>A maps to NM_006043.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:13400017 G>A maps to NM_006042.1 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:13400017 G>A maps to NM_006042.1 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:14204912 G>A maps to NM_006041.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:14205041 C>T maps to NM_006041.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr17:14248368 C>T maps to NM_006041.1 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:14204936 G>A maps to NM_006041.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr16:25704307 C>T maps to NM_006040.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr16:26147517 C>A maps to NM_006040.2 Y440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:26147211 G>A maps to NM_006040.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:25704427 G>A maps to NM_006040.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr16:26147400 A>G maps to NM_006040.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:114378681 C>T maps to NM_153612.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:1962138 G>A maps to ENST00000454677 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr16:1961986 G>A maps to ENST00000454677 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr16:1961698 C>T maps to ENST00000454677 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:1961935 G>A maps to ENST00000454677 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:1961986 G>A maps to ENST00000454677 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:129025948 G>A maps to NM_004807.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:129026305 C>T maps to NM_004807.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:129075789 G>A maps to NM_004807.2 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:132091163 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:132090882 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:132090965 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:131762867 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:132091107 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:132090965 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:131762994 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:131762947 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:131762597 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr13:96743550 C>T maps to NM_153456.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:96743259 G>A maps to NM_153456.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:29141961 A>G maps to NM_172002.3 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr1:209880330 T>G maps to NM_005525.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:67470746 C>T maps to NM_000196.3 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:67470812 A>G maps to NM_000196.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:67469996 C>T maps to NM_000196.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:40705487 G>A maps to NM_000413.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:40705463 C>T maps to NM_000413.2 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:43861601 C>T maps to NM_016142.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr11:43876698 G>A maps to NM_016142.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:88234975 T>G maps to NM_178135.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:49316485 G>A maps to NM_016246.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:82131905 C>T maps to NM_002153.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr16:82131836 G>A maps to NM_002153.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:99064278 C>T maps to NM_000197.1 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:118792053 T>C maps to NM_000414.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:118861612 T>C maps to NM_000414.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:57167905 C>T maps to NM_003725.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:162762613 G>A maps to NM_016371.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:162769540 A>G maps to NM_016371.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:120056676 C>T maps to ENST00000235547 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:120054204 C>T maps to ENST00000235547 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:120056673 C>T maps to ENST00000235547 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr1:119964588 G>A maps to NM_000198.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr1:119958040 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:119962128 C>T maps to NM_000198.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:30999230 C>T maps to NM_025193.3 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr16:84163758 G>A maps to NM_031463.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:84163847 G>A maps to NM_031463.4 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:115166289 T>C maps to NM_032303.4 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr9:115221774 G>T maps to NM_032303.4 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:145533579 G>A maps to NM_005526.2 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:145535504 C>T maps to NM_005526.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:145535771 C>T maps to NM_005526.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:145535771 C>T maps to NM_005526.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr8:145535202 G>A maps to NM_005526.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:122753115 C>T maps to NM_004506.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:122743434 T>C maps to NM_004506.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr21:44949699 G>A maps to NM_007031.1 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:56565281 G>A maps to NM_001080439.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:102568316 G>A maps to NM_001017963.2 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:44216455 T>C maps to NM_007355.2 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:104326615 G>T maps to NM_003299.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:118439099 C>T maps to NM_025015.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr10:118434849 C>A maps to NM_025015.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr10:118434573 C>T maps to NM_025015.2 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:3719362 C>T maps to NM_052970.4 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:3725644 C>T maps to NM_052970.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr20:3726147 C>A maps to NM_052970.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:3732584 C>T maps to NM_052970.4 C611C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr21:15746180 T>C maps to NM_006948.4 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:15746384 A>G maps to NM_006948.4 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:14896174 G>A maps to NM_016299.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr10:14896242 T>A maps to NM_016299.2 L285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr6:31785227 G>C maps to NM_005345.5 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:31783568 C>T maps to NM_005345.5 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:31785383 C>T maps to NM_005345.5 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:31795921 C>T maps to NM_005346.4 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr6:31779056 A>G maps to NM_005527.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr6:31779554 G>A maps to NM_005527.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:31778621 C>T maps to NM_005527.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:31777883 G>A maps to NM_005527.3 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr6:31778312 C>T maps to NM_005527.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:31779131 T>C maps to NM_005527.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:31779557 A>G maps to NM_005527.3 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:31779491 T>C maps to NM_005527.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:31778570 C>T maps to NM_005527.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr14:65008769 G>A maps to NM_021979.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:65008910 C>T maps to NM_021979.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:65008403 G>A maps to NM_021979.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:65009255 C>T maps to NM_021979.3 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr14:65008904 C>T maps to NM_021979.3 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:65008541 C>T maps to NM_021979.3 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:65008541 C>T maps to NM_021979.3 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr14:65009231 G>T maps to NM_021979.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:65007662 C>T maps to NM_021979.3 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:132428414 A>G maps to NM_002154.3 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:128732616 T>C maps to ENST00000438626 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:128724794 T>C maps to ENST00000438626 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr4:128716933 C>T maps to ENST00000438626 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr4:128725222 A>G maps to ENST00000438626 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:128751950 A>G maps to ENST00000438626 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:128722949 G>A maps to ENST00000438626 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:127998918 G>A maps to NM_005347.4 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr9:127999056 G>C maps to NM_005347.4 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:128003291 G>T maps to NM_005347.4 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:128001309 C>T maps to NM_005347.4 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr9:128003157 C>A maps to NM_005347.4 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:161495323 C>T maps to NM_002155.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:161495881 G>A maps to NM_002155.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:161495323 C>T maps to NM_002155.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:161495032 C>T maps to NM_002155.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:161495095 T>C maps to NM_002155.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:161495587 C>T maps to NM_002155.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:122928609 T>C maps to NM_006597.3 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:137892146 G>A maps to NM_004134.6 Y652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:137903346 C>T maps to NM_004134.6 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:137892158 G>A maps to NM_004134.6 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr7:75932121 G>A maps to NM_001540.3 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:54405716 G>A maps to NM_016126.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:53751771 G>A maps to NM_006308.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr5:53751846 C>T maps to NM_006308.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:16344392 G>A maps to ENST00000375714 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:16344392 G>T maps to ENST00000375714 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:16342092 C>T maps to ENST00000375714 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:119617263 C>T maps to NM_014365.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:55773977 A>G maps to NM_012267.4 *360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr19:55790946 G>A maps to NM_012267.4 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:55776757 C>A did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr2:64685501 G>A maps to NM_014181.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:64685462 T>C maps to NM_014181.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr2:198353800 G>C maps to NM_199440.1 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:198353797 T>C maps to NM_199440.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr2:198351916 C>G maps to NM_199440.1 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:22150184 G>A maps to NM_005529.5 V4309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:22178101 G>A maps to NM_005529.5 P2365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:22191362 C>T maps to NM_005529.5 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:22150130 G>A maps to NM_005529.5 N4327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr1:22188575 G>A maps to NM_005529.5 C1591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr1:22166043 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:22183649 G>A maps to NM_005529.5 N1811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr1:22203130 C>A maps to NM_005529.5 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:22160047 T>C maps to NM_005529.5 S3630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:22217178 G>A maps to NM_005529.5 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:22154538 G>A maps to NM_005529.5 G4172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:22173012 G>A maps to NM_005529.5 C2748C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:22170712 G>A maps to NM_005529.5 C2848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:22174253 G>A maps to NM_005529.5 C2651C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:22176958 C>T maps to NM_005529.5 A2397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:22179504 C>T maps to NM_005529.5 G2166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:22150205 G>A maps to NM_005529.5 G4302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr1:22178377 G>A maps to NM_005529.5 A2304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:22216951 G>A maps to NM_005529.5 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr1:22216488 G>A maps to NM_005529.5 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:22181916 T>C maps to NM_005529.5 Q1959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:22205551 G>A maps to NM_005529.5 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr1:22168591 G>A maps to NM_005529.5 T3032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:22161427 C>T maps to NM_005529.5 S3488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:22167695 G>A maps to NM_005529.5 A3137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:22222725 G>A maps to NM_005529.5 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:31717997 T>C maps to NM_006644.2 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr13:31725790 T>C maps to NM_006644.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:31718003 A>G maps to NM_006644.2 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:31725097 G>A maps to NM_006644.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr13:31722525 G>C maps to NM_006644.2 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:20385902 G>A maps to NM_001098520.1 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:20398123 A>G did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr11:20403747 G>T maps to NM_001098520.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:20385852 T>C maps to NM_001098520.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:135593612 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:135582955 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135593205 A>T did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:135581813 G>A did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr4:70920040 C>T maps to NM_002159.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:63256781 A>G maps to NM_000524.2 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:63257303 G>A maps to NM_000524.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:63256880 C>T maps to NM_000524.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:63257081 C>T maps to NM_000524.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr5:63256625 C>A maps to NM_000524.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:63257399 G>A maps to NM_000524.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr5:63256316 C>T maps to NM_000524.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr5:63256772 C>T maps to NM_000524.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:63256559 G>A maps to NM_000524.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:63256964 G>T maps to NM_000524.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:63256802 C>T maps to NM_000524.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:63256880 C>T maps to NM_000524.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:63256582 C>A maps to NM_000524.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:63257450 G>A maps to NM_000524.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:78172949 C>T maps to NM_000863.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr6:78172595 G>A maps to NM_000863.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:78172718 A>G maps to NM_000863.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr6:78172799 G>A maps to NM_000863.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:78172721 G>A maps to NM_000863.1 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:78172571 C>T maps to NM_000863.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:23520193 C>T maps to NM_000864.4 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:87725456 G>A maps to NM_000865.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr6:87725915 G>A maps to NM_000865.2 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr6:87725621 G>A maps to NM_000865.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr6:87725375 C>A maps to NM_000865.2 C108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:87725672 C>T maps to NM_000865.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:88040784 G>T maps to NM_000866.3 G296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr3:88040703 A>C maps to NM_000866.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr3:88040874 G>T maps to NM_000866.3 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:88040618 A>G maps to NM_000866.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr13:47409676 G>A maps to NM_000621.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:114141455 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:113965895 G>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:114141350 C>T did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:114141784 T>A did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:114141191 A>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:114141412 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:114082758 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:113965891 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr23:114141533 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:114141261 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:113965832 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:113965794 G>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:114141642 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr23:114082669 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:113860365 C>T maps to NM_213621.3 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr11:113857316 C>A maps to NM_213621.3 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:113853934 C>A maps to NM_213621.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:113857682 C>T maps to NM_213621.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr3:183774680 G>A maps to NM_130770.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:183756362 G>A maps to NM_001145143.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:183823623 C>T maps to NM_182589.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:183824456 C>T maps to NM_182589.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:147928373 C>T maps to NM_001040173.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:147889350 A>G maps to NM_001040173.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:147902809 A>G maps to NM_001040173.2 F151F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4201-01A-01D-1126-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:154863076 C>T maps to NM_024012.2 C156C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-7707-01A-11D-2053-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:154863211 C>T maps to NM_024012.2 A201A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-A4QL-01A-31D-A25D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CG-4306-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:154862908 C>T maps to NM_024012.2 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr7:154863076 C>T maps to NM_024012.2 C156C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HF-7132-01A-11D-2053-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:154862986 G>A maps to NM_024012.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:154863286 T>C maps to NM_024012.2 A226A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-A4GQ-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:154862881 G>A maps to NM_024012.2 A91A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IN-AB1X-01A-11D-A397-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:154863037 C>A maps to NM_024012.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr7:154862725 C>T maps to NM_024012.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:19992866 C>A maps to NM_000871.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr1:20005854 G>A maps to NM_000871.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:19992503 C>T maps to NM_000871.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:19992827 C>T maps to NM_000871.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:92617293 C>T maps to NM_019859.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:92509260 G>A maps to NM_019859.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr10:124273781 C>T maps to NM_002775.4 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:124266283 G>A maps to NM_002775.4 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:124273781 C>T maps to NM_002775.4 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:74759793 G>A maps to NM_013247.4 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:74757165 C>T maps to NM_013247.4 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:74759793 G>A maps to NM_013247.4 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:74757944 T>A maps to NM_013247.4 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:8293206 C>T maps to NM_053044.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:8305988 G>A maps to NM_053044.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:8271766 G>A maps to NM_053044.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr4:8288323 C>T maps to NM_053044.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:8304223 G>A maps to NM_053044.3 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:38832616 G>A maps to NM_153692.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:38835653 T>C maps to NM_153692.3 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:38840068 T>C maps to NM_153692.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:38834062 C>T maps to NM_153692.3 H192H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:38839285 G>T maps to NM_153692.3 G372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:3234903 G>A maps to NM_002111.6 A2760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:3215860 C>T maps to NM_002111.6 A2317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr4:3230454 G>A maps to NM_002111.6 T2654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:3201627 C>T maps to NM_002111.6 T1846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr4:3134613 C>T maps to NM_002111.6 C823C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:3219639 C>T maps to NM_002111.6 R2401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:3088672 G>T maps to NM_002111.6 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:3184143 C>T maps to NM_002111.6 R1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:3214390 T>C maps to NM_002111.6 P2243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:3137630 G>A maps to NM_002111.6 R878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:3109035 G>A maps to NM_002111.6 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:3215824 C>A maps to NM_002111.6 C2305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr4:3240696 C>T maps to NM_002111.6 V3069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:3146956 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:3134559 G>A maps to NM_002111.6 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:3149909 C>T maps to NM_002111.6 D1158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr4:3149762 G>A maps to NM_002111.6 W1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr21:33318456 C>T maps to NM_014586.1 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr21:33370837 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:656845 G>A maps to NM_148959.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:656488 G>T maps to NM_148959.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:656932 G>A maps to NM_148959.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:656446 C>T maps to NM_148959.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:656755 G>A maps to NM_148959.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:656857 G>T maps to NM_148959.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:656554 G>A maps to NM_148959.3 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:656425 C>T maps to NM_148959.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:656884 G>A maps to NM_148959.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:53569477 G>A did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:53655774 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:53630413 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:53674332 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:53600834 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:53586421 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:53590730 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53607903 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:53574995 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:53586415 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:53566004 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:53573483 G>A did not map to a codon.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr23:53672406 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:53574767 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:53588850 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:53574689 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:53613487 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:53590778 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:53622291 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:53657954 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:53575079 T>C did not map to a codon.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr23:53564519 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:53563520 C>T did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:53655785 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:53586337 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:53631666 A>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:53674485 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:53562433 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:53575176 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:53565986 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:53561649 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr23:53571558 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:111089063 G>A maps to NM_001040107.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:111088011 G>A maps to NM_001040107.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:50340360 G>A maps to NM_153281.1 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr3:50355619 A>G maps to NM_033158.4 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr3:50357456 G>T maps to NM_033158.4 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr3:50355685 G>C maps to NM_033158.4 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:123516941 C>T maps to NM_012269.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:123517153 C>A maps to NM_012269.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:70867803 G>A maps to NM_032821.2 G4554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:70989428 G>A maps to NM_032821.2 S2054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr16:70934954 G>T maps to NM_032821.2 Y2999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr16:70843796 C>T maps to NM_032821.2 T4923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:70972544 G>A maps to NM_032821.2 Q2322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:71054190 G>A maps to NM_032821.2 Y1072Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:70852298 G>A maps to NM_032821.2 C4867C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr16:70902553 G>A maps to NM_032821.2 P3742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:70993580 G>A maps to NM_032821.2 I2036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:71025986 T>C maps to NM_032821.2 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr16:70917970 G>A maps to NM_032821.2 S3276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:71218772 G>A maps to NM_032821.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr16:70986527 T>G maps to NM_032821.2 A2108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr16:71015345 G>A maps to NM_032821.2 S1485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:70867809 G>A maps to NM_032821.2 N4552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:70941282 T>C maps to NM_032821.2 S2835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:71019096 C>T maps to NM_032821.2 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr16:70902514 G>A maps to NM_032821.2 D3755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr16:70917862 G>A maps to NM_032821.2 A3312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr16:70906011 G>T maps to NM_032821.2 V3672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:125769524 A>C maps to NM_001134793.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:125769530 C>T maps to NM_001134793.1 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:118921764 G>A maps to NM_001130991.1 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:118919523 G>A maps to NM_001130991.1 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:9628457 G>A maps to NM_001039613.1 *249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:95007333 G>A maps to ENST00000375660 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:95040153 A>T maps to ENST00000375660 Y297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:95030530 T>C maps to ENST00000375660 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:95033315 G>A maps to ENST00000375660 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:95025291 C>T maps to ENST00000375660 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:220300108 C>A maps to NM_018060.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:220280449 T>C maps to NM_018060.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr1:220284128 T>A maps to NM_018060.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:220284280 T>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:88732602 C>T maps to NM_004967.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr4:88731867 G>A maps to NM_004967.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr4:88732665 A>G maps to NM_004967.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:88732677 C>T maps to NM_004967.3 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr4:88732539 A>G maps to NM_004967.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:82936962 G>T maps to NM_015525.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:82950020 G>T maps to NM_015525.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:82933167 C>T maps to NM_015525.2 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr6:82925889 G>A maps to NM_015525.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:82912315 A>G maps to NM_015525.2 Y886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:203693594 A>G maps to NM_138468.4 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:10394790 C>T maps to NM_000201.2 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:10385678 A>G maps to NM_000201.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr19:10394178 G>A maps to NM_000201.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:10395520 C>T maps to NM_000201.2 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr19:10449618 G>A maps to NM_002162.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:10446425 G>A maps to NM_002162.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:10398393 T>C maps to NM_001544.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:10404791 T>C maps to NM_003259.3 C596C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:10401748 G>A maps to NM_003259.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:10405143 C>T maps to NM_003259.3 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:52869976 G>A maps to NM_016513.4 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:52871164 G>A maps to NM_016513.4 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr6:52905947 C>A maps to NM_016513.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr6:52897371 G>A maps to NM_016513.4 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr21:45657062 G>A maps to ENST00000400379 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr21:45655434 G>A maps to ENST00000400379 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr21:45657074 C>T maps to ENST00000400379 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:73015810 T>G maps to NM_001545.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:19838300 C>T maps to NM_001546.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:94294396 A>G maps to NM_004969.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:94294387 A>G maps to NM_004969.3 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr10:94223572 A>G maps to NM_004969.3 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:94221001 A>G maps to NM_004969.3 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:209113131 T>C maps to NM_005896.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:209116254 G>A maps to NM_005896.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr15:90628286 C>T maps to NM_002168.2 W375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr15:78454613 C>T maps to NM_005530.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:78453995 C>T maps to NM_005530.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:78452549 T>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:2639085 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:2640406 G>A maps to NM_006899.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:2640690 G>A maps to NM_006899.2 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:2641139 G>T maps to NM_006899.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:153053555 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:153053044 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153052988 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153052284 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:153052939 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153052969 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:1088621 G>A maps to NM_004508.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:1070564 G>T maps to NM_033261.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:1065709 C>T maps to NM_033261.2 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:39872859 C>T maps to NM_194294.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:39872904 T>C maps to NM_194294.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:39871155 C>T maps to NM_194294.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:148564575 A>G did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:148577904 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:148579679 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:148579805 G>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:148579642 G>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:148579704 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:148564564 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:148585689 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:148586601 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:996133 T>C maps to NM_000203.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:996112 C>T maps to NM_000203.3 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:996127 C>T maps to NM_000203.3 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:997814 C>T maps to NM_000203.3 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:997871 G>A maps to NM_000203.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:13264527 C>T maps to NM_004907.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:181059003 A>G maps to NM_016545.4 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:131939118 A>T maps to NM_203434.2 *405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:6650772 C>T maps to NM_001193457.1 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:6650742 G>A maps to NM_001193457.1 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:159019337 C>A maps to ENST00000295809 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:159021881 A>G maps to ENST00000295809 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:159021771 C>T maps to ENST00000295809 R657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:159021771 C>T maps to ENST00000295809 R657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:158988416 A>G maps to ENST00000295809 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:94568187 G>A maps to NM_206949.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:94568277 C>T maps to NM_206949.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:94595892 A>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:18286419 C>T maps to NM_006332.3 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:41166274 G>T maps to NM_005533.4 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr17:41166234 C>T maps to NM_005533.4 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:79120722 C>A maps to NM_006417.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:79125146 C>T maps to NM_006417.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:79101175 T>C did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr1:79093938 G>T maps to NM_006820.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:79107130 C>A maps to NM_006820.2 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:27992915 G>A maps to NM_022873.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:163134116 G>A maps to NM_022168.2 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr2:163174423 T>G maps to NM_022168.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:163128887 G>A maps to NM_022168.2 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:163138978 T>C maps to NM_022168.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:163139082 G>A maps to NM_022168.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:91162181 C>G maps to NM_001548.3 Y50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr10:91162118 C>T maps to NM_001548.3 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:91143708 T>C maps to NM_001010987.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr10:91143417 T>G maps to NM_001010987.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:91143906 G>A maps to NM_001010987.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:91066702 T>C maps to NM_001547.4 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:91066054 G>A maps to NM_001547.4 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:91098637 C>T maps to NM_001549.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:91177660 A>G maps to NM_012420.2 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:21206630 C>A maps to NM_002171.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:21206985 G>A maps to NM_002171.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr9:21367520 A>G maps to NM_006900.3 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:21367438 A>G maps to NM_006900.3 *191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:21367454 T>C maps to NM_006900.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:21367853 G>A maps to NM_006900.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:21217076 G>T maps to NM_002173.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr9:21304766 T>A maps to NM_002169.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:21304714 A>G maps to NM_002169.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr9:21350352 T>C maps to NM_021002.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:21409396 T>A maps to NM_002170.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:21409547 C>T maps to NM_002170.3 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr21:34721568 G>T maps to NM_000629.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:34725188 C>T maps to NM_000629.2 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr9:21077679 C>T maps to NM_002176.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:21077643 G>A maps to NM_002176.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr9:21077391 G>C maps to NM_002176.2 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr9:21077643 G>A maps to NM_002176.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr9:21077517 G>A maps to NM_002176.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:137528209 A>G maps to NM_000416.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:137519584 A>G maps to NM_000416.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr21:34793837 T>C maps to ENST00000381995 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:21141077 C>T maps to NM_002177.1 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:21141089 G>A maps to NM_002177.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:112095821 C>T maps to NM_001007245.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:112112913 A>C maps to NM_001007245.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:50328081 C>T maps to ENST00000336089 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:50329819 C>T maps to ENST00000336089 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:129185900 C>T maps to NM_052985.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:129233273 T>C maps to NM_052985.2 G1061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:129185774 C>T maps to NM_052985.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:129211007 C>T maps to NM_052985.2 R724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:129202443 G>A maps to NM_052985.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:1642177 G>A maps to NM_014714.3 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:1616232 G>A maps to NM_014714.3 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:1561151 C>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:1637197 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:1576691 C>T maps to NM_014714.3 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:27679391 G>A maps to NM_015662.1 H1119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:27682681 G>A maps to NM_015662.1 R846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:27684327 T>C maps to NM_015662.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:27702964 C>T maps to NM_015662.1 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:27703941 G>C maps to NM_015662.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:27688650 G>A maps to NM_015662.1 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:27683909 G>A maps to NM_015662.1 C831C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr2:27684225 C>G maps to NM_015662.1 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:27681050 G>A maps to NM_015662.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:118427697 A>G maps to NM_020153.3 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:42232530 T>C did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr20:42252655 G>A maps to NM_016004.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:42264652 G>A maps to NM_016004.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:107938289 T>C maps to ENST00000457963 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:107910403 T>C maps to ENST00000457963 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:26984557 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:27009016 G>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:26984354 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:160021773 C>T maps to ENST00000483754 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr3:160099333 C>T maps to ENST00000326448 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:159997079 G>A maps to ENST00000483754 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:69385716 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:69354475 C>T did not map to a codon.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr23:69366562 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr23:69366607 T>C did not map to a codon.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr23:69366607 T>C did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:69366607 T>C did not map to a codon.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr23:69366607 T>C did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr15:65623873 G>A maps to NM_004884.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:65628286 C>T maps to NM_004884.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr15:65623493 G>A maps to NM_004884.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr15:65622984 G>T maps to NM_004884.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:65681221 C>T maps to NM_020962.1 E877E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:65681619 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:65702607 G>A maps to NM_020962.1 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:102869550 C>T maps to NM_001111285.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr15:99434707 G>A maps to NM_000875.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr15:99452111 C>T maps to NM_000875.3 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:99434644 C>T maps to NM_000875.3 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:99442757 G>A maps to NM_000875.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:99491898 C>T maps to NM_000875.3 G1228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:99486213 C>T maps to NM_000875.3 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr15:99500475 C>T maps to NM_000875.3 V1303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr15:99467875 G>A maps to NM_000875.3 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:99491898 C>T maps to NM_000875.3 G1228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:99251055 C>T maps to NM_000875.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:99251013 C>A maps to NM_000875.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:99442793 C>T maps to NM_000875.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:99482584 C>T maps to NM_000875.3 I1151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:99486164 G>A maps to NM_000875.3 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:99486272 G>A maps to NM_000875.3 S1193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:2154746 C>T maps to NM_001127598.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr11:2154255 G>A maps to NM_001127598.1 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:2156624 G>A maps to NM_001127598.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:2156702 G>T maps to NM_001127598.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:47075283 T>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:185375139 G>A maps to NM_006548.4 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:185407312 G>T maps to NM_006548.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:185416115 G>A maps to NM_006548.4 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr3:185393610 T>C maps to NM_006548.4 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr3:185369932 G>A maps to NM_006548.4 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:185404891 G>A maps to NM_006548.4 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:185367232 G>T maps to NM_006548.4 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:23509591 G>A maps to NM_006547.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:23509591 G>A maps to NM_006547.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:23387307 C>T maps to NM_006547.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:23358754 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:23352016 A>T maps to NM_006547.2 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:23352440 A>G maps to NM_006547.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr7:23358874 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:23508117 C>T maps to NM_006547.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:160523628 C>T maps to NM_000876.2 G2307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:160469472 C>T maps to NM_000876.2 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:160493902 C>T maps to NM_000876.2 C1559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:160517597 C>T maps to NM_000876.2 H2261H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:160501182 T>C maps to NM_000876.2 C1903C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:160466819 C>T maps to NM_000876.2 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr6:160526044 C>T maps to NM_000876.2 Q2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:160468903 C>T maps to NM_000876.2 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:160494500 G>A maps to NM_000876.2 A1649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:1840990 G>A maps to NM_001146006.1 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr16:1841398 A>G maps to NM_001146006.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:1842220 C>T maps to NM_001146006.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:45932599 C>T maps to NM_000596.2 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:45928277 C>T maps to NM_000596.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:45931545 G>T maps to NM_000596.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr7:45931539 C>T maps to NM_000596.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:217525349 C>T maps to NM_000597.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:45957022 G>T maps to NM_001013398.1 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:57907022 G>A maps to NM_001553.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:57898657 C>A maps to NM_001553.1 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:46543645 C>T maps to NM_001002923.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:46543795 G>C maps to NM_001002923.1 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:68704491 C>T maps to NM_002180.2 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:68704521 G>A maps to NM_002180.2 Q858Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:68703984 G>A maps to NM_002180.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:68705746 A>C maps to NM_002180.2 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:68707030 C>A maps to NM_002180.2 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr11:68679025 G>C maps to NM_002180.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:68701932 C>T maps to NM_002180.2 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr11:68675676 C>T maps to NM_002180.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr4:71522132 G>T maps to NM_144646.3 C131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr4:71522075 G>C maps to NM_144646.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:71527815 G>A maps to NM_144646.3 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:23915548 C>T maps to NM_020070.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr22:23915476 C>T maps to NM_020070.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:51826933 C>T maps to NM_001101372.1 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:51826933 C>T maps to NM_001101372.1 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:130415704 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:130408788 T>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:130410939 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:130410035 A>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:130419220 C>T did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr23:130419220 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:130408637 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:130416640 T>C did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:130408767 G>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:130408802 T>A did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:130416653 T>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:130417038 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:130409636 T>C did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:130412055 T>A did not map to a codon.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr23:130408108 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr23:130412568 G>A did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:130416663 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:130411031 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:130411956 T>G did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:130417041 G>A did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:130412102 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:130419878 G>A did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr23:130410117 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:130419314 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr23:130409204 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:130419305 C>T did not map to a codon.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr23:130410205 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:130411039 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:151176329 C>T maps to NM_178822.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:151164675 C>T maps to NM_178822.4 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr3:151163064 A>G maps to NM_178822.4 S1568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr3:151165491 C>A maps to NM_178822.4 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:151165877 T>G maps to NM_178822.4 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr3:151155061 G>C maps to NM_178822.4 G2429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr3:151176380 C>T maps to NM_178822.4 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr3:151156234 G>A maps to NM_178822.4 A2038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:151155547 T>C maps to NM_178822.4 P2267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr3:151161457 G>A maps to NM_178822.4 S1759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:151163493 G>A maps to NM_178822.4 A1425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr3:151165454 G>A maps to NM_178822.4 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:118621665 C>A maps to NM_152538.2 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr3:118645023 C>T maps to NM_152538.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr3:118645002 A>G maps to NM_152538.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:118645002 A>C maps to NM_152538.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr3:118644975 G>T maps to NM_152538.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:118621465 T>C maps to NM_152538.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:118649027 G>A maps to NM_152538.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:18738329 G>A maps to NM_173588.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:18736148 G>A maps to NM_173588.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr11:18736136 G>A maps to NM_173588.3 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:18741300 T>G maps to NM_173588.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr11:18738296 T>C maps to NM_173588.3 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:117142761 G>T maps to NM_001542.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:117156492 G>A maps to NM_001542.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:117127666 G>A maps to NM_001542.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:117146450 C>T maps to NM_001542.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr1:117156428 G>T maps to NM_001542.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:117156548 G>A maps to NM_001542.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:117142914 G>A maps to NM_001542.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:117150720 G>A maps to NM_001542.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:117150810 G>A maps to NM_001542.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:117122209 G>A maps to NM_001542.2 G1066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:117156663 C>T maps to NM_001542.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr1:117158923 G>A maps to NM_001542.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:117146633 G>A maps to NM_001542.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:117122236 G>A maps to NM_001542.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr1:117156620 G>A maps to NM_001542.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr21:41151083 T>C maps to NM_001080444.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:21654457 A>G maps to NM_005849.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:160062177 G>A maps to NM_052868.2 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:160064938 A>G maps to NM_052868.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr1:160062788 G>A maps to NM_052868.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:160062275 G>A maps to NM_052868.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:159907503 G>A maps to NM_001135050.1 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:159902364 G>T maps to NM_001135050.1 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:159901372 G>T maps to NM_001135050.1 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr1:159901335 G>A maps to NM_001135050.1 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:159912852 C>T maps to NM_001135050.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:159899183 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:133791084 C>T maps to NM_014987.1 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:133794727 G>A maps to NM_014987.1 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:133790517 C>T maps to NM_014987.1 G1034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:133800876 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:133814113 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:133790637 G>A maps to NM_014987.1 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:133791084 C>T maps to NM_014987.1 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr11:133801564 C>A maps to NM_014987.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:133792518 G>T maps to NM_014987.1 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:133789707 C>T maps to NM_014987.1 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:219920498 G>A maps to NM_002181.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:219920564 C>T maps to NM_002181.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr2:219925066 T>C maps to NM_002181.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr5:140039371 C>A maps to NM_006083.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:140039780 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr5:140033631 C>T maps to NM_006083.3 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr12:99020373 C>T maps to NM_153687.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr12:99007734 C>T maps to NM_201612.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:111663937 G>A maps to NM_003640.3 D626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:111689700 G>T maps to NM_003640.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:111663738 G>A maps to NM_003640.3 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:42129708 C>T maps to NM_001556.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:42178299 C>A maps to NM_001556.2 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:42151028 T>C maps to NM_001556.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:42178356 C>T maps to NM_001556.2 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:42178257 C>T maps to NM_001556.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:42162711 G>A maps to NM_001556.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:206669459 A>G maps to NM_014002.3 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:153770625 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:50444306 G>A maps to NM_006060.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:50467673 C>T maps to NM_006060.3 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr7:50459469 G>T maps to NM_006060.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr7:50450355 C>T maps to NM_006060.3 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr7:50468285 G>A maps to NM_006060.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:50468282 G>A maps to NM_006060.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr7:50459523 C>T maps to NM_006060.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:50450373 C>T maps to NM_006060.3 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:50468105 C>T maps to NM_006060.3 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:50468285 G>A maps to NM_006060.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:50459496 C>T maps to NM_006060.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:213872277 C>A maps to ENST00000342002 G469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr2:213878644 T>C maps to ENST00000342002 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:213872793 G>A maps to ENST00000342002 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:37948989 G>A maps to NM_012481.3 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:37949115 T>A maps to NM_012481.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:37922576 C>T maps to NM_012481.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:56415291 C>T maps to NM_022465.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:56428547 T>C maps to NM_022465.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:206943239 C>T did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr11:117866364 C>T maps to NM_001558.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:117869863 C>T maps to NM_001558.3 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr11:117869668 C>T maps to NM_001558.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:158747326 G>A maps to NM_002187.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:158750308 C>T maps to NM_002187.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr5:158750329 G>C maps to NM_002187.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:158743806 C>A maps to NM_002187.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:18187107 A>G maps to NM_005535.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:18183095 G>A maps to NM_005535.1 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr19:18179265 G>C maps to NM_005535.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:67787283 G>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:67786105 C>T maps to NM_001559.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:67861594 C>T maps to NM_001559.2 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:67795413 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:67838167 A>G maps to NM_001559.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:67855786 C>T maps to NM_001559.2 C674C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:67833650 C>T maps to NM_001559.2 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:117895239 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:117907897 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:117910471 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:117925752 A>G did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:117895117 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr23:117883715 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:114249137 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:114239868 A>G did not map to a codon.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr23:114239847 C>T did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:114249022 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:114238660 T>G did not map to a codon.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr23:114249029 T>G did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:114239784 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:142651088 A>G maps to NM_000585.3 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:81601117 C>T maps to NM_172217.3 T1326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr15:81589339 C>T maps to NM_172217.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr15:81565489 C>T maps to NM_172217.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:81585074 G>A maps to NM_172217.3 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr15:81584949 C>T maps to NM_172217.3 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:81585002 C>A maps to NM_172217.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:81592331 C>T maps to NM_172217.3 R889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:148754009 C>T maps to NM_014443.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr5:148754003 C>T maps to NM_014443.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:21295831 C>T maps to NM_138284.1 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:17590313 G>A maps to NM_014339.5 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:17590409 C>T maps to NM_014339.5 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr22:17577949 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr22:17589440 C>T maps to NM_014339.5 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:17589281 C>T maps to NM_014339.5 Y391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:17578807 C>T maps to NM_014339.5 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:17583053 C>T maps to NM_014339.5 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:53899037 C>T maps to NM_018725.3 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:53899190 C>T maps to NM_018725.3 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:53883766 T>C maps to NM_018725.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:9970061 C>T maps to NM_153461.2 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:9959027 T>A maps to NM_153461.2 L10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:57136540 C>T maps to NM_017563.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:57132278 G>T maps to NM_017563.3 C484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr3:57131678 C>T maps to NM_017563.3 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:57131969 A>C maps to NM_017563.3 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:57132101 G>A maps to NM_017563.3 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:57132008 G>A maps to NM_017563.3 Y574Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:9950917 G>A maps to NM_153483.2 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:9952627 C>T maps to NM_153483.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr3:9948409 T>A maps to NM_153483.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:50437775 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:103010927 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:103006645 A>G maps to NM_003855.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:102998140 A>G maps to NM_003855.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:103013312 A>G maps to NM_003855.2 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:103053709 C>T maps to NM_003853.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr1:206972262 G>A maps to NM_153758.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:113591056 C>T maps to NM_000576.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:113593778 C>A maps to NM_000576.2 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:113591100 G>A maps to NM_000576.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr2:113590380 C>T maps to NM_000576.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:190366253 C>A maps to NM_002182.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:190326849 T>C maps to NM_002182.3 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:29973259 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:29973571 A>T did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:29414373 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:29301172 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:29973786 T>C did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:29301158 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:29973750 C>T did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:29935667 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:29301314 C>T did not map to a codon.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr23:29301097 A>C did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:29973642 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:29959765 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:29973925 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr23:29417400 A>C did not map to a codon.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr23:29973585 T>G did not map to a codon.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr23:104728345 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:104999215 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:104984564 A>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:104512144 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:105011053 C>T did not map to a codon.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr23:105011213 A>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:104999177 G>T did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:104512216 A>C did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:104512135 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:105011291 T>G did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:104478506 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:104984675 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:104440309 A>C did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr23:104999222 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:102965662 C>A maps to NM_016232.4 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:102968038 G>A maps to NM_016232.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:102955438 A>G maps to NM_016232.4 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr2:102842400 G>A maps to NM_003854.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:102849495 C>T maps to NM_003854.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:113890255 C>T maps to NM_173841.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:113877667 A>T maps to NM_173841.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:113890279 C>T maps to NM_173841.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:137322793 G>T maps to NM_014432.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:137323027 C>T maps to NM_014432.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:136701097 G>A maps to NM_144717.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr3:136714376 G>A maps to NM_144717.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:27448865 G>A maps to NM_181079.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:24447501 G>A maps to NM_021258.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:24447435 A>G maps to NM_021258.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr6:137476153 G>A maps to NM_052962.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr1:67666557 G>T maps to NM_144701.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:67635286 G>A maps to NM_144701.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:67685298 G>T maps to NM_144701.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:207076325 C>T maps to NM_001185156.1 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:68595795 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:28515225 G>A maps to NM_145659.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr16:28518120 C>T maps to NM_145659.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:14162494 C>T maps to NM_004843.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:14162972 G>A maps to NM_004843.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:39760406 G>A maps to NM_172138.1 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:39759368 C>T maps to NM_172138.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:39735457 C>T maps to ENST00000392072 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:39734752 C>T maps to ENST00000392072 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:39734728 A>G maps to ENST00000392072 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:39734704 A>G maps to ENST00000392072 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:24484051 G>A maps to NM_170743.2 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:24486012 C>T maps to NM_170743.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:39789107 C>T maps to NM_172140.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:37524249 G>T maps to ENST00000406505 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:37524762 C>T maps to ENST00000406505 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:37533716 G>A maps to ENST00000406505 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:70327620 C>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:70331289 C>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:70329101 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:131396446 C>T maps to NM_000588.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:131398084 C>T maps to NM_000588.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:122658458 G>A maps to NM_001014336.1 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:55203250 C>G maps to NM_139017.4 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:55164655 C>A maps to NM_139017.4 Y64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr5:55203250 C>G maps to NM_139017.4 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr5:55203250 C>G maps to NM_139017.4 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr5:55203250 C>G maps to NM_139017.4 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:70688477 G>A maps to NM_152456.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:1471218 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:1471116 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1471267 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:1471218 C>T did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:1460717 G>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:1499987 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:132009877 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:50393016 C>T maps to NM_172374.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:50393801 G>A maps to NM_172374.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr19:50393268 A>G maps to NM_172374.1 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:50397557 C>T maps to NM_172374.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr19:50397634 T>A maps to NM_172374.1 K175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr19:50398323 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:50392932 C>T maps to NM_172374.1 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:27353455 T>C maps to NM_000418.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:27374121 T>G maps to NM_000418.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:3118290 A>G maps to NM_000564.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:3137114 A>G maps to NM_000564.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:3139715 G>A maps to NM_000564.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:154437708 C>T maps to NM_000565.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:55247856 G>A maps to NM_002184.3 N533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr5:55238561 C>T maps to NM_002184.3 W652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:55237206 A>G maps to NM_002184.3 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:55236978 C>T maps to NM_002184.3 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:35873659 C>T maps to NM_002185.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:135229822 T>C maps to NM_000590.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:155232610 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:155232626 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:155239770 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:155234162 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:155239512 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:155239701 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:121712305 T>C maps to ENST00000344209 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:166927240 G>T maps to NM_199351.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:153642707 T>C did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:6630784 C>T maps to NM_001014795.1 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:239079275 G>A maps to NM_030768.2 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:239092728 G>A maps to NM_030768.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr19:15226969 G>A maps to NM_006844.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:15227319 G>T maps to NM_006844.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr19:15233934 G>A maps to NM_006844.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr11:31484781 G>C maps to NM_144981.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:86371632 C>A maps to NM_006839.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:131102230 C>T maps to NM_033416.1 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr17:43923420 G>T maps to NM_175882.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr17:43924089 C>T maps to NM_175882.2 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr17:43922820 C>T maps to NM_175882.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:43922862 A>G maps to NM_175882.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr17:43923435 C>T maps to NM_175882.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr18:12028894 C>T maps to NM_014214.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:22007893 T>C maps to NM_018439.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr8:57905925 G>A maps to NM_017813.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:128038479 G>A maps to NM_000883.3 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr7:128038596 G>A maps to NM_000883.3 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:76657070 G>A maps to NM_001563.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:76744487 T>C maps to NM_001563.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:76731853 G>A maps to NM_001563.2 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:76713644 G>A maps to NM_001563.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr6:76751765 C>A maps to NM_001563.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr6:76640785 C>T maps to NM_001563.2 E709E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:100949960 G>A maps to NM_016247.2 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:100964715 C>T maps to NM_016247.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr3:100951809 A>G maps to NM_016247.2 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:100972551 C>T maps to NM_016247.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:100951710 G>T maps to NM_016247.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr10:105037930 G>A maps to NM_032727.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:105037207 G>A maps to NM_032727.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:62594565 C>T maps to NM_176877.2 H1740H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:62503675 C>T maps to NM_176877.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:62228823 G>A maps to NM_176877.2 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:62516731 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:62574143 G>A maps to NM_176877.2 G1471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr1:62516709 G>T maps to NM_176877.2 E1369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:62257033 T>C maps to NM_176877.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr1:62594610 C>A maps to NM_176877.2 I1755I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr17:4891774 C>T maps to NM_001167987.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:61919279 G>A maps to NM_001040694.1 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:61916007 G>T maps to NM_001040694.1 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:61908214 C>T maps to NM_001040694.1 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr11:61917560 G>A maps to NM_001040694.1 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:61895677 T>C maps to NM_001040694.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:105169514 C>T maps to ENST00000252520 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:105169687 C>T maps to ENST00000252520 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr14:105174316 G>A maps to ENST00000252520 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr14:105177495 C>T maps to ENST00000252520 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:111371951 C>T maps to NM_005537.3 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr13:111372026 A>C maps to NM_005537.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr13:111371945 C>T maps to NM_005537.3 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr13:111367990 T>G maps to NM_005537.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:184432039 G>T maps to NM_001564.2 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:120593418 A>G maps to NM_019071.2 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:120604801 C>T maps to NM_019071.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:242662668 G>A maps to NM_032329.4 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:220439917 T>C maps to NM_002191.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:41729418 T>C maps to NM_002192.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:41729811 G>A maps to NM_002192.2 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:121104066 C>T maps to NM_002193.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:121104165 C>T maps to NM_002193.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr12:57843600 A>C maps to NM_005538.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:57843558 C>T maps to NM_005538.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:57843580 C>T maps to NM_005538.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:30795373 A>G maps to NM_006774.4 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:30795376 G>A maps to NM_006774.4 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr7:30795205 C>T maps to NM_006774.4 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:30795468 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:30795439 T>C maps to NM_006774.4 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:30795286 C>T maps to NM_006774.4 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:41366687 G>A maps to NM_017553.1 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:41387798 C>T maps to NM_017553.1 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:41277579 G>A maps to NM_017553.1 R1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:41364222 G>A maps to NM_017553.1 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:41276448 G>A maps to NM_017553.1 D1341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:41388077 C>T maps to NM_017553.1 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr18:33077703 C>T maps to NM_001098817.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:206921057 G>A maps to NM_017759.4 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:99172075 C>T maps to NM_001134224.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr2:99204052 C>T maps to NM_001134224.1 Y972Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:99155398 C>T maps to NM_001134224.1 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr2:99180036 C>T maps to NM_001134224.1 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr2:99182627 G>T maps to NM_001134224.1 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:99204008 C>T maps to NM_001134224.1 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:99170939 C>T maps to NM_001134224.1 H523H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr4:143094841 A>G maps to NM_003866.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:143181672 T>G maps to NM_003866.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:143045800 C>T maps to NM_003866.2 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:143067053 G>A maps to NM_003866.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:134463964 C>T maps to NM_005539.3 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:134563058 C>T maps to NM_005539.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr10:134563058 C>T maps to NM_005539.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:38351482 G>A maps to ENST00000373026 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:38411519 C>T maps to ENST00000373026 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:38330096 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:234072452 C>T maps to ENST00000359570 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:234102497 G>A maps to ENST00000359570 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:234072494 G>A maps to ENST00000359570 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:139329212 G>T maps to NM_019892.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:139325452 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:121567529 T>C maps to NM_014937.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:121582626 C>T maps to NM_014937.2 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:121551117 G>A maps to NM_014937.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr10:121586985 G>A maps to NM_014937.2 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:121582586 T>C maps to NM_014937.2 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:121586928 G>A maps to NM_014937.2 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:121587267 C>T maps to NM_014937.2 C1125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:121586727 C>T maps to NM_014937.2 D945D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:121582626 C>T maps to NM_014937.2 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:31523362 C>T maps to ENST00000331075 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:31522406 C>T maps to ENST00000331075 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:31524008 C>T maps to ENST00000331075 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr22:31520865 C>T maps to ENST00000331075 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:31522652 G>A maps to ENST00000331075 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:71942234 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:71946493 C>T maps to NM_001567.3 Y886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:71948326 C>T maps to NM_001567.3 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr11:71946755 G>A maps to NM_001567.3 K899K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr11:2182156 G>T maps to NM_001042376.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:2170468 G>A maps to NM_001042376.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:2170495 C>T maps to NM_001042376.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:15247375 T>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:5233696 T>C maps to NM_002195.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:5231549 G>A maps to NM_002195.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr1:67266856 G>T maps to NM_005478.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr20:20350143 C>T maps to NM_002196.2 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr20:20349828 C>T maps to NM_002196.2 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:20348949 C>A maps to NM_002196.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:36004684 C>T maps to NM_032594.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:36003562 G>A maps to NM_032594.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:36003661 G>A maps to NM_032594.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:36004594 G>A maps to NM_032594.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:36004420 C>T maps to NM_032594.3 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:36003676 G>A maps to NM_032594.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:36005035 G>A maps to NM_032594.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:36004801 C>T maps to NM_032594.3 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:36005108 G>T maps to NM_032594.3 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:7167977 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:7141701 G>A maps to NM_000208.2 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:7125521 C>T maps to NM_000208.2 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:7152852 C>T maps to NM_000208.2 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr19:7132310 G>A maps to NM_000208.2 V900V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:7170608 T>A maps to NM_000208.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:7150505 A>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:7184544 G>A maps to NM_000208.2 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr19:7184577 G>T maps to NM_000208.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:7152780 C>T maps to NM_000208.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:156812270 G>A maps to NM_014215.2 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:156814012 G>A maps to NM_014215.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr1:156816536 G>A maps to NM_014215.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:156816355 G>A maps to NM_014215.2 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:156823940 G>A maps to NM_014215.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:156812192 T>C maps to NM_014215.2 A1078A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:156819053 G>A maps to NM_014215.2 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:156823913 G>A maps to NM_014215.2 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:1529296 G>A maps to ENST00000389470 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:1538053 C>T maps to ENST00000389470 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:1538425 G>A maps to ENST00000389470 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:1539892 G>A maps to ENST00000389470 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:1513959 G>T maps to ENST00000389470 R2105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:1538924 G>A maps to ENST00000389470 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:1511206 C>T maps to ENST00000389470 S2299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:1533408 C>T maps to ENST00000389470 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:1535864 G>A maps to ENST00000389470 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:1523450 G>A maps to ENST00000389470 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:1518140 C>T maps to ENST00000389470 V1712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:1511248 G>A maps to ENST00000389470 D2285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr7:1535798 T>C maps to ENST00000389470 E696E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:1539534 G>A maps to ENST00000389470 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:1510497 G>A maps to ENST00000389470 Y2361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:1518026 G>A maps to ENST00000389470 S1750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:1538479 C>T maps to ENST00000389470 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:1539931 G>A maps to ENST00000389470 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:1525027 C>A maps to ENST00000389470 G1185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:1510812 G>A maps to ENST00000389470 N2315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr7:1538053 C>T maps to ENST00000389470 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:1512731 G>A maps to ENST00000389470 R2230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:1536890 C>T maps to ENST00000389470 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:19677152 C>T maps to NM_018142.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:19679997 G>T maps to NM_018142.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr4:106614631 G>A maps to NM_020395.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:59989017 A>G maps to NM_020748.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:59967231 C>T maps to NM_020748.2 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:153744814 G>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:153745682 G>A maps to ENST00000428986 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:153735838 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:153736607 G>A maps to ENST00000428986 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:153732006 T>C maps to ENST00000428986 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:153736610 G>A maps to ENST00000428986 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:77672169 C>T maps to NM_033547.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:77669838 A>G maps to NM_033547.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr11:77602876 G>T maps to NM_033547.3 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr11:77639468 C>T maps to NM_033547.3 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:62416570 G>A maps to NM_030628.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:62416783 A>G maps to NM_030628.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:62415760 C>T maps to NM_030628.1 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:62417002 A>G maps to NM_030628.1 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr11:62416321 C>T maps to NM_030628.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:62416159 C>T maps to NM_030628.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:62415085 G>A maps to NM_030628.1 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:52004495 C>T maps to NM_012141.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:212161318 A>G maps to NM_015434.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:212142037 T>C maps to NM_015434.3 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:212161323 G>A maps to NM_015434.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:212180669 C>T maps to NM_015434.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:212141283 G>A maps to NM_015434.3 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr1:212126027 T>C maps to NM_015434.3 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:95886788 C>T maps to NM_017864.2 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:95877853 C>T maps to NM_017864.2 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:128627709 A>G maps to NM_015693.3 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr4:128564846 G>A maps to NM_015693.3 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:128554305 T>C maps to NM_015693.3 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:128627892 A>G maps to NM_015693.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr4:128632185 C>T maps to NM_015693.3 Q830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:102988441 C>T maps to NM_014425.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:103054968 C>T maps to NM_014425.2 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:103035176 G>T maps to NM_014425.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr9:103015322 A>T maps to NM_014425.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:103002491 C>T maps to NM_014425.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:103035331 A>G maps to NM_014425.2 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:103009028 G>A maps to NM_014425.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:49765664 G>A maps to NM_153273.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:48732352 G>T maps to ENST00000443964 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:48732685 G>A maps to ENST00000395509 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:48725852 A>G maps to ENST00000395509 D401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:33703226 G>A maps to NM_054111.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:154481145 G>A maps to NM_001130700.1 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:154489164 G>A maps to NM_001130700.1 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr6:154489164 G>A maps to NM_001130700.1 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:154520862 A>G maps to NM_001130700.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:154542443 A>G maps to NM_001130700.1 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr6:154520838 G>T maps to NM_001130700.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:59986901 T>C did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:61747670 C>T maps to NM_001134779.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:61763068 C>T maps to NM_001134779.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:44433042 C>T maps to NM_014652.3 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:44432663 T>C maps to NM_014652.3 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:44432282 C>T maps to NM_014652.3 R812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr1:44424236 C>A maps to NM_014652.3 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:44424483 C>T maps to NM_014652.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr1:44422611 G>A maps to NM_014652.3 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:24654688 C>A maps to ENST00000458132 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:9446770 C>T maps to NM_006391.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:9456520 A>G maps to NM_006391.2 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:9459746 C>T maps to NM_006391.2 N870N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:30837275 A>G maps to NM_006390.3 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:30833413 A>G did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:30816462 A>G maps to NM_006390.3 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:30792612 A>G maps to NM_006390.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:30814170 A>G maps to NM_006390.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:30815389 A>G maps to NM_006390.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr12:30834693 C>T maps to NM_006390.3 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr12:30819132 A>G maps to NM_006390.3 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr9:95411815 G>A maps to NM_022755.5 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:95420957 G>A maps to NM_022755.5 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:95378326 C>T maps to NM_022755.5 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr9:95418776 G>T maps to NM_022755.5 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:95397510 C>T maps to NM_022755.5 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:237272541 G>A maps to ENST00000457693 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:121500636 G>A maps to NM_001023570.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:32672878 G>A maps to NM_001160042.1 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:32673019 C>T maps to NM_001160042.1 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:32673400 G>A maps to NM_001160042.1 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:32673632 G>T maps to NM_001160042.1 G531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:32672878 G>A maps to NM_001160042.1 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr7:2617907 G>A maps to NM_152558.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:2622221 C>T maps to NM_152558.3 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr3:51897242 C>T maps to NM_203424.1 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:197618325 G>A maps to NM_001134435.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:197665522 G>A maps to NM_001134435.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:197670672 G>A maps to NM_001134435.1 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:197670852 G>A maps to NM_001134435.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:67664606 C>T maps to NM_001031715.2 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:19800165 G>A maps to NM_153208.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:91040461 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:91035844 C>T maps to NM_003870.3 Y1510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:90972888 A>G maps to NM_003870.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr15:90996482 A>G maps to NM_003870.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:75954395 A>G maps to NM_006633.2 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr5:75967730 G>A maps to NM_006633.2 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:75871585 C>T maps to NM_006633.2 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:75989260 G>A maps to NM_006633.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:156521763 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:156498799 G>T maps to NM_178229.4 G1493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:156500055 T>C maps to NM_178229.4 T1415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:156518532 A>G maps to NM_178229.4 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr1:156524091 G>A maps to NM_178229.4 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr1:156508623 A>G maps to NM_178229.4 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:156513773 T>C maps to NM_178229.4 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:156533002 G>A maps to NM_178229.4 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr1:156517990 G>C maps to NM_178229.4 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:156517927 C>T maps to NM_178229.4 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:156521535 G>A maps to NM_178229.4 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:156508825 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:156510582 G>A maps to NM_178229.4 R886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:156535836 G>A maps to NM_178229.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:12944316 G>A maps to ENST00000429247 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:53280262 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53268435 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53279870 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53280311 G>A did not map to a codon.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr23:53280268 C>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:53279576 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:53284023 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:53285132 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:53285091 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:53265547 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:53285132 C>G did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:53279784 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:53265540 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:274931 G>A maps to NM_001170738.1 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:247674 G>T maps to NM_001170738.1 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:248328 C>T maps to NM_001170738.1 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:248454 G>A maps to NM_001170738.1 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:248346 C>T maps to NM_001170738.1 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:248073 G>A maps to NM_001170738.1 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr12:280290 C>G maps to NM_001170738.1 A1026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:234813 C>A maps to NM_001170738.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:266232 C>T maps to NM_001170738.1 D732D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:266726 T>C maps to NM_001170738.1 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:123109381 C>T maps to NM_178827.4 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:123109359 C>A maps to NM_178827.4 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:123142740 A>G maps to NM_178827.4 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:123109381 C>T maps to NM_178827.4 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:153282483 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:153278859 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:153278549 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:153281507 G>A did not map to a codon.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr23:153284491 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:153278090 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:153282397 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:153282030 T>C did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr3:10283809 T>G maps to NM_001570.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:10280463 G>A maps to NM_001570.3 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:66605355 T>C maps to NM_007199.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:66620618 T>C did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr12:66641719 C>T maps to NM_007199.2 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:66641587 T>C maps to NM_007199.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr12:66638316 C>G maps to NM_007199.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:78755307 C>T maps to NM_004136.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:78768645 T>C maps to NM_004136.2 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:78764093 A>G maps to NM_004136.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr5:131823675 C>T maps to NM_002198.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr5:131822698 G>T maps to NM_002198.2 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr5:131819645 C>T maps to NM_002198.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:185329429 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:185350181 C>A maps to NM_002199.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:185309953 C>T maps to NM_002199.3 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr19:46388027 G>T maps to NM_015649.1 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:50166693 G>A maps to NM_001571.5 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:50165517 C>T maps to NM_001571.5 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr19:50163006 G>A maps to NM_001571.5 H394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:50165475 C>T maps to NM_001571.5 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:394996 A>G maps to NM_002460.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:394867 G>A maps to NM_002460.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr6:398915 C>T maps to NM_002460.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:401688 C>T maps to NM_002460.3 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:394847 C>T maps to NM_002460.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:405051 G>A maps to NM_002460.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr6:401484 C>T maps to NM_002460.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:398831 C>T maps to NM_002460.3 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr6:401655 G>A maps to NM_002460.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:128587395 C>T maps to NM_001098629.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:209961989 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:209965705 C>T maps to NM_006147.2 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:209964011 G>A maps to NM_006147.2 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:209964019 G>A maps to NM_006147.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:209963053 C>T maps to NM_006147.2 W379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:209968683 C>T maps to NM_006147.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:85948112 C>T maps to NM_002163.2 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr16:85948115 G>A maps to NM_002163.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:85948085 G>A maps to NM_002163.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr16:85948094 G>A maps to NM_002163.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:24632716 T>C maps to NM_006084.4 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr19:44223717 C>T maps to NM_019612.3 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:44223738 C>G maps to NM_019612.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:44222892 C>T maps to NM_019612.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:44223342 C>T maps to NM_019612.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr19:44097365 G>A maps to NM_001007561.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:227660940 C>T maps to NM_005544.2 Q838Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:227662527 G>A maps to NM_005544.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:227663079 C>T maps to NM_005544.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:227663052 G>A maps to NM_005544.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr2:227662668 A>G maps to NM_005544.2 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:227660073 G>A maps to NM_005544.2 G1127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr2:227662550 G>A maps to NM_005544.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr2:227662032 G>A maps to NM_005544.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr2:227661351 G>A maps to NM_005544.2 N701N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:227662739 G>A maps to NM_005544.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:227662209 C>T maps to NM_005544.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr13:110434787 G>A maps to NM_003749.2 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr13:110436795 G>A maps to NM_003749.2 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:110434416 G>A maps to NM_003749.2 H1328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:110436711 C>T maps to NM_003749.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:107977612 T>C did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:107978571 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:107978723 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:107979482 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:107976464 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:107978365 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:107979096 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:107976204 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:107979508 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:107977351 T>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:107976158 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:107976444 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:107978695 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr23:107979401 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:107979541 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:107978668 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:107978395 C>T did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:107978447 C>T did not map to a codon.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr23:107977193 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:107976680 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr23:107975885 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr23:107978367 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:107978312 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:107978480 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:107977918 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:107976124 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr23:107977571 T>G did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr23:107977166 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:107979182 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:107979334 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:107978751 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:107978081 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr23:107977174 A>G did not map to a codon.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr5:3599409 T>C maps to NM_024337.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr5:3599409 T>G maps to NM_024337.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:3601108 G>A maps to NM_024337.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr5:3600108 G>A maps to NM_024337.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:3599721 C>T maps to NM_024337.3 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:3599820 C>T maps to NM_024337.3 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:2748540 C>T maps to NM_033267.4 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:2749020 C>T maps to NM_033267.4 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:2748585 A>C maps to NM_033267.4 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:2748624 G>A maps to NM_033267.4 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr5:2748984 C>T maps to NM_033267.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr5:2748954 G>A maps to NM_033267.4 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:2749035 G>A maps to NM_033267.4 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr5:2748624 G>A maps to NM_033267.4 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr5:2749118 C>A maps to NM_033267.4 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:54317652 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:54319006 C>T maps to NM_024336.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:1879903 C>T maps to NM_016358.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:1879765 C>T maps to NM_016358.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:1878802 G>A maps to NM_016358.2 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:54967667 C>T maps to NM_005853.5 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr16:54967388 C>G maps to NM_005853.5 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:54966465 C>T maps to NM_005853.5 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:54967710 T>C maps to NM_005853.5 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:54966627 C>T maps to NM_005853.5 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr16:55363167 G>A maps to NM_024335.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:55362816 C>T maps to NM_024335.2 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:55360396 C>T maps to NM_024335.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr16:55361503 C>T maps to NM_024335.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:55363089 C>T maps to NM_024335.2 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:55362702 C>T maps to NM_024335.2 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr12:108961018 T>C maps to NM_213595.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr1:949722 G>A maps to NM_005101.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr1:156696910 C>T maps to NM_030980.1 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr1:156694023 G>A maps to NM_030980.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:76632884 G>A maps to NM_145805.1 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr15:76629256 G>A maps to NM_145805.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr15:74467618 C>T maps to NM_201526.1 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:74427111 C>T maps to NM_001130137.1 Q673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:74426147 C>T maps to NM_001130137.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:74425790 G>A maps to NM_001130137.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:74425463 C>T maps to NM_001130137.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:74427272 C>T maps to NM_001130137.1 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr15:74425595 C>T maps to NM_001130137.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:74425934 C>T maps to NM_001130137.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:74426789 C>A maps to NM_001130137.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:74425313 C>T maps to NM_001130137.1 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:74427107 C>T maps to NM_001130137.1 D671D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:74425172 C>T maps to NM_001130137.1 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:74425133 T>G maps to NM_001130137.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:74426537 G>A maps to NM_001130137.1 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:13279874 C>T maps to NM_080826.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:13279772 C>T maps to NM_080826.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:77948914 C>T maps to NM_199296.2 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:16445838 G>A maps to NM_001101426.3 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr22:35481613 T>G maps to NM_001008494.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr19:18546940 C>T maps to NM_016368.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:33026405 C>T maps to ENST00000262650 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:33030036 C>T maps to ENST00000262650 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:32996529 T>C maps to ENST00000262650 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr16:47345221 G>T maps to NM_030790.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr16:47494836 C>T maps to NM_030790.3 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:2930008 T>A maps to NM_018463.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:2929297 G>T maps to NM_018463.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:2929960 G>A maps to NM_018463.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr16:304606 C>T maps to NM_032039.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:52227933 G>A maps to NM_181501.1 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr5:52145262 G>A maps to NM_181501.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:52216276 T>G maps to NM_181501.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr5:52204855 G>A maps to NM_181501.1 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:52177730 C>T maps to NM_181501.1 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:52214675 A>G maps to NM_181501.1 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:52183697 C>T maps to NM_181501.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:145535839 G>A maps to NM_003637.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:145534183 T>C maps to NM_003637.3 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:145530912 T>C maps to NM_003637.3 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:145537741 G>A maps to NM_003637.3 E860E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:68661609 G>A maps to ENST00000423218 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:68617467 C>T did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr15:68649511 C>T maps to ENST00000423218 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:68624343 T>G maps to ENST00000423218 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:68619069 G>A maps to ENST00000423218 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr5:52366068 C>T maps to NM_002203.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:52367772 C>A maps to NM_002203.3 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr17:42455110 C>T maps to NM_000419.3 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:42466709 G>A maps to NM_000419.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:42457459 C>T maps to NM_000419.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:42452961 G>A maps to NM_000419.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:42463277 G>A maps to NM_000419.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:42461007 C>A maps to NM_000419.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:48145497 C>T maps to NM_002204.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr17:48156528 G>A maps to NM_002204.2 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:48158768 G>A maps to NM_002204.2 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:48155489 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:48148759 C>T maps to NM_002204.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:182399097 G>A did not map to a codon.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr2:182360533 C>T maps to NM_000885.4 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:182394351 C>T maps to NM_000885.4 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr2:182374425 T>C maps to NM_000885.4 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr2:182350606 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:182323027 C>T maps to NM_000885.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:182323027 C>T maps to NM_000885.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:182322997 C>A maps to NM_000885.4 C91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr12:54799106 G>A maps to NM_002205.2 D356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:173344452 G>A maps to ENST00000264106 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr12:56082735 G>A maps to ENST00000347027 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:56101280 C>T maps to ENST00000347027 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:56088255 C>T maps to ENST00000347027 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:56091498 A>G maps to ENST00000347027 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr12:56092215 G>A maps to ENST00000347027 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:15720762 G>A maps to NM_003638.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:15760806 C>A maps to NM_003638.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:15600165 G>A maps to NM_003638.1 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:15628611 G>A maps to NM_003638.1 I781I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr10:15639292 A>G maps to NM_003638.1 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr10:15650282 A>C maps to NM_003638.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr10:15634287 G>A maps to NM_003638.1 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:15590531 A>G maps to NM_003638.1 C934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:15628599 C>T maps to NM_003638.1 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:15649741 G>A maps to NM_003638.1 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:15761560 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:37559044 G>A maps to NM_002207.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:37560808 T>C maps to NM_002207.2 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:37670703 G>A maps to NM_002207.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:37567541 C>T maps to NM_002207.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:37574879 C>T maps to NM_002207.2 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr3:37555267 C>T maps to NM_002207.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr3:37845378 C>T maps to NM_002207.2 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr3:37695242 C>G maps to NM_002207.2 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:31422506 C>G maps to ENST00000444228 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:31426275 G>A maps to ENST00000444228 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr16:31405554 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:31405650 C>T maps to ENST00000444228 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:31434452 G>A maps to ENST00000444228 K949K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:3665217 G>A maps to NM_002208.4 H102H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:3660313 G>A maps to NM_002208.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:3660326 C>T maps to NM_002208.4 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:3660418 C>A maps to NM_002208.4 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:30529991 C>T maps to NM_002209.2 N1060N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:30507870 C>T maps to NM_002209.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:31336658 C>A maps to NM_001145808.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr16:31283289 G>A maps to NM_001145808.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:31277141 G>A maps to NM_001145808.1 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:31283277 G>T maps to NM_001145808.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr16:31336625 G>C maps to NM_001145808.1 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:31336582 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:31332934 T>C maps to NM_001145808.1 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:31341633 C>A maps to NM_001145808.1 C1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:187541574 G>A maps to NM_002210.3 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr2:187503012 C>A maps to NM_002210.3 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:187520983 G>T maps to NM_002210.3 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr2:187521023 C>T maps to NM_002210.3 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:31391663 C>A maps to NM_000887.3 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31383730 C>T maps to NM_000887.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31384581 G>A maps to NM_000887.3 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:31383748 G>A maps to NM_000887.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr16:31371108 C>T maps to NM_000887.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:31374257 C>T maps to NM_000887.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr16:31382720 G>A maps to NM_000887.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:31373184 C>T maps to NM_000887.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:31368596 C>T maps to NM_000887.3 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr16:31368359 G>T maps to NM_000887.3 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:31383829 C>T maps to NM_000887.3 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr16:31383943 C>T maps to NM_000887.3 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:33214796 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:9548268 G>A maps to NM_004763.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:9547004 T>C maps to NM_004763.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:70522260 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:70523137 C>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:70523492 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:70523124 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:70524390 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr21:46326962 C>T maps to NM_000211.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:46313381 G>A maps to NM_000211.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr21:46330673 C>A maps to NM_000211.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr21:46311734 G>A maps to NM_000211.3 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:46309279 G>A maps to NM_000211.3 C596C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:46321484 G>A maps to NM_000211.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:46330638 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr21:46321415 G>A maps to NM_000211.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:46323289 G>A maps to NM_000211.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:46323304 G>A maps to NM_000211.3 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr21:46321618 G>A maps to NM_000211.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr21:46320285 G>A maps to NM_000211.3 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:46309914 G>A maps to NM_000211.3 N545N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:63920099 G>T maps to ENST00000371092 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr17:73727403 C>T maps to NM_001005619.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:73747157 C>T maps to NM_001005619.1 Y1253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:73733712 T>C maps to NM_001005619.1 C736C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:73729675 C>T maps to NM_001005619.1 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:73748641 C>T maps to NM_001005619.1 S1364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:73745106 C>A maps to NM_001005619.1 T1099T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:73736899 C>T maps to NM_001005619.1 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:73728293 C>T maps to NM_001005619.1 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:73751202 T>C maps to NM_001005619.1 S1472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:73727939 G>A maps to NM_001005619.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:124578266 G>T maps to NM_002213.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:160993948 G>A maps to NM_000888.3 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:161052046 G>A maps to NM_000888.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:160994242 G>A maps to NM_000888.3 C454C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr2:160994709 C>A maps to NM_000888.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:160994275 G>T maps to NM_000888.3 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:161052031 G>A maps to NM_000888.3 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr12:53587071 C>T maps to NM_000889.1 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr12:53586644 C>T maps to NM_000889.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:53585641 C>T did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr7:20438595 A>G maps to NM_002214.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:20444333 C>T maps to NM_002214.2 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr13:102235689 T>C maps to NM_004791.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:102105270 G>A maps to NM_004791.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr3:52824908 G>A maps to NM_002215.2 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8364-01A-11D-2340-08 chr3:52819115 C>T maps to NM_002215.2 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:52821009 C>T maps to NM_002215.2 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr3:52822069 C>T maps to NM_002215.2 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:52824812 C>T maps to NM_002215.2 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:52824843 C>T maps to NM_002215.2 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:52824863 G>T maps to NM_002215.2 S807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:52825533 G>A maps to NM_002215.2 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:7785223 T>C did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr10:7759714 C>T maps to NM_002216.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:7786852 C>A maps to NM_002216.2 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:52831834 C>T maps to NM_002217.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:52836762 C>T maps to NM_002217.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:52831900 C>T maps to NM_002217.3 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:52835032 C>T maps to NM_002217.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:52861194 G>T maps to ENST00000485816 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:52861146 G>A maps to ENST00000485816 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:7618458 G>A maps to ENST00000256861 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:7608185 A>G maps to ENST00000256861 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:7618578 G>A maps to ENST00000256861 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr10:7621728 C>T maps to ENST00000256861 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr10:7618704 T>G maps to ENST00000256861 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:7618869 G>A maps to ENST00000256861 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:7618674 G>A maps to ENST00000256861 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr10:7614340 C>A maps to NM_001001851.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:7708804 C>T maps to ENST00000256861 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:7627909 G>A maps to ENST00000256861 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:54781450 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:54784874 C>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:54815024 A>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:54776439 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:54800552 A>G did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:54814955 A>C did not map to a codon.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr23:54785303 C>T did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:54785173 T>C did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:54823453 A>T did not map to a codon.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr23:54817435 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:54783778 T>C did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:54785376 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:54776524 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:54780117 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:54780159 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:54784483 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:54784080 C>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:54783865 T>C did not map to a codon.
Sequencing variant TCGA-RD-A8N0-01A-12D-A364-08 chr23:54783555 A>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:54784865 A>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:156672938 G>A maps to NM_005546.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr5:156635913 G>A maps to NM_005546.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:156649961 C>T maps to NM_005546.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:160917763 G>A maps to NM_080878.2 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:160914968 C>A maps to NM_080878.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:78622665 T>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:231740378 C>T maps to NM_030926.4 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:231740483 C>T maps to NM_030926.4 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:231741675 C>T maps to NM_030926.4 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr2:231742257 G>A maps to NM_030926.4 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:231742167 G>A maps to NM_030926.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:3204041 C>T maps to NM_033453.2 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:93412765 G>A maps to NM_014216.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:41794293 G>A maps to NM_002220.1 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:226924811 G>A maps to NM_002221.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:226923839 G>A maps to NM_002221.3 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:226924475 C>T maps to NM_002221.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr1:226825433 C>T maps to NM_002221.3 R857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:226924067 G>A maps to NM_002221.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:226925054 C>T maps to NM_002221.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:4808339 G>T maps to ENST00000356617 G1887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:4856236 G>A maps to ENST00000356617 P2562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:4842130 G>A maps to ENST00000356617 S2316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:4821277 C>T maps to ENST00000356617 H2110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:4859883 C>T maps to ENST00000356617 T2660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:4810192 A>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:4829714 C>T maps to ENST00000356617 R2232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr3:4709209 G>T maps to ENST00000356617 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:4715041 G>A maps to ENST00000356617 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:4715059 C>T maps to ENST00000356617 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:4853059 C>T maps to ENST00000356617 L2460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr12:26551881 G>A maps to NM_002223.2 I2541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:26784906 G>A maps to NM_002223.2 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:26839487 C>T maps to NM_002223.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:26551953 T>C maps to NM_002223.2 R2517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:26493201 G>A maps to NM_002223.2 G2639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:26848567 G>A maps to NM_002223.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:26775333 C>A maps to NM_002223.2 E1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:26811001 C>A maps to NM_002223.2 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IZ-01A-32D-A25D-08 chr12:26648091 C>T maps to NM_002223.2 Q1725Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:26580932 A>G maps to NM_002223.2 G2286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:26634089 G>A maps to NM_002223.2 R2033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:26572038 C>T maps to NM_002223.2 A2351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:26749968 A>G maps to NM_002223.2 D1367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr12:26732986 G>A maps to NM_002223.2 P1494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:26750043 C>T maps to NM_002223.2 V1342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr12:26864159 C>T maps to NM_002223.2 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:33654202 C>T maps to ENST00000374316 H1962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:33648140 C>T maps to ENST00000374316 C1420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:33638468 G>A maps to ENST00000374316 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr6:33655295 G>A maps to ENST00000374316 P2073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:33662759 C>T maps to ENST00000374316 G2615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:33656439 G>A maps to ENST00000374316 P2192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr6:33632879 A>G maps to ENST00000374316 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr6:33656556 A>T maps to ENST00000374316 T2231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:33659476 G>A maps to ENST00000374316 S2437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr6:33632703 T>C maps to ENST00000374316 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:33643503 C>T maps to ENST00000374316 G1051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:33653882 G>A maps to ENST00000374316 T1907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:33623606 G>A maps to ENST00000374316 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:33638468 G>A maps to ENST00000374316 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:33631648 C>T maps to ENST00000374316 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:33641486 C>T maps to ENST00000374316 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr6:33653465 G>A maps to ENST00000374316 S1843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:33656502 G>A maps to ENST00000374316 V2213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:106074504 C>A maps to NM_033397.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:106075560 G>A maps to NM_033397.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr10:106074372 G>A maps to NM_033397.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:19126265 C>T maps to NM_001034841.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr16:19127265 C>A maps to NM_001034841.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:35195846 C>T maps to NM_003024.2 Q1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:35127703 T>C did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr21:35209290 G>A maps to NM_001001132.1 *1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr21:35154337 A>G maps to NM_003024.2 K575K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr21:35166670 A>G maps to NM_003024.2 Q617Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:24426494 C>A maps to NM_006277.2 *1698Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:40699904 C>T maps to NM_002225.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:152883823 C>T maps to NM_005547.2 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:152882473 A>G maps to NM_005547.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:152882755 G>A maps to NM_005547.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr1:152883949 G>T maps to NM_005547.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr1:185277942 G>T maps to NM_006469.4 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:128253654 C>G maps to NM_017969.2 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:128249665 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:150715264 T>A maps to NM_203395.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr6:150710674 G>A maps to NM_203395.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:49246782 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:49247734 G>T maps to NM_182575.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:10620232 C>T maps to NM_000214.2 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:10622290 G>A maps to NM_000214.2 C911C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:10621533 A>G maps to NM_000214.2 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:10625788 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:10620391 C>T maps to NM_000214.2 K1137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:10620526 G>A maps to NM_000214.2 C1092C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:10625878 C>T maps to NM_000214.2 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:10628734 A>G maps to NM_000214.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr20:10629247 G>A maps to NM_000214.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:105618516 G>A maps to NM_002226.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:105622216 G>A maps to NM_002226.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr14:105609472 G>A maps to NM_002226.3 S1092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:105612832 G>A maps to NM_002226.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr14:105617713 C>T maps to NM_002226.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:105615280 G>A maps to NM_002226.3 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr3:9934634 C>G maps to NM_032492.3 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr3:9934907 C>T maps to NM_032492.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:65344790 G>A maps to NM_002227.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:65323362 G>A maps to NM_002227.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:65304183 G>C maps to NM_002227.2 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:65335079 G>A maps to NM_002227.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:65313280 A>C maps to NM_002227.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:65307254 C>T maps to NM_002227.2 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr1:65303750 G>T maps to NM_002227.2 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:5050705 C>T maps to NM_004972.3 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:5080259 T>C maps to NM_004972.3 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:5064998 C>T maps to NM_004972.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:5022091 A>T maps to NM_004972.3 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:5022213 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:5089750 G>A maps to NM_004972.3 K883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr9:5069140 G>A maps to NM_004972.3 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:5054661 G>A maps to NM_004972.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:17943457 G>A maps to NM_000215.3 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:6080671 C>T maps to NM_001099433.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:6066723 C>A maps to NM_001099433.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr4:6107559 G>A maps to NM_001099433.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:6107670 C>T maps to NM_001099433.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr4:6082036 T>C maps to NM_001099433.1 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr4:6086630 G>T maps to NM_001099433.1 S299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr4:6043884 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:6087299 G>A maps to NM_001099433.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:6107370 C>T maps to NM_001099433.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr4:6083436 C>A maps to NM_001099433.1 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr4:6064092 G>A maps to NM_001099433.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr4:6082024 T>A maps to NM_001099433.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:147012251 T>C maps to NM_014790.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:147019215 G>A maps to NM_014790.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:147040711 C>A maps to NM_014790.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:133930822 C>T maps to NM_001105521.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:133963529 C>T maps to NM_001105521.2 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:133963535 C>T maps to NM_001105521.2 N666N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr11:134014822 G>A maps to NM_032801.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:15507633 C>T maps to NM_004973.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:15496889 A>G maps to NM_004973.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:15512569 C>T maps to NM_004973.2 T1028T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:15520331 C>T maps to NM_004973.2 C1197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:15512545 C>T maps to NM_004973.2 C1020C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:15496925 G>A maps to NM_004973.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:15496979 G>A maps to NM_004973.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr6:15501507 C>T maps to NM_004973.2 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:15487610 C>T maps to NM_004973.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:15501606 C>T maps to NM_004973.2 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr7:139829296 A>G maps to NM_030647.1 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr14:59954531 C>T maps to ENST00000356057 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:59965468 C>T maps to ENST00000356057 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:64979727 G>A maps to NM_032776.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:64979740 G>A maps to NM_032776.1 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:64968899 T>C maps to NM_032776.1 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:64958333 A>G maps to NM_032776.1 G1810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr10:64960411 T>C maps to NM_032776.1 K1700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:64967738 T>C maps to NM_032776.1 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:64975327 G>A maps to NM_032776.1 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:227920623 G>A maps to NM_023007.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:227920367 T>G maps to NM_023007.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:227920194 C>T maps to NM_023007.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:227922491 G>A maps to NM_023007.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:227920188 G>A maps to NM_023007.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:27221728 C>T maps to NM_001145348.1 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:27232029 G>T maps to NM_001145348.1 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:74719968 G>A maps to NM_001081461.1 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:42127218 C>T maps to NM_005090.3 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:42138434 A>G maps to NM_005090.3 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:42139593 G>A maps to NM_005090.3 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:42134086 T>A maps to NM_005090.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr15:42138150 C>T maps to NM_005090.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:42139593 G>A maps to NM_005090.3 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:42139946 C>T maps to NM_005090.3 D976D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:78608245 T>C maps to NM_152405.4 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr5:78610474 C>T maps to NM_152405.4 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr5:78595998 A>G maps to NM_152405.4 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:75171671 G>A maps to NM_020647.2 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:75227697 G>A maps to NM_020647.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:75227796 G>A maps to NM_020647.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:75233262 G>T maps to NM_020647.2 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr8:75157410 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:75227607 G>A maps to NM_020647.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:75227622 C>T maps to NM_020647.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr20:42744649 C>A maps to NM_020433.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:42744670 C>T maps to NM_020433.4 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:42788478 G>A maps to NM_020433.4 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr20:42744523 C>T maps to NM_020433.4 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:42789003 G>A maps to NM_020433.4 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:42815039 G>A maps to NM_020433.4 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:87723328 C>T maps to NM_020655.2 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:87677939 C>T maps to NM_020655.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:87678419 C>T maps to NM_020655.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:87723915 C>T maps to NM_020655.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:87678281 C>T maps to NM_020655.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:24045099 G>A maps to NM_032452.2 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:24040253 C>T maps to NM_032452.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr14:24040544 G>T maps to NM_032452.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:143747297 C>T maps to NM_003724.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:143746319 C>T maps to NM_003724.2 W386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:143747243 C>T maps to NM_003724.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr8:143747315 G>A maps to NM_003724.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr11:96125231 G>A maps to NM_003772.3 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr11:96124154 A>G maps to NM_003772.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:2255301 T>A maps to NM_144616.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:2252759 C>T maps to NM_144616.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:2255289 C>T maps to NM_144616.3 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:2252348 G>A maps to NM_144616.3 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:153947256 G>A maps to NM_006694.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:153949674 C>T maps to NM_006694.3 W18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:12902620 C>T maps to NM_002229.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:12902770 C>T maps to NM_002229.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8209-01A-11D-2340-08 chr19:18391901 G>A maps to NM_005354.4 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:39919525 C>A maps to NM_021991.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:39925732 G>A maps to NM_021991.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:24358031 G>A maps to NM_181337.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:8555944 A>G did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:8555927 A>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:8555952 T>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:8522075 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:8522074 T>C did not map to a codon.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr23:8591677 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:8538694 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:8555938 A>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:8502391 C>T did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:8555988 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:8522052 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:8504916 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:8503691 C>T did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:8555952 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:8538576 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:8503631 G>A did not map to a codon.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr23:8538712 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:8553427 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:8565133 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:8504930 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:8507772 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:8699939 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr23:8507758 T>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:711848 G>A maps to NM_015158.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:711134 C>A maps to NM_015158.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:744579 C>A maps to NM_015158.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr9:712604 C>T maps to NM_015158.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:676998 C>T maps to NM_015158.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:742368 G>A maps to NM_015158.2 L1287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr9:742405 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:738433 C>T maps to NM_015158.2 N1161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:11280722 C>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr19:11289025 G>A maps to NM_015493.6 N513N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr19:11289370 C>T maps to NM_015493.6 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:11304230 G>T maps to NM_015493.6 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:11304272 G>A maps to NM_015493.6 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:11289277 C>T maps to NM_015493.6 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr19:11303897 G>A maps to NM_015493.6 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr19:8389404 G>A maps to NM_198471.2 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:62728926 C>T maps to NM_181712.4 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:62733981 T>C maps to NM_181712.4 E736E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:62732401 A>G did not map to a codon.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr1:62704050 A>C maps to NM_181712.4 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:75669878 C>T maps to NM_001130089.1 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:75665395 G>A maps to NM_001130089.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr16:75669925 G>A maps to NM_001130089.1 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:40265765 G>A maps to NM_021078.2 R805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:40266538 C>T maps to NM_021078.2 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:40272727 G>T maps to NM_021078.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:20164247 C>T maps to NM_003884.4 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:20113952 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:20187854 T>G maps to NM_003884.4 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:20181823 G>T maps to NM_003884.4 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:65481994 G>A maps to NM_182710.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr6:149916258 C>T maps to NM_007044.2 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:149918301 G>A maps to NM_007044.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr6:149924460 G>A maps to NM_007044.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:30857758 C>T maps to NM_032116.3 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr13:30805516 C>T maps to NM_032116.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:44627352 C>T maps to ENST00000356157 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:57789829 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:57789030 C>T maps to NM_005886.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:57787092 G>T maps to NM_005886.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:15390078 C>T maps to NM_201628.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:15441016 C>T maps to NM_201628.2 F738F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr1:15386798 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:15386752 G>A maps to NM_201628.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:15390069 C>T maps to NM_201628.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:14925621 C>T maps to NM_201628.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:170367064 C>T maps to NM_006063.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:127642065 T>A maps to NM_207335.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr7:32909211 T>C maps to NM_015483.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:32909213 G>A maps to NM_015483.2 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:32914663 A>G maps to NM_015483.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:32909148 C>T maps to NM_015483.2 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr7:32909936 A>G maps to NM_015483.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr7:32909325 A>G maps to NM_015483.2 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:105929632 C>T maps to NM_198439.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr11:105924368 A>G maps to NM_198439.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:47599014 A>G maps to NM_018095.4 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:47594871 A>G maps to NM_018095.4 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr11:47594625 G>A maps to NM_018095.4 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:42727820 C>T maps to NM_152393.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:42727235 C>T maps to NM_152393.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr3:42733379 C>T maps to NM_152393.2 N587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:42727727 C>T maps to NM_152393.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr3:42730381 C>A maps to NM_152393.2 C481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:41705320 G>A maps to NM_152903.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:41706251 A>T maps to NM_152903.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:41768039 G>A maps to NM_032138.4 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:41767958 G>A maps to NM_032138.4 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:41766824 A>G maps to NM_032138.4 D523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr13:41768159 C>T maps to NM_032138.4 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:41767066 G>A maps to NM_032138.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:67058347 G>T maps to NM_032505.2 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:67058676 T>A maps to NM_032505.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:85276639 A>G maps to NM_020122.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:85276645 C>T maps to NM_020122.4 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr2:85276555 C>T maps to NM_020122.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr12:5020810 C>T maps to NM_000217.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr12:5021266 C>T maps to NM_000217.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr12:5021647 G>A maps to NM_000217.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:5020648 C>T maps to NM_000217.2 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr12:5021221 G>A maps to NM_000217.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:5021704 C>T maps to NM_000217.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:5020675 C>T maps to NM_000217.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:5020657 C>T maps to NM_000217.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:5020591 G>A maps to NM_000217.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:111060062 A>G maps to NM_005549.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:111060926 G>T maps to NM_005549.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr1:111059875 A>C maps to NM_005549.2 *512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:111147187 G>A maps to NM_004974.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:111216141 G>A maps to NM_002232.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:111216252 C>T maps to NM_002232.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:111216270 G>A maps to NM_002232.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:111216960 G>A maps to NM_002232.3 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:111216087 G>A maps to NM_002232.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:111217062 G>A maps to NM_002232.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:111217182 G>A maps to NM_002232.3 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:111217086 G>A maps to NM_002232.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:111217182 G>A maps to NM_002232.3 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:111217308 C>T maps to NM_002232.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:111216711 G>A maps to NM_002232.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:111216189 G>A maps to NM_002232.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:111216387 G>A maps to NM_002232.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:111216000 G>A maps to NM_002232.3 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr11:30033280 C>T maps to NM_002233.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:30034021 G>A maps to NM_002233.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr11:30033592 G>A maps to NM_002233.2 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:30033223 G>A maps to NM_002233.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr12:5154806 G>A maps to NM_002234.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:5154983 C>T maps to NM_002234.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:5154542 C>A maps to NM_002234.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr12:5153795 C>T maps to NM_002234.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:5154230 G>A maps to NM_002234.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:5154773 G>A maps to NM_002234.2 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:4920571 C>T maps to NM_002235.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:4919239 G>A maps to NM_002235.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:4919518 C>T maps to NM_002235.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr12:4920526 G>A maps to NM_002235.3 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:4920010 G>A maps to NM_002235.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr12:4919302 C>T maps to NM_002235.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:49573445 A>G maps to NM_031886.2 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:49575416 C>T maps to NM_031886.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:49575335 G>A maps to NM_031886.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:49573325 T>C maps to NM_031886.2 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:49573430 A>T maps to NM_031886.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:49575416 C>T maps to NM_031886.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:49573328 G>A maps to NM_031886.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:156232929 G>A maps to NM_172159.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:156170726 T>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:155838426 G>A maps to NM_172160.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:156232160 C>T maps to NM_172159.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:156009836 G>A maps to NM_172159.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:156009836 G>A maps to NM_172159.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr3:155838600 G>A maps to NM_172160.2 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:6155400 C>A maps to NM_003636.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:7826434 C>T maps to NM_004732.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr17:7826434 C>T maps to NM_004732.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:7827317 G>A maps to NM_004732.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:48098561 G>A maps to NM_004975.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr20:47989960 C>T maps to NM_004975.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr20:47990302 G>A maps to NM_004975.2 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr20:47990461 G>C maps to NM_004975.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr20:48098750 C>T maps to NM_004975.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:47991256 G>A maps to NM_004975.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:47991403 G>A maps to NM_004975.2 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr20:47991256 G>A maps to NM_004975.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr20:47990119 A>G maps to NM_004975.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:47990545 C>T maps to NM_004975.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:73480199 C>T maps to NM_004770.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:73848885 A>G maps to NM_004770.2 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:73480259 T>C maps to NM_004770.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr8:73850022 C>T maps to NM_004770.2 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr8:73480085 C>A maps to NM_004770.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:73480199 C>T maps to NM_004770.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:73480328 C>T maps to NM_004770.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:73849350 C>T maps to NM_004770.2 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:73849680 C>T maps to NM_004770.2 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:73480223 C>T maps to NM_004770.2 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:17793375 T>C maps to NM_001112741.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:17793705 C>T maps to NM_001112741.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:17793390 C>T maps to NM_001112741.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:17793501 G>A maps to NM_001112741.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:17758046 C>T maps to NM_001112741.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:17757938 C>T maps to NM_001112741.1 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:75444650 A>G maps to NM_139137.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr12:75444467 A>G maps to NM_139137.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:75601556 C>T maps to NM_139137.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr12:75444551 G>A maps to NM_139137.2 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:75444610 C>A maps to NM_139137.2 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:75601436 G>A maps to NM_139137.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:75601373 G>A maps to NM_139137.2 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr12:75601379 G>A maps to NM_139137.2 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr12:75601256 G>A maps to NM_139137.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:75441990 T>C maps to NM_139137.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:75444467 A>C maps to NM_139137.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:50826916 G>A maps to NM_004977.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:110766269 C>T maps to NM_004978.4 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:110754480 C>T maps to NM_004978.4 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:110765857 C>T maps to NM_004978.4 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:110765764 C>T maps to NM_004978.4 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:110754324 C>T maps to NM_004978.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:48826128 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48826002 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:48826045 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:48826018 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:48825825 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:48823396 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:48826373 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:48826139 T>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:48820065 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:48826157 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:48826002 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:48826075 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:48826285 G>A did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:48826173 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:119915141 G>A maps to NM_012281.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:119915474 T>C maps to NM_012281.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:119915717 C>T maps to NM_012281.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr7:120387762 G>T maps to NM_012281.2 E582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:119915438 G>A maps to NM_012281.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:120373104 C>T maps to NM_012281.2 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:119915483 C>T maps to NM_012281.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr7:119915480 C>T maps to NM_012281.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:112318755 G>A maps to ENST00000315987 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:112525165 G>C maps to ENST00000315987 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:112323323 C>T maps to ENST00000315987 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:112524250 G>T maps to ENST00000315987 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:108868074 C>T did not map to a codon.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr23:108868161 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:223917919 C>T maps to NM_080671.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:223918057 C>A maps to NM_080671.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:11053817 G>A maps to NM_002236.4 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:11053196 C>T maps to NM_002236.4 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:11052923 C>T maps to NM_002236.4 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr20:49620992 G>A maps to NM_002237.3 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr20:49626830 C>T maps to NM_002237.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:49626347 G>A maps to NM_002237.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:49626524 G>A maps to NM_002237.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:49626566 G>A maps to NM_002237.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:49621004 G>A maps to NM_002237.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:49620976 G>A maps to NM_002237.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:49626812 G>A maps to NM_002237.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr20:49620923 G>A maps to NM_002237.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr20:49626317 G>A maps to NM_002237.3 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:49626560 G>A maps to NM_002237.3 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr20:49626860 C>T maps to NM_002237.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:77659089 C>T maps to NM_012283.1 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr18:77659614 G>A maps to NM_012283.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:77659161 G>A maps to NM_012283.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:77659755 C>T maps to NM_012283.1 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:77659545 G>A maps to NM_012283.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr18:77623822 C>T maps to NM_012283.1 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr18:77623864 C>T maps to NM_012283.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:42720440 C>A maps to NM_133329.5 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr16:84270602 C>A maps to NM_172347.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:84256425 G>A maps to NM_172347.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:84270674 G>A maps to NM_172347.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:84256029 C>T maps to NM_172347.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr16:84270704 G>A maps to NM_172347.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr16:84256364 G>A maps to NM_172347.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:84256128 C>T maps to NM_172347.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:210970964 C>A maps to NM_172362.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:210977368 C>T maps to NM_172362.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:210857159 G>A maps to NM_172362.2 H811H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:210857459 G>A maps to NM_172362.2 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:210971060 G>A maps to NM_172362.2 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:211192541 A>G maps to NM_172362.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:210948743 G>T maps to NM_172362.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:210857060 G>A maps to NM_172362.2 C844C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr7:150654534 G>A maps to NM_000238.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:150647277 G>A maps to NM_000238.2 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr7:150648899 C>T maps to NM_000238.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:150648020 G>T maps to NM_000238.2 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:49934784 C>T maps to NM_012284.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:49944110 A>G maps to NM_012284.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:49933273 G>A maps to NM_012284.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:49951216 G>A maps to NM_012284.1 A911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:49934802 C>A maps to NM_012284.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:40330907 G>A maps to NM_012285.2 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:40330387 C>A maps to NM_012285.2 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:40312255 C>T maps to NM_012285.2 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:40330964 G>T maps to NM_012285.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:40315667 G>C maps to NM_012285.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:40321494 C>T maps to NM_012285.2 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:40332933 C>T maps to NM_012285.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:40323976 A>G maps to NM_012285.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr14:63416923 G>A maps to NM_139318.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:63483610 G>A maps to NM_139318.3 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:63269209 C>T maps to NM_139318.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr14:63447745 G>T maps to NM_139318.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr14:63511892 G>T maps to NM_139318.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:63269269 T>C maps to NM_139318.3 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr14:63417124 G>A maps to NM_139318.3 C365C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr14:63447895 A>G maps to NM_139318.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:61622450 C>T maps to NM_030779.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr17:61601588 C>T maps to NM_030779.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:61615880 C>T maps to NM_030779.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:61607782 G>A maps to NM_030779.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:61607902 G>A maps to NM_030779.2 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:61619794 C>T maps to NM_030779.2 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:61611293 G>A maps to NM_030779.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:61613292 G>A maps to NM_030779.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:163292017 G>A maps to NM_033272.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:163228391 C>A maps to NM_033272.2 G1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:163241449 C>T did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr2:163374465 G>T maps to NM_033272.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:163279955 G>A maps to NM_033272.2 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr2:163250982 G>A maps to NM_033272.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:19389260 T>C maps to NM_144633.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:19575179 A>G maps to NM_144633.2 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:19389428 C>T maps to NM_144633.2 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:19554719 G>T maps to NM_144633.2 E780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:19491652 C>T maps to NM_144633.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr3:19498311 G>A maps to NM_144633.2 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr3:19384206 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:19479671 G>A maps to NM_144633.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:19575323 G>A maps to NM_144633.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr3:19479729 C>T maps to NM_144633.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr3:19574897 G>A maps to NM_144633.2 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:19322765 G>A maps to NM_144633.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:19479729 C>T maps to NM_144633.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr3:19479761 G>A maps to NM_144633.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:170147329 C>T maps to NM_001034837.1 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr10:103603253 C>T maps to NM_014591.4 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr10:103587925 G>A maps to NM_014591.4 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:20734354 A>T maps to ENST00000382152 Y197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr4:20751287 G>A maps to ENST00000382152 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:160011932 G>A maps to NM_002241.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr1:160011395 G>A maps to NM_002241.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:160011275 G>A maps to NM_002241.4 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:160012246 G>A maps to NM_002241.4 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:17408963 G>A maps to NM_000525.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr17:21318689 C>A maps to NM_021012.4 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr17:21319794 C>T maps to NM_021012.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:21318707 C>T maps to NM_021012.4 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:21319868 C>T maps to NM_021012.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:48967754 C>T maps to NM_170720.1 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr19:48967992 C>T maps to NM_170720.1 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:39671200 C>T maps to NM_170736.1 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr21:39671293 C>T maps to NM_170736.1 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr21:39671578 C>A maps to NM_170736.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr21:39671473 C>T maps to NM_170736.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:68128527 C>T maps to NM_018658.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:68128881 C>T maps to NM_018658.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:68129338 C>T maps to NM_018658.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr17:68172061 C>T maps to NM_000891.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr17:68171974 C>T maps to NM_000891.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:68171275 C>T maps to NM_000891.2 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:68171192 C>T maps to NM_000891.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:155555562 C>T maps to NM_002239.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:155711596 A>G maps to NM_002239.2 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:155555961 C>T maps to NM_002239.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:155711630 C>T maps to NM_002239.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:155555856 C>T maps to NM_002239.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:155711245 T>G maps to NM_002239.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:38823342 G>A maps to NM_152868.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr22:38823393 G>A maps to NM_152868.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr22:38823135 T>C maps to NM_152868.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:38823342 G>A maps to NM_152868.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:38823564 C>T maps to NM_152868.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:38823825 G>A maps to NM_152868.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr22:38823738 C>T maps to NM_152868.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr22:38823525 C>T maps to NM_152868.1 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:38823978 C>T maps to NM_152868.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:38823342 G>A maps to NM_152868.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:38823102 C>T maps to NM_152868.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:38823825 G>A maps to NM_152868.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:128781941 C>T maps to NM_000890.3 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:128781632 A>G maps to NM_000890.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:128781365 C>T maps to NM_000890.3 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:39087186 G>A maps to NM_002240.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:38997768 G>A maps to NM_002240.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr12:21918911 G>T maps to NM_004982.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:21926412 C>T maps to NM_004982.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:21926430 G>A maps to NM_004982.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:160053936 C>T maps to NM_004983.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:160054210 C>T maps to NM_004983.2 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:233802518 G>A maps to NM_002245.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr1:233802386 C>T maps to NM_002245.3 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:233802512 G>A maps to NM_002245.3 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:88729809 C>T maps to NM_138318.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:88652429 G>A maps to NM_138318.2 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr14:90651176 C>T maps to NM_022054.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr14:90651235 C>T maps to NM_022054.2 N372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:90650905 C>T maps to NM_022054.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr14:90651133 C>T maps to NM_022054.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr14:90650596 G>A maps to NM_022054.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr14:90651109 C>T maps to NM_022054.2 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:43379274 G>A maps to ENST00000372861 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr6:39285600 G>A maps to NM_032115.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:39290199 C>T maps to NM_032115.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr6:39282791 C>A maps to NM_032115.3 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:39284135 C>T maps to NM_032115.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:39272336 G>A maps to NM_031460.3 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:39267229 G>A maps to NM_031460.3 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:118960781 G>A maps to NM_181840.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:215342542 A>T maps to NM_001017425.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr1:215342581 A>C maps to NM_001017425.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:215179290 T>C maps to NM_001017424.2 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:215345500 T>C maps to NM_001017425.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:26950775 C>T maps to NM_002246.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:26950640 G>A maps to NM_002246.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:26915808 C>T maps to NM_002246.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr11:64064726 C>T maps to ENST00000422670 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:64066925 C>T maps to ENST00000422670 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:39158872 G>A maps to NM_003740.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:38818030 C>T maps to NM_004823.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:38817378 C>T maps to NM_004823.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:65361211 T>A maps to NM_033347.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:65360995 G>A maps to NM_033347.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:65361009 G>A maps to NM_033347.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:140631310 C>T maps to NM_016601.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr8:140631115 C>T maps to NM_016601.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:140631268 C>T maps to NM_016601.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:140715169 G>A maps to NM_016601.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:140630971 C>T maps to NM_016601.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:140631238 G>A maps to NM_016601.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr8:140714995 G>A maps to NM_016601.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:78799283 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:78846313 G>A maps to NM_001161352.1 R458*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GH-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr5:169805758 G>A maps to NM_004137.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:178546004 G>A maps to NM_005832.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:178546037 C>T maps to NM_005832.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:178560439 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:70760699 C>T maps to NM_014505.4 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:18092606 C>T maps to ENST00000222249 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:18085947 G>A maps to ENST00000222249 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr5:113740478 C>T maps to NM_021614.2 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:113698753 C>T maps to NM_021614.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:113798823 T>G maps to NM_021614.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:113698876 C>T maps to NM_021614.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr5:113699631 C>A maps to NM_021614.2 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:113822860 C>T maps to NM_021614.2 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:113698591 C>T maps to NM_021614.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:113831788 C>T maps to NM_021614.2 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr5:113740481 A>C maps to NM_021614.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:154841702 G>A maps to NM_002249.4 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:154842329 T>C maps to NM_002249.4 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:44278354 G>A maps to NM_002250.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:2549241 C>T maps to NM_000218.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:2798260 A>C maps to NM_000218.2 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:62070959 C>T maps to NM_172107.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:62044867 G>A maps to NM_172107.2 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr20:62038566 G>A maps to NM_172107.2 H683H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr20:62076113 C>T maps to NM_172107.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr20:62073779 C>T maps to NM_172107.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:62038257 C>T maps to NM_172107.2 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:62046406 C>T maps to NM_172107.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr20:62044876 G>A maps to NM_172107.2 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr8:133187702 G>A maps to NM_004519.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:133142093 G>A maps to NM_004519.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:133150154 G>A maps to NM_004519.2 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:133196584 G>A maps to NM_004519.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr8:133141889 C>G maps to NM_004519.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:133142015 A>G maps to NM_004519.2 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr8:133150172 C>T maps to NM_004519.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr8:133492524 G>A maps to NM_004519.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:133492425 C>T maps to NM_004519.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:133150208 G>A maps to NM_004519.2 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:133492533 C>T maps to NM_004519.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr8:133175737 T>C maps to NM_004519.2 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr8:133196523 G>A maps to NM_004519.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr8:133198391 G>T maps to NM_004519.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:41289876 G>A maps to NM_004700.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:73879484 C>T maps to NM_001160133.1 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:73902308 A>G maps to NM_001160133.1 K596K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:73904254 C>T maps to NM_001160133.1 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:73902415 T>C did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr6:73900346 A>T maps to NM_001160133.1 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:73332153 C>T maps to NM_001160133.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:73902286 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr13:50590126 G>A maps to NM_173605.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:43726482 A>G maps to NM_002251.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:43727238 G>A maps to NM_002251.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:43727031 G>A maps to NM_002251.3 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr20:43726422 G>A maps to NM_002251.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:99440938 C>A maps to NM_020697.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr8:99441349 C>T maps to NM_020697.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr8:99441397 A>G maps to NM_020697.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:99440302 G>A maps to NM_020697.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr2:18112835 C>T maps to NM_002252.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:18112823 C>T maps to NM_002252.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:138594205 C>T maps to ENST00000298480 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:138662708 C>T maps to ENST00000298480 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:138667191 C>T maps to ENST00000298480 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:138678158 C>T maps to ENST00000298480 D1098D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr9:138683643 C>T maps to ENST00000298480 D1189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr9:138642851 C>T maps to ENST00000298480 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:138594139 C>T maps to ENST00000298480 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:138642881 C>T maps to ENST00000298480 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr9:138683694 G>A maps to ENST00000298480 P1206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:138677160 C>T maps to ENST00000298480 H1054H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:138657598 C>T maps to ENST00000298480 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:138651626 C>T maps to ENST00000298480 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:196395021 G>A maps to NM_198503.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:196300296 T>G maps to NM_198503.2 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:196342339 A>G maps to NM_198503.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:196303053 C>T maps to NM_198503.2 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:196438180 C>T maps to NM_198503.2 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:196205113 A>G did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr1:196342280 G>T maps to NM_198503.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr1:196303014 A>G maps to NM_198503.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr1:196309468 A>C did not map to a codon.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr1:196274443 G>A maps to NM_198503.2 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:196227453 T>C maps to NM_198503.2 K1027K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr1:196398802 A>T maps to NM_198503.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:196309597 A>G maps to NM_198503.2 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:36780101 G>A maps to NM_001031836.2 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr8:36780062 C>G maps to NM_001031836.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:36644861 A>G maps to NM_001031836.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:36675179 C>T maps to NM_001031836.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:36780116 C>T maps to NM_001031836.2 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr8:36675179 C>T maps to NM_001031836.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:36766905 G>A maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:36788638 C>T maps to NM_001031836.2 H969H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr8:36780116 C>T maps to NM_001031836.2 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr8:36788587 G>A maps to NM_001031836.2 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr8:110986296 C>T maps to NM_014379.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:110984529 C>T maps to NM_014379.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr8:110986308 G>A maps to NM_014379.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:110984985 A>C maps to NM_014379.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:2718572 G>A maps to NM_133497.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:2729453 C>A maps to NM_133497.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:2718785 G>A maps to NM_133497.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:2718053 C>T maps to NM_133497.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:2718572 G>A maps to NM_133497.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr9:2718542 C>G maps to NM_133497.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr18:24035754 C>T maps to NM_001142730.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr18:24056601 A>G maps to NM_001142730.1 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr18:24035838 T>C maps to NM_001142730.1 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:24039685 G>A maps to NM_001142730.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:109889606 G>A maps to NM_031954.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:109895794 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr12:109889531 C>T maps to NM_031954.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:7256533 C>T maps to NM_001002914.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:29922370 G>A maps to NM_178863.2 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr16:29922418 G>T maps to NM_178863.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:77728067 G>A maps to NM_023930.3 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:34302405 G>A maps to ENST00000422820 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:34302306 C>T maps to ENST00000422820 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:34302405 G>A maps to ENST00000422820 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:34292184 C>T maps to ENST00000422820 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:143853253 C>T maps to NM_020768.3 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:143586873 C>A maps to NM_020768.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:143587109 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:143853253 C>T maps to NM_020768.3 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr5:143853556 C>A maps to NM_020768.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr5:143587083 A>T maps to NM_020768.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:37457577 G>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:201371661 C>T maps to NM_152387.2 R26R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4G9-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:201354987 T>A maps to NM_152387.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr16:67325600 C>T maps to NM_001100915.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr16:67325657 G>A maps to NM_001100915.1 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr16:67329236 C>G maps to NM_001100915.1 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr16:67329220 G>A maps to NM_001100915.1 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:67328047 G>A maps to NM_001100915.1 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:36442764 G>A maps to NM_173562.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:77885447 A>C maps to NM_001029859.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:215792266 C>A maps to NM_016121.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:215792498 A>C maps to NM_016121.3 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:45768255 G>A maps to NM_198404.2 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:45768414 T>C maps to NM_198404.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:2752388 C>T maps to NM_018992.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:2732701 C>T maps to NM_018992.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:58484480 A>G did not map to a codon.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr3:58487061 C>T maps to NM_153331.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:44450158 C>A maps to NM_198353.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr4:44449772 G>A maps to NM_198353.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:44450165 G>A maps to NM_198353.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:44449850 C>T maps to NM_198353.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr8:25287388 G>C maps to NM_017634.3 S385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:25296816 T>C maps to NM_017634.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr13:103443451 C>T maps to NM_024089.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:103443277 T>C maps to NM_024089.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:103443738 G>A maps to NM_024089.2 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr13:103450843 C>G maps to NM_024089.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:108351904 A>G did not map to a codon.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr11:108361829 G>A maps to NM_153705.4 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr11:108350174 A>T maps to NM_153705.4 Y382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:48892968 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:6505846 G>A maps to NM_006854.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:23409680 C>T maps to NM_001009999.2 R819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:23399802 A>G maps to NM_001009999.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:23382483 C>A maps to NM_001009999.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:23398630 A>G maps to NM_001009999.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:23405510 C>T maps to NM_001009999.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:18161562 G>A maps to ENST00000388870 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:67017571 G>T maps to NM_012308.2 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:67017750 T>C maps to NM_012308.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:67017888 A>T maps to NM_012308.2 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:67018077 A>G maps to NM_012308.2 E859E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:67018167 C>T maps to NM_012308.2 D889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr12:121987460 G>A maps to ENST00000377071 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:121958856 G>A maps to ENST00000377071 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:121878619 T>C maps to ENST00000377071 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:121878637 C>T maps to ENST00000377071 P1197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:121891033 G>A maps to ENST00000377071 C616C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:121970819 G>A maps to ENST00000377071 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:121881880 A>G maps to ENST00000377071 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:86677061 C>T maps to NM_001146688.1 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:86705120 C>T maps to NM_001146688.1 C687C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr2:86669283 C>T maps to NM_001146688.1 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:86683980 C>T maps to NM_001146688.1 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:86712113 G>A maps to NM_001146688.1 W1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:86669238 C>T maps to NM_001146688.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr2:86712977 T>G maps to NM_001146688.1 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:86697396 C>T maps to NM_001146688.1 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:86716692 C>T maps to NM_001146688.1 R1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:137717275 C>T maps to NM_016604.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:137722192 A>G maps to NM_016604.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:137708478 C>T maps to NM_016604.3 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:137713488 A>G maps to NM_016604.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr5:137762665 C>A maps to NM_016604.3 R1472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:44131408 C>T maps to NM_014663.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:5082430 C>T maps to NM_015015.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:5040023 T>C did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:5039896 C>T maps to NM_015015.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr19:5077396 G>A maps to NM_015015.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr19:5033011 G>A maps to NM_015015.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:5144078 C>T maps to NM_015015.2 H884H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:7015919 G>A maps to NM_015061.3 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:7013987 A>G maps to NM_015061.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:6888044 T>C maps to NM_015061.3 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr9:7174615 A>T maps to NM_015061.3 R1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:7174665 C>T maps to NM_015061.3 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr9:6893232 G>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:6986410 T>C maps to NM_015061.3 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:94732107 A>C maps to NM_018039.2 *524Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr11:94731168 T>C maps to NM_018039.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:94730889 C>T maps to NM_018039.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:94759242 A>G maps to NM_001161630.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:94759566 C>T maps to NM_001161630.1 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:94759422 C>A maps to NM_001161630.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:430228 C>A maps to NM_001042603.1 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:422353 C>T maps to NM_001042603.1 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr12:498206 T>C maps to NM_001042603.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:416988 G>A maps to NM_001042603.1 S1187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr12:432347 G>A maps to NM_001042603.1 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:427453 G>A maps to NM_001042603.1 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:427486 C>T maps to NM_001042603.1 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:420107 C>T maps to NM_001042603.1 W1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:464321 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:202709803 G>A maps to ENST00000367264 Q1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:202704711 G>A maps to ENST00000367264 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:202746174 C>T maps to ENST00000367264 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:202711577 G>A maps to ENST00000367264 Q880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:202700078 C>T maps to ENST00000367264 Q1414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:202702810 A>G maps to ENST00000367264 I1245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:202722104 C>T maps to ENST00000367264 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr1:202715451 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:202724445 A>G maps to ENST00000367264 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:53227953 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:53247023 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:53228051 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:53227771 A>G did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:53231065 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53230898 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53244982 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53247566 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:53247092 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:53241076 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:53246350 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:53240992 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:53227712 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:53247012 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:53222405 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:53245078 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr23:53243870 C>T did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:53224445 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:53225095 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:53226000 T>C did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:53230891 C>T did not map to a codon.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr23:53222342 C>G did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr23:53241007 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr23:53230785 C>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:53222179 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:53240001 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr24:21869170 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:21906375 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr24:21894487 G>C did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr23:44922784 G>C did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:44928860 C>G did not map to a codon.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr23:44942723 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:44949993 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:44879952 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr23:44733192 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:44879905 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:44966692 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:44937699 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:7751759 C>T maps to NM_001080424.1 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:7756422 C>A maps to NM_001080424.1 A1572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:7750892 G>A maps to NM_001080424.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:7751579 C>T maps to NM_001080424.1 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:7750589 C>T maps to NM_001080424.1 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:7750658 C>T maps to NM_001080424.1 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:7749497 T>C maps to NM_001080424.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:7748988 C>T maps to NM_001080424.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:7752899 G>C maps to NM_001080424.1 G1098G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr17:7752758 C>T maps to NM_001080424.1 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:55958788 G>A maps to NM_002253.2 R1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:55972862 T>C maps to NM_002253.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:55962480 A>G maps to NM_002253.2 A881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr4:55980319 G>A maps to NM_002253.2 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr4:55984780 G>C maps to NM_002253.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr4:55979621 T>C maps to NM_002253.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:55971023 C>T maps to NM_002253.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:55980355 A>G maps to NM_002253.2 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:10610091 G>A maps to NM_203500.1 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:10610475 G>A maps to NM_203500.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:10610651 G>A maps to NM_203500.1 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr19:10610424 G>T maps to NM_203500.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:10610265 G>A maps to NM_203500.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:142638383 T>C maps to NM_000420.2 A718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:142640414 G>A maps to NM_000420.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:142651348 C>A maps to NM_000420.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:91449950 A>G maps to NM_007035.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:91449223 G>A maps to NM_007035.3 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:32503448 G>T maps to NM_006559.1 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:62887149 G>A maps to NM_152688.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:62442600 C>T maps to NM_152688.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr6:62611270 G>T maps to NM_152688.2 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:62688108 T>C maps to NM_152688.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr6:62611215 C>A maps to NM_152688.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:27322320 C>T maps to NM_006488.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:27322380 C>T maps to NM_006488.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr2:27317347 T>C maps to NM_000221.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:24905386 T>C did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr19:6417054 G>C maps to NM_003685.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr9:2811527 A>G maps to NM_014878.4 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:2831329 G>A maps to NM_014878.4 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:2807899 A>T maps to NM_014878.4 C576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:19566467 T>C maps to NM_015047.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:19546112 G>A maps to NM_015047.1 R918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:19549973 G>A maps to NM_015047.1 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:26943182 C>T maps to NM_014680.2 E2107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:26960767 C>T maps to NM_014680.2 S1088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:26959180 A>G maps to NM_014680.2 S1294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:26962261 A>G maps to NM_014680.2 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr17:26961093 C>T maps to NM_014680.2 R1027R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr17:26970286 C>T maps to NM_014680.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr17:26961874 T>C maps to NM_014680.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr15:64673155 C>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:141309271 A>T maps to NM_014773.3 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:141305076 G>A maps to NM_014773.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:48309036 C>T maps to NM_001080394.1 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:48613000 G>A maps to NM_001080394.1 W574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:73484940 G>A maps to ENST00000375248 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:73491707 C>T maps to ENST00000375248 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:73482482 C>T maps to ENST00000375248 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:73487137 G>A maps to ENST00000375248 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr17:73493925 C>T maps to ENST00000375248 Q1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:126044599 C>T maps to ENST00000377985 W1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:126062901 A>G maps to ENST00000377985 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:126051079 G>A maps to ENST00000377985 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:126088706 T>G maps to ENST00000377985 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:126087248 G>C maps to ENST00000377985 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:197444991 G>A maps to NM_014687.1 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:6865063 G>A maps to NM_014743.2 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:6863905 T>C maps to NM_014743.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:42796382 C>T maps to NM_015349.1 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:42796577 G>A maps to NM_015349.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:70171405 C>T maps to NM_014734.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:105349143 C>A maps to ENST00000453495 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:105344247 G>A maps to ENST00000453495 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:105353080 C>T maps to ENST00000453495 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:105353974 C>T maps to ENST00000453495 D1134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:105360681 G>A maps to ENST00000453495 E1480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr14:105346655 C>T maps to ENST00000453495 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr14:105353626 G>A maps to ENST00000453495 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:105353506 G>A maps to ENST00000453495 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:105353893 G>A maps to ENST00000453495 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr14:75142934 G>A maps to NM_001039479.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:24588854 C>T maps to NM_014809.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:24588956 G>A maps to NM_014809.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:24547485 G>A maps to NM_014809.3 S1042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:24596334 C>T maps to NM_014809.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr6:24596436 C>T maps to NM_014809.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:24578459 A>G maps to NM_014809.3 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:24564428 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:24596739 G>A maps to NM_014809.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:34830834 C>T maps to NM_014686.3 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:34838948 T>C did not map to a codon.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr19:34824688 T>A maps to NM_014686.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:34791599 C>T maps to NM_014686.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:114199318 G>A maps to NM_001080398.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:114145501 A>G maps to NM_001080398.1 V1442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:114131333 C>T maps to NM_001080398.1 P1876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:114145513 G>A maps to NM_001080398.1 T1438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:114246711 C>T maps to NM_001080398.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:114246941 C>T maps to NM_001080398.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:114172449 G>T maps to NM_001080398.1 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:114137449 G>A maps to NM_001080398.1 G1529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:114124384 A>G maps to NM_001080398.1 T1993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:114204599 C>T maps to NM_001080398.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:35739648 C>T maps to NM_014672.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:36640051 G>A maps to NM_014657.1 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:36627619 G>A maps to NM_014657.1 D921D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:36612041 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr20:36641192 A>G maps to NM_014657.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:127767936 A>G maps to NM_014702.4 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr6:127775077 C>A maps to NM_014702.4 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:127767708 C>T maps to NM_014702.4 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:127770988 G>A maps to NM_014702.4 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:127775048 G>A maps to NM_014702.4 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr6:127768230 A>G maps to NM_014702.4 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:4825181 C>T maps to ENST00000450194 D1044D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:4830443 T>C maps to ENST00000450194 C1404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:4823847 C>T maps to ENST00000450194 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:4824581 C>T maps to ENST00000450194 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:4823985 G>T maps to ENST00000450194 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:4830329 G>A maps to ENST00000450194 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:4821213 C>T maps to ENST00000450194 C776C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:4826032 A>C maps to ENST00000450194 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr18:46343629 C>T maps to NM_001142397.1 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr18:46163043 C>A maps to NM_001142397.1 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:46163032 C>T maps to NM_001142397.1 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:15704907 G>A maps to NM_014647.3 I1225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr16:15703511 T>C maps to NM_014647.3 Q1274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:15718922 C>T maps to NM_014647.3 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:15690711 C>T maps to NM_014647.3 S1689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:43896332 C>T maps to NM_015284.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:43904427 G>A maps to NM_015284.2 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:43906257 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:43903370 G>A maps to NM_015284.2 S1233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:43908488 G>T did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:43904433 C>T maps to NM_015284.2 D1292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:43908168 G>A maps to NM_015284.2 A1778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr1:43913550 C>T maps to NM_015284.2 R2259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:43908277 C>T maps to NM_015284.2 R1815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:43909432 C>T maps to NM_015284.2 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:43903493 C>T maps to NM_015284.2 S1244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:43893399 C>T maps to NM_015284.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:43896974 A>G maps to NM_015284.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:43908169 C>T maps to NM_015284.2 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr1:43916081 C>G maps to NM_015284.2 V2511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:47154078 G>A maps to NM_014774.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:47149029 T>C maps to NM_014774.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:47144225 A>G maps to NM_014774.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:3662382 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr16:85111160 G>A maps to NM_014732.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:85106595 G>A maps to NM_014732.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:22624383 G>T maps to ENST00000446597 C769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:22677507 C>A maps to ENST00000446597 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:27751546 C>A maps to NM_015202.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:27709700 C>T maps to NM_015202.2 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:27585251 G>A maps to NM_015202.2 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:27765528 C>T maps to NM_015202.2 V1196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:27710865 A>G maps to NM_015202.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:27761439 G>A maps to NM_015202.2 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr16:27789225 C>A maps to NM_015202.2 V1579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:3755626 T>C maps to NM_014704.3 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:3732034 G>A maps to NM_014704.3 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:3751487 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:3754079 G>A maps to NM_014704.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:42303702 T>A maps to NM_015058.1 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:42457537 C>T maps to NM_015058.1 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr13:42189136 G>A maps to NM_015058.1 G1565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr13:42465632 A>G maps to NM_015058.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:42407529 C>T maps to NM_015058.1 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr13:42144797 C>T maps to NM_015058.1 T1805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:42245134 G>A maps to NM_015058.1 R1520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:42407523 C>T maps to NM_015058.1 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr13:42393518 G>A maps to NM_015058.1 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr13:42465630 C>T maps to NM_015058.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr13:42267045 G>A maps to NM_015058.1 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr14:58915173 T>C maps to ENST00000354386 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:58943921 A>C maps to ENST00000354386 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:58917321 G>T maps to ENST00000354386 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr14:58934501 C>G maps to ENST00000354386 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:138376877 G>A maps to NM_014811.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:138379961 C>T maps to NM_014811.3 G1202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:138376418 G>A maps to NM_014811.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:138378947 C>T maps to NM_014811.3 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr9:138377177 G>A maps to NM_014811.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:138376814 C>T maps to NM_014811.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:138378032 G>A maps to NM_014811.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:138379775 C>T maps to NM_014811.3 D1140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:138379875 C>T maps to NM_014811.3 R1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr11:46686424 G>A maps to NM_001142673.1 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:2607757 G>A maps to NM_015229.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:2603764 G>A maps to NM_015229.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr12:55356378 T>A maps to NM_001098815.1 K435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:55360194 G>A maps to NM_001098815.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:55357524 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:55356580 T>C maps to NM_001098815.1 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:6515340 G>A maps to NM_014804.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:6498334 G>A maps to NM_014804.2 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:6511777 T>C maps to NM_014804.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:6493253 G>A maps to NM_014804.2 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:39879386 G>A maps to NM_015038.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:39878978 C>A maps to NM_015038.1 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:96974274 T>C maps to NM_015323.4 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:96974250 T>C maps to NM_015323.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:96997629 G>A maps to NM_015323.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:96986655 C>T maps to NM_015323.4 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:8784834 C>T maps to ENST00000456698 D935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr18:8783802 G>A maps to ENST00000456698 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:8720349 A>G maps to ENST00000456698 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:8798181 C>T maps to ENST00000456698 R1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:8825986 G>A maps to ENST00000456698 S1812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:8825899 G>A maps to ENST00000456698 L1783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr18:8825986 G>A maps to ENST00000456698 S1812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr18:8824699 G>A maps to ENST00000456698 A1383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr18:8813125 C>T maps to ENST00000456698 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr18:8825584 G>A maps to ENST00000456698 S1678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr18:8825455 G>A maps to ENST00000456698 T1635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:55836528 G>A maps to NM_014924.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:55836546 G>A maps to NM_014924.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr14:55864145 G>A maps to NM_014924.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:55848755 C>T maps to NM_014924.3 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:55848811 G>A maps to NM_014924.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:55848902 G>A maps to NM_014924.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:55836609 C>T maps to NM_014924.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:55836375 C>T maps to NM_014924.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr14:55847307 G>A maps to NM_014924.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:19446962 A>G maps to NM_015329.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:36423467 C>A maps to NM_001100425.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:36366482 G>A maps to NM_001100425.1 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:155886462 T>C maps to NM_014949.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr10:75548518 G>A maps to NM_015037.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr10:75557208 C>T maps to NM_015037.2 R1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:75550768 G>A maps to NM_015037.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr4:154519771 C>T maps to NM_001131007.1 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr4:154525487 G>A maps to NM_001131007.1 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:154508907 T>G maps to NM_001131007.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:154519884 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:154512226 C>T maps to NM_001131007.1 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:154553945 C>T maps to NM_001131007.1 N1428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:154544212 C>T maps to NM_001131007.1 D1341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr4:154505987 A>T maps to NM_001131007.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:154525457 C>A maps to NM_001131007.1 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:5461450 G>A maps to NM_015325.1 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:5463037 T>C maps to NM_015325.1 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:5466526 C>T maps to NM_015325.1 H1991H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:5460962 C>T maps to NM_015325.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:5469043 G>A maps to NM_015325.1 R2055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:5462905 G>A maps to NM_015325.1 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:5476115 G>A maps to NM_015325.1 W2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:5462806 C>T maps to NM_015325.1 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:5461195 C>T maps to NM_015325.1 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:5464736 C>A maps to NM_015325.1 R1764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:5463610 C>T maps to NM_015325.1 C1388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:5462461 C>T maps to NM_015325.1 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:84913716 T>C maps to NM_014895.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:84930883 T>C maps to NM_014895.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:29429624 G>A maps to NM_014939.3 H1213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr18:29410771 A>G maps to NM_014939.3 F1418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:29410885 A>G maps to NM_014939.3 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:29488793 G>A maps to NM_014939.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:79749838 A>G maps to NM_015206.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:79749907 C>T maps to NM_015206.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:79749038 G>T maps to NM_015206.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:79748860 G>A maps to NM_015206.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr15:79750765 C>T maps to NM_015206.2 D759D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:79750189 T>C maps to NM_015206.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr15:79760593 C>T maps to NM_015206.2 Y873Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr12:105553926 G>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:105540905 G>A maps to NM_015275.1 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:105514940 T>C maps to NM_015275.1 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr12:105534781 C>T maps to NM_015275.1 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:34977118 C>T maps to NM_015297.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr9:34977147 C>A maps to NM_015297.1 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:123107275 T>C maps to NM_015312.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:123193561 T>C did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr4:123161242 T>G maps to NM_015312.3 L1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr4:123260415 A>T maps to NM_015312.3 K4069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:123156179 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:123170764 C>T maps to NM_015312.3 R1880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:123283309 C>T maps to NM_015312.3 L4976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:44803034 G>A maps to NM_020696.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:141386387 A>G maps to NM_001080392.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:34371042 G>A maps to NM_020702.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:34371726 G>A maps to NM_020702.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:34372047 A>G maps to NM_020702.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:34372002 G>A maps to NM_020702.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr9:34371579 G>T maps to NM_020702.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:34371969 G>A maps to NM_020702.3 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:34371858 G>A maps to NM_020702.3 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:34370859 C>A maps to NM_020702.3 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:34370907 G>A maps to NM_020702.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr9:34371924 C>T maps to NM_020702.3 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:34371198 G>A maps to NM_020702.3 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr5:175774614 G>A maps to NM_020444.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:175777654 G>A maps to NM_020444.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr5:175774948 C>T maps to NM_020444.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr15:81241150 C>T maps to NM_018689.1 F1324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:81181893 T>G maps to NM_018689.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr15:81234300 C>T maps to NM_018689.1 G1173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr23:118221163 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:118222232 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:118222606 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:118221819 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:118223447 A>T did not map to a codon.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr23:118220734 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:118223524 G>A did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:118222007 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:118230471 C>A did not map to a codon.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr23:118219448 G>T did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:118221481 T>C did not map to a codon.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr23:118221771 G>A did not map to a codon.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr23:118223449 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:118222369 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:118222627 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:118220919 G>T did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr23:118223120 G>T did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:118222913 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr23:118239096 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:118222648 T>G did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:118284424 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:118220518 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr23:118223517 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:57180789 G>A maps to NM_020722.1 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr4:57181918 C>T maps to NM_020722.1 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:57182055 G>A maps to NM_020722.1 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:24833917 C>T maps to NM_019590.3 S1740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:24835180 C>T maps to NM_019590.3 S1920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:24833340 C>T maps to NM_019590.3 P1714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:24833184 C>A maps to NM_019590.3 T1662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:24831888 A>C maps to NM_019590.3 S1230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:24825773 C>T maps to NM_019590.3 H1162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr10:24832058 C>A maps to NM_019590.3 S1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:24832503 C>T maps to NM_019590.3 V1435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr10:24832185 C>T maps to NM_019590.3 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:24832164 C>T maps to NM_019590.3 H1322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:24783527 G>A maps to NM_019590.3 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr10:24820923 T>C did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr10:24790440 C>T maps to NM_019590.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:24833917 C>T maps to NM_019590.3 S1740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:138657550 C>T maps to NM_020340.4 T2154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:138655784 C>T maps to NM_020340.4 G1934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:138655223 G>A maps to NM_020340.4 T1747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:138619828 T>C maps to NM_020340.4 N1245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:138531150 C>T maps to NM_020340.4 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:138584110 C>T maps to NM_020340.4 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:138601239 A>C maps to NM_020340.4 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:138582701 A>G maps to NM_020340.4 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:138655838 C>T maps to NM_020340.4 T1952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:138566719 C>T maps to NM_020340.4 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr6:138640957 C>T maps to NM_020340.4 H1531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:138584542 G>A maps to NM_020340.4 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:128706567 T>C maps to NM_020741.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:128696933 C>T maps to NM_020741.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:44115974 G>A maps to NM_015443.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:44115974 G>A maps to NM_015443.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:44116578 G>A maps to NM_015443.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr17:44109658 G>T maps to NM_015443.3 Y948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:44248448 A>T maps to NM_015443.3 L354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:44248641 G>A maps to NM_015443.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:44249239 A>G maps to NM_015443.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:44249125 C>T maps to NM_015443.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr10:72297652 T>C maps to NM_014431.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:72292381 C>T maps to NM_014431.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:72299394 C>T maps to NM_014431.2 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:72298757 C>T maps to NM_014431.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:97268531 G>T maps to ENST00000421845 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:109740118 C>T maps to NM_020775.3 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:109735345 C>A maps to NM_020775.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:109742805 T>C maps to NM_020775.3 C918C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:109741245 C>T maps to NM_020775.3 R817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr1:109734024 G>T maps to NM_020775.3 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:109727748 C>T maps to NM_020775.3 N345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:109707265 C>T maps to NM_020775.3 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:86522241 G>A maps to NM_001142749.2 Q954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr7:86542516 T>A maps to NM_001142749.2 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr7:86522398 C>T maps to NM_001142749.2 W901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:52901973 T>C maps to NM_019600.2 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr15:52902399 C>T maps to NM_019600.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:52877020 G>A maps to NM_019600.2 Q1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:101834522 G>A maps to NM_020802.2 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:101833872 G>T maps to NM_020802.2 G703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:101818759 A>G did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr11:101849100 C>T maps to NM_020802.2 R957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:101815142 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:101834309 C>T maps to NM_020802.2 H848H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:232941434 C>T maps to NM_019090.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr1:232941161 G>A maps to NM_019090.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:232942229 C>A maps to NM_019090.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr3:113699558 G>A maps to NM_020817.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:113761604 T>C maps to NM_020817.1 S120S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:113772455 T>C maps to NM_020817.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr14:94088837 G>A maps to ENST00000393153 S1775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:94088105 G>A maps to ENST00000393153 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:94103625 A>G maps to ENST00000393153 G1988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:94087970 A>G maps to ENST00000393153 E1486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr14:94088363 G>A maps to ENST00000393153 S1617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:94069684 T>C maps to ENST00000393153 R1225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr14:94088123 C>T maps to ENST00000393153 D1537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:94046500 T>C maps to ENST00000393153 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr14:94063795 C>T maps to ENST00000393153 C1094C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr14:94173132 G>A maps to ENST00000393153 S2619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr14:94173132 G>A maps to ENST00000393153 S2619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr14:94120099 C>T maps to ENST00000393153 P2093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr14:94088465 C>T maps to ENST00000393153 S1651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:94158099 C>T maps to ENST00000393153 S2487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:94007039 C>T maps to ENST00000393153 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr14:94160685 A>G maps to ENST00000393153 V2553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:95531574 A>G maps to NM_015496.3 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr8:95539022 G>A maps to NM_015496.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr8:95500938 G>A maps to NM_015496.3 R1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:95523694 C>T maps to NM_015496.3 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:95547124 T>A maps to NM_015496.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:95556068 G>A maps to NM_015496.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:95539213 A>G maps to NM_015496.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:95524311 G>A maps to NM_015496.3 I919I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:186112158 A>G maps to NM_020827.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:5765509 C>T maps to ENST00000414202 R980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:5765700 C>T maps to ENST00000414202 R1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:5769249 C>T maps to ENST00000414202 R1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:30318026 C>T maps to NM_020848.2 P350P. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:30316207 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr10:30318556 G>A maps to NM_020848.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:30316193 A>G maps to NM_020848.2 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:30336507 G>A maps to NM_020848.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:13232856 C>T maps to NM_020853.1 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:13229018 G>A maps to NM_020853.1 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:13215854 C>T maps to NM_020853.1 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr12:13229045 C>A maps to NM_020853.1 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:59855208 C>T maps to NM_020854.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:59895675 A>G maps to NM_020854.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:226447575 G>A maps to NM_020864.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:226447269 G>A maps to NM_020864.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:226446930 C>T maps to NM_020864.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:226447215 G>A maps to NM_020864.1 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:226446978 C>T maps to NM_020864.1 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:226447161 C>T maps to NM_020864.1 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:226446681 C>T maps to NM_020864.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr2:226446837 G>A maps to NM_020864.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:33236613 A>T maps to NM_020888.2 K612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:33236270 T>C maps to NM_020888.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:108276165 C>T maps to NM_020890.2 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:108295156 T>C maps to NM_020890.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:100119940 A>G maps to ENST00000375206 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:100056270 C>T maps to ENST00000375206 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr9:100085178 C>T maps to ENST00000375206 C591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr9:100053766 G>C maps to ENST00000375206 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:100070317 C>T maps to ENST00000375206 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:100057268 G>A maps to ENST00000375206 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:100105644 A>G maps to ENST00000375206 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:100128908 C>T maps to ENST00000375206 C1361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:100137831 C>T maps to ENST00000375206 G1590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100070306 C>T maps to ENST00000375206 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100080822 C>T maps to ENST00000375206 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100088876 G>A maps to ENST00000375206 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:1348915 C>T maps to NM_020894.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr4:1369242 G>A maps to NM_020894.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:1345606 G>A maps to NM_020894.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:35107926 G>A maps to NM_025182.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:35107419 G>T maps to NM_025182.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:35108145 C>T maps to NM_025182.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:35106308 C>T maps to NM_025182.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:7682714 G>A maps to NM_001080429.2 T1201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:7675434 C>A maps to NM_001080429.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr19:7677721 G>A maps to NM_001080429.2 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:7670157 C>T maps to NM_001080429.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:7676635 C>T maps to NM_001080429.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:7676007 G>A maps to NM_001080429.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:138604035 C>T maps to NM_001164665.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:138603264 C>T maps to NM_001164665.1 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:138602724 C>T maps to NM_001164665.1 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:138546181 G>A maps to NM_001164665.1 A1650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:138556001 A>G maps to NM_001164665.1 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:138603417 A>G maps to NM_001164665.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:138603523 A>T maps to NM_001164665.1 L283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:138566237 C>T maps to NM_001164665.1 A1375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:138601983 C>T maps to NM_001164665.1 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:138602922 C>T maps to NM_001164665.1 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr7:138546175 C>G maps to NM_001164665.1 V1652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:138601632 A>G maps to NM_001164665.1 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:138603297 A>G maps to NM_001164665.1 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:138555947 G>A maps to NM_001164665.1 P1502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:138602901 G>A maps to NM_001164665.1 I490I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-A4GP-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:138602844 G>A maps to NM_001164665.1 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:56917833 T>C maps to NM_020931.2 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr6:56918082 T>G maps to NM_020931.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr6:56919486 A>T maps to NM_020931.2 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:118738811 G>A maps to NM_001127211.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr10:118713646 A>G maps to NM_001127211.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:118661436 G>A maps to NM_001127211.1 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:118674915 G>A maps to NM_001127211.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:84520636 C>T maps to NM_020947.3 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:84516206 C>T maps to NM_020947.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:84522881 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:84520282 G>A maps to NM_020947.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr16:84520429 G>A maps to NM_020947.3 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:180886021 C>T maps to NM_020950.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr1:180885844 G>A maps to NM_020950.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:180904526 C>T maps to NM_020950.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:180904928 G>A maps to NM_020950.1 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr18:43497753 T>C maps to NM_020964.2 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:43532381 A>G maps to NM_020964.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr18:43481064 C>T maps to NM_020964.2 P1514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:43469906 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:43496006 G>A maps to NM_020964.2 D1183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:44681392 G>A maps to NM_001099294.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:44681393 C>T maps to NM_001099294.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:18376402 C>T maps to NM_001145304.1 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:18378124 C>T maps to NM_001145304.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:18368001 C>T maps to NM_001145304.1 W1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:18375880 C>T maps to NM_001145304.1 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:18368202 C>T maps to NM_001145304.1 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr19:18376588 A>G maps to NM_001145304.1 H587H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:18375781 A>G maps to NM_001145304.1 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr19:18376066 C>T maps to NM_001145304.1 Q761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr19:18378192 G>A maps to NM_001145304.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:18377587 G>A maps to NM_001145304.1 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr19:18368166 G>A maps to NM_001145304.1 S1309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:45602032 T>C maps to NM_018559.2 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:175231101 T>C maps to NM_001145314.1 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:175229931 A>G maps to NM_001145314.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:176794703 C>T maps to NM_030650.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:176857065 G>A maps to NM_030650.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:176857024 C>T maps to NM_030650.1 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:1919972 C>A maps to ENST00000434971 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:36841596 G>A maps to NM_001029864.1 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:36848100 A>C maps to NM_001029864.1 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:36848127 G>A maps to NM_001029864.1 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:20988424 C>T maps to NM_017794.3 D1667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:20923739 C>T maps to NM_017794.3 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:20885230 T>C did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:20874756 C>T maps to NM_017794.3 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:20944774 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:20990120 G>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr9:20995573 A>G maps to NM_017794.3 R1784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:20758163 A>C maps to NM_017794.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:20770059 G>A maps to NM_017794.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr9:20923661 G>A maps to NM_017794.3 E952E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr9:20988424 C>T maps to NM_017794.3 D1667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:20944745 C>T maps to NM_017794.3 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr9:20866977 A>T maps to NM_017794.3 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:233518333 G>T maps to NM_032435.2 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:233497843 C>T maps to NM_032435.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:233514947 G>T maps to NM_032435.2 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:105881194 C>T maps to NM_032424.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:105880395 G>A maps to NM_032424.1 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:61343162 A>G maps to NM_001129993.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:61319640 C>T maps to NM_001129993.1 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:61304054 G>A maps to NM_001129993.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:111583578 T>C maps to NM_153369.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr6:111587265 T>C maps to NM_153369.2 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr6:111587790 T>A maps to NM_153369.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:111587418 T>C maps to NM_153369.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:30653468 T>C maps to NM_133471.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:30653306 G>A maps to NM_133471.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr6:30652349 A>C maps to NM_133471.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:30652837 C>A maps to NM_133471.3 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:115421991 G>A maps to NM_133465.2 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:22476528 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:139694926 G>A maps to NM_001039374.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:139699854 C>T maps to NM_001039374.4 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:11983511 C>T maps to ENST00000376576 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:113375206 A>C maps to NM_001009899.2 A1774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:113375914 T>C maps to NM_001009899.2 L1538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:113376118 C>T maps to NM_001009899.2 Q1470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:113379373 A>G maps to NM_001009899.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:113376124 C>T maps to NM_001009899.2 Q1468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:113376997 T>C maps to NM_001009899.2 K1177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:113376115 C>T maps to NM_001009899.2 Q1471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:113374107 C>A maps to NM_001009899.2 E2141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr3:113377642 T>G maps to NM_001009899.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:73959958 C>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:73961201 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:73961873 G>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:73961038 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:73963609 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:73964287 A>G did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:73960012 T>G did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:73961293 T>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:73961405 T>C did not map to a codon.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr23:73963016 A>T did not map to a codon.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr23:73961094 T>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:73963788 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:73965453 G>A did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:73961053 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:73963004 T>C did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr23:73961322 A>C did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:73959939 T>G did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:73962103 A>C did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:73960012 T>C did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:73960251 C>A did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:73962730 A>C did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:73961615 T>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:73963910 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:73963420 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:73963373 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:73960012 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:73964075 C>T did not map to a codon.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr23:73960054 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr23:73964226 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:73964201 G>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr23:73961846 C>A did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr9:5968973 G>A maps to NM_001017969.2 H419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:6007370 C>T maps to NM_001017969.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr9:6007499 G>A maps to NM_001017969.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:5968409 T>C maps to NM_001017969.2 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr9:5923016 T>G maps to NM_001017969.2 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:8934030 T>A maps to NM_020738.2 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:8957837 C>T maps to NM_020738.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr2:8919263 T>C maps to NM_020738.2 R792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:8946398 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:8871791 G>A maps to NM_020738.2 I1458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:94392364 T>C maps to NM_004523.3 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:94409744 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr10:94372844 G>A maps to NM_004523.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:116854655 A>G maps to ENST00000259410 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:17826309 C>T maps to NM_022113.4 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:17826299 G>A maps to NM_022113.4 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:17764688 G>A maps to NM_022113.4 S1690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr6:17987358 G>T maps to NM_022113.4 T24T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B7-A5TN-01A-21D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:29025012 C>T maps to NM_015254.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr8:28999694 T>C maps to NM_015254.3 K771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:28976393 A>G maps to NM_015254.3 H1217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:28974485 G>A maps to NM_015254.3 G1233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:29035014 C>T maps to NM_015254.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:29006249 G>A maps to NM_015254.3 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:28991586 C>T maps to NM_015254.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:28991586 C>T maps to NM_015254.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:200539048 T>A maps to NM_014875.2 S1217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:200522566 G>A maps to NM_014875.2 S1632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:44816776 C>T maps to NM_020242.2 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr3:44879786 C>T maps to NM_020242.2 D1064D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:44828023 T>C maps to NM_020242.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:16496225 T>C maps to NM_024704.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:16493496 A>G maps to NM_024704.4 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr20:16336989 G>A maps to NM_024704.4 F1202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:16359925 G>A maps to NM_024704.4 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:21031183 C>T maps to NM_020816.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:20998557 C>T maps to NM_020816.2 Q865Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:21044007 G>A maps to NM_020816.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:20992757 G>A maps to NM_020816.2 R954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:21031054 C>T maps to NM_020816.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:21011474 C>T maps to NM_020816.2 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:21044070 G>A maps to NM_020816.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:21014027 C>T maps to NM_020816.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:28104446 T>C maps to NM_031217.3 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:28058200 T>C maps to NM_031217.3 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:28119440 T>C maps to NM_031217.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:43004358 C>T maps to ENST00000438933 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:43011404 G>A maps to ENST00000438933 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:43005671 G>T maps to ENST00000438933 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr17:72350361 G>A maps to NM_153209.3 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:72346663 C>T maps to NM_153209.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:72344013 C>T maps to NM_153209.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:72345393 C>T maps to NM_153209.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:72338809 C>T maps to NM_153209.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:241726673 G>A maps to ENST00000373308 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:241689867 G>A maps to ENST00000373308 R985R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr2:241726727 G>A maps to ENST00000373308 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:241726715 G>A maps to ENST00000373308 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:241659197 G>A maps to ENST00000373308 R1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:241708579 G>A maps to ENST00000373308 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr2:241710438 G>A maps to ENST00000373308 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr1:10363931 G>T maps to NM_183416.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:10336424 T>C maps to ENST00000377086 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:10420985 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:10381866 C>T maps to ENST00000377086 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:10386384 C>T maps to ENST00000377086 Y964Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr1:10399859 G>A maps to ENST00000377086 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:10363627 C>T maps to NM_183416.3 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:10384887 C>T maps to ENST00000377086 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:10407833 G>C maps to ENST00000377086 V1271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:4917018 C>T maps to NM_006612.5 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:4925493 C>T maps to NM_006612.5 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:4905793 A>C maps to NM_006612.5 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4925838 T>C maps to NM_006612.5 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:137518868 C>T maps to NM_005733.2 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr5:137521737 G>A maps to NM_005733.2 Q738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr5:137521328 C>T maps to NM_005733.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:91483732 T>C maps to ENST00000416354 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:91483812 T>C maps to ENST00000416354 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr10:91533795 A>G maps to ENST00000416354 T1848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:91477456 T>C maps to ENST00000416354 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:91484800 G>A maps to ENST00000416354 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:91498279 G>T maps to ENST00000416354 E1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:39756910 G>T maps to ENST00000395670 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:39752102 G>A maps to ENST00000395670 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr12:39735370 C>T maps to ENST00000395670 E619E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:39716467 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:39716542 C>A maps to ENST00000395670 E1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:39726210 C>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:200960843 G>A maps to NM_017596.2 R799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:200944026 C>T maps to NM_017596.2 A1530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:200974804 G>T maps to NM_017596.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:200968581 G>A maps to NM_017596.2 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:200948727 G>A maps to NM_017596.2 S1352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:200956131 G>T maps to NM_017596.2 G1202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:200944728 G>A maps to NM_017596.2 Y1491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:200960073 C>T maps to NM_017596.2 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:200969636 G>A maps to NM_017596.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:200977956 G>A maps to NM_017596.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:200971337 G>A maps to NM_017596.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:200978483 G>A maps to NM_017596.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr16:29815361 G>A maps to NM_007317.1 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:29809920 G>A maps to NM_007317.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr16:29809730 G>A maps to NM_007317.1 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:69728954 C>T maps to NM_138555.1 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:69737151 C>T maps to NM_138555.1 N801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:69728918 C>T maps to NM_138555.1 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:69728002 C>T maps to NM_138555.1 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:34256007 T>C maps to NM_194313.2 V1199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:34256529 G>A maps to NM_194313.2 N1025N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:34286629 C>A maps to NM_194313.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:34297076 C>T maps to NM_194313.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:168439367 A>G maps to NM_030615.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:168443280 G>A maps to NM_030615.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:168440762 G>A maps to NM_030615.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr14:104624225 G>A maps to NM_015656.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:104641908 C>T maps to NM_015656.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr14:104641833 T>C maps to NM_015656.1 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:245849620 C>T maps to NM_018012.3 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:245848973 C>T maps to NM_018012.3 Q897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:245765974 T>C maps to NM_018012.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:245704074 C>A maps to NM_018012.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:245704125 T>G maps to NM_018012.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:245849095 C>T maps to NM_018012.3 D937D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr1:245849033 G>T maps to NM_018012.3 E917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:245809567 A>G maps to NM_018012.3 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:245775156 C>T maps to NM_018012.3 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:245848858 C>T maps to NM_018012.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:245850604 G>A maps to NM_018012.3 P1440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:245583005 G>A maps to NM_018012.3 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr1:245850349 C>A maps to NM_018012.3 A1355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:245772772 G>A maps to NM_018012.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:245704239 G>T maps to NM_018012.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:86504087 G>A maps to NM_017576.1 H630H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:86503401 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:86482714 G>A maps to NM_017576.1 Q940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:86506374 C>A maps to NM_017576.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:61669520 G>T maps to NM_001098511.1 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:61642999 T>C maps to NM_001098511.1 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:51901020 G>A maps to NM_032559.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:51901323 G>A maps to NM_032559.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:51901716 C>T maps to NM_032559.4 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr17:51900726 C>T maps to NM_032559.4 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:51900666 G>A maps to NM_032559.4 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr17:51900904 C>T maps to NM_032559.4 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr17:51901629 T>G maps to NM_032559.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:51901221 C>T maps to NM_032559.4 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr17:51901629 T>G maps to NM_032559.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:132070140 G>A maps to ENST00000403231 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:132037892 G>A maps to ENST00000403231 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr20:30898020 C>A maps to NM_004798.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:30919088 T>G maps to NM_004798.3 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr20:30897660 G>A maps to NM_004798.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:30915465 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:26203384 G>A maps to NM_002254.6 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:26203670 G>A maps to NM_002254.6 N372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:26203973 G>A maps to NM_002254.6 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:26204117 A>G maps to NM_002254.6 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:69615825 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:69639531 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:69639928 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:69626770 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:69606470 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:69519001 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:69637774 G>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:154395129 C>T maps to NM_001099293.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:154396038 C>T maps to NM_001099293.1 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:154394630 T>C maps to NM_001099293.1 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:154396976 T>C maps to NM_001099293.1 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:57957310 T>C did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:57962771 C>T maps to NM_004984.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr12:57963827 G>A maps to NM_004984.2 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr12:57972097 G>A maps to NM_004984.2 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:57966493 C>T maps to NM_004984.2 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:57963881 G>A maps to NM_004984.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:57957970 T>C maps to NM_004984.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:32329380 T>C maps to NM_004521.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr10:32317436 T>C maps to NM_004521.2 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr10:32323762 G>C maps to NM_004521.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:32311964 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:149853787 C>T maps to NM_004522.1 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:149864535 C>A maps to NM_004522.1 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:149679725 C>T maps to NM_004522.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:39507856 G>A maps to NM_145027.4 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:39693055 T>G maps to NM_145027.4 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr6:39563909 G>A maps to NM_145027.4 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:90171796 C>T maps to NM_198525.2 Q1295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:90176437 G>A maps to NM_198525.2 I884I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:47277591 G>A maps to NM_182902.3 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:47282447 A>G maps to NM_182902.3 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:47318858 A>G maps to NM_182902.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr1:170007466 G>A maps to NM_014970.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:170024464 G>A maps to NM_014970.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:33365927 C>T maps to NM_002263.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr6:33373065 C>T maps to NM_002263.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr6:33374040 A>T maps to NM_002263.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:145692674 G>A maps to NM_145754.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:57803605 C>T maps to NM_005550.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr16:57795041 G>C maps to NM_005550.3 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:57798090 G>A maps to NM_005550.3 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:57800798 G>A maps to NM_005550.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:7829836 C>T maps to NM_012311.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr10:7798105 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:55282337 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:55286905 C>T maps to ENST00000291633 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr19:55285061 C>T maps to ENST00000291633 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:55253678 C>A maps to NM_015868.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:55263119 T>C maps to NM_015868.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:55263952 T>C maps to NM_015868.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr19:55250953 G>A maps to NM_015868.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:55333225 G>T maps to ENST00000355608 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:55341404 G>A maps to NM_013289.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:55329953 G>A maps to ENST00000355608 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:55301702 C>T maps to NM_001015070.1 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr1:158045981 G>A maps to ENST00000368173 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:158061242 C>T maps to ENST00000368173 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr1:158064483 T>C maps to ENST00000368173 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:36357366 C>T maps to NM_199180.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr19:36357138 C>T maps to NM_199180.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr19:36357075 C>T maps to NM_199180.2 Y603Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr19:36351835 G>A maps to NM_199180.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:36351525 C>T maps to NM_199180.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr11:126396493 G>A maps to NM_032531.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:126396433 T>C maps to NM_032531.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:126294612 G>A maps to NM_032531.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:126314937 G>A maps to NM_032531.3 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:126396493 G>A maps to NM_032531.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:126343329 G>C maps to NM_032531.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:126306784 G>A maps to NM_032531.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:126305199 T>C did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:126318958 A>G maps to NM_032531.3 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:126391267 G>A maps to NM_032531.3 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr11:126294780 G>A maps to NM_032531.3 N677N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:920351 C>T maps to NM_032551.4 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:55592139 G>A maps to NM_000222.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr4:55594073 C>T maps to NM_000222.2 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:55569972 G>A maps to NM_000222.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:88910186 A>G maps to NM_000899.4 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:88912497 C>T maps to NM_000899.4 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:33635903 C>T maps to NM_004795.3 N896N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:33590991 G>A maps to NM_004795.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:33635255 C>T maps to NM_004795.3 H680H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr13:33591183 C>T maps to NM_004795.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:33590826 C>T maps to NM_004795.3 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr13:33635846 C>T maps to NM_004795.3 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:33590919 G>A maps to NM_004795.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:39409171 A>G maps to NM_175737.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr4:39448220 C>T maps to NM_175737.3 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:39435904 G>T maps to NM_175737.3 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:39409015 T>C maps to NM_175737.3 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:104121163 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:104135936 T>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:66026205 C>T maps to NM_022822.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr19:45852835 C>T maps to NM_177417.2 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:43033371 C>T maps to NM_201523.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:12996890 G>T maps to NM_006563.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:12997909 G>A maps to NM_006563.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:103664220 C>T maps to NM_005655.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:103663668 C>T maps to NM_005655.2 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:10188507 C>G maps to NM_003597.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:74420072 G>A maps to NM_007249.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr13:74269808 C>A did not map to a codon.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr13:74419994 C>T maps to NM_007249.4 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr13:74387317 C>A maps to NM_007249.4 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr13:74420435 C>T maps to NM_007249.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:130418140 G>A maps to NM_138693.2 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:126070901 G>T maps to NM_014079.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr3:126071069 C>T maps to NM_014079.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:1854667 G>A maps to NM_031918.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:1854670 C>A maps to NM_031918.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr4:38696528 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:38690381 G>A maps to NM_016531.5 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:38691350 A>G maps to NM_016531.5 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:38690342 G>A maps to NM_016531.5 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:110250403 G>A maps to NM_004235.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:110249777 C>T maps to NM_004235.4 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr13:73636261 G>A maps to NM_001730.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:3821739 C>T maps to NM_001300.5 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:3824016 G>A maps to NM_001300.5 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:207953237 C>T maps to NM_003709.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:207953303 A>G maps to NM_003709.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:56276692 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:56296709 A>G did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr23:56295827 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:56259772 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:73002895 C>T maps to NM_001206.2 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:129764311 T>C maps to NM_014997.3 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:129770478 C>T maps to NM_014997.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:50249175 G>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr14:50246975 A>G maps to NM_014315.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:42985305 G>A maps to NM_057161.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr6:42987056 C>T maps to NM_057161.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:42985380 C>T maps to NM_057161.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:87744969 C>T maps to NM_017566.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:87760451 C>T maps to NM_017566.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:27950951 C>T maps to NM_020782.1 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:18809628 C>T maps to NM_152375.2 C718C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:18809259 C>T maps to NM_152375.2 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:18809661 A>G maps to NM_152375.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:18808479 A>G maps to NM_152375.2 Q335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:18809470 A>T maps to NM_152375.2 K666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:18809343 C>T maps to NM_152375.2 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:18809181 G>A maps to NM_152375.2 W569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:50988016 C>T maps to NM_138433.3 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr1:205308334 G>A maps to NM_018203.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr1:205312624 G>A maps to NM_018203.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr3:49212501 G>A maps to NM_173546.2 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr13:70370968 G>A maps to NM_020866.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr13:70681468 G>A maps to NM_020866.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr13:70549921 G>T maps to NM_020866.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr13:70413189 A>C maps to NM_020866.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:40001940 C>A maps to NM_152467.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:39994258 C>A maps to NM_152467.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:39998197 G>A maps to NM_152467.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr17:40001937 C>T maps to NM_152467.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:40001628 C>T maps to NM_152467.3 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:40011389 C>T maps to NM_018143.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:40010507 C>T maps to NM_018143.1 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:40010210 C>T maps to NM_018143.1 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:40021245 G>A maps to NM_018143.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:202894139 G>A maps to NM_021633.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:202880241 T>C maps to NM_021633.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:117053537 A>G did not map to a codon.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr23:117033039 C>T did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:117043898 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr23:117032968 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:117043338 G>A did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:117079444 T>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:117043782 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr23:117043383 G>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:30321989 G>A maps to NM_020805.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:30260414 C>T maps to NM_020805.1 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:30275441 G>A maps to NM_020805.1 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:30350455 G>A maps to NM_020805.1 C33C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F1-6177-01A-11D-1800-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-F1-A448-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr18:30349900 G>A maps to ENST00000426194 S43S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-8602-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:24006407 T>G did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:24006434 T>G did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr23:24024571 G>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:24006747 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:24006373 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr23:24007015 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:897042 G>A maps to NM_198317.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:898537 G>A maps to NM_198317.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:899514 C>T maps to NM_198317.2 Y491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:899372 C>T maps to NM_198317.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr3:47378199 G>A maps to NM_025010.4 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr3:47378130 C>T maps to NM_025010.4 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:47361165 C>T maps to NM_025010.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:166215607 T>G maps to NM_001161521.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:166159927 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:166160008 T>C maps to NM_001161521.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:166232670 T>A maps to NM_001161521.1 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:166218823 C>T maps to NM_001161521.1 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:166160047 A>G maps to NM_001161521.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:166231876 T>C maps to NM_001161521.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:166238987 A>G maps to NM_001161521.1 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:166160008 T>C maps to NM_001161521.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr4:166226803 T>C maps to NM_001161521.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:173720976 C>T maps to NM_014458.3 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:173702864 C>T maps to NM_014458.3 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:173726130 T>C maps to NM_014458.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:6659417 G>A maps to NM_014851.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:6662469 G>A maps to NM_014851.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:6659213 G>A maps to NM_014851.2 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr1:6653645 C>A maps to NM_014851.2 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:20819359 G>A maps to NM_032775.3 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:20796662 G>A maps to NM_032775.3 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:20819311 G>A maps to NM_032775.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:20796461 C>T maps to NM_032775.3 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:20825699 G>T maps to NM_032775.3 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:20812181 G>A maps to NM_032775.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:170591737 G>T maps to NM_144711.5 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr2:170606067 C>T maps to NM_144711.5 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr15:86311858 C>A maps to NM_022480.3 G395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:86312669 G>A maps to NM_022480.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr15:86311916 C>T maps to NM_022480.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:86311598 A>G maps to NM_022480.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr15:86311421 G>A maps to NM_022480.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:18779088 G>A maps to NM_018316.1 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:18779601 G>A maps to NM_018316.1 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:18779454 C>T maps to NM_018316.1 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:18778858 C>T maps to NM_018316.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:18779691 C>T maps to NM_018316.1 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr14:45414825 C>T maps to ENST00000355081 Q116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:45400590 G>A maps to ENST00000355081 Y513Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr14:45414993 A>T maps to ENST00000355081 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:136964109 G>A maps to NM_017415.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:137056164 A>G maps to NM_017415.2 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:136974735 C>T maps to NM_017415.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:136964058 G>A maps to NM_017415.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:137013310 C>A maps to NM_017415.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:239050087 C>T maps to NM_198582.3 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:239049817 C>T maps to NM_198582.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr6:53516914 C>G maps to NM_001003760.4 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:97562323 C>A maps to NM_052904.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:97562221 G>A maps to NM_052904.3 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:97562107 T>C maps to NM_052904.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:97578818 C>T maps to NM_052904.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:97562308 G>A maps to NM_052904.3 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:21674082 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:21675115 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:21675791 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:21674963 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:21675777 G>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:21675536 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:21675008 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:21674116 A>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:21675212 C>T did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:21674199 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:21674641 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr23:21675867 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:21675898 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:21675003 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr11:75134733 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:75136620 G>A maps to NM_001039548.2 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr16:84693457 G>A maps to NM_024731.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:84690643 C>T maps to NM_024731.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:84695451 C>T maps to NM_024731.2 Q522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr16:84690913 C>T maps to NM_024731.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:84690727 C>T maps to NM_024731.2 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:84691315 C>T maps to NM_024731.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr16:84691069 G>A maps to NM_024731.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr8:124663888 G>A maps to NM_001081675.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:124663888 G>A maps to NM_001081675.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr8:124664440 C>A maps to NM_001081675.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:124658209 C>T maps to NM_001081675.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:124663912 G>A maps to NM_001081675.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr23:86868965 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:86919767 G>T did not map to a codon.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr23:86887302 T>G did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr23:86924352 T>G did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:86877392 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:86890731 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:86888891 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:86888821 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:86880694 T>G did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:86773289 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:86887420 T>C did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr23:86880643 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:86887302 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:86880676 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:86877404 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:86890616 C>A did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:86877277 T>G did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:86877392 T>G did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:86868965 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:86868927 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:86887245 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:86919924 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:39083780 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:39077614 C>A maps to NM_015990.4 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr4:39116777 G>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:183226230 A>G maps to NM_130446.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:183209879 G>A maps to NM_130446.2 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:183225900 T>C maps to NM_130446.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:183245659 C>A maps to NM_130446.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:23205475 C>T maps to NM_001031710.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:88116473 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:88085027 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:21333733 C>T maps to NM_018847.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr19:51322565 G>A maps to NM_002257.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:51518082 C>T maps to NM_001077500.1 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:51518124 C>T maps to NM_001077500.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:51520526 G>T maps to NM_001077500.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:51520421 G>A maps to NM_001077500.1 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:51535219 G>A maps to NM_019598.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:51537327 C>T maps to NM_019598.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:51537252 C>T maps to NM_019598.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr19:51535213 T>C maps to NM_019598.2 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr19:51561827 G>A maps to NM_015596.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr19:51559975 C>T maps to NM_015596.1 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr19:51581383 T>C maps to NM_022046.4 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr19:51582847 G>A maps to NM_022046.4 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:51361283 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:51411928 G>A maps to NM_004917.3 S127S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GU-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:51453226 G>A maps to NM_012427.4 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr19:51455844 G>A maps to NM_012427.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:51455907 A>G maps to NM_012427.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr19:51501057 G>T maps to NM_144505.1 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr19:51503866 G>A maps to NM_144505.1 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:51503765 C>T maps to NM_144505.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr19:51503768 C>T maps to NM_144505.1 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr19:51509978 C>T maps to NM_012315.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:51512560 G>A maps to NM_012315.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:48692091 C>T maps to NM_001135629.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:48722900 T>C maps to NM_001135629.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr2:48687038 C>T maps to NM_001135629.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:48718300 T>C maps to NM_001135629.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:10603632 C>T maps to NM_213658.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr12:9994999 T>G maps to NM_016523.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:9144877 G>A maps to NM_005810.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:139168321 C>A maps to NM_198508.2 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:139167662 G>A maps to NM_198508.2 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:139168211 G>A maps to NM_198508.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:139167677 C>T maps to NM_198508.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr7:139168250 G>A maps to NM_198508.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:139168283 G>A maps to NM_198508.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:10532362 G>A maps to NM_007360.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:241695794 C>A maps to NM_003679.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:241712983 A>T maps to NM_003679.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:135010566 C>T maps to ENST00000368572 C580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:134999949 G>A maps to ENST00000368572 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr10:135011859 C>T maps to ENST00000368572 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:135015098 A>G maps to ENST00000368572 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:135009294 G>A maps to ENST00000368572 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:135015104 C>T maps to ENST00000368572 F1032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr10:135000075 C>T maps to ENST00000368572 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr10:135015104 C>T maps to ENST00000368572 F1032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:135026341 C>T maps to ENST00000368572 C1455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:135032587 C>T maps to ENST00000368572 A1620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:134981024 G>A maps to ENST00000368572 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr10:134980917 C>A maps to ENST00000368572 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:134981758 C>T maps to ENST00000368572 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:135025033 C>T maps to ENST00000368572 S1341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:186459741 G>A maps to NM_001102416.2 W519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:186437925 C>T maps to NM_001102416.2 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:186442910 C>T maps to NM_001102416.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:186445039 G>A maps to NM_001102416.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:123042004 C>A maps to NM_014708.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:123082319 T>C maps to NM_014708.4 I1466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:123087722 A>G maps to NM_014708.4 L1678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:123060421 A>G maps to NM_014708.4 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:123055440 T>C maps to NM_014708.4 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr12:123087725 C>T maps to NM_014708.4 L1679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr12:123068995 A>C maps to NM_014708.4 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr12:123060344 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:123099620 G>A maps to NM_014708.4 L1987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:122152608 T>C maps to NM_002264.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:66036861 C>G maps to NM_002266.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:66039401 C>T maps to NM_002266.2 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:66033571 T>C maps to NM_002266.2 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr6:117053377 C>G maps to NM_002269.2 Y504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:32635509 A>G maps to NM_012316.4 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:32628092 C>T maps to NM_012316.4 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:32628101 C>T maps to NM_012316.4 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:32626256 T>A maps to NM_012316.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:45734320 G>A maps to NM_002265.4 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr17:45750504 C>T maps to NM_002265.4 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:152732435 G>A maps to NM_001025231.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:152733356 T>C maps to NM_001025231.1 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:152732492 T>G maps to NM_001025231.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152732459 C>T maps to NM_001025231.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:152733755 C>A maps to NM_001025231.1 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:152733486 C>T maps to NM_001025231.1 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:152732600 C>T maps to NM_001025231.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr1:152732375 T>G maps to NM_001025231.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr19:47981012 A>G maps to NM_007059.2 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:149430493 C>T maps to NM_032534.2 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr7:149430832 T>A maps to NM_032534.2 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:149426384 G>A maps to NM_032534.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:8272949 G>A maps to NM_213597.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:88327338 C>T maps to NM_016618.1 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:29534822 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:29494864 C>T maps to NM_032045.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr22:29538078 C>T maps to NM_032045.4 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr19:10665848 C>T maps to NM_023008.3 E571E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:10670351 G>A maps to NM_023008.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:10670505 C>A maps to NM_023008.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr7:91863881 A>G maps to NM_194456.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr7:91864761 A>G maps to NM_194456.1 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:91830632 T>C maps to NM_194456.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:75900125 T>C maps to NM_007043.6 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:75900335 A>C maps to NM_007043.6 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:53069129 G>A maps to NM_006121.3 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:53070144 G>A maps to NM_006121.3 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:53069360 G>A maps to NM_006121.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:38975865 C>A maps to NM_000421.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr17:39019793 G>A maps to NM_000223.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:39019475 T>A maps to NM_000223.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr17:39023096 C>T maps to NM_000223.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr17:39020062 G>A maps to NM_000223.3 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:39019562 G>A maps to NM_000223.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr17:39661550 A>G maps to NM_153490.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr17:39659305 C>T maps to NM_153490.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:39661385 C>T maps to NM_153490.2 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:39659655 G>A maps to NM_153490.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:39743059 G>T maps to NM_000526.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:39674626 G>A maps to NM_002275.3 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr17:39767455 G>A maps to NM_005557.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:39767341 A>G maps to NM_005557.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:39767416 G>A maps to NM_005557.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:39780473 G>T maps to NM_000422.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr17:39776786 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:53344641 C>T maps to NM_000224.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:39680723 G>A maps to NM_002276.4 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:39680054 G>A maps to NM_002276.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:53040720 G>A maps to NM_000423.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr12:53043706 C>T maps to NM_000423.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:39041119 G>A maps to NM_019010.2 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:39092831 G>A maps to NM_015515.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:39092615 G>A maps to NM_015515.3 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:38859801 G>A maps to NM_019016.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:38855781 G>A maps to NM_019016.2 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:38911502 A>G maps to NM_181534.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:38907470 G>A maps to NM_181534.3 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr17:38907470 G>A maps to NM_181534.3 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr17:38910186 C>T maps to NM_181534.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:38928170 A>G maps to NM_181539.4 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr17:38927473 G>A maps to NM_181539.4 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:38926122 C>T maps to NM_181539.4 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:38936089 C>A maps to NM_181537.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:38936016 G>A maps to NM_181537.3 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:38938568 G>A maps to NM_181537.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr17:38938424 C>T maps to NM_181537.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:38936050 G>A maps to NM_181537.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:38935849 G>A maps to NM_181537.3 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr17:38933502 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:38938373 T>C maps to NM_181537.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr17:38935957 G>A maps to NM_181537.3 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:38933951 G>A maps to NM_181537.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:38955914 G>A maps to NM_181535.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:38953224 G>A maps to NM_181535.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr17:38953224 G>A maps to NM_181535.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:38953224 G>A maps to NM_181535.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr17:38954573 G>A maps to NM_181535.3 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr17:38953380 G>A maps to NM_181535.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr12:53185087 C>T maps to ENST00000309505 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr17:39553196 G>A maps to ENST00000393998 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:39623343 G>A maps to NM_002278.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:39622022 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:39616433 G>A maps to NM_002278.3 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:39622144 C>T maps to NM_002278.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr17:39616421 G>A maps to NM_002278.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:39502731 C>T maps to NM_004138.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr17:39505635 G>A maps to NM_004138.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:39506941 G>A maps to NM_004138.2 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:39521646 C>T maps to ENST00000394004 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:39520150 G>T maps to ENST00000394004 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr17:39521763 G>A maps to ENST00000394004 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:39521128 C>T maps to ENST00000394004 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:39525759 G>A maps to ENST00000394004 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:39535676 G>A maps to NM_021013.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:39535280 G>A maps to NM_021013.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:39535727 G>T maps to NM_021013.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:39634621 C>T maps to NM_002280.4 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr17:39633825 G>C maps to NM_002280.4 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr17:39633455 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:39643623 C>T maps to NM_003771.4 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr17:39643638 G>A maps to NM_003771.4 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:39645759 C>T maps to NM_003771.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:39580042 C>T maps to NM_003770.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:39593777 C>T maps to NM_006771.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:39596888 A>G maps to NM_006771.3 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:39596906 A>G maps to NM_006771.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:39123063 T>C maps to NM_213656.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:39122753 G>A maps to NM_213656.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:39116717 C>T maps to NM_213656.3 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr17:39116588 G>T maps to NM_213656.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:39122765 G>A maps to NM_213656.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:53202625 G>T maps to NM_002272.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:53207947 C>T maps to NM_002272.2 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr12:53207644 A>G maps to NM_002272.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:39137373 G>A maps to NM_182497.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:39137108 G>A maps to NM_182497.3 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr17:39134526 C>G maps to NM_182497.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:39140441 G>A maps to NM_182497.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:39140459 T>C maps to NM_182497.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr17:39135120 G>A maps to NM_182497.3 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr12:52908758 G>A maps to NM_000424.3 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:52913954 A>G maps to NM_000424.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:52885322 C>A maps to NM_005554.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr12:52886594 G>T maps to NM_005554.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:52881871 G>A maps to NM_005554.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:52881689 G>A maps to NM_005554.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr12:52886438 G>A maps to NM_005554.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:52841347 G>A maps to NM_005555.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:52845640 C>A maps to NM_005555.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr12:52844236 G>A maps to NM_005555.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr12:52840976 G>A maps to NM_005555.3 H564H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr12:52842676 G>A maps to NM_005555.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:52863219 G>A maps to NM_173086.4 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:52865983 C>T maps to NM_173086.4 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr12:52864969 G>A maps to NM_173086.4 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr12:52865202 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:52629018 C>T maps to NM_005556.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:52635263 A>G maps to NM_005556.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr12:52943835 G>A maps to NM_033448.2 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr12:52946762 C>T maps to NM_033448.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:52981584 G>A maps to NM_080747.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr12:52981500 A>G maps to NM_080747.2 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr12:53002162 G>A maps to NM_175068.2 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:53010155 G>A maps to NM_175068.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:53004417 G>A maps to NM_175068.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:53009981 G>A maps to NM_175068.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr12:53009981 G>A maps to NM_175068.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr12:53007513 G>C maps to NM_175068.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:52967138 C>T maps to NM_175053.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr12:52964497 G>A maps to NM_175053.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr12:52964593 G>A maps to NM_175053.3 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:52967360 G>A maps to NM_175053.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:52826979 C>T maps to ENST00000252245 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:52818456 G>A maps to ENST00000252245 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:52818447 G>A maps to ENST00000252245 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:53165876 C>T did not map to a codon.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr12:53169374 C>T maps to NM_015848.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr12:53170703 T>C maps to NM_015848.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr12:53170706 A>T maps to NM_015848.4 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:53170982 G>A maps to NM_015848.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:53086239 G>A maps to NM_175078.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:53097188 C>T maps to NM_175078.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:53091566 G>A maps to NM_175078.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr12:53091599 G>T maps to NM_175078.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:53086544 C>T maps to NM_175078.2 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:53097077 A>T maps to NM_175078.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:53233705 G>A maps to NM_173352.2 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:53227816 G>A maps to NM_175834.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:53227573 G>A maps to NM_175834.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:53295003 C>A did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr12:53291265 G>A maps to NM_002273.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:52567500 G>A maps to NM_182507.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:52681484 C>A maps to NM_002281.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:52685195 G>A maps to NM_002281.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:52794310 C>T maps to NM_033033.3 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:52799985 G>T maps to NM_033033.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:52799668 G>A maps to NM_033033.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:52788848 G>A maps to NM_033033.3 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr12:52714936 G>A maps to NM_002282.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:52776271 G>A maps to NM_033045.3 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:52774337 C>T maps to NM_033045.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr12:52761120 A>C maps to NM_002283.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:52761183 C>T maps to NM_002283.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:52757944 G>A maps to NM_002283.3 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:52754648 G>C maps to NM_002283.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:52758882 G>A maps to NM_002283.3 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:52760961 G>A maps to NM_002283.3 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:52760898 G>A maps to NM_002283.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr12:52695750 C>A maps to NM_002284.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr12:52698792 G>C maps to NM_002284.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:52695705 T>C maps to NM_002284.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:39727638 G>T maps to NM_000226.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:39728025 G>A maps to NM_000226.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr17:39728196 C>T maps to NM_000226.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:46057372 C>T maps to NM_181688.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr21:46066845 T>C maps to NM_198692.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr21:46117691 C>T maps to NM_198699.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:45971167 G>A maps to NM_198693.2 C58C. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:45978502 A>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr21:45978127 G>A maps to NM_198696.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:45978565 G>A maps to NM_198696.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr21:45993823 G>A maps to NM_198687.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:45993646 C>A maps to NM_198687.1 C4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr21:46000422 G>A maps to NM_198694.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:45999795 G>A maps to NM_198694.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:46011723 G>A maps to NM_198688.2 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:46011354 C>T maps to NM_198688.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr21:46047348 G>A maps to NM_198690.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:46047213 C>T maps to NM_198690.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr21:46047096 G>A maps to NM_198690.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr21:32253378 G>A maps to NM_175858.2 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr21:32253375 C>T maps to NM_175858.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr21:46078066 C>T maps to NM_198697.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr21:31768880 T>G maps to NM_181599.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr21:31744375 G>A maps to NM_181621.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr21:31797957 A>G maps to NM_181622.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr21:31797957 A>G maps to NM_181622.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr21:31797957 A>T maps to NM_181622.1 S91S. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:31802767 A>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr21:31812842 T>G maps to NM_181623.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr21:31852450 G>A maps to NM_181607.1 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr21:31852624 G>A maps to NM_181607.1 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr21:31852612 G>A maps to NM_181607.1 Y8Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:31859628 G>A maps to NM_181608.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr21:31864197 G>A maps to NM_181609.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr21:31869359 A>G maps to ENST00000433652 Y23Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr21:31869350 G>T maps to ENST00000433652 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:31933569 G>A maps to ENST00000437381 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr21:31933431 A>C maps to NM_181614.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:32007650 C>T maps to NM_181616.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr21:32007683 C>T maps to NM_181616.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr21:32127678 G>A maps to NM_181619.1 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr21:32127675 G>T maps to NM_181619.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:32119421 G>T maps to NM_181617.1 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:31973468 C>T maps to NM_181620.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr21:31720882 G>A maps to NM_181624.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr21:31654857 G>A maps to NM_001085455.1 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr21:31654506 G>A maps to NM_001085455.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr21:31691972 C>T maps to NM_203405.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr21:31709740 G>T maps to NM_001077711.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr21:31709494 C>T maps to NM_001077711.1 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:31709602 G>T maps to NM_001077711.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr21:31709566 A>G maps to NM_001077711.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr21:31709740 G>A maps to NM_001077711.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:39155889 C>T maps to NM_031959.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr17:39340974 G>T maps to ENST00000458321 C40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:39334155 T>C maps to ENST00000458321 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr17:39334305 G>T maps to ENST00000458321 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr17:39323896 C>T maps to NM_033187.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:39316817 C>T maps to NM_032524.1 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:39305581 G>A maps to NM_033188.3 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr17:39305929 G>T maps to NM_033188.3 C30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:39240614 C>T maps to ENST00000377731 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:39253832 G>T maps to NM_031960.2 A168A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8686-01A-11D-2394-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-A4IU-01A-22D-A25D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CD-A4MG-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CG-4442-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:1643095 G>A maps to ENST00000359229 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:1651483 C>A maps to NM_001001480.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:1651135 G>A maps to NM_001001480.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:1651321 T>C maps to NM_001001480.2 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:71238366 C>T maps to ENST00000422553 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:71249202 C>T maps to ENST00000422553 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:71249433 A>G maps to NM_021046.2 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr21:31965057 C>T maps to NM_181605.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr21:32185382 G>A maps to NM_175857.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr17:39383334 C>G maps to NM_031961.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr17:39383202 C>G maps to NM_031961.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:39406319 C>A maps to NM_033191.2 C116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:39406136 T>G maps to NM_033191.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr17:39394377 C>G maps to NM_031963.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:39394686 C>G maps to NM_031963.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:39412119 C>T maps to ENST00000431129 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:35979568 G>A maps to NM_207392.1 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:25919447 C>T maps to ENST00000268763 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr17:25932710 C>T maps to ENST00000268763 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:25935008 G>A maps to ENST00000268763 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr17:25924412 G>A maps to ENST00000268763 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:25909963 G>A maps to ENST00000268763 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:118105366 G>A maps to ENST00000339824 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:117909124 G>T maps to ENST00000339824 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:118198970 C>T maps to ENST00000339824 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr12:118298218 G>C maps to ENST00000339824 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:117962691 G>A maps to ENST00000339824 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr12:118105459 G>T maps to ENST00000339824 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:119207828 A>G maps to NM_152305.2 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:119209484 T>C maps to NM_152305.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:119211257 T>C maps to NM_152305.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:119204223 C>T maps to NM_152305.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr14:56107658 T>A maps to NM_001079521.1 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr14:56079047 T>C maps to NM_001079521.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:56101376 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:134322425 G>A maps to NM_178554.4 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr3:134322495 G>A maps to NM_178554.4 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:143718340 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:143718340 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:143715235 T>C maps to NM_003937.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:143685242 T>C maps to NM_003937.2 H102H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr2:143799644 A>G maps to NM_003937.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:143742716 G>A maps to NM_003937.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr23:153129906 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153128276 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:153130651 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153132190 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153133890 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153136294 C>A did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:153134382 G>A did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:153137609 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:153128939 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153135050 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153130377 C>T did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:153129809 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153133494 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153131205 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:153129871 G>A did not map to a codon.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr23:153136335 G>A did not map to a codon.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr23:153134081 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:153128279 A>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:153135592 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:153137619 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:153128216 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:153135084 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:153133799 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:153129000 T>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:153134359 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr23:153135927 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153134320 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:62675693 A>G maps to NM_019079.4 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:62676143 T>C maps to NM_019079.4 H566H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:62675693 A>G maps to NM_019079.4 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:50734514 G>T maps to NM_024884.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:42143745 G>A maps to NM_032107.4 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:42162976 G>A maps to NM_032107.4 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:42169671 A>G maps to NM_032107.4 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr20:42168806 C>T maps to NM_032107.4 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr20:42165075 G>A maps to NM_032107.4 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:41620172 C>T maps to NM_031488.4 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:41625569 C>T maps to NM_031488.4 R639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:41620733 C>T maps to NM_031488.4 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr6:130407340 C>T maps to NM_032438.2 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:130454681 C>A maps to NM_032438.2 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr18:5969415 T>C maps to NM_173464.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:108677979 G>T maps to NM_145315.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:63433781 T>C maps to NM_032857.3 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:63421744 T>C maps to NM_032857.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:201355651 C>T maps to NM_005558.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:201358400 C>T maps to NM_005558.3 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:201351408 G>A maps to NM_005558.3 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:6882044 G>A maps to NM_002286.5 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:6887522 G>A maps to NM_002286.5 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:6887525 C>G maps to NM_002286.5 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153706394 C>T did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:153706703 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr23:153706666 C>G did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:54876411 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:54872730 C>T maps to NM_002287.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:54872718 T>C maps to NM_002287.3 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:55020281 C>T maps to NM_002288.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:6964746 G>A maps to NM_005559.2 G2417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:7046312 G>A maps to NM_005559.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:6943248 G>A maps to NM_005559.2 G2999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr18:6997770 T>C maps to NM_005559.2 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr18:6942107 G>A maps to NM_005559.2 F3066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr18:7049220 A>G maps to NM_005559.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:6999504 G>T maps to NM_005559.2 A1534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr18:7049124 G>A maps to NM_005559.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:7037642 G>A maps to NM_005559.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:6959368 C>T maps to NM_005559.2 A2583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr18:7013870 G>A maps to NM_005559.2 C1102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr18:6958567 G>A maps to NM_005559.2 Y2624Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr18:7049075 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr18:7016643 G>A maps to NM_005559.2 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr18:7032151 G>A maps to NM_005559.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr18:7037693 C>T maps to NM_005559.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:7037642 G>A maps to NM_005559.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:6976070 G>A maps to NM_005559.2 V2118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:6986330 T>C maps to NM_005559.2 L1728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr18:7026102 C>T maps to NM_005559.2 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:6947160 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:7014023 C>T maps to NM_005559.2 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:7044751 C>T maps to NM_005559.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr18:7044733 G>A maps to NM_005559.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:6955368 C>T maps to NM_005559.2 Q2730Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr18:7013888 C>T maps to NM_005559.2 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr18:7023202 G>A maps to NM_005559.2 D887D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr18:7013849 G>A maps to NM_005559.2 C1109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr18:7011406 C>G maps to NM_005559.2 G1193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr18:6986279 T>C maps to NM_005559.2 V1745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr18:7080030 G>T maps to NM_005559.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr18:6999932 G>A maps to NM_005559.2 G1482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:6985270 G>A maps to NM_005559.2 A1875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:7050728 G>T maps to NM_005559.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr18:7034563 A>G maps to NM_005559.2 D655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:129465080 C>T maps to NM_000426.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:129781431 C>T maps to NM_000426.3 R2319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:129663523 C>T maps to NM_000426.3 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr6:129634197 A>T maps to NM_000426.3 K1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr6:129475705 A>C maps to NM_000426.3 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:129608989 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:129511426 C>T maps to NM_000426.3 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr6:129513973 G>A maps to NM_000426.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr6:129634004 G>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:129371151 A>T maps to NM_000426.3 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr6:129663594 G>A maps to NM_000426.3 L1473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:129511375 T>C maps to NM_000426.3 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:129419457 T>C maps to NM_000426.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:129621927 C>T maps to NM_000426.3 R1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:129381042 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:21413907 G>A maps to ENST00000416669 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr18:21407421 C>T maps to ENST00000416669 S940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:21396418 C>T maps to ENST00000416669 C707C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:21404476 C>A maps to ENST00000416669 S842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:21364089 C>T maps to ENST00000416669 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:21390462 C>T maps to ENST00000416669 C581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:21402304 A>G maps to ENST00000416669 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:21461970 C>T maps to ENST00000416669 H1730H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:112462561 T>C maps to NM_001105206.1 E937E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr6:112528343 G>A maps to NM_001105206.1 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:112461979 T>A maps to NM_001105206.1 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:112463467 G>A maps to NM_001105206.1 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:112496513 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:112439089 G>T maps to NM_001105206.1 I1611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:60887001 G>A maps to NM_005560.3 Y3203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr20:60909065 G>C maps to NM_005560.3 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:60903406 G>T maps to NM_005560.3 P1514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr20:60887022 G>A maps to NM_005560.3 F3196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr20:60887485 G>A maps to NM_005560.3 G3110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:60911480 G>A maps to NM_005560.3 C746C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:60927303 G>A maps to NM_005560.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:60912691 C>T maps to NM_005560.3 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:60887228 C>T maps to NM_005560.3 P3168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:60885487 T>C maps to NM_005560.3 G3529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:60904111 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr20:60887583 G>A maps to NM_005560.3 R3078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:60897442 G>A maps to NM_005560.3 A2076A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:60892477 C>T maps to NM_005560.3 A2478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:60886293 G>A maps to NM_005560.3 R3338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:60885619 G>A maps to NM_005560.3 V3485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:60887967 C>T maps to NM_005560.3 P3018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr20:60885269 C>T maps to NM_005560.3 T3566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:60885269 C>T maps to NM_005560.3 T3566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr20:60887315 G>A maps to NM_005560.3 N3139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:107575973 G>A maps to NM_002291.2 D1358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:107642155 G>A maps to NM_002291.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:107566693 G>T maps to NM_002291.2 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:107599830 A>G maps to NM_002291.2 C851C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:107615541 A>G maps to NM_002291.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:107615526 A>C maps to NM_002291.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:107621182 G>A maps to NM_002291.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:107572744 C>T maps to NM_002291.2 E1422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:49163222 G>T maps to NM_002292.3 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:49159272 A>G maps to NM_002292.3 G1648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:49162013 C>T maps to NM_002292.3 P1047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:49162266 A>G maps to NM_002292.3 I992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr3:49162317 G>A maps to NM_002292.3 D975D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:49161198 G>T maps to NM_002292.3 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr3:49167419 G>A maps to NM_002292.3 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:49168415 G>A maps to NM_002292.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr3:49160320 C>A maps to NM_002292.3 L1463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:49159633 A>G maps to NM_002292.3 R1581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:49161294 C>T maps to NM_002292.3 T1221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:209811924 A>G maps to NM_000228.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:209800772 C>T maps to NM_000228.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:209799326 T>A maps to NM_000228.2 K548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr1:209800301 G>T maps to NM_000228.2 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:209799234 G>A maps to NM_000228.2 C578C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:209799126 C>G maps to NM_000228.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:209788708 C>T maps to NM_000228.2 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:209790918 G>A maps to NM_000228.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:107671310 G>A maps to NM_007356.2 H1644H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr7:107732088 G>T maps to NM_007356.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:107708574 C>A maps to NM_007356.2 G778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:107671339 G>A maps to NM_007356.2 Q1635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:107671352 T>C maps to NM_007356.2 G1630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:183111831 C>T maps to NM_002293.3 I1579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:183086545 C>T maps to NM_002293.3 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:183099509 G>A maps to NM_002293.3 Q1104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:183079646 C>T maps to NM_002293.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:183100471 C>T maps to NM_002293.3 N1175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:183090855 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr1:183097818 G>T maps to NM_002293.3 E1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:183208691 T>C maps to NM_005562.2 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:183197578 T>C maps to NM_005562.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:183205612 C>T maps to NM_005562.2 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr1:183201455 G>A maps to NM_005562.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr1:183208625 C>T maps to NM_005562.2 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:183207509 C>T maps to NM_005562.2 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:133946995 C>T maps to ENST00000355048 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:133951289 G>A maps to ENST00000355048 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:133901810 C>T maps to ENST00000355048 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:133952675 A>G maps to ENST00000355048 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr9:133901753 C>T maps to ENST00000355048 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr9:133932370 G>A maps to ENST00000355048 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:133901810 C>T maps to ENST00000355048 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:133920994 C>T maps to ENST00000355048 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr9:133914362 C>T maps to ENST00000355048 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:133914602 C>T maps to ENST00000355048 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:133911696 C>A maps to ENST00000355048 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:133928326 C>T maps to ENST00000355048 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:133936464 A>G maps to ENST00000355048 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:133901768 G>A maps to ENST00000355048 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr9:133960932 G>T maps to ENST00000355048 R1363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr9:133914320 C>T maps to ENST00000355048 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:133901753 C>T maps to ENST00000355048 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:113965126 G>A maps to NM_005561.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:113975974 G>A maps to NM_005561.3 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:113973832 G>A maps to NM_005561.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr13:113974718 C>T maps to NM_005561.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr23:119575714 C>G did not map to a codon.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr23:119573034 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:182858383 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:211319879 G>A maps to NM_001136575.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr7:55492978 C>G maps to NM_018697.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr7:55493071 G>T maps to NM_018697.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:55498928 C>T maps to NM_018697.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr7:55479696 C>G maps to NM_018697.3 S308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:37526605 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:37431372 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:17586687 G>A maps to NM_015907.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr4:17609193 C>T maps to NM_015907.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:31206722 C>T maps to NM_006762.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:31208094 G>T maps to NM_006762.2 C208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:31214495 G>A maps to NM_006762.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:33733730 A>G maps to NM_133642.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:34157418 C>T maps to NM_133642.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:33670583 G>A maps to NM_133642.3 N700N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:154179463 C>T maps to ENST00000377643 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr5:154172295 G>T maps to ENST00000377643 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:154092574 C>T maps to NM_015315.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:154181658 G>A maps to ENST00000377643 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:50867241 G>A maps to ENST00000429001 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:50847268 T>C maps to ENST00000429001 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:909764 C>T maps to NM_015155.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:875435 C>T maps to NM_015155.1 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:860913 G>A maps to NM_015155.1 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:930434 A>G maps to NM_015155.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr10:875401 G>A maps to NM_015155.1 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:875655 C>A maps to NM_015155.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr15:71128780 C>T maps to NM_018357.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:71124945 G>A maps to NM_018357.2 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:113568023 T>C maps to ENST00000509061 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr5:145532786 A>G maps to NM_020117.9 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:145539996 G>T maps to NM_020117.9 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:45436076 G>A maps to NM_015340.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:45554624 A>C did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:45435950 T>G maps to NM_015340.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:45527187 C>T maps to NM_015340.3 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:45561787 G>A maps to NM_015340.3 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:64744083 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:64749525 G>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:64749748 A>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:64738168 G>A did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr23:64754490 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:64743992 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:64738226 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:64734802 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:64734800 C>T did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr1:150940918 G>A maps to NM_181746.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:150941395 C>T maps to NM_181746.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:150940935 G>A maps to NM_181746.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr15:100942974 T>C maps to ENST00000394113 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:101009656 C>T maps to ENST00000394113 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:8320600 T>C maps to NM_024552.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:8321558 C>T maps to NM_024552.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr12:50561071 T>A maps to NM_147190.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:28997879 C>T maps to NM_014387.3 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:73638399 A>G maps to NM_032464.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr7:73638355 C>T maps to NM_032464.2 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:73634117 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:150016246 T>A maps to NM_004690.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:150001446 G>A maps to NM_004690.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr6:150004715 T>C maps to NM_004690.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:150004382 A>G maps to NM_004690.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:150005720 C>T maps to NM_004690.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:150023030 A>G maps to NM_004690.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:21562754 C>T maps to NM_014572.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:21557369 G>A maps to NM_014572.2 Y825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:21557771 G>A maps to NM_014572.2 H691H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:21562885 G>A maps to NM_014572.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:21549230 G>A maps to NM_014572.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr13:21562160 G>A maps to NM_014572.2 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:21549269 G>A maps to NM_014572.2 F1002F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:21562394 G>A maps to NM_014572.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:111431077 C>T maps to ENST00000375615 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr11:111420375 C>T maps to ENST00000375615 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:30480465 G>A maps to NM_030915.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr20:36975023 C>T maps to NM_004139.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr20:36993354 C>T maps to NM_004139.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr1:225605727 C>T maps to NM_194442.1 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:225599125 A>G maps to NM_194442.1 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:225598067 G>A maps to NM_194442.1 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:225594396 C>T maps to NM_194442.1 W484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:102987488 C>T maps to NM_006562.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:102988545 C>A maps to NM_006562.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr10:102988410 G>A maps to NM_006562.4 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:74725185 G>C maps to NM_001009812.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:74725092 C>T maps to NM_001009812.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:68118333 G>A maps to ENST00000380035 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:68119416 C>T maps to ENST00000380035 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr15:68118708 C>T maps to ENST00000380035 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:68119725 A>G maps to ENST00000380035 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr15:68118660 G>A maps to ENST00000380035 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:68120208 C>T maps to ENST00000380035 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:68118414 C>T maps to ENST00000380035 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:68119563 C>T maps to ENST00000380035 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:80197137 C>T maps to NM_181714.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:80196803 G>A maps to NM_181714.3 R671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:80223189 G>A maps to NM_181714.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr6:80203349 G>A maps to NM_181714.3 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:40783698 G>A maps to NM_152505.3 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr21:40778530 T>C maps to NM_152505.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:152799956 C>T maps to NM_178348.2 C3C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:152785236 C>T maps to NM_178349.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:152777849 A>C maps to NM_178351.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr1:152777876 G>C maps to NM_178351.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:152777633 G>A maps to NM_178351.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr1:152777810 G>A maps to NM_178351.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:152770395 C>A maps to NM_178352.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:152770557 G>A maps to NM_178352.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:152759796 C>T maps to NM_178353.1 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:152759975 C>T maps to ENST00000417924 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:152749083 C>T maps to NM_178354.2 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:152748990 C>T maps to ENST00000439693 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:152748993 A>G maps to ENST00000439693 G49G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P3-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:152671466 T>A maps to NM_178428.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:152648550 T>C maps to NM_178429.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:152648652 C>T maps to NM_178429.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:152595540 C>T maps to NM_178431.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:152595411 C>T maps to NM_178431.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:152552262 G>A maps to NM_032563.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:32745575 C>T maps to ENST00000373562 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:30748622 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:30682531 C>T maps to NM_182551.3 N18N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:43620631 G>A maps to NM_014793.4 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:43622495 C>T maps to NM_014793.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:43622546 G>C maps to NM_014793.4 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:43621730 G>A maps to NM_014793.4 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr15:43621364 A>G maps to NM_014793.4 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:138413363 C>T maps to NM_002297.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:139637343 C>T maps to NM_001001712.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:130913979 G>A maps to ENST00000373013 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:130913967 C>T maps to ENST00000373013 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:139639194 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:138557548 C>T maps to ENST00000277526 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr9:138556087 C>T maps to ENST00000277526 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr9:139878085 C>T maps to NM_207510.3 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:98714928 A>T maps to NM_001170765.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:98715024 C>T maps to NM_001170765.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr13:46718574 A>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:169689853 T>C maps to NM_005565.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:169714972 C>T did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:169680149 A>C maps to NM_005565.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:169693821 G>T maps to NM_005565.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:169679510 G>T maps to NM_005565.3 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:169714972 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:136547159 G>A maps to NM_002299.2 H1848H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:136567246 T>C maps to NM_002299.2 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:136567186 G>A maps to NM_002299.2 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:136566592 G>A maps to NM_002299.2 Y1108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:136567156 G>A maps to NM_002299.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:136566100 G>A maps to NM_002299.2 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:136547366 A>C maps to NM_002299.2 A1779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:136548300 C>T maps to NM_002299.2 Q1754Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:136561665 C>A maps to NM_002299.2 T1499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:136566637 T>G maps to NM_002299.2 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:136567156 G>A maps to NM_002299.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:136562435 G>T maps to NM_002299.2 R1455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr15:66850102 G>T maps to NM_207338.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr10:103871258 C>T maps to NM_001113407.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr10:103869243 G>A maps to NM_001113407.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr10:103869413 C>T maps to NM_001113407.1 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:103868035 G>A maps to NM_001113407.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:16597435 G>A maps to NM_001290.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:16900029 G>A maps to NM_001290.3 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr11:18424399 C>T maps to NM_001165414.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr11:18428746 G>T maps to NM_001165414.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:18428719 G>A maps to NM_001165414.1 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:59499249 G>A maps to NM_033195.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr15:59499720 T>C maps to NM_033195.1 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr12:21807506 A>T maps to NM_002300.6 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr11:18456455 T>G maps to NM_017448.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:75149233 G>A maps to NM_153486.3 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr16:75147703 C>T maps to NM_153486.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:75149236 C>T maps to NM_153486.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:75148723 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:11241982 C>T maps to NM_000527.4 D858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr19:11218183 G>T maps to NM_000527.4 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:11241982 C>T maps to NM_000527.4 D858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:22140918 G>A maps to NM_001013693.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:22141089 G>A maps to NM_001013693.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:22140996 C>T maps to NM_001013693.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:22142502 C>A maps to NM_001013693.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr11:36250769 A>G maps to NM_174902.2 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:36119922 C>T maps to NM_174902.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:36057668 C>T maps to NM_174902.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr11:36248917 G>A maps to NM_174902.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:25893404 C>T maps to NM_015627.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:25883727 C>T maps to NM_015627.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:140271019 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:140271028 C>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:140271009 T>A did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:140271114 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr22:44892764 G>A maps to NM_032287.2 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:53282676 A>C maps to NM_007015.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr13:53277900 G>A maps to NM_007015.2 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr13:53286890 A>G maps to NM_007015.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:135283097 C>T maps to NM_002302.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr5:135286987 A>G maps to NM_002302.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr4:108991887 A>G maps to NM_016269.4 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:226127113 G>A maps to NM_003240.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:226125284 C>T maps to NM_003240.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:226125158 T>C maps to NM_003240.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:226127158 G>A maps to NM_003240.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr3:156763475 T>G maps to NM_001004316.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:153177275 C>T maps to NM_001010857.1 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:205388356 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:205350917 G>A maps to ENST00000367153 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:65609821 A>G maps to NM_014319.4 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:65564318 G>T maps to NM_014319.4 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:65639550 T>C maps to NM_014319.4 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:65633991 C>T maps to NM_014319.4 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:54660649 G>A maps to NM_024316.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:54967521 C>T maps to ENST00000431846 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:54966184 T>C maps to ENST00000431846 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:54969364 T>C maps to ENST00000431846 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:54966170 C>T maps to ENST00000431846 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:54968978 C>T maps to ENST00000431846 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:54967826 G>A maps to ENST00000431846 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:54967256 G>A maps to ENST00000431846 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:54967958 G>A maps to ENST00000431846 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:54967271 G>A maps to ENST00000431846 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:54973656 A>G maps to NM_198988.1 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:54973331 G>A maps to NM_198988.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:52244163 C>T maps to NM_138792.2 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr7:127894644 G>T maps to NM_000230.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:66102559 C>A maps to NM_002303.5 C1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:66088618 G>A maps to NM_002303.5 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:66081709 C>A maps to NM_002303.5 S672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:66101926 T>C maps to NM_002303.5 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:66102610 T>G maps to NM_002303.5 T1137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:66081740 C>T maps to NM_002303.5 N682N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:66031253 T>C maps to NM_002303.5 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:66075939 T>C maps to NM_002303.5 D652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:43224592 T>C maps to NM_022356.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:43221292 G>A maps to NM_022356.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:43221308 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:43223474 G>C maps to NM_022356.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:43223531 G>A maps to NM_022356.3 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:189713204 T>C maps to NM_018192.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:189690756 G>A maps to NM_018192.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:189691760 T>C maps to NM_018192.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:189700849 G>A maps to NM_018192.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:29963353 C>T maps to NM_015344.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:1843250 C>T maps to NM_012318.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:1843475 G>T maps to NM_012318.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:1843331 G>A maps to NM_012318.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:38264557 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:51450007 C>T maps to ENST00000448283 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr22:38075623 C>T maps to NM_002305.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr22:38074507 C>T maps to NM_002305.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:63283103 A>G maps to NM_001142535.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:40197274 G>A maps to NM_203471.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:40197238 A>G maps to NM_203471.1 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:76968443 G>T maps to NM_005567.3 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:76968460 G>A maps to NM_005567.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:76968443 G>A maps to NM_005567.3 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:20361660 G>A maps to ENST00000324290 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:20354886 A>G maps to ENST00000324290 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:20354895 A>G maps to ENST00000324290 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr10:95557277 G>A maps to NM_005097.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:95556816 C>T maps to NM_005097.2 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:25005660 C>A maps to NM_018176.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:25020787 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:25005582 C>T maps to NM_018176.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:22012933 C>T maps to NM_139278.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:22012137 G>A maps to NM_139278.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:22005797 G>A maps to NM_139278.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:22009059 G>A maps to NM_139278.2 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:22005870 C>A maps to NM_139278.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:22012915 C>T maps to NM_139278.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:35617395 G>A maps to NM_139284.2 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr14:93176157 G>A maps to NM_005606.6 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr14:93178265 C>A maps to NM_005606.6 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:27389977 C>T maps to NM_018490.2 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:71974203 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:71977877 C>T maps to NM_003667.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:71977665 C>T maps to NM_003667.2 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:202287752 C>T maps to NM_001017403.1 H774H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:202276472 C>T maps to NM_001017403.1 N408N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:202287078 G>T did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr6:63990177 G>A maps to NM_016571.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr6:63990393 C>T maps to NM_016571.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:206782789 A>G maps to NM_006893.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:206772932 C>T maps to NM_006893.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr19:49519854 T>G maps to NM_000894.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:48915275 G>A maps to NM_000233.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr13:40175340 G>A maps to NM_005780.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:111914339 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:111914428 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:111914250 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:111914413 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:111914298 C>T did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr7:104377348 G>T maps to NM_199000.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:103969412 C>T maps to NM_199000.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr7:103969640 C>A maps to NM_199000.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:103969529 C>T maps to NM_199000.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:35773524 C>T maps to NM_182548.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:35773710 C>A maps to NM_182548.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:35773518 C>T maps to NM_182548.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:35773659 C>T maps to NM_182548.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr6:35773557 C>T maps to NM_182548.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr6:35773617 G>A maps to NM_182548.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:126186603 G>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:126172752 G>A maps to NM_022126.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:126172752 G>A maps to NM_022126.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr10:126301904 G>A maps to NM_022126.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:126186675 G>A maps to NM_022126.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr17:35300352 G>A maps to NM_005568.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:35298006 G>A maps to NM_005568.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:139092501 G>A maps to NM_014564.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:139089227 G>A maps to NM_014564.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:139091566 G>A maps to NM_014564.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:139090567 G>A maps to NM_014564.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:139091593 G>A maps to NM_014564.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:139096804 G>A maps to NM_178138.4 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr9:139092518 T>A maps to NM_014564.3 K59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:180235535 C>T maps to NM_033343.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:180235619 C>A maps to NM_033343.3 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:180243368 C>T maps to NM_033343.3 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:180241137 C>T maps to NM_033343.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:180240566 G>A maps to NM_033343.3 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:113907131 G>A maps to NM_022363.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:113906171 G>A maps to NM_022363.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:113909231 C>T maps to NM_022363.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:124979347 G>A maps to NM_014368.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:197890757 G>A maps to NM_020204.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:197889163 G>A maps to NM_020204.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:197890646 G>A maps to NM_020204.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:39472856 A>G maps to NM_006859.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr22:30639660 G>A maps to NM_002309.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr22:30640887 T>C maps to NM_002309.3 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:38484883 G>A maps to NM_002310.5 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:38506630 A>G maps to NM_002310.5 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:38490327 A>G maps to NM_002310.5 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr5:38484944 G>A maps to NM_002310.5 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:48620960 G>A maps to NM_000234.1 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:48660364 C>T maps to NM_000234.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr19:48624486 G>A maps to NM_000234.1 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr19:48626467 G>A maps to NM_000234.1 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:48640805 G>A maps to NM_000234.1 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr17:33331398 G>A maps to NM_013975.3 Q968Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:33323670 A>T maps to NM_013975.3 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:33326359 C>T maps to NM_013975.3 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:33323126 C>T maps to NM_013975.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:33329792 G>A maps to NM_013975.3 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:108861846 C>T maps to NM_001098268.1 W590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:108862650 A>G maps to NM_001098268.1 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:108863307 T>C maps to NM_001098268.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr13:108862196 C>A maps to NM_001098268.1 G474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr13:108861687 G>A maps to NM_001098268.1 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr19:55107774 G>A maps to NM_006863.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:55107771 G>A maps to NM_006863.1 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:55098812 A>G maps to NM_001130917.1 *484W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:55086420 G>A maps to NM_001130917.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:55086396 C>T maps to NM_001130917.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr19:55086957 T>C maps to NM_001130917.1 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr19:55085957 C>T maps to NM_001130917.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr19:54803094 C>T maps to ENST00000251375 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr19:54802684 G>A maps to ENST00000251375 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:54802621 G>T maps to ENST00000251375 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr19:54802026 C>T maps to ENST00000251375 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr19:54848674 G>A maps to NM_012276.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:54849823 T>C maps to NM_012276.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:54848403 A>G maps to NM_012276.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:54849399 C>T maps to NM_012276.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:54844947 A>G maps to NM_012276.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:54848965 G>A maps to NM_012276.3 G219G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-4460-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr19:54818814 G>A maps to NM_021250.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:54744363 C>A maps to ENST00000419410 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:54744914 G>A maps to ENST00000245620 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:54742957 G>A maps to NM_024318.2 H439H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr19:54746094 C>T maps to ENST00000407860 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:54745899 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:55143617 C>T maps to ENST00000427581 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:55148283 C>A maps to ENST00000427581 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:55143557 G>A maps to ENST00000427581 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr19:55148075 G>A maps to ENST00000427581 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:55145092 G>C maps to ENST00000427581 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:55143957 C>A maps to ENST00000427581 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:55145092 G>C maps to ENST00000427581 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:54783434 G>T maps to ENST00000391747 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:54782341 G>A maps to ENST00000391747 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:54783691 G>A maps to ENST00000391747 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr19:54783278 C>T maps to ENST00000391747 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:54783646 T>G maps to ENST00000391747 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:54720982 G>A maps to NM_001081450.1 Y626Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:54720970 G>A maps to NM_001081450.1 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr19:54725991 G>A maps to NM_001081450.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:55177748 C>T maps to ENST00000391733 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:55176584 C>T maps to ENST00000391733 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:55177748 C>T maps to ENST00000391733 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr19:55175266 G>A maps to ENST00000391733 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:55174490 C>A maps to ENST00000391733 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:55179346 G>A maps to ENST00000391733 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr19:55179193 C>T maps to ENST00000391733 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:54759152 G>A maps to NM_001081442.1 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:54760845 G>A maps to NM_001081442.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:50594643 G>A maps to NM_001113546.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:50575790 G>A maps to NM_001113546.1 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:41607972 G>A maps to NM_014988.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr3:45677681 C>G maps to NM_014240.2 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:45637135 C>T maps to NM_014240.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr3:45677681 C>G maps to NM_014240.2 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:45637564 G>A maps to NM_014240.2 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:45677681 C>G maps to NM_014240.2 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr3:45677681 C>G maps to NM_014240.2 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr3:45677681 C>G maps to NM_014240.2 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:45677681 C>G maps to NM_014240.2 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:45637762 G>A maps to NM_014240.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:45636835 G>A maps to NM_014240.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:61776055 G>A maps to NM_030576.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:73535597 C>T maps to NM_002314.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:73513361 C>T maps to NM_002314.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr7:73530166 G>A maps to NM_002314.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:73510957 T>C maps to NM_002314.2 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr7:73534913 C>T maps to NM_002314.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:31663868 A>G maps to NM_001031801.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:31672999 C>T maps to NM_001031801.1 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:31669456 G>A maps to NM_001031801.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:31672810 C>T maps to NM_001031801.1 C582C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-6452-01A-12D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:128398500 G>T maps to NM_017980.4 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:26752822 C>T maps to NM_024674.4 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:26751894 C>T maps to NM_024674.4 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr6:105526495 C>T maps to NM_001004317.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:105526474 T>C maps to NM_001004317.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:83891602 A>G maps to NM_194282.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:83905919 A>G maps to NM_194282.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:83849452 C>T maps to NM_194282.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:83852118 T>A maps to NM_194282.2 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:81331468 C>T maps to NM_004664.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:81331456 C>T maps to NM_004664.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr19:49619587 G>A maps to NM_022165.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:27520240 C>T maps to NM_018362.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr11:27528281 T>C maps to NM_018362.3 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:27523053 G>A maps to NM_018362.3 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr1:226475498 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:226420810 G>A maps to ENST00000366807 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr15:77906538 G>A maps to NM_032808.5 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:77906694 C>T maps to NM_032808.5 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:77907657 C>T maps to NM_032808.5 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr15:77907219 A>G maps to NM_032808.5 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:27950564 A>G maps to NM_152570.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:27949022 G>T maps to NM_152570.1 C549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr9:27949697 G>A maps to NM_152570.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:27950585 G>A maps to NM_152570.1 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:27949355 C>T maps to NM_152570.1 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr9:27950156 C>T maps to NM_152570.1 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr9:27949052 T>C maps to NM_152570.1 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:2291559 G>A maps to NM_001101391.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:2290755 C>T maps to NM_001101391.1 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:151773686 C>T maps to NM_001004432.2 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:151774478 C>T maps to NM_001004432.2 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:151774637 C>T maps to NM_001004432.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:151774631 G>A maps to NM_001004432.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr15:101114417 G>A maps to NM_001040616.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:101110169 G>T maps to NM_001040616.2 S516*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8487-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:58840556 C>T maps to NM_000236.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:42911547 G>A maps to NM_005357.2 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:42914695 C>A maps to NM_005357.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:42914869 G>A maps to NM_005357.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:42911533 C>T maps to NM_005357.2 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:42914842 C>T maps to NM_005357.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:42930554 C>T maps to NM_005357.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr10:90435383 T>G maps to NM_001198829.1 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr10:90427342 T>C maps to NM_001198829.1 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:90428384 G>A maps to NM_001198829.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr18:47101748 T>G maps to NM_006033.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:47110075 A>G maps to NM_006033.2 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:185252633 A>G maps to NM_139248.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr21:15561477 T>C maps to NM_198996.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr21:15517045 G>C maps to NM_198996.2 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr21:15579145 G>A maps to NM_198996.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:90354522 T>C maps to NM_001010939.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:90353787 C>T maps to NM_001010939.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:90492015 C>T maps to NM_001080518.1 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr10:90522040 C>T maps to NM_001102469.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr10:90522040 C>T maps to NM_001102469.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:99778418 G>A did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr2:99778960 T>C maps to NM_015929.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr16:11650388 C>A maps to NM_001136472.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:96430679 G>T maps to NM_153234.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:96460265 A>G maps to NM_153234.4 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:18140895 C>T maps to NM_004140.3 H571H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:18140982 T>A maps to NM_004140.3 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:18145265 G>T maps to NM_004140.3 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:73568033 C>T maps to NM_001031803.1 D783D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:73566222 C>T maps to NM_001031803.1 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr17:73566075 G>A maps to NM_001031803.1 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:73552158 C>T maps to NM_001031803.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr17:73569676 C>T maps to NM_001031803.1 N947N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:57006141 T>C maps to NM_005570.3 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:57013238 A>C maps to NM_005570.3 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:57020468 G>A maps to NM_005570.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:57020529 G>A maps to NM_005570.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:75117870 G>A maps to NM_021819.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:75117888 C>A maps to NM_021819.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:75108769 C>T maps to NM_021819.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr5:176765498 G>A maps to NM_006816.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:97377618 G>A maps to NM_001142292.1 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:97400257 A>T maps to NM_001142292.1 C104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:156518498 C>T maps to ENST00000354505 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr12:49497521 C>T maps to NM_018113.2 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:70423554 G>A maps to NM_018368.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:70428895 A>G maps to NM_018368.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:36142605 T>C maps to NM_001007527.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr5:36104204 A>C maps to NM_001007527.1 Y677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:8590438 C>T maps to NM_014583.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr22:50942824 G>T maps to NM_033200.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr22:50943865 A>G maps to NM_033200.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr3:197723128 C>T maps to NM_001136049.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:197701944 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:156106820 T>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:156105024 G>A maps to NM_170707.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr1:156100521 G>T maps to NM_170707.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:126168435 G>A maps to NM_005573.3 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:126156661 T>C maps to NM_005573.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:126145903 G>A maps to NM_005573.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:2434860 C>T maps to NM_032737.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr19:2433889 A>G maps to NM_032737.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:2433910 G>A maps to NM_032737.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:2431599 C>T maps to NM_032737.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:2434869 C>A maps to NM_032737.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:8248583 C>T maps to ENST00000428101 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:33881012 G>A maps to NM_005574.3 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:16704206 C>T maps to ENST00000441439 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:16713447 G>A maps to ENST00000441439 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:16713456 C>T maps to ENST00000441439 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr1:87805290 G>T maps to NM_006769.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:76391407 G>A maps to ENST00000357063 W616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:76427230 C>T maps to ENST00000357063 G1386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:76407185 G>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:76378449 A>G maps to ENST00000357063 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr13:76427386 G>A maps to ENST00000357063 R1438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr13:76408360 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr1:201868802 G>T maps to NM_012134.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr7:123302308 C>T maps to NM_207163.1 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:123302860 C>T maps to NM_207163.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GJ-01A-11D-A25D-08 chr7:123302917 T>C maps to NM_207163.1 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:69167996 T>C maps to NM_198271.3 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:69171387 C>A maps to NM_198271.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr3:69168782 C>A maps to NM_198271.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:69168700 C>A maps to NM_198271.3 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:69171377 G>A maps to NM_198271.3 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:97823049 G>A maps to NM_014916.3 T1091T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:97823865 A>G maps to NM_014916.3 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:97820057 T>G maps to NM_014916.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr7:97823364 C>T maps to NM_014916.3 D1196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:97800878 C>T maps to NM_014916.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr7:97800977 C>T maps to NM_014916.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:97821333 C>T maps to NM_014916.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:97822374 G>A maps to NM_014916.3 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:97822647 C>T maps to NM_014916.3 D957D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:97822956 C>T maps to NM_014916.3 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:97821423 C>T maps to NM_014916.3 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:97821732 C>T maps to NM_014916.3 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:49001493 C>T maps to NM_001080434.1 A973A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:48994446 C>A maps to NM_001080434.1 P1457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:49001484 C>A maps to NM_001080434.1 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:49012112 C>T maps to NM_001080434.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:49000698 T>C maps to NM_001080434.1 R1238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:165322398 G>A maps to NM_177398.3 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:165182924 G>A maps to NM_177398.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr1:165182991 A>G maps to NM_177398.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:165218651 T>C maps to NM_177398.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:165182973 G>A maps to NM_177398.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:129455843 C>T maps to NM_001174147.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr9:129453291 C>T maps to NM_001174147.1 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:100148608 T>C maps to ENST00000489752 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:96363451 C>A maps to NM_005575.2 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr5:96320900 C>T maps to NM_005575.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:96333776 T>C maps to NM_005575.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:96358075 C>T maps to NM_005575.2 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:96342193 G>A maps to NM_005575.2 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:54364903 G>A maps to NM_001126328.1 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:54327148 G>A maps to NM_001126328.1 C704C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:54440033 G>A maps to NM_001126328.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr13:28136827 G>A maps to NM_153371.3 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:28155572 T>A maps to NM_153371.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:28130442 A>G maps to NM_153371.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:22546265 C>T maps to NM_001135865.1 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr5:135188427 C>T maps to ENST00000420621 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:96906417 C>A maps to NM_001037228.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr11:193134 C>T maps to NM_145651.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr12:12514146 T>G maps to NM_058169.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:12588661 T>C maps to NM_058169.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:5711820 G>A maps to NM_004793.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr19:5694791 G>A maps to NM_004793.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:5696692 G>T maps to NM_004793.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr19:5693353 C>T maps to NM_004793.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:48303975 C>T maps to NM_031490.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:48368166 T>C maps to NM_031490.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:12598380 A>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr8:12586496 T>C maps to NM_152271.3 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:12586436 G>A maps to NM_152271.3 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr2:100906806 C>T maps to NM_198461.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:100916227 G>A maps to NM_198461.3 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:118108895 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:118145830 C>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:118109313 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:118147117 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:118108784 T>C did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr5:121405746 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:121409722 A>G maps to NM_002317.5 C340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr15:74239440 C>T maps to NM_005576.2 Y461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:23191024 G>A maps to NM_002318.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr8:23167239 G>A maps to NM_002318.2 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:23159644 G>A maps to NM_002318.2 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:23159566 G>A maps to NM_002318.2 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:74761464 G>A maps to NM_032603.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:74779706 G>A maps to NM_032603.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:74777344 G>C maps to NM_032603.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:100021878 A>G maps to NM_032211.6 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:100017915 C>T maps to NM_032211.6 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:100016574 G>A maps to NM_032211.6 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:100017801 G>A maps to NM_032211.6 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:160977181 G>T maps to NM_005577.2 C1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr6:161015129 G>A maps to NM_005577.2 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:161032712 G>A maps to NM_005577.2 H828H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:161054903 G>A maps to NM_005577.2 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:161022105 T>C maps to NM_005577.2 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr6:161027566 A>G maps to NM_005577.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:160953679 A>G maps to NM_005577.2 G1948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:161032592 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:161007490 A>C maps to NM_005577.2 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:160999615 C>T maps to NM_005577.2 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:113637838 G>A maps to NM_057159.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:113704449 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:113637775 G>T maps to NM_057159.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:19735184 G>A maps to NM_004720.5 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:19737729 G>A maps to NM_004720.5 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:85279837 G>A maps to NM_012152.2 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:85331458 A>C maps to NM_012152.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:85331254 G>A maps to NM_012152.2 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:85331364 G>A maps to NM_012152.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:78010973 A>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:78010579 A>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:78010798 C>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:78011060 G>A did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:78011421 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:78011339 A>C did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:78010421 G>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:6729439 C>T maps to ENST00000435659 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr12:6729979 C>T maps to ENST00000435659 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:1466902 G>A maps to NM_024830.3 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr5:1466948 G>A maps to NM_024830.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:1466999 G>A maps to NM_024830.3 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr16:55583230 C>T maps to NM_017839.4 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:55584911 G>A maps to NM_017839.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr16:55559523 T>C maps to NM_017839.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr15:34654981 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:34652411 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:14269308 C>T maps to NM_001008701.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:14273430 G>A maps to NM_001008701.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:14272388 C>T maps to NM_001008701.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:14266919 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:14270397 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:14267939 G>A maps to NM_001008701.2 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:14288488 G>A maps to NM_001008701.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:14268254 G>A maps to NM_001008701.2 N856N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:14288437 G>A maps to NM_001008701.2 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:14273895 G>A maps to NM_001008701.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr1:82372879 C>T maps to ENST00000370717 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:82409062 G>T maps to ENST00000370717 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr4:62845475 C>T maps to ENST00000506720 R1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:62862014 G>A maps to ENST00000506720 W1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:62758467 G>A maps to ENST00000506720 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr4:62452948 C>T maps to ENST00000506720 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:11924027 G>A maps to ENST00000396099 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:11944580 C>T maps to ENST00000396099 D688D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:11905730 C>T maps to ENST00000396099 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:2937882 C>T maps to NM_014646.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:2926767 C>T maps to NM_014646.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:39977797 G>A maps to NM_022896.1 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:39980774 T>C maps to NM_022896.1 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:39976274 G>A maps to NM_022896.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:39976199 T>C maps to NM_022896.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:39987093 C>A maps to NM_022896.1 R775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr8:19813349 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:19811790 G>A maps to NM_000237.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:19813403 C>T maps to NM_000237.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr8:19805706 C>T maps to NM_000237.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:56342192 C>A maps to NM_006151.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:104075141 C>T maps to NM_017753.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:11468408 C>T maps to NM_001170635.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:11471929 C>T maps to NM_001170635.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:814917 G>A maps to NM_024888.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:812971 C>T maps to NM_024888.1 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:813079 C>T maps to NM_024888.1 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:99771299 C>T maps to NM_014839.4 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:99772445 C>T maps to NM_014839.4 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:99771803 C>T maps to NM_014839.4 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:99771788 G>A maps to NM_014839.4 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:99771803 C>T maps to NM_014839.4 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr1:99767365 C>T maps to NM_014839.4 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:99380467 G>A maps to NM_001037317.1 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr1:99470146 C>T maps to NM_001037317.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:99358628 C>A maps to NM_001037317.1 *322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:99469993 G>A maps to NM_001037317.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:99470206 C>T maps to NM_001037317.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr1:99470041 G>C maps to NM_001037317.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:99418624 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:99380374 T>C maps to NM_001037317.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:155665741 G>A maps to NM_004744.3 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:155665561 C>T maps to NM_004744.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr4:155670289 T>G did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr4:155665549 C>T maps to NM_004744.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr4:155670187 C>A maps to NM_004744.3 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:155665615 C>T maps to NM_004744.3 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr4:151836803 G>A maps to NM_006726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:151814244 A>G maps to NM_006726.3 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:151773633 A>G maps to NM_006726.3 S1076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:151770150 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr4:151511863 C>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:47315827 C>T maps to NM_001164211.1 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:114419018 T>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:114422933 C>T did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:114357665 C>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:114384421 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:114357647 G>A did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr23:114468293 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:114384408 A>C did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:100175013 T>C did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:100179466 T>C maps to NM_002319.3 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:803459 C>T maps to NM_145886.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:800160 C>T maps to NM_145886.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:800555 G>A maps to NM_145886.3 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:39804818 G>A maps to NM_020862.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr19:39805106 G>A maps to NM_020862.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr19:39805433 C>T maps to NM_020862.1 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:39798593 G>A maps to NM_020862.1 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:39798458 G>A maps to NM_020862.1 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:39799103 C>T maps to NM_020862.1 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:40359768 G>A maps to NM_020737.1 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr6:40360101 C>T maps to NM_020737.1 K650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:40360463 G>A maps to NM_020737.1 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr6:40400075 G>A maps to NM_020737.1 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:40359879 G>A maps to NM_020737.1 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:36435743 C>T maps to NM_024509.1 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:36431205 C>T maps to NM_024509.1 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:66625382 T>C maps to NM_024036.4 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:42356769 T>C maps to NM_152447.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:42357186 T>A maps to NM_152447.3 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:42356184 C>T maps to NM_152447.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:42360854 C>T maps to NM_152447.3 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:42355860 T>A maps to NM_152447.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:42356778 A>G maps to NM_152447.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:4538911 C>A maps to NM_052972.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:133859328 G>T maps to NM_144648.1 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:133884087 A>G maps to NM_144648.1 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:133943140 C>T maps to NM_144648.1 T777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr3:66457881 G>A maps to NM_015541.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:66467668 G>A maps to NM_015541.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:66430684 A>C did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:66467668 G>A maps to NM_015541.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:66448588 C>T maps to NM_015541.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:66430713 C>T maps to NM_015541.2 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:66431996 G>A maps to NM_015541.2 C892C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:66434451 G>A maps to NM_015541.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr3:66436707 G>A maps to NM_015541.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr3:66430782 G>A maps to NM_015541.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:113653185 T>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:113657400 T>C maps to NM_014813.1 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:113653182 T>C maps to NM_014813.1 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr12:59279647 T>C maps to NM_153377.3 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:59266596 A>G maps to NM_153377.3 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:59308080 T>C maps to NM_153377.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:86001150 C>T maps to NM_015613.2 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:85997426 G>A maps to NM_015613.2 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:85992426 G>A maps to NM_015613.2 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:85997321 G>T maps to NM_015613.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:85984650 C>T maps to NM_001017924.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr10:85981786 C>T maps to NM_001017924.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:85981858 G>A maps to NM_001017924.2 C490C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr10:85982203 C>T maps to NM_001017924.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:85984620 C>T maps to NM_001017924.2 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:110790876 G>A maps to NM_198506.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:25232352 A>G maps to ENST00000354454 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:25232194 C>T maps to ENST00000354454 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr12:25260804 T>A maps to ENST00000354454 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr12:25260795 C>T maps to ENST00000354454 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:57566978 T>C maps to NM_002332.2 T1064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:57595584 C>T maps to NM_002332.2 D3497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:57605716 C>A maps to NM_002332.2 A4422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:57571368 C>T maps to NM_002332.2 D1452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:57592012 C>T maps to NM_002332.2 C3119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:57569405 C>T maps to NM_002332.2 C1237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr12:57605025 C>T maps to NM_002332.2 C4328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr12:57560824 G>A maps to NM_002332.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr12:57578890 C>T maps to NM_002332.2 R2122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr12:57589507 C>T maps to NM_002332.2 F2835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:57552350 C>A maps to NM_002332.2 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:57587451 C>T maps to NM_002332.2 D2596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:57577934 C>A maps to NM_002332.2 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:57600316 C>G maps to NM_002332.2 G3884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr12:57605722 C>T maps to NM_002332.2 I4424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr12:57574522 C>T maps to NM_002332.2 S1820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:57589751 C>T maps to NM_002332.2 D2889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:57592030 C>A maps to NM_002332.2 T3125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:57595681 G>T maps to NM_002332.2 E3530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr12:57579488 C>T maps to NM_002332.2 H2213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr12:57549992 C>T maps to NM_002332.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:57567662 G>A maps to NM_002332.2 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:57602544 G>A maps to NM_002332.2 A4030A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:150164194 G>A maps to NM_032832.5 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:105521171 A>G maps to NM_013437.4 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:105601047 G>A maps to NM_013437.4 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:105601077 C>T maps to NM_013437.4 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr8:105503071 T>C maps to NM_013437.4 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:105509435 G>A maps to NM_013437.4 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:105509305 T>A maps to NM_013437.4 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr8:105503140 A>G maps to NM_013437.4 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr8:105502951 T>C maps to NM_013437.4 E843E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:141291694 G>A maps to NM_018557.2 R2553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr2:141707813 A>G maps to NM_018557.2 C1042C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr2:141272220 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:140990804 C>A maps to NM_018557.2 E4584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:141665467 G>A maps to NM_018557.2 G1166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr2:141201952 A>G maps to NM_018557.2 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:141202147 A>G maps to NM_018557.2 S3386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr2:141283857 T>C maps to NM_018557.2 A2608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr2:141299516 C>T maps to NM_018557.2 G2406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:141680552 C>T maps to NM_018557.2 K1100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr2:141208231 T>G did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr2:141081581 C>A maps to NM_018557.2 G4132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:141260672 C>A did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr2:141946114 A>G maps to NM_018557.2 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:141143549 G>A maps to NM_018557.2 F3481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:141291620 G>A maps to NM_018557.2 C2577C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:141474371 G>A maps to NM_018557.2 I1924I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:141474385 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:141812692 G>T maps to NM_018557.2 S515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr2:141128300 A>G maps to NM_018557.2 S3662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr2:141607715 G>A maps to NM_018557.2 R1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr2:141092115 C>T maps to NM_018557.2 W4043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:141806633 G>A maps to NM_018557.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr2:141122308 A>G maps to NM_018557.2 S3684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr2:141459401 G>A maps to NM_018557.2 N2105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:141299346 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:141751622 C>T maps to NM_018557.2 W862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr2:141641402 A>T maps to NM_018557.2 A1384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:141643705 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:141232881 G>A maps to NM_018557.2 C3150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:140990804 C>A maps to NM_018557.2 E4584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:141598626 C>T maps to NM_018557.2 W1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:141143492 G>A maps to NM_018557.2 D3500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:141660582 G>A maps to NM_018557.2 C1224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:141202173 C>A maps to NM_018557.2 G3378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:141253203 A>C maps to NM_018557.2 T2988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:141773396 C>T maps to NM_018557.2 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr2:141259338 T>A maps to NM_018557.2 R2923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:141114003 C>A maps to NM_018557.2 G3813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr2:141459801 C>T maps to NM_018557.2 E2070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr2:141130575 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:141473671 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr2:141473666 G>A maps to NM_018557.2 N1966N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr2:141298622 A>G maps to NM_018557.2 L2478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:170081875 A>G maps to NM_004525.2 L1828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:170048451 G>A maps to NM_004525.2 G2974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:170058335 G>A maps to NM_004525.2 R2752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:170099925 A>G maps to NM_004525.2 D1179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:170066148 G>A maps to NM_004525.2 R2095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:170103434 C>T maps to NM_004525.2 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:169996080 C>T maps to NM_004525.2 A4413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:170088298 G>A maps to NM_004525.2 Q1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:170129473 G>A maps to NM_004525.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr2:170012823 C>T maps to NM_004525.2 T4037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr2:170063038 G>A maps to NM_004525.2 S2397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:170103434 C>T maps to NM_004525.2 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:170062855 T>C maps to NM_004525.2 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:170135889 T>C maps to NM_004525.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:170063433 C>A maps to NM_004525.2 E2266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:170127417 G>C maps to NM_004525.2 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr2:170099464 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:186288368 C>A maps to ENST00000362004 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr4:186299313 G>C maps to ENST00000362004 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:186299232 A>G did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:33687651 C>T maps to NM_002333.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:33696461 C>T maps to NM_002333.3 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:33697148 C>T maps to NM_002333.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr19:33693820 C>T maps to NM_002333.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:46880598 G>A maps to ENST00000256991 R1930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:46910971 G>T maps to ENST00000256991 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr11:46886048 G>A maps to ENST00000256991 L1776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr11:46890211 G>A maps to ENST00000256991 A1675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:46907917 A>G maps to ENST00000256991 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:46900581 T>C maps to ENST00000256991 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:46894693 G>A maps to ENST00000256991 L1559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr11:46920142 C>T maps to ENST00000256991 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:46880542 G>A maps to ENST00000256991 S1948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:46918462 G>A maps to ENST00000256991 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:68201163 C>T maps to NM_002335.2 C1286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:68192761 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:68153967 G>A maps to NM_002335.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:68125147 G>A maps to NM_002335.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:68197118 C>A maps to NM_002335.2 C1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr11:68153889 C>T maps to NM_002335.2 H374H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:68183971 C>T maps to NM_002335.2 R1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr11:68179068 C>T maps to NM_002335.2 I828I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:68115450 C>A maps to NM_002335.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:25750562 C>A maps to NM_001135772.1 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:12278294 G>A maps to NM_002336.2 R1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:12317328 G>A maps to NM_002336.2 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:53715090 C>T maps to NM_004631.3 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:3516637 G>A maps to NM_002337.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr4:3521918 G>C maps to NM_002337.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:3526676 G>A maps to NM_002337.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:44200830 C>T maps to NM_133259.3 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:44171033 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:44187749 A>G maps to NM_133259.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:44126408 G>A maps to NM_133259.3 F1258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:53785558 G>T maps to NM_018214.4 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr6:53764635 T>A maps to NM_018214.4 L245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:53785468 C>A maps to NM_018214.4 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr6:53706990 C>T maps to NM_018214.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:53660206 G>A maps to NM_018214.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr12:70003952 A>G maps to NM_201550.2 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:145745256 T>C maps to NM_014665.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:145746832 C>T maps to NM_014665.2 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr8:145746158 C>G maps to NM_014665.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:194841 C>T maps to NM_001080478.1 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:192309 G>A maps to NM_001080478.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:194080146 G>A maps to NM_001135057.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:194081220 G>A maps to NM_001135057.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:194080098 G>A maps to NM_001135057.2 C564C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:194080701 G>A maps to NM_001135057.2 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr6:25554281 G>A maps to NM_017640.5 V850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:25540215 G>A maps to NM_017640.5 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:25600665 C>T maps to NM_017640.5 R1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:25581666 G>A maps to NM_017640.5 A1002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:25450637 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:25529040 C>T maps to NM_017640.5 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:24532579 C>T maps to NM_138360.3 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr14:24528102 C>T maps to NM_138360.3 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:24534214 G>A maps to NM_138360.3 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:24537874 C>A maps to NM_138360.3 L1255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr14:24535791 G>A maps to NM_138360.3 K1203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:24532726 A>G maps to NM_138360.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:102574473 C>T maps to NM_001031692.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:102574618 C>T maps to NM_001031692.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:102584825 G>A maps to NM_001031692.2 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:102584867 G>A maps to NM_001031692.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:26995767 A>G maps to NM_022901.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr9:26995659 T>C maps to NM_022901.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr3:46586646 C>T maps to NM_024512.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:46593060 G>T maps to NM_024512.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:7019088 G>A maps to NM_201650.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:7016488 C>T maps to NM_201650.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr8:145749545 G>A maps to NM_001024678.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:18507560 G>A maps to NM_145256.2 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:18507698 G>A maps to NM_145256.2 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:134188715 A>G maps to NM_030626.2 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:99926274 C>T maps to NM_144598.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:99901564 C>T maps to NM_144598.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr21:45876919 C>T maps to NM_030891.3 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:7231915 C>T maps to NM_001105581.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr18:7231996 C>G maps to NM_001105581.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:169572613 G>A maps to NM_024727.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:169578489 A>G maps to NM_024727.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:169587561 C>A maps to NM_024727.2 G12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:76371655 A>G maps to NM_001128922.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:196388523 C>T maps to NM_198565.1 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:196387397 C>A maps to NM_198565.1 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:196387173 C>T maps to NM_198565.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:196387311 G>A maps to NM_198565.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr3:196386900 C>T maps to NM_198565.1 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:67410681 G>A maps to NM_018296.5 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr16:67409241 C>G maps to NM_018296.5 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr16:67401082 A>G maps to NM_018296.5 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:67401313 G>A maps to NM_018296.5 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:44626101 C>T maps to NM_001006607.2 N1199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr17:44626380 G>A maps to NM_001006607.2 T1292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr17:44590245 G>A maps to NM_001006607.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:62892244 C>T maps to NM_199340.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr17:62893201 C>T maps to NM_199340.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:62856576 G>A maps to NM_199340.2 N1229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:62893279 T>C maps to NM_199340.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:62852004 G>T maps to NM_199340.2 I1604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr17:62892244 C>T maps to NM_199340.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:30348560 A>G maps to ENST00000327564 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:30348992 G>A maps to ENST00000327564 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr17:30349599 C>T maps to ENST00000327564 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:30348266 G>A maps to ENST00000327564 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:30376228 C>A maps to ENST00000327564 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:100614639 G>A maps to NM_144620.2 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr1:100614639 G>A maps to NM_144620.2 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:127669217 C>T maps to NM_022143.4 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:127669904 G>A maps to NM_022143.4 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:127669673 G>A maps to NM_022143.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:127669829 C>T maps to NM_022143.4 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr7:127670417 G>A maps to NM_022143.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:127669622 G>A maps to NM_022143.4 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:127669502 G>T maps to NM_022143.4 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:46744535 A>G maps to ENST00000254454 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:46751469 G>A maps to ENST00000254454 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:46768844 G>A maps to ENST00000254454 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr1:46746842 C>G maps to ENST00000254454 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:54433548 A>G maps to NM_052940.3 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:54433605 C>T maps to NM_052940.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:122667813 C>T maps to NM_001098519.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr12:122684792 C>T maps to NM_001098519.1 Y469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:122685453 G>A maps to NM_001098519.1 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:122677437 G>A maps to NM_001098519.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr12:122676080 C>T maps to NM_001098519.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr12:122685459 T>G maps to NM_001098519.1 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:122667813 C>T maps to NM_001098519.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:122676080 C>T maps to NM_001098519.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:122677464 G>A maps to NM_001098519.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:45913837 C>T maps to NM_033413.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:45913055 A>G maps to NM_033413.3 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr1:3712476 G>A maps to NM_020710.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:17900947 G>A maps to NM_031294.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:71193354 C>T maps to NM_017691.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:71276444 T>C maps to NM_017691.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:71185960 G>A maps to NM_017691.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:51021313 C>T maps to NM_001080457.1 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:51021442 C>T maps to NM_001080457.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr19:51021775 C>T maps to NM_001080457.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:51021574 G>A maps to NM_001080457.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:51020884 G>A maps to NM_001080457.1 H695H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr19:51022344 G>A maps to NM_001080457.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:51021142 G>A maps to NM_001080457.1 H609H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:40136705 T>C maps to NM_020929.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:40136486 A>T maps to NM_020929.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr11:40136912 C>A maps to NM_020929.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr11:40136012 T>A maps to NM_020929.1 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:84211350 C>T maps to NM_178452.4 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr16:84193341 C>T maps to NM_178452.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:165513784 T>A maps to NM_001005214.3 C84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr1:165513565 G>A maps to NM_001005214.3 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr1:165514099 C>T maps to NM_001005214.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:165532863 C>T maps to NM_001005214.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:165514019 C>T maps to NM_001005214.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:165513571 C>T maps to NM_001005214.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:165513721 C>T maps to NM_001005214.3 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:165533032 C>A maps to NM_001005214.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr1:165513877 G>A maps to NM_001005214.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr1:165532958 G>A maps to NM_001005214.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr11:56954950 C>A maps to NM_001005210.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:42840346 C>T maps to NM_153260.2 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:42839647 C>T maps to NM_153260.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:120067694 G>A maps to NM_001099678.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr17:48462539 G>A maps to NM_018509.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:150034225 A>G maps to NM_023942.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:150034531 C>T maps to NM_023942.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:150034579 C>T maps to NM_023942.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:52861189 T>G maps to NM_001024611.1 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr4:52883455 T>C maps to NM_001024611.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr4:52862041 T>G maps to NM_001024611.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:52861525 G>A maps to NM_001024611.1 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:52861930 C>T maps to NM_001024611.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:52861789 G>A maps to NM_001024611.1 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:67922970 G>A maps to ENST00000421742 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:70478694 C>T maps to NM_020794.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:70257796 T>C maps to NM_020794.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:70503936 G>A maps to NM_020794.2 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:70503936 G>A maps to NM_020794.2 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr1:70503882 T>C maps to NM_020794.2 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:70504914 G>T maps to NM_020794.2 V1098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:70505178 G>A maps to NM_020794.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr1:70501915 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:70504368 G>A maps to NM_020794.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:70505178 G>A maps to NM_020794.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr1:70505052 C>A maps to NM_020794.2 G1144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr1:70504188 C>T maps to NM_020794.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr1:70541926 A>T maps to NM_020794.2 G1428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:70505250 C>T maps to NM_020794.2 Y1210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:131670816 C>T maps to NM_001127244.1 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:131670897 G>A maps to NM_001127244.1 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:90048781 G>A maps to NM_015350.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:90048283 C>T maps to NM_015350.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:90049768 T>C maps to NM_015350.2 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:90178422 C>T maps to NM_032270.4 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:90178605 C>A maps to NM_032270.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:90179604 C>T maps to NM_032270.4 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:90179052 C>T maps to NM_032270.4 C308C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:90400498 A>G maps to NM_001134479.1 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:90400153 T>C maps to NM_001134479.1 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:90400676 C>T maps to NM_001134479.1 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:90399382 A>G maps to NM_001134479.1 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:90399961 A>G maps to NM_001134479.1 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:90398725 T>C maps to NM_001134479.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:90399415 T>C maps to NM_001134479.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr19:7965350 C>T maps to NM_025061.3 H648H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:7965620 G>A maps to NM_025061.3 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr19:7965137 C>T maps to NM_025061.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:7965098 C>T maps to NM_025061.3 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:7964276 G>A maps to NM_025061.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:7963907 C>T maps to NM_025061.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:86049697 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:86035829 C>T maps to NM_033402.4 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr8:86041520 A>G maps to NM_033402.4 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr8:86047188 G>T maps to NM_033402.4 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:86027608 G>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:238668756 C>T maps to NM_001137552.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:37095347 C>T maps to NM_006309.2 Q720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:85547849 G>A maps to NM_001079910.1 S1566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:85450661 A>T maps to NM_001079910.1 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:85449485 A>G maps to NM_001079910.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:85466853 T>C maps to NM_001079910.1 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:85518279 T>C maps to NM_001079910.1 I1330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr12:85450034 A>C maps to NM_001079910.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr12:85638607 T>C maps to NM_001079910.1 F1686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:74649284 T>C maps to NM_001105659.1 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:74649218 G>A maps to NM_001105659.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:74649221 G>A maps to NM_001105659.1 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr1:74648524 G>A maps to NM_001105659.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:101528929 G>A maps to NM_024652.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:101567505 C>T maps to NM_024652.3 R816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:101609037 T>A maps to NM_024652.3 T2011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr15:101569257 C>T maps to NM_024652.3 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr15:101562792 G>A maps to NM_024652.3 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr15:101593606 C>T maps to NM_024652.3 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:101549172 C>A maps to NM_024652.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:101569366 C>T maps to NM_024652.3 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:101602776 A>C did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr15:101589893 A>G maps to NM_024652.3 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:101464887 G>A maps to NM_024652.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:101464932 C>T maps to NM_024652.3 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr12:40687444 C>T maps to NM_198578.3 Q930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr12:40740651 T>G maps to NM_198578.3 T2069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:40677741 A>G maps to NM_198578.3 Q769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:40672042 G>T maps to NM_198578.3 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:40645121 G>A maps to NM_198578.3 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:40714946 C>A maps to NM_198578.3 I1709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr12:40740624 T>G maps to NM_198578.3 G2060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:40653407 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:40645113 T>C maps to NM_198578.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:40681201 T>C maps to NM_198578.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:40740561 T>C maps to NM_198578.3 R2039R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr12:40629470 T>C maps to NM_198578.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:40758799 T>C maps to NM_198578.3 R2446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr12:40618971 G>A maps to NM_198578.3 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:40758784 T>A maps to NM_198578.3 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:40722216 T>C maps to NM_198578.3 A1904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr12:40699584 A>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:3888175 C>A maps to NM_020873.5 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:3887324 C>T maps to NM_020873.5 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:3887632 C>T maps to NM_020873.5 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr3:3886559 T>C maps to NM_020873.5 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr3:3887101 G>T maps to NM_020873.5 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr1:204587179 C>T maps to NM_201630.1 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:204588802 C>T maps to NM_201630.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:204588667 G>A maps to NM_201630.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:204587071 A>G maps to NM_201630.1 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:204587212 A>G maps to NM_201630.1 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:204588976 G>A maps to NM_201630.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:204588976 G>A maps to NM_201630.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:204588370 G>A maps to NM_201630.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:204588726 G>A maps to NM_201630.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr1:204587486 C>T maps to NM_201630.1 W545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:110764282 C>T maps to NM_018334.4 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr7:110762918 C>A maps to NM_018334.4 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:110764824 T>A maps to NM_018334.4 L666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:110763254 C>T maps to NM_018334.4 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:110763754 A>G maps to NM_018334.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:110763370 T>C maps to NM_018334.4 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:110763829 C>A maps to NM_018334.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr7:110764040 C>T maps to NM_018334.4 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:110762968 T>C maps to NM_018334.4 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:110763693 T>A maps to NM_018334.4 L289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:6022630 C>T maps to NM_152611.3 W420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:6022102 C>T maps to NM_152611.3 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:6022501 G>A maps to NM_152611.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:6022018 C>T maps to NM_152611.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:6022873 G>A maps to NM_152611.3 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:6031512 G>A maps to NM_152611.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:62455767 G>A maps to NM_203422.2 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:62455515 G>A maps to NM_203422.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:62455515 G>A maps to NM_203422.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:80530308 G>A maps to NM_178839.4 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:80530586 G>A maps to NM_178839.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:80529714 G>A maps to NM_178839.4 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:80529699 G>A maps to NM_178839.4 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:80529903 G>A maps to NM_178839.4 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:80530110 G>T maps to NM_178839.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:80530419 A>G maps to NM_178839.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr2:80530431 G>A maps to NM_178839.4 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:80530713 G>T maps to NM_178839.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:80529621 G>A maps to NM_178839.4 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr2:80529509 G>A maps to NM_178839.4 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:80529384 G>A maps to NM_178839.4 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:138209436 T>C maps to NM_015564.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:138208712 C>A maps to NM_015564.2 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:138210078 G>A maps to NM_015564.2 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:138209268 G>A maps to NM_015564.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:68686784 C>T maps to NM_178011.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:77746781 G>A maps to NM_001134745.1 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:77746703 A>G maps to NM_001134745.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:77746529 G>A maps to NM_001134745.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:77746549 G>A maps to NM_001134745.1 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:130251731 C>T maps to NM_001005374.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:130223459 C>T maps to NM_001005374.2 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:130224622 C>T maps to NM_001005374.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr9:130219653 G>A maps to NM_001005374.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:54952503 A>G maps to NM_020678.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:54959014 A>G maps to NM_020678.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:54952710 G>A maps to NM_020678.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr3:54952776 A>T maps to NM_020678.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:54959069 A>G maps to NM_020678.2 N60N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:71806463 C>T maps to NM_145309.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:102108750 C>T maps to NM_152892.1 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:102109079 C>T maps to NM_152892.1 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr3:115805189 T>C maps to NM_002338.3 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:115561348 C>T maps to NM_002338.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr3:115571348 T>C maps to NM_002338.3 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:194379823 G>A maps to NM_018385.2 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:194387290 A>G maps to NM_018385.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:38027334 G>A maps to NM_014462.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:38027435 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:34710755 T>C maps to NM_001114093.1 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:14239579 C>T maps to NM_014463.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:18420587 G>A maps to NM_012321.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr19:18420551 G>A maps to NM_012321.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:18420512 G>A maps to NM_012321.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:35752846 T>C maps to NM_205834.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr19:35757793 C>T maps to NM_205834.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:35753458 C>T maps to NM_205834.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:35741296 T>C maps to NM_205834.2 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr21:47635653 G>A maps to NM_002340.5 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr21:47633707 G>A maps to NM_002340.5 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr21:47636353 G>A maps to NM_002340.5 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:47635155 G>A maps to NM_002340.5 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr21:47615618 G>A maps to NM_002340.5 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:47625757 C>T maps to NM_002340.5 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:21242841 A>T maps to ENST00000381541 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr12:21200086 T>G maps to ENST00000381541 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr12:21201652 C>T maps to ENST00000381541 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:21207463 A>T maps to ENST00000381541 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:21201649 C>G maps to ENST00000381541 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr12:21205068 T>G maps to ENST00000381541 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:21174421 T>C maps to ENST00000381541 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr12:21205042 A>T maps to ENST00000381541 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:21176222 T>C did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:31556428 C>T maps to NM_007161.3 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:31541349 G>A maps to NM_000595.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:96394808 G>A maps to NM_000895.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:31548542 G>A maps to NM_002341.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr14:24785117 G>C maps to NM_181657.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:33488370 A>G maps to ENST00000354476 E844E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:33588553 G>A maps to ENST00000354476 T1457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr2:33589409 G>A maps to ENST00000354476 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr2:33589404 C>T maps to ENST00000354476 R1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:33487838 C>A maps to ENST00000354476 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr2:33623443 C>T maps to ENST00000354476 C1667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:33360020 C>T maps to ENST00000354476 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:33572509 C>T maps to ENST00000354476 C1312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr2:33246090 G>A maps to ENST00000354476 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:33589400 T>C maps to ENST00000354476 C1507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr2:33505200 C>T maps to ENST00000354476 R1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr2:33413914 A>G maps to ENST00000354476 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:33585766 G>A maps to ENST00000354476 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:33589322 C>T maps to ENST00000354476 G1481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:33623443 C>T maps to ENST00000354476 C1667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:33623575 C>T maps to ENST00000354476 T1711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr14:75052600 C>T maps to NM_000428.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:74971791 C>T maps to NM_000428.2 A1421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:75078161 C>T maps to NM_000428.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:75022287 G>A maps to NM_000428.2 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:74969584 G>A maps to NM_000428.2 A1647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:74995321 G>A maps to NM_000428.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:74978020 G>A maps to NM_000428.2 C985C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:74995222 C>T maps to NM_000428.2 T777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr14:75078311 C>T maps to NM_000428.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:74995348 G>A maps to NM_000428.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:74970716 C>T maps to NM_000428.2 P1498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:75002695 C>T maps to NM_000428.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:75019031 G>A maps to NM_000428.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:74995670 C>T maps to NM_000428.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:74999144 C>T maps to NM_000428.2 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:75078512 C>T maps to NM_000428.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:65307099 C>A did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr11:65321231 G>A maps to NM_001130144.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:41111032 T>C maps to ENST00000308370 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:41114168 C>G maps to ENST00000308370 Y467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:41105348 C>T maps to ENST00000308370 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:46484978 G>A maps to NM_002343.3 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:46480909 G>A maps to NM_002343.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:41804948 C>T maps to NM_002344.5 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:144184651 T>A maps to NM_032860.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:144184234 C>T maps to NM_032860.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:144178444 C>T maps to NM_032860.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:258085 A>G maps to NM_201412.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr7:139106913 C>G maps to NM_016019.2 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr17:48817691 A>G maps to ENST00000393227 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:23417972 G>A maps to NM_001142546.1 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:23419293 C>T maps to NM_001142546.1 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:24998138 G>A maps to NM_001009909.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr11:25004700 T>G maps to NM_001009909.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:24750762 G>A maps to NM_001009909.2 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:24518833 G>A maps to NM_001009909.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:24518845 C>T maps to NM_001009909.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr11:24927589 C>T maps to NM_001009909.2 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:114536675 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:114540907 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:114541132 G>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:114537965 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:114524365 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:114540913 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:114540852 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:144102850 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:144103049 C>T maps to NM_002346.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:144103049 C>T maps to NM_002346.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr6:31686896 G>C maps to NM_025261.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:31683366 G>A maps to ENST00000375834 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:31675768 C>T maps to ENST00000375834 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:31678135 G>A maps to NM_001003693.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr8:143784758 C>T maps to ENST00000292430 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:160714969 C>T maps to NM_001198759.1 W762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:160731975 G>A maps to NM_001198759.1 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:160738647 T>C maps to NM_001198759.1 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:160667103 A>G maps to NM_001198759.1 G1544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:160663583 A>G maps to NM_001198759.1 S1630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:160793288 C>A maps to ENST00000263285 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:160771610 C>A maps to NM_001033667.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr1:160771607 C>T maps to NM_001033667.1 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:74922306 G>T maps to NM_015364.4 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:99907720 G>A maps to NM_174898.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:56863305 T>C maps to NM_002350.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:56910921 A>T maps to NM_002350.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:143856710 G>A maps to NM_177457.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr2:133403680 G>A maps to ENST00000409034 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr2:133403722 G>A maps to ENST00000409034 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr8:143831772 G>A maps to NM_205545.1 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:43968516 G>A maps to NM_014400.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:42342318 A>G maps to NM_173506.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr2:150064895 C>T maps to NM_177964.3 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:54978306 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:219366531 G>A maps to NM_138794.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr1:219347303 G>T maps to NM_138794.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:151134222 T>C maps to NM_212551.4 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr15:52017114 G>T maps to NM_153374.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:89820955 G>A maps to NM_198273.1 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:235971801 G>A maps to NM_000081.2 D772D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:235920622 G>A maps to NM_000081.2 L2339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:235884190 T>C maps to NM_000081.2 V3110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:235904747 G>A maps to NM_000081.2 R2778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:235971774 C>T maps to NM_000081.2 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:235993567 T>G maps to NM_000081.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:235929421 G>A maps to NM_000081.2 Y2026Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:235887375 G>T maps to NM_000081.2 I3089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:235944235 C>A maps to NM_000081.2 E1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:235972914 T>C maps to NM_000081.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:235922882 A>G maps to NM_000081.2 N2090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:235969040 A>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:235884028 A>G maps to NM_000081.2 P3164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:235976334 C>T maps to NM_000081.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:235920595 T>C maps to NM_000081.2 Q2348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:235971942 A>G maps to NM_000081.2 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:235976349 A>G maps to NM_000081.2 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:235866228 G>A maps to NM_000081.2 R3398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr1:235918902 A>G maps to NM_000081.2 D2368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:10585562 C>T maps to NM_006691.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:69743885 A>G did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr10:30915178 C>T maps to NM_183058.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:21348039 T>C maps to NM_006767.3 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr22:21346540 C>T maps to NM_006767.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:21343940 C>T maps to NM_006767.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:20107709 G>A maps to NM_021020.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:20110739 G>A maps to NM_021020.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:20110460 C>T maps to NM_021020.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:20110715 C>T maps to NM_021020.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:20107709 G>A maps to NM_021020.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr8:20107747 G>A maps to NM_021020.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:20110460 C>T maps to NM_021020.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:20110844 G>T maps to NM_021020.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:20110931 C>T maps to NM_021020.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:20112439 G>A maps to NM_021020.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:102766798 C>T maps to NM_032429.2 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:102763508 C>T maps to NM_032429.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:102763508 C>T maps to NM_032429.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr10:102763673 T>C maps to NM_032429.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:9094485 T>A maps to NM_002355.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr13:36049996 T>G maps to NM_005584.4 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr13:36049747 G>A maps to NM_005584.4 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:36049858 C>T maps to NM_005584.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:151504408 G>T maps to NM_006439.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr4:151504537 G>A maps to NM_006439.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr4:151505062 G>A maps to NM_006439.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:151504300 C>T maps to NM_006439.4 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:20180648 C>A maps to NM_182762.3 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr7:20198396 A>T maps to NM_182762.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr7:20198240 G>A maps to NM_182762.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr1:39797926 G>A maps to ENST00000289893 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:39549961 A>T maps to ENST00000361689 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:39844181 C>T maps to ENST00000361689 Y2359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:39919405 C>T maps to ENST00000361689 R4865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:39753192 C>T maps to ENST00000361689 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:39888400 G>T did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr1:39801199 G>A maps to ENST00000289893 V1420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:39910507 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:39757661 G>A maps to ENST00000361689 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:39801292 C>A maps to ENST00000289893 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:39907926 C>T maps to ENST00000361689 R4236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:39910338 C>T maps to ENST00000361689 L4420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:39798124 C>T maps to ENST00000289893 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:39749099 A>C maps to ENST00000361689 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:39844152 G>T maps to ENST00000361689 G2350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:39758497 C>T maps to ENST00000361689 Q664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:39893907 C>T maps to ENST00000361689 F3522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:39800560 C>T maps to ENST00000289893 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:63782730 G>A maps to NM_014067.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:15210619 C>T maps to ENST00000310348 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:14665513 C>T maps to ENST00000310348 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr20:15866407 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:15948228 C>T maps to ENST00000310348 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:15866409 C>T maps to ENST00000310348 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:2262371 G>A maps to NM_003550.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:2255799 C>T maps to NM_003550.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:2108876 G>A maps to NM_003550.2 H390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr7:2020095 G>A maps to NM_003550.2 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:2255913 C>T maps to NM_003550.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:2054220 G>A maps to NM_003550.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:1976413 G>A maps to NM_003550.2 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:2020095 G>A maps to NM_003550.2 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:120983143 A>C maps to NM_002358.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:11736990 T>C maps to ENST00000376669 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr19:501810 G>A maps to NM_130760.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:47296131 C>T maps to NM_003682.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:47308065 G>A maps to NM_003682.3 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:47348330 C>T maps to NM_003682.3 R1589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:47310990 C>T maps to NM_003682.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr11:47306679 G>A maps to NM_003682.3 E782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr11:47330174 G>T maps to NM_003682.3 E1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:47296159 C>T maps to NM_003682.3 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:1309204 C>T maps to ENST00000505177 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr4:1330743 C>T maps to ENST00000505177 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:166985521 G>A did not map to a codon.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr1:166985521 G>A did not map to a codon.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr1:166974587 C>T maps to NM_032858.1 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:79632968 C>T maps to NM_005360.4 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:79633682 G>A maps to NM_005360.4 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:79632790 G>A maps to NM_005360.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145161331 C>T maps to NM_032272.4 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:39316980 C>T maps to NM_005461.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:39316587 G>A maps to NM_005461.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:39317103 G>A maps to NM_005461.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:39317280 C>T maps to NM_005461.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:39317181 C>T maps to NM_005461.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:38610473 G>A maps to NM_012323.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:35793405 G>A maps to NM_002361.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:35800864 G>A maps to NM_002361.3 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:35801065 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:35801451 C>T maps to NM_002361.3 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:35800978 G>A maps to NM_002361.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:35791236 C>T maps to NM_002361.3 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:35786696 G>A maps to NM_002361.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:152482986 C>T did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:152482313 C>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:152482677 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:152482578 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:152482875 C>A did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:152482526 C>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:151303088 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:151303861 A>G did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:151303020 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:151303513 T>A did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:151303169 T>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:151303921 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:151303074 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:151304050 T>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:148797292 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:148797264 T>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:148797715 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:148797492 G>A did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:148797473 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:148798034 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:151900641 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:151900175 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:151899915 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:151900065 C>T did not map to a codon.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr23:151900230 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:151900085 A>T did not map to a codon.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr23:151900011 G>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:151900303 A>G did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:151900056 T>C did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:151935736 G>T did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:151935780 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:151935621 A>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:151935503 G>C did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr23:151935400 G>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:151935273 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:151935398 C>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:151935798 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:151935284 A>G did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:151092438 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:151092383 A>G did not map to a codon.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr23:151092503 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:151092877 A>G did not map to a codon.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr23:151092839 G>A did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:151092882 A>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:151092777 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:151092866 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:151283726 T>C did not map to a codon.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr23:151869825 C>A did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:151869965 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:151870217 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:151870232 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:151869696 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:151870147 G>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:151870139 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:151870024 T>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:149013851 C>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:149013370 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:149013558 A>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:149013070 C>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:149013705 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:30269408 C>T did not map to a codon.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr23:30269582 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:30268696 C>T did not map to a codon.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr23:30269231 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:30268937 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:30269561 C>T did not map to a codon.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr23:30269611 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:30268873 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:30269110 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:30269102 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:27840425 C>T did not map to a codon.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr23:27840217 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:27840118 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:27839446 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:27840404 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr23:27839809 A>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:35821241 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:35820608 C>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:35821200 A>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:35820768 T>C did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:35820606 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:35820535 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:35820337 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:26157823 G>T did not map to a codon.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr23:26157599 A>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:26157453 T>G did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:26157255 T>C did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr23:26157453 T>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:26157682 T>A did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr23:26158022 G>C did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:26157427 A>G did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:26157987 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:30236809 C>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:30237446 A>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:30237407 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:30237220 G>A did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:30237208 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:30236742 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:30237206 A>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:30254157 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:30254422 A>T did not map to a codon.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr23:30254144 A>G did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:30254228 A>G did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:30254144 A>T did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:30254216 G>A did not map to a codon.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr23:30254928 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:30254058 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:30254477 A>G did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:30260840 A>C did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:30260942 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:30260339 C>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:30260313 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:30260374 T>A did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:30261267 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr23:30261022 C>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:26212472 C>T did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr23:26212638 C>T did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr23:26212112 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:26212499 C>T did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:26212098 C>T did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:26212088 A>C did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:26212460 T>C did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:26212864 G>A did not map to a codon.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr23:26212896 G>A did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:26212527 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:26212528 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:26212995 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:26212380 C>A did not map to a codon.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr23:26212037 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:140993584 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:140996353 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:140995997 G>T did not map to a codon.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr23:140996327 A>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:140995627 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:140995835 A>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:140995298 C>A did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:140996140 C>A did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr23:140996299 T>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:140994647 C>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:140993746 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:140994227 C>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:140994233 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:140994240 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:140994246 A>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:140996505 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:140995431 T>A did not map to a codon.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr23:140995302 C>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:140994813 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:140996571 G>T did not map to a codon.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr23:140995214 T>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:140994235 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:140995605 G>T did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:140995049 A>T did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:140995250 T>G did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:140993255 T>C did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:140993322 G>A did not map to a codon.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr23:140994529 T>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:140993324 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr23:140993376 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:140996327 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:140996373 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr23:140993284 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:140995042 G>T did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr23:140996081 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:140996081 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:140994080 T>G did not map to a codon.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr23:140995000 A>T did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:140996329 T>G did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:140996472 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr23:140996327 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr23:140994423 A>G did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr23:141291457 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:141291101 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr23:141290909 C>T did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:141291506 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:141290906 C>A did not map to a codon.
Sequencing variant TCGA-CG-5716-01A-21D-1800-08 chr23:141291625 A>T did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:141290852 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:141290964 G>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:140926120 G>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:140953267 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:140969267 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:140985385 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:140953282 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:140985570 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:140985150 G>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:140953385 T>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:140953267 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:140967038 T>G did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:140953350 A>T did not map to a codon.
Sequencing variant TCGA-BR-A4IZ-01A-32D-A25D-08 chr23:140984462 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:140984912 G>T did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:140953338 G>C did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:140983060 T>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:140984486 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:140983058 G>A did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:140985098 G>T did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:140983167 C>T did not map to a codon.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr23:140984591 C>A did not map to a codon.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr23:140969410 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr23:140969447 A>G did not map to a codon.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr23:140984482 C>G did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:140984901 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:140953352 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:140969356 A>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:51639695 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:51637832 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:51639597 A>G did not map to a codon.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr23:51640686 G>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:51640095 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:51637864 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:51639797 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:51638631 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:51641390 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:51638835 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:51639616 G>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:51640304 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:51638685 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:51638745 G>A did not map to a codon.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr23:51644766 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:51638288 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:54841882 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:54838667 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:54837341 T>C did not map to a codon.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr23:54836551 C>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:54836446 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:54837467 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:75649388 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:75649861 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:75650755 C>A did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:75648561 T>G did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:75650041 A>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:75648365 G>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:75650836 G>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:75649352 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:75649450 G>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:75648335 A>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:75649839 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr23:75650026 C>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:75649081 T>C did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:75650722 A>G did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:75650660 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:75649436 G>A did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:75649974 T>G did not map to a codon.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr23:75650125 T>G did not map to a codon.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr23:75650188 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:75649599 C>A did not map to a codon.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr23:75650234 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:75648848 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr23:75649508 G>A did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:75004269 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:75004552 A>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:75004643 C>T did not map to a codon.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr23:75004702 C>A did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:75004528 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:184428772 G>A maps to NM_022149.4 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:184428949 C>T maps to NM_022149.4 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr23:55478887 C>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:55479096 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:55479458 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:55478848 A>G did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:55479466 A>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:55479393 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:55479175 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr23:55478926 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:23890195 G>A maps to NM_019066.4 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:23890345 C>T maps to NM_019066.4 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:23889178 G>A maps to NM_019066.4 D1237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:65344807 G>A maps to NM_015520.1 I1246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr3:65344794 T>G maps to NM_015520.1 R1251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:65342133 C>T maps to NM_001033057.1 Q1436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:65342508 G>A maps to NM_001033057.1 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:65342796 G>A maps to NM_001033057.1 S1215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:65425595 G>A maps to NM_001033057.1 Q410*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HJ-7597-01A-21D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:77824370 G>A maps to NM_012301.3 R697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:78636480 G>A maps to NM_012301.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:77708269 C>A maps to NM_012301.3 E1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:77789471 G>T maps to NM_012301.3 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr7:77973215 T>A maps to NM_012301.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:77824200 A>C maps to NM_012301.3 Y753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:77789516 G>A maps to NM_012301.3 Y890Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:77756555 G>A maps to NM_012301.3 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:77762324 C>T maps to NM_012301.3 A1028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr7:78256457 G>A maps to NM_012301.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr7:77998504 G>A maps to NM_012301.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr7:77797389 G>A maps to NM_012301.3 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr7:77789453 G>A maps to NM_012301.3 F911F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr7:77998504 G>A maps to NM_012301.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:78150951 G>A maps to NM_012301.3 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:114092137 C>T maps to NM_001142782.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:114128213 C>T maps to NM_001142782.1 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr1:114196494 A>G maps to NM_001142782.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:114225543 G>A maps to NM_001142782.1 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr1:114225852 G>A maps to NM_001142782.1 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr1:114225543 G>A maps to NM_001142782.1 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:114201837 G>T maps to NM_001142782.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:49019248 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:49021224 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:49022483 T>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:49021218 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:49021126 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr23:49021420 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:77112975 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:77111077 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:77150867 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:77096752 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:77112908 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:77150882 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:77131012 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:10809074 C>T maps to NM_005906.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:10802141 G>A maps to NM_005906.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:10796272 C>T maps to NM_005906.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:10796374 T>C maps to NM_005906.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:10830845 G>A maps to NM_005906.3 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr6:10796389 G>A maps to NM_005906.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:10775639 G>T maps to NM_005906.3 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:33346652 C>T maps to NM_032509.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:33354772 C>T maps to NM_032509.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr2:95715447 C>T maps to NM_002371.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:110849314 G>A maps to NM_005434.4 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:110849254 C>T maps to NM_005434.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr18:56376641 C>T maps to NM_006785.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr9:72758552 T>C maps to NM_153267.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr9:72785542 G>C maps to NM_153267.4 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:139749901 G>A maps to ENST00000392881 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:139754411 C>T maps to ENST00000392881 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:139748064 C>T maps to ENST00000392881 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:139749901 G>A maps to ENST00000392881 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:139748022 C>T maps to ENST00000392881 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr9:139747812 C>T maps to ENST00000392881 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:139753496 C>T maps to ENST00000392881 G1082G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:139751826 C>T maps to ENST00000392881 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:179195921 C>T maps to NM_014757.4 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:179195994 T>C maps to NM_014757.4 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:95712231 G>A maps to NM_032427.1 N1117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:95724694 G>A maps to NM_032427.1 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:95724830 G>A maps to NM_032427.1 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:95724790 G>A maps to NM_032427.1 Q746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:95712333 C>T maps to NM_032427.1 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr11:95825796 A>G maps to NM_032427.1 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:95825409 C>T maps to NM_032427.1 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:95712333 C>T maps to NM_032427.1 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:95826234 G>A maps to NM_032427.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:95825913 C>T maps to NM_032427.1 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:140640938 G>A maps to ENST00000509479 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:140811419 C>T maps to ENST00000509479 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr4:140811122 T>C maps to ENST00000509479 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:140640518 G>A maps to ENST00000509479 D1125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:140811116 C>T maps to ENST00000509479 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:140811599 G>A maps to ENST00000509479 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:149639051 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:149638866 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:149671695 C>A did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:149638239 A>T did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:149639246 T>C did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:149639019 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:149671654 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:149671776 C>T did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:149638352 C>T did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:149641984 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:149639572 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:149639605 C>A did not map to a codon.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:149638530 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:149671787 G>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:149639681 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:149671584 C>T did not map to a codon.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:49217245 C>A maps to NM_001130915.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:119670100 G>A maps to NM_005907.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:119569512 G>A maps to NM_005907.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr6:119670146 C>T maps to NM_005907.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:119669654 G>A maps to NM_005907.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:117944903 T>C maps to NM_006699.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:117944918 G>A maps to NM_006699.3 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:118065573 C>T maps to NM_006699.3 R641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:117910864 G>A maps to NM_006699.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:26013010 C>T maps to NM_020379.2 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:26104702 C>T maps to NM_020379.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:26110216 C>T maps to NM_020379.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:26104648 C>A maps to NM_020379.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:109103320 T>C maps to NM_002372.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:109155378 C>T maps to NM_002372.2 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:109183455 C>T maps to NM_002372.2 R981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:109181594 G>A maps to NM_002372.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:109091158 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:109103234 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:91448605 C>T maps to NM_006122.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:91454613 G>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr15:91455875 G>A maps to NM_006122.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:12774529 C>T maps to NM_000528.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:12760205 C>T maps to NM_000528.3 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:6611523 G>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:6611011 C>T maps to NM_015274.1 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:75648755 G>A maps to NM_006715.2 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:75648485 C>T maps to NM_006715.2 W987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr15:75648551 G>A maps to NM_006715.2 S965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr15:75648716 G>C maps to NM_006715.2 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:75651070 G>A maps to NM_006715.2 D740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:75648255 C>T maps to NM_006715.2 P1038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:75656379 T>C maps to NM_006715.2 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:103557138 A>G maps to NM_005908.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:103553302 G>A maps to NM_005908.3 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:96052732 C>T maps to NM_024641.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:96034416 T>C maps to NM_024641.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:96054017 C>T maps to NM_024641.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:12491443 G>A maps to NM_018050.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:12483887 A>G maps to NM_018050.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:12491411 G>A maps to NM_018050.2 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr23:43603731 A>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:43603381 C>T did not map to a codon.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr23:43603413 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:43591071 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:43662604 G>T did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:43662580 T>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:43656371 C>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:43816367 C>A maps to ENST00000382031 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:43820987 T>C maps to ENST00000382031 T2677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:43814150 C>T maps to ENST00000382031 C398C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:43818212 G>A maps to ENST00000382031 T1752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:43819208 G>A maps to ENST00000382031 V2084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:43819856 T>C maps to ENST00000382031 V2300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr15:43815306 C>T maps to ENST00000382031 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:43815947 G>A maps to ENST00000382031 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr15:43821401 G>A maps to ENST00000382031 V2815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:71491780 C>T maps to NM_005909.3 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:71490957 G>A maps to NM_005909.3 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr5:71495206 G>T maps to NM_005909.3 E2009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:71494146 G>A maps to NM_005909.3 E1655E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr5:71492952 G>A maps to NM_005909.3 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:71494695 C>T maps to NM_005909.3 F1838F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr5:71489952 C>T maps to NM_005909.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:71491092 G>A maps to NM_005909.3 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr5:71495727 C>T maps to NM_005909.3 D2182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:71495781 A>G maps to NM_005909.3 P2200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:71490624 G>A maps to NM_005909.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr5:71495358 C>T maps to NM_005909.3 Y2059Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:172942523 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:172945100 G>A maps to NM_199227.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:33147563 G>A maps to NM_181509.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:242159680 G>A maps to NM_001004343.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr1:242159614 G>A maps to NM_001004343.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:17844194 C>T maps to NM_018174.4 D994D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:17845107 G>A maps to NM_018174.4 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr19:17836660 G>A maps to NM_018174.4 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:17838442 G>A maps to NM_018174.4 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:210559704 G>A maps to NM_002374.3 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:210518128 C>T maps to NM_002374.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:210558201 T>C maps to NM_002374.3 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:210574734 T>G maps to NM_002374.3 S1610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr2:210560637 G>T maps to NM_002374.3 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:210559926 C>T maps to NM_002374.3 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:210560532 G>A maps to NM_002374.3 T1213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:210557418 A>C maps to NM_002374.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:210559224 A>G maps to NM_002374.3 E777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:210570372 C>T maps to NM_002374.3 R1552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:210558966 T>A maps to NM_002374.3 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr2:210560979 T>C maps to NM_002374.3 S1362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:210560784 C>T maps to NM_002374.3 T1297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:210574734 T>A maps to NM_002374.3 S1610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:210595033 G>A maps to NM_002374.3 S1799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr2:210557511 T>G maps to NM_002374.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:210560124 C>T maps to NM_002374.3 D1077D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr2:210557511 T>G maps to NM_002374.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:210559606 C>T maps to NM_002374.3 R905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr2:210557574 G>C maps to NM_002374.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr2:210517906 C>A maps to NM_002374.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr2:210559323 A>G maps to NM_002374.3 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:210557553 A>G maps to NM_002374.3 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr2:210559323 A>G maps to NM_002374.3 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:66774156 C>T maps to NM_002755.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:4099373 C>A maps to NM_030662.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:4117449 C>T maps to NM_030662.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:4117503 G>A maps to NM_030662.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:4099310 C>T maps to NM_030662.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:4117560 C>T maps to NM_030662.3 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HB-01A-12D-A25D-08 chr19:4110644 G>A maps to NM_030662.3 H104H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-4201-01A-01D-1126-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:21201725 A>G maps to ENST00000316920 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:21204190 C>T maps to NM_145109.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:21207774 C>T maps to NM_145109.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:21206532 G>A maps to NM_145109.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:21216801 A>G did not map to a codon.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr17:21203933 G>A maps to NM_145109.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:21215542 G>A maps to NM_145109.2 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:21202198 G>A maps to NM_145109.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:11984730 C>T maps to ENST00000415385 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:11984781 C>T maps to ENST00000415385 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:12016622 G>A maps to ENST00000415385 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:12028689 T>C did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr17:67519769 A>G maps to NM_002758.3 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:7975259 T>C did not map to a codon.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr19:7976323 G>T maps to ENST00000425613 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr19:7976132 A>T did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr19:7976133 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:56155649 C>T maps to NM_005921.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:56179351 A>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:56179394 G>A maps to NM_005921.1 P1236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr5:56178645 C>T maps to NM_005921.1 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:40718827 C>T maps to NM_002446.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:40698258 G>T maps to NM_002446.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:40712064 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:40721045 C>T maps to NM_002446.3 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:65375800 G>A maps to NM_002419.3 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:65365878 T>G maps to NM_002419.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:65365884 C>T maps to NM_002419.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr11:65365944 C>T maps to NM_002419.3 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr11:65380600 G>A maps to NM_002419.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:53880256 G>A maps to NM_001193511.1 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:53878988 G>A maps to NM_001193511.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr12:53879108 G>T maps to NM_001193511.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:185191525 C>T maps to NM_004721.3 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:185198017 A>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:43362235 G>A maps to ENST00000344686 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:43348436 C>T maps to ENST00000344686 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:43363911 G>A maps to ENST00000344686 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:43343976 G>A maps to ENST00000344686 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:19475113 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:19413306 C>T did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:19410171 A>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:19389098 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:19410569 C>T did not map to a codon.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr23:19390934 C>T did not map to a codon.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr23:19475122 C>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:19431561 G>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:19475044 C>T did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:19431477 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:19391782 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:19391802 G>A did not map to a codon.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr23:19387273 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:19398293 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr23:19425333 A>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:128065337 C>T maps to NM_006609.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:128083332 A>G maps to NM_006609.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr2:128075264 A>G maps to NM_006609.3 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:128084283 G>A maps to NM_006609.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:61770977 C>T maps to NM_203351.1 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:61759259 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:61768553 T>G maps to NM_203351.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:61770953 G>A maps to NM_203351.1 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:161501971 G>A maps to NM_005922.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:161523017 C>T maps to NM_005922.2 R1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:161470749 C>T maps to NM_005922.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr6:161470482 C>T maps to NM_005922.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:161527592 C>T maps to NM_005922.2 R1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:137018440 T>C maps to NM_005923.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:136904863 C>T maps to NM_005923.3 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:136923030 A>G maps to NM_005923.3 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:136926361 T>C maps to NM_005923.3 Q888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:136913615 G>A maps to NM_005923.3 C1005C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:27688703 G>T maps to NM_004672.3 C431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:27683214 C>T maps to NM_004672.3 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:91269916 T>C maps to NM_145331.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:91260184 A>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:30748326 G>A maps to NM_005204.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:30748254 A>G maps to NM_005204.2 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:30739266 C>T maps to NM_005204.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr10:30749641 G>A maps to NM_005204.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:30739257 G>A maps to NM_005204.2 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr14:71215716 G>A maps to NM_033141.2 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:71199484 G>A maps to NM_033141.2 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:71197171 G>A maps to NM_033141.2 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:71199760 G>A maps to NM_033141.2 C789C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:71199958 G>A maps to NM_033141.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:71227783 C>T maps to NM_033141.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:39108028 G>A maps to NM_001042600.1 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:64566892 C>T maps to NM_004579.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:64564486 G>C maps to NM_004579.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:64567830 G>T maps to NM_004579.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:64570354 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr2:102460758 C>T maps to NM_145686.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:50911876 C>T maps to NM_198794.1 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr14:50906791 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:75298475 A>G maps to NM_033063.1 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr11:75298496 T>C maps to NM_033063.1 Q683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:75316959 C>T maps to NM_033063.1 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:75298880 T>C maps to NM_033063.1 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:136698971 G>A maps to NM_001198609.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:136732782 T>C maps to NM_001198609.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:36641818 C>T maps to NM_018067.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:36636749 C>T maps to NM_018067.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:36645159 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:20082869 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr23:20081623 G>A did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:20081623 G>A did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:20028954 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:20043093 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:135313711 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:135313851 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:135314316 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135308163 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:135310893 C>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:135314038 G>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:135313819 C>A did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:135314088 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:135307004 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:135314370 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:135301781 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:135303040 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:135313014 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:135318404 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:135314104 T>C did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:135310824 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:135318439 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:135328223 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:135314152 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:156289782 T>C maps to NM_001039580.1 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:87024398 T>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:87080617 T>C maps to NM_138982.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr22:50694076 C>T maps to NM_002969.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:50693731 C>T maps to NM_002969.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:50693746 C>T maps to NM_002969.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr6:36104268 G>A maps to NM_002754.3 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:36106832 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr18:48190610 C>T maps to NM_002747.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:48255701 G>A maps to NM_002747.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:48241531 C>T maps to NM_002747.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:48256133 C>T maps to NM_002747.3 D558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr18:48255713 C>T maps to NM_002747.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:48256037 G>A maps to NM_002747.3 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:52356398 C>T maps to NM_002748.3 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:52339142 G>A maps to NM_002748.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:52356197 T>C maps to NM_002748.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:19286516 T>G maps to NM_139034.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:19286235 C>T maps to NM_139034.2 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:19284295 G>A maps to NM_139034.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:19284208 G>A maps to NM_139034.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:19284577 T>C maps to NM_139034.2 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:19284835 G>A maps to NM_139034.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:49635187 T>C did not map to a codon.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr11:45924103 G>A maps to NM_005456.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr22:51045177 C>T maps to ENST00000329492 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:1817231 C>T maps to NM_015133.3 Y1056Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:1818553 G>A maps to NM_015133.3 S1272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:1797262 C>T maps to NM_015133.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:1818734 C>T maps to NM_015133.3 G1307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:1810416 C>A maps to NM_015133.3 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:1818598 C>T maps to NM_015133.3 G1287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:1818371 G>A maps to NM_015133.3 S1244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:179663506 G>A maps to NM_002752.4 N384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:179668087 G>A maps to NM_002752.4 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:128347880 C>T maps to NM_001006617.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:128246827 C>T maps to NM_001006617.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:128322030 G>T maps to NM_001006617.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr3:50679759 C>T maps to NM_004635.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:42105235 G>A maps to NM_001128608.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:42110260 T>C maps to NM_001128608.1 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr15:42105152 C>T maps to NM_001128608.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr15:42115795 C>A maps to NM_001128608.1 A1256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr15:42116180 T>C maps to NM_001128608.1 L1385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:42107545 G>A maps to NM_001128608.1 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr15:42105823 A>G maps to NM_001128608.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr18:32706942 A>T maps to NM_014268.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:44101485 C>T maps to NM_001123066.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr17:44073912 G>A maps to NM_001123066.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr17:44101419 G>A maps to NM_001123066.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:44039744 C>T maps to NM_001123066.3 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:44101482 G>A maps to NM_001123066.3 Q759Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr4:164466832 G>A maps to ENST00000514618 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:60879030 C>T maps to NM_152598.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:60802446 G>A maps to NM_152598.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:60837268 T>C maps to NM_152598.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:60814661 A>G maps to NM_152598.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:60879084 G>A maps to NM_152598.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:16091067 C>T maps to NM_001102562.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:8491552 G>A maps to NM_016496.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:126250639 T>C maps to NM_178450.3 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr2:217142428 G>A maps to NM_020814.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr2:217142482 A>C maps to NM_020814.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr10:94100523 G>A maps to NM_017824.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr5:10402500 G>A maps to NM_005885.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:10391769 G>A maps to NM_005885.2 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:10417410 G>A maps to NM_005885.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:10387154 G>A maps to NM_005885.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:160605007 C>T maps to NM_022826.2 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr2:160602344 A>C maps to NM_022826.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:160599594 G>A maps to NM_022826.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr2:160604514 G>A maps to NM_022826.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr2:160585643 T>C maps to NM_022826.2 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:45956825 G>T maps to NM_145021.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:45959709 C>T maps to NM_145021.4 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr12:58151952 G>A maps to NM_138396.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:114181337 C>T maps to NM_002356.5 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr6:114181208 G>A maps to NM_002356.5 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:119752089 C>T maps to NM_006770.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr2:119751969 G>A maps to NM_006770.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:119726814 C>T maps to NM_006770.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr2:119750045 G>T maps to NM_006770.3 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:119726814 C>T maps to NM_006770.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:119699941 C>T maps to NM_006770.3 H22H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr1:220825397 C>T maps to NM_018650.3 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:220826556 A>G maps to NM_018650.3 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:220791773 C>T maps to NM_018650.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:220809208 C>A maps to NM_018650.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:220835357 C>T maps to NM_018650.3 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr11:63672269 G>A maps to NM_001039469.2 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:63667548 C>T maps to NM_001039469.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:63670253 G>A maps to NM_001039469.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr14:103928797 G>A maps to ENST00000335102 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:103958243 C>T maps to ENST00000335102 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr14:103871564 A>G maps to ENST00000335102 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:45762389 T>C maps to NM_031417.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:45805629 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:45766417 G>A maps to NM_031417.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr19:45767969 G>A maps to NM_031417.3 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:57906609 G>A maps to NM_004990.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr12:57898028 C>T maps to NM_004990.2 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr2:198570227 C>T maps to NM_138395.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:198571289 T>C maps to NM_138395.3 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr5:68715517 G>A maps to NM_001038603.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:68715901 G>A maps to NM_001038603.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:68728391 A>G maps to NM_001038603.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:71674725 C>T maps to NM_001017967.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:71668201 C>T maps to NM_052858.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:71674500 C>T maps to NM_001017967.2 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:71668549 C>T maps to NM_052858.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr6:160328817 T>A maps to NM_002377.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr6:160328009 C>A maps to NM_002377.2 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:29454569 C>T maps to NM_052967.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:29455511 C>A maps to NM_052967.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr6:29455076 A>C maps to NM_052967.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:186953693 G>A maps to NM_139125.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:186953744 C>T maps to NM_139125.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:186954046 G>A maps to NM_139125.3 R538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr3:186943166 T>C maps to NM_001879.5 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:186943262 T>C maps to NM_001879.5 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr1:11087138 C>A maps to NM_006610.2 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:11103524 C>T maps to NM_006610.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:11097869 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:11087238 G>A maps to NM_006610.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:11097751 G>A maps to NM_006610.2 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:12984810 C>T maps to NM_014975.2 G1280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:12984645 G>A maps to NM_014975.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:12962927 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:12984254 G>A maps to NM_014975.2 S1127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:12985335 G>A maps to NM_014975.2 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:12979550 G>A maps to NM_014975.2 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:12978558 G>A maps to NM_014975.2 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:12985200 G>A maps to NM_014975.2 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:46496748 C>T maps to NM_015112.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:46497991 T>G maps to NM_015112.2 A1110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:46496356 G>T maps to NM_015112.2 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:46497965 A>C maps to NM_015112.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:46498027 C>T maps to NM_015112.2 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:46496690 G>A maps to NM_015112.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:18252810 G>A maps to NM_015016.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:18248127 C>T maps to NM_015016.1 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:18252738 C>T maps to NM_015016.1 F722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr19:18234440 C>T maps to NM_015016.1 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:18256011 C>T maps to NM_015016.1 D975D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:18245775 C>T maps to NM_015016.1 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:66430463 C>T maps to NM_001164664.1 C780C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr5:66429353 C>T maps to NM_001164664.1 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr5:66430463 C>T maps to NM_001164664.1 C780C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:66445329 C>T maps to NM_001164664.1 R1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:27459729 C>T maps to NM_001172303.1 C614C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:82033575 G>A maps to NM_000429.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:82036320 G>A maps to NM_000429.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:82034358 G>T maps to NM_000429.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:85769749 T>C maps to NM_005911.4 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:85769743 T>C maps to NM_005911.4 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr2:85770888 A>G maps to NM_005911.4 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:162945227 A>G maps to NM_013283.3 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:162943692 G>A maps to NM_013283.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:3778396 G>A maps to NM_002378.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:3784120 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:3779045 G>A maps to NM_002378.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:31194314 G>A maps to NM_002379.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:31189676 G>A maps to NM_002379.3 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr1:31188061 C>T maps to NM_002379.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr1:31189634 A>G did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:98943433 G>A maps to ENST00000254898 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:99039746 A>C maps to ENST00000254898 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:20196997 G>T maps to NM_002381.4 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:20206009 C>T maps to NM_002381.4 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:43933294 G>A maps to ENST00000372754 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:43933090 A>G maps to ENST00000372754 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:43933213 G>A maps to ENST00000372754 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr20:43933363 C>T maps to ENST00000372754 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:43926645 C>T maps to ENST00000372754 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:43926972 G>A maps to ENST00000372754 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:43927167 C>T maps to ENST00000372754 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:43927119 C>A maps to ENST00000372754 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:138658650 A>T maps to ENST00000394800 K715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:138658373 C>T maps to ENST00000394800 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr5:138655021 G>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:3842923 G>A maps to NM_020746.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:29818096 C>T maps to NM_001042539.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr16:29818186 C>T maps to NM_001042539.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:29821440 G>A maps to NM_002383.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:29821440 G>T maps to NM_002383.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr18:47803199 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:47803029 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr18:47796136 G>A maps to NM_015845.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:51731393 G>A maps to NM_003927.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:1578341 G>A maps to NM_003926.5 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr19:1578404 G>A maps to NM_003926.5 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:1592611 C>A maps to NM_003926.5 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:1581155 G>A maps to NM_003926.5 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:8953875 G>A maps to NM_145208.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:129152935 G>A maps to NM_003925.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:149247136 C>T maps to ENST00000404807 G1312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:149247532 G>A maps to ENST00000404807 K1444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr2:149247082 G>A maps to ENST00000404807 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr2:149227247 T>G maps to ENST00000404807 L579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:57920919 C>T maps to NM_052897.3 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:57919677 G>A maps to NM_052897.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr12:57918173 C>T maps to NM_052897.3 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:54530478 A>G maps to NM_000242.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:89757253 G>A maps to NM_203406.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:89757036 G>A maps to NM_203406.1 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr13:97995277 C>T maps to ENST00000376673 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:97995268 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:131524938 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:131540406 C>T did not map to a codon.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr23:131540372 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:131540286 A>G did not map to a codon.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr6:20113187 C>T maps to NM_001080480.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:9017243 A>G maps to NM_138799.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr2:9002809 C>T maps to NM_138799.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:9017343 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:9013331 A>G maps to NM_138799.2 H263H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:9002809 C>T maps to NM_138799.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr2:9008632 G>A maps to NM_138799.2 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:8998937 A>G maps to NM_138799.2 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:54677779 G>A maps to NM_024298.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:54677812 A>G maps to NM_024298.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr19:54678009 G>A maps to NM_024298.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:54678100 G>A maps to NM_024298.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:84103625 T>C maps to NM_003791.2 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:84094377 C>T maps to NM_003791.2 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:84101342 C>T maps to NM_003791.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:21871620 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:21887617 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:21896665 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:21896712 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:21896784 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:89986037 C>A maps to ENST00000304984 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:89985929 C>T maps to ENST00000304984 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:89986082 C>T maps to ENST00000304984 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:13884950 G>A maps to NM_000529.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:13884977 C>T maps to NM_000529.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr18:13885436 C>T maps to NM_000529.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr20:54824579 C>T maps to ENST00000371389 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:54824312 C>T maps to ENST00000371389 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:54824414 C>T maps to ENST00000371389 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:54824426 C>T maps to ENST00000371389 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr18:58038751 A>G maps to NM_005912.2 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:58038673 T>C maps to NM_005912.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr18:13825820 C>T maps to NM_005913.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:13826186 C>T maps to NM_005913.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr18:13826228 G>A maps to NM_005913.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:119185612 G>A maps to NM_006500.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr11:119183093 G>A maps to NM_006500.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:119183609 G>T maps to NM_006500.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:29340012 T>C maps to NM_001034172.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr18:29340009 C>T maps to NM_001034172.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:103349892 C>T did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:103349654 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:103349128 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:43533209 G>A maps to NM_173467.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:112676241 C>A maps to NM_001085377.1 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:112824009 G>A maps to NM_001085377.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:112364689 G>A maps to NM_001085377.1 S940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:112364668 T>C maps to NM_001085377.1 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr5:112406813 C>T maps to NM_001085377.1 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr5:112478958 C>T maps to NM_001085377.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:112403792 G>A maps to NM_001085377.1 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:112420982 G>A maps to NM_001085377.1 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:112418624 G>A maps to NM_001085377.1 Y572Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:182735068 G>A maps to NM_020166.3 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:182755191 A>G maps to NM_020166.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:70944922 G>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:71351377 C>T maps to NM_032601.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr23:138698451 G>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:138698520 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:138697060 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:138713568 C>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:138714594 A>C did not map to a codon.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr23:138689887 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:138689851 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:138729030 A>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:138713595 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr23:138699693 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr23:138708380 G>A did not map to a codon.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr23:138724647 C>A did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:138708373 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:113728774 C>T maps to NM_001112732.1 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:183013085 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:183013130 T>C maps to NM_015078.2 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:182946140 C>A maps to NM_015078.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:182947566 T>A maps to NM_015078.2 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:47135053 C>T maps to NM_001171506.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:47136202 G>A maps to NM_001171506.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:41075619 A>G maps to NM_005297.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:41077106 C>T maps to NM_005297.3 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr22:41077139 C>A maps to NM_005297.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr22:41077262 C>A maps to NM_005297.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:100368815 C>T maps to NM_032503.2 *341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:100390835 G>A maps to NM_032503.2 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr6:100390874 G>A maps to NM_032503.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:150549865 T>C maps to NM_021960.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr10:13234490 G>A maps to NM_182751.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:13213235 C>T maps to NM_182751.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:13213033 C>T maps to NM_182751.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr10:13217564 G>T maps to NM_182751.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:127335931 G>T maps to NM_004526.2 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr6:52142411 G>C maps to ENST00000419835 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr21:47662777 A>G maps to NM_003906.3 V1788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:47665033 G>A maps to NM_003906.3 Y1575Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:47671502 C>T maps to NM_003906.3 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr21:47680750 G>A maps to NM_003906.3 R1179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr21:47685899 G>A maps to NM_003906.3 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:47684122 C>A maps to NM_003906.3 A1081A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr21:47685983 G>A maps to NM_003906.3 V962V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:47676878 G>A maps to NM_003906.3 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:47697477 G>A maps to NM_003906.3 Y607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr21:47663637 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:48874073 A>C did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr8:48883435 G>A maps to NM_182746.1 K600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr8:48889313 T>C maps to NM_182746.1 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:48878897 C>T maps to NM_182746.1 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr8:48874863 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:48878897 C>T maps to NM_182746.1 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:48883153 C>T maps to NM_182746.1 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:35808653 C>A maps to NM_006739.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:35817309 G>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:136614441 G>A maps to NM_005915.4 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:136602246 G>A maps to NM_005915.4 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:136626254 G>A maps to NM_005915.4 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:99693746 C>T maps to NM_005916.3 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:99690626 C>T maps to NM_005916.3 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:99691936 C>T maps to NM_005916.3 K569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr20:5948581 G>A maps to NM_032485.4 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:5966644 G>A maps to NM_032485.4 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr20:5958553 T>A maps to NM_032485.4 Y476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr20:5963628 C>A maps to NM_032485.4 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:5966633 C>A maps to NM_032485.4 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:119238738 G>A maps to ENST00000316316 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:119238765 G>A maps to ENST00000316316 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr19:7593840 C>T maps to NM_020533.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:85424295 A>C maps to NM_153259.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr1:85510983 G>A maps to NM_018298.9 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:6302422 C>T maps to NM_024596.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:6302631 C>T maps to NM_024596.3 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:6302586 T>C maps to NM_024596.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:6266827 A>G maps to NM_024596.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr8:6500542 C>T maps to NM_024596.3 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:6302319 A>G maps to NM_024596.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:6357398 C>T maps to NM_024596.3 H721H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:6302004 C>T maps to NM_024596.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:94267672 C>T maps to NM_024717.4 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:94942206 G>A maps to NM_018349.3 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:94841700 C>T maps to NM_018349.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr15:94884107 G>C maps to NM_018349.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:94858781 T>C maps to NM_018349.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr15:94913350 C>T maps to NM_018349.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:119742204 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:119742167 T>G did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:30672219 A>G maps to NM_014641.2 P1580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:30671880 C>T maps to NM_014641.2 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:30673670 C>A maps to NM_014641.2 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:41613963 C>A maps to NM_005586.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:41617444 G>T maps to NM_005586.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:114655772 G>A maps to NM_199072.4 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:37619916 G>A maps to ENST00000297153 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:37623658 T>C maps to ENST00000297153 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr14:47426670 G>A maps to NM_001113498.2 Y665Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:47343400 C>A maps to NM_001113498.2 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr14:47314967 C>T did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr14:47504253 G>A maps to NM_001113498.2 N593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr14:47426817 C>T maps to NM_001113498.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:63824674 A>C maps to NM_005917.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr2:207619946 C>T maps to NM_001039845.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:207620120 T>C maps to NM_001039845.1 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:207619811 G>A maps to NM_001039845.1 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr2:207620042 C>T maps to NM_001039845.1 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:207620230 T>C did not map to a codon.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr7:75687380 C>T maps to NM_005918.2 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:75694213 C>A maps to NM_005918.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:68696397 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:68709979 C>T maps to NM_017440.4 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:68724911 C>T maps to NM_017440.4 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:69229703 C>T maps to NM_002392.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:69233298 T>C maps to NM_002392.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:69233334 T>G maps to NM_002392.3 Y400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:90453363 G>A maps to NM_014611.1 C1416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:90372630 G>A maps to NM_014611.1 G4764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:90405416 G>A maps to NM_014611.1 S3226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:90422949 G>A maps to NM_014611.1 R2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:90499579 C>T maps to NM_014611.1 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:90494778 A>T maps to NM_014611.1 Y467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:90354753 A>G maps to NM_014611.1 L5528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:90409954 T>C maps to NM_014611.1 S2899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:90428118 T>C maps to NM_014611.1 R2183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:90504396 T>C maps to NM_014611.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:90418230 C>A maps to NM_014611.1 E2628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:90360518 C>T maps to NM_014611.1 A5321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:90402710 C>T maps to NM_014611.1 L3346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr6:90368580 C>T maps to NM_014611.1 E4923E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:90428704 C>T maps to NM_014611.1 P2034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:90402779 G>A maps to NM_014611.1 Y3323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:90428227 C>T maps to NM_014611.1 W2147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:90395560 G>A maps to NM_014611.1 Q3902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:90399784 G>A maps to NM_014611.1 G3609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:90448143 C>A maps to NM_014611.1 E1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:90428682 G>A maps to NM_014611.1 L2042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr6:90425373 G>A maps to NM_014611.1 F2286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:90354840 G>A maps to NM_014611.1 R5499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr6:90459387 C>T maps to NM_014611.1 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:90422426 C>A maps to NM_014611.1 G2433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:90359802 C>T maps to NM_014611.1 Q5382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:90377777 G>A maps to NM_014611.1 G4683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr6:90403851 C>T maps to NM_014611.1 L3274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:83926225 A>G maps to NM_002395.4 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:83921762 C>T maps to NM_002395.4 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr6:83926270 C>A maps to NM_002395.4 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr6:83926279 T>C maps to NM_002395.4 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr6:83933649 T>A maps to NM_002395.4 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr6:83947438 A>G maps to NM_002395.4 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:83947464 G>A maps to NM_002395.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:48458684 C>T maps to NM_002396.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr18:48442540 A>G maps to NM_002396.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr18:48434456 C>T maps to NM_002396.4 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:86161429 G>A maps to NM_001014811.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:86209064 G>A maps to NM_001014811.1 C215C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:86267647 C>T maps to NM_001014811.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr11:86158220 C>T maps to NM_001014811.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:86161399 C>T maps to NM_001014811.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:37961519 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:168833262 T>C maps to NM_004991.3 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr3:168845678 C>T maps to NM_004991.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:168838892 C>T maps to NM_004991.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr3:168807857 C>A maps to NM_004991.3 E1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:168833508 C>T maps to NM_004991.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:168840365 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:169099148 G>A maps to NM_004991.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:153297979 G>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:153296470 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153296141 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153295905 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153297999 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153363099 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153297718 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153296752 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:153295822 T>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:153296056 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153296090 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:37565281 A>G maps to NM_004774.3 T1064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr17:37564294 G>A maps to NM_004774.3 I1393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:37564723 T>A maps to NM_004774.3 G1250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:37566691 G>A maps to NM_004774.3 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:37564789 A>G maps to NM_004774.3 G1228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:37564729 C>T maps to NM_004774.3 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:37564678 G>T maps to NM_004774.3 S1265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr17:37571509 G>A maps to NM_004774.3 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:70349623 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:70348473 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:70353000 A>G did not map to a codon.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr23:70349257 C>T did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:70357075 C>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:70349688 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:70360634 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:70360646 A>G did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr23:70341240 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:70356409 A>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:70360613 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:70360622 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:70360646 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:70348158 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:70356309 C>T did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:70361777 G>A did not map to a codon.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr23:70344685 G>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:70340969 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:70347217 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:70341605 T>C did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr23:70360607 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:70356269 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:70341236 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:70341448 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:70349680 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:151093845 T>C maps to NM_053002.4 P1264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:150845682 A>G maps to NM_053002.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:151082764 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:151127056 C>A maps to NM_053002.4 L1914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr3:151129178 G>A maps to NM_053002.4 P1973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr3:151095919 T>G maps to NM_053002.4 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:60030382 A>G maps to NM_005121.2 T2020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:60043997 A>G maps to NM_005121.2 G1402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:60072700 A>G maps to NM_005121.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:60032890 C>T maps to NM_005121.2 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:60042386 C>T maps to NM_005121.2 P1608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:60033125 A>G maps to NM_005121.2 C1899C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr17:60042585 G>C maps to NM_005121.2 S1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:60042386 C>T maps to NM_005121.2 P1608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr17:60028344 A>G maps to NM_005121.2 D2044D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:116428978 A>G maps to NM_015335.4 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr12:116434871 T>C maps to NM_015335.4 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr12:116424992 C>T maps to NM_015335.4 R1345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:116429758 G>A maps to NM_015335.4 N1000N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:116457116 A>G maps to NM_015335.4 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:116446527 G>A maps to NM_015335.4 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:116429674 G>T maps to NM_015335.4 A1028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:40571543 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:40522274 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:40542152 C>T did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:40513616 T>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:40547714 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:40572273 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:40518547 G>T did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:40511085 A>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:40552102 A>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:40562800 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:40542143 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:40569343 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:40551963 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:20891433 A>G maps to NM_001003891.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:20929470 C>T maps to NM_001003891.1 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr22:20920869 A>G maps to NM_001003891.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:20940111 C>T maps to NM_001003891.1 Y743Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr22:20939221 C>T maps to NM_001003891.1 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr22:20922843 C>T maps to NM_001003891.1 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:871998 C>T maps to NM_005481.2 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:889761 C>T maps to NM_005481.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:868169 C>T maps to NM_005481.2 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:93545199 T>C maps to NM_004268.4 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr11:93529608 C>G maps to NM_004268.4 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:93530715 T>C maps to NM_004268.4 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:57472561 A>G maps to ENST00000431606 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr11:57472642 G>C maps to ENST00000431606 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:41884625 C>T maps to NM_004275.3 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:41884547 C>T maps to NM_004275.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:131914222 A>C maps to ENST00000403834 V1113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:131912628 A>G maps to ENST00000403834 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:131929184 G>C maps to ENST00000403834 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:131919757 G>C maps to ENST00000403834 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:131919552 T>G maps to ENST00000403834 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:131944544 A>G maps to ENST00000403834 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr6:131940973 G>T maps to ENST00000403834 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:38175814 G>A maps to NM_014815.3 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:38182434 C>T maps to NM_014815.3 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr17:38185182 C>A maps to NM_014815.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:38185221 C>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:50332235 G>T maps to NM_030973.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:50335365 G>A maps to NM_030973.3 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr19:16688409 C>T maps to NM_004831.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:16688382 C>T maps to NM_004831.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:16687473 C>T maps to NM_004831.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:16688493 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:134955186 G>A maps to NM_004269.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:17616360 G>A maps to NM_025205.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr8:118552169 C>T maps to NM_080651.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr17:6554833 G>T maps to NM_016060.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:6547900 C>T maps to NM_016060.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:6547975 G>A maps to NM_016060.2 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:48651316 A>G maps to NM_014166.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr14:71064346 A>T maps to ENST00000430055 L57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:156566346 G>T maps to NM_004270.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:156566376 C>T maps to NM_004270.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr17:17394652 G>A maps to NM_018019.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:17394784 C>T maps to NM_018019.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:100250897 C>T maps to ENST00000338042 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:88100420 G>A maps to NM_002397.4 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr5:88018546 G>A maps to NM_002397.4 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:156452227 C>T did not map to a codon.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr1:156446839 G>A maps to NM_005920.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr1:156437997 A>G maps to NM_005920.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:3299586 G>A maps to NM_000243.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr16:3293245 A>G maps to NM_000243.2 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr16:3304410 G>A maps to NM_000243.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:3306385 G>A maps to NM_000243.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:3304677 G>A maps to NM_000243.2 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:3304218 C>T maps to NM_000243.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:3306392 G>A maps to NM_000243.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:3304437 C>T maps to NM_000243.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:126746113 C>T maps to NM_032446.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:126783247 G>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:126776467 G>A maps to NM_032446.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:126746173 C>T maps to NM_032446.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:126754876 C>T maps to NM_032446.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr15:66416313 C>T maps to NM_032445.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:66206165 C>T maps to NM_032445.2 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr15:66262945 G>A maps to NM_032445.2 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:66416289 G>T maps to NM_032445.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:66273115 C>T maps to NM_032445.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr15:66209283 G>A maps to NM_032445.2 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:66191138 C>T maps to NM_032445.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:66222090 G>A maps to NM_032445.2 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:66249935 G>A maps to NM_032445.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:3431981 G>A maps to ENST00000452816 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:3424476 C>T maps to ENST00000452816 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr1:3427383 G>A maps to ENST00000452816 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:3425194 G>A maps to ENST00000452816 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:3425663 G>A maps to ENST00000452816 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:3428234 G>A maps to ENST00000452816 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:3410410 G>A maps to ENST00000452816 D1512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr1:3440795 G>T maps to ENST00000452816 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:3417774 G>A maps to ENST00000452816 C879C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:3428618 G>A maps to ENST00000452816 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:42880242 C>T maps to ENST00000251268 G2618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr19:42860251 C>T maps to ENST00000251268 I1470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:42862422 C>T maps to ENST00000251268 R1713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:42880470 C>T maps to ENST00000251268 S2694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:42861647 G>A maps to ENST00000251268 P1641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr19:42853691 G>A maps to ENST00000251268 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:42839278 C>T maps to ENST00000251268 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:42847701 T>C maps to ENST00000251268 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:42095565 G>A maps to NM_152513.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:42139161 G>A maps to NM_152513.3 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:42095613 C>T maps to NM_152513.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr10:15014612 C>T maps to NM_001080836.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr2:66796233 C>T maps to NM_002398.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:66667070 C>T maps to ENST00000407092 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:37184484 G>A maps to NM_170675.2 H441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:37184484 G>A maps to NM_170675.2 H441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:37388528 G>A maps to NM_170675.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:37390289 G>A maps to NM_170675.2 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:37375969 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:37390265 C>T maps to NM_170675.2 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr19:47912429 G>A maps to NM_020160.1 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:47910637 C>T maps to NM_020160.1 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:36589612 G>A maps to NM_014791.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:36589561 T>C maps to NM_014791.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:32094942 T>G maps to NM_015955.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:32093438 C>T maps to NM_015955.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr11:64575025 G>A maps to NM_130804.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:41719378 G>A maps to NM_004527.3 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr7:15652167 C>T maps to NM_005924.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:15725655 C>T maps to NM_005924.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:46803148 C>T maps to NM_005588.2 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:46803247 C>T maps to NM_005588.2 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:46800838 C>T maps to NM_005588.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:29788118 A>G maps to NM_005925.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:29790530 T>C maps to NM_005925.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr18:29793259 G>A maps to NM_005925.2 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:29797784 C>T maps to NM_005925.2 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:100028447 C>T maps to NM_019606.5 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:88766640 A>G maps to ENST00000395102 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:88766898 T>C maps to ENST00000395102 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:112733041 T>C maps to NM_006343.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:112686910 G>A maps to NM_006343.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr2:112786253 G>A maps to NM_006343.2 W938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:112767591 C>T maps to NM_006343.2 Y676Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:112705142 A>G maps to NM_006343.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:81295493 C>T maps to NM_022566.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:81282060 T>C maps to NM_015154.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:81271766 G>A maps to NM_015154.1 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr15:90320184 A>G maps to NM_001039958.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr7:130144837 C>T maps to NM_002402.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:116339389 C>T maps to NM_001127500.1 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:116339812 T>C maps to NM_001127500.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:116423355 A>G did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr7:116339155 G>T maps to NM_001127500.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr7:116397505 T>G maps to NM_001127500.1 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:116435767 C>T maps to NM_001127500.1 D1304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:116436021 G>A maps to NM_001127500.1 A1357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:116436096 G>A maps to NM_001127500.1 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:116339278 C>T maps to NM_001127500.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr7:116436060 G>A maps to NM_001127500.1 V1370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:116397717 G>A maps to NM_001127500.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:116381016 C>T maps to NM_001127500.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:116435961 C>A maps to NM_001127500.1 C1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:99960601 C>T maps to NM_015143.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:99960601 C>T maps to NM_015143.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:95887858 T>C maps to NM_006838.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:767233 C>T maps to NM_024042.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:81052064 G>A maps to NM_001004431.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:81052109 G>A maps to NM_001004431.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:2324090 G>C maps to NM_024086.3 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:2323875 T>C maps to NM_024086.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr17:2323551 C>T maps to NM_024086.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:2324150 T>G maps to NM_024086.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:2324129 G>A maps to NM_024086.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:132396541 G>A maps to NM_014064.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:171753043 G>A maps to NM_015935.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:171761376 T>C did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:171755118 T>C maps to NM_015935.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:171763605 G>A maps to NM_015935.4 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:119631198 A>G maps to NM_020961.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:60503763 C>T maps to NM_181725.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:60503711 C>T maps to NM_181725.3 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr14:21979359 C>T maps to NM_019852.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr18:2539061 C>T maps to NM_022840.3 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr18:2544688 G>A maps to NM_022840.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:2547406 C>A maps to NM_022840.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr12:56075988 C>T maps to NM_152637.2 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:21623994 C>T maps to NM_016025.3 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr16:21666561 G>T maps to NM_016025.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:156047021 G>A maps to NM_001093725.1 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:156046579 G>A maps to NM_001093725.1 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:156047099 G>A maps to NM_001093725.1 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:82336433 G>A maps to NM_032246.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:82336952 A>G maps to NM_032246.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:82336391 C>T maps to NM_032246.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:82336562 G>A maps to NM_032246.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr15:82335986 G>A maps to NM_032246.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr15:82336070 G>A maps to NM_032246.3 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:82335956 C>T maps to NM_032246.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:82335713 G>T maps to NM_032246.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:82335695 G>T maps to NM_032246.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:1556758 C>T maps to NM_001174118.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:1556728 G>A maps to NM_001174118.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:1556716 C>T maps to NM_001174118.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:1556758 C>T maps to NM_001174118.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:17303032 T>C maps to NM_017459.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:153432961 C>T maps to NM_005927.4 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:170912708 C>T maps to NM_021647.6 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr4:170913335 G>A maps to NM_021647.6 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:170912624 T>C maps to NM_021647.6 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr4:170912681 A>C maps to NM_021647.6 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr4:170913248 G>T maps to NM_021647.6 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:228195479 C>T maps to NM_020194.4 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:228220471 C>T maps to NM_020194.4 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:228211947 A>G maps to NM_020194.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:89453091 G>A maps to NM_005928.2 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:8654932 G>A maps to NM_004225.2 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:196736657 G>A maps to NM_005929.5 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:196736546 G>A maps to NM_005929.5 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:196746550 G>A maps to NM_033316.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:196748317 G>A maps to NM_005929.5 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:196748317 G>A maps to NM_005929.5 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:196735804 C>T maps to NM_005929.5 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:196737602 G>A maps to NM_005929.5 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:179085363 G>A maps to NM_033540.2 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:179066689 G>A maps to NM_033540.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:179095136 A>G maps to NM_033540.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:12061829 C>T maps to NM_014874.3 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:12067171 C>T maps to NM_014874.3 Y645Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr1:12062116 C>T maps to NM_014874.3 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:12065912 C>T maps to NM_014874.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:12065912 C>T maps to NM_014874.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr22:37872992 A>T maps to NM_002405.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:37870635 G>A maps to NM_002405.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr22:37876305 C>T maps to NM_002405.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:119213673 C>T maps to NM_031433.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:119217081 G>A maps to NM_031433.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:119212401 G>A maps to NM_031433.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:119216152 A>T maps to NM_031433.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:119214607 G>A maps to NM_031433.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:158520105 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:158538070 T>C maps to NM_022736.2 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:2933847 C>T maps to NM_001146069.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:2934850 C>T maps to NM_001146069.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:74737080 T>C maps to NM_024311.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr17:74740461 T>A maps to NM_024311.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:40430969 C>T maps to NM_001136493.1 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:40433329 C>T maps to NM_001136493.1 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:24247036 C>T maps to ENST00000338315 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:24247036 C>T maps to ENST00000338315 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr2:24240391 C>T maps to ENST00000338315 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:145735315 C>A maps to NM_138431.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:205548986 G>A maps to NM_181644.4 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:53647542 C>T maps to NM_001170790.1 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:191301045 A>G maps to NM_017694.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:191301591 T>G maps to NM_017694.3 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr17:8701292 G>A maps to NM_152599.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:8701550 C>T maps to NM_152599.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:8700836 C>T maps to NM_152599.3 W534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:8701913 G>A maps to NM_152599.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr17:8700938 G>A maps to NM_152599.3 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:8701010 C>A maps to NM_152599.3 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:8700710 A>G maps to NM_152599.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:8700926 A>G maps to NM_152599.3 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:677075 G>A maps to ENST00000404286 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:676597 C>T maps to ENST00000404286 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:677114 G>T maps to ENST00000404286 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:679629 C>T maps to ENST00000404286 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr4:680389 G>C maps to ENST00000404286 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:128878706 G>A maps to NM_152778.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:103334878 C>T maps to NM_032718.3 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:41988755 T>C maps to ENST00000219905 N516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:42028758 C>T maps to ENST00000219905 Q1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:42053966 C>T maps to ENST00000219905 Q2526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:42021439 C>T maps to ENST00000219905 R1246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr15:42003114 T>G maps to ENST00000219905 Y884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:42058412 G>A maps to ENST00000219905 V2760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:42057186 G>T maps to ENST00000219905 V2665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:42005390 C>T maps to ENST00000219905 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:141750600 A>G maps to ENST00000475668 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:141752696 C>T maps to ENST00000475668 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:141759708 C>T maps to ENST00000475668 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:141797430 C>T maps to ENST00000475668 R2578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:141805633 T>C maps to ENST00000475668 T2736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:141747668 G>A maps to ENST00000475668 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr7:141759273 T>C maps to ENST00000475668 D1274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:141747659 T>C maps to ENST00000475668 N858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:141754636 A>G maps to ENST00000475668 Q1081Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:141708378 C>T maps to ENST00000475668 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:141752212 C>A maps to ENST00000475668 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:141731568 A>G maps to ENST00000475668 Q520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:141795514 T>C did not map to a codon.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr7:141727495 G>A maps to ENST00000475668 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:141719018 C>T maps to ENST00000475668 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:180218990 C>T maps to NM_001114617.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:180219104 G>A maps to NM_001114617.1 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:180218921 C>T maps to NM_001114617.1 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:180219452 C>T maps to NM_001114617.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:180219399 C>T maps to NM_001114617.1 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:180218735 C>T maps to NM_001114617.1 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr5:180219899 C>G maps to NM_001114617.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr5:180218744 C>T maps to NM_001114617.1 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:50088552 A>G maps to NM_002408.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr22:39884326 C>T maps to NM_001098270.1 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr22:39884749 C>T maps to NM_001098270.1 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr22:39884755 G>A maps to NM_001098270.1 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr22:39883516 G>A maps to NM_001098270.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr22:39884755 G>A maps to NM_001098270.1 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:39884005 C>T maps to NM_001098270.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr22:39883370 A>T maps to NM_001098270.1 K7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:99294913 G>A maps to NM_012214.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:99260499 C>T maps to NM_012214.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr5:179229074 C>A maps to NM_054013.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:86373638 A>G maps to ENST00000393205 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:86373299 G>A maps to ENST00000393205 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:135102525 C>T maps to NM_002410.3 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:135095864 T>C maps to NM_002410.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:135095924 C>T maps to NM_002410.3 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:135206336 C>T maps to NM_002410.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:74936836 G>A maps to NM_198955.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:74942513 C>T maps to NM_198955.1 H644H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:74878308 C>T maps to NM_198955.1 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:74942477 C>T maps to NM_198955.1 Y632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr17:74922696 C>T maps to NM_198955.1 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr7:88423658 A>G maps to NM_152706.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:88424141 G>A maps to NM_152706.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:43280417 C>T maps to NM_153361.2 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:43280272 C>T maps to NM_153361.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr7:22534433 C>T maps to ENST00000441815 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:22532993 G>A maps to ENST00000441815 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:22533350 G>A maps to ENST00000441815 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:103553731 G>A maps to NM_012215.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:103560140 A>G maps to NM_012215.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:127441311 G>A maps to NM_007283.5 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:4731600 G>A maps to NM_015246.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:16516860 C>A maps to NM_145764.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:16516815 C>A maps to NM_145764.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:165623554 C>T maps to ENST00000367886 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:165624621 C>T maps to ENST00000367886 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:39722039 G>A maps to NM_054024.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:39716572 G>A maps to NM_054024.3 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:39716612 G>T maps to NM_054024.3 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:39716692 A>G maps to NM_054024.3 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:39717064 G>A maps to NM_054024.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:222832159 T>G maps to NM_198551.2 T1568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:222838879 G>A maps to NM_198551.2 P1881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr18:19418418 T>G maps to NM_020774.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr18:19427011 T>A maps to NM_020774.2 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:19418352 A>G maps to NM_020774.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr18:19383900 C>T maps to NM_020774.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:31378915 G>A maps to NM_000247.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr6:109775344 G>A maps to NM_022765.3 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:109771646 T>C maps to NM_022765.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:109770678 T>G maps to NM_022765.3 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:12237833 C>T maps to NM_014632.2 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:12241974 C>T maps to NM_014632.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:12245001 C>T maps to NM_014632.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:12225870 C>T maps to NM_014632.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:12225942 T>C maps to NM_014632.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:12281403 C>T maps to NM_014632.2 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:18310434 C>T maps to NM_015241.2 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:18363979 G>A maps to NM_001136004.1 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr22:18324715 G>A maps to NM_015241.2 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:18379716 G>A maps to NM_015241.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr22:18300776 C>T maps to NM_015241.2 W1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:18301232 C>T maps to NM_015241.2 P1398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:12315407 C>T maps to NM_032867.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr11:12345545 A>C maps to NM_032867.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:12316003 C>A maps to NM_032867.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr22:38322051 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:1484709 C>T maps to NM_182924.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:1479612 G>A maps to NM_182924.3 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:1484997 G>A maps to NM_182924.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr7:1484295 C>T maps to NM_182924.3 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:1484823 C>T maps to NM_182924.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:31473918 G>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:31474170 C>T maps to NM_005931.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:10535113 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:10437779 G>A did not map to a codon.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr23:10450559 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:10437742 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:10427834 G>A did not map to a codon.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr23:10535578 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:10534990 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:10427779 G>A did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:10535200 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:10535363 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:38664475 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:38664470 A>G did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr23:38664501 C>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:107148790 T>C did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr23:107084450 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:107169388 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:107167579 T>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:107147195 T>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:107084613 A>C did not map to a codon.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr23:107167698 G>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:1257207 C>T maps to NM_177401.4 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:1254308 T>C maps to NM_177401.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr19:1257093 G>C maps to NM_177401.4 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:67411923 A>G maps to NM_001077700.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:327208 C>T maps to NM_017550.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr19:334462 G>A maps to NM_017550.1 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:56219146 G>T maps to ENST00000381226 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:56219755 A>G maps to ENST00000381226 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:56231564 A>G maps to ENST00000381226 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:12081866 G>A maps to NM_021933.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr1:12091804 G>A maps to NM_021933.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:12091855 G>A maps to NM_021933.2 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:12091810 G>A maps to NM_021933.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr17:4794767 G>A maps to NM_153827.4 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:4796055 C>T maps to NM_153827.4 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:4787719 C>T maps to NM_153827.4 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4796589 C>T maps to NM_170663.4 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4797866 G>A maps to NM_153827.4 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:89272953 T>C maps to NM_004897.4 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:89265088 G>A maps to NM_004897.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:7612321 T>C maps to NM_019005.3 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:7636048 G>A maps to NM_019005.3 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:7612651 A>G maps to NM_019005.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:50928040 C>T maps to NM_017584.5 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:50928212 G>A maps to NM_017584.5 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:50927725 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:56847527 C>T maps to NM_012064.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr12:56847485 C>T maps to NM_012064.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:56847485 C>T maps to NM_012064.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:24415536 C>A maps to NM_005932.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:37736308 G>A maps to NM_001195296.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:37737949 A>C maps to NM_001195296.1 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr14:37838736 C>T maps to NM_001195296.1 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr14:37969169 T>C maps to NM_001195296.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:99786045 A>T maps to NM_138798.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:69998212 G>A maps to ENST00000448226 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:226413383 T>C maps to NM_031944.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr10:129905498 G>C maps to NM_002417.4 G1535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:129901496 C>T maps to NM_002417.4 T2869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:129901517 T>C maps to NM_002417.4 T2862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:129907157 G>A maps to NM_002417.4 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:129901619 T>C maps to NM_002417.4 S2828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:129902378 T>C maps to NM_002417.4 S2575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr10:129908756 C>T maps to NM_002417.4 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:129906398 A>G maps to NM_002417.4 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:129902695 C>A maps to NM_002417.4 E2470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:129907237 G>A maps to NM_002417.4 Q956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:129913861 G>A maps to NM_002417.4 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:129905282 G>A maps to NM_002417.4 N1607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr10:129902576 C>T maps to NM_002417.4 T2509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr10:129913473 G>A maps to NM_002417.4 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr20:10389281 C>T maps to NM_170784.1 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:40807696 A>G maps to NM_020831.3 H831H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:40827406 A>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr22:40814584 C>T maps to NM_020831.3 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:40819671 C>T maps to NM_020831.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:40814986 C>T maps to NM_020831.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:40815357 G>A maps to NM_020831.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr22:40814950 G>C maps to NM_020831.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr22:40831517 G>A maps to NM_020831.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:40859225 C>T maps to NM_020831.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:14312821 G>A maps to NM_014048.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:131113828 A>G maps to NM_013255.4 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr7:131151137 T>G maps to NM_013255.4 L631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:131122563 G>A maps to NM_013255.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:47030769 A>G maps to NM_003684.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:2046620 G>A maps to NM_199054.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr19:2043499 A>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:2046390 G>A maps to NM_199054.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:2041037 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:140158905 G>A maps to NM_013446.3 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:140156540 G>A maps to NM_013446.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:140158983 T>C maps to NM_013446.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:140155023 C>T maps to NM_013446.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:140159028 C>T maps to NM_013446.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:12611710 C>T maps to NM_014160.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:12610388 T>C maps to NM_014160.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr15:23811828 G>A maps to NM_005664.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr15:23811447 G>A maps to NM_005664.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr15:23811375 C>T maps to NM_005664.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr15:23812251 C>T maps to NM_005664.3 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:56288384 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:28024159 T>C maps to NM_173576.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:28030414 C>G maps to NM_173576.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr22:50515883 C>T maps to NM_015166.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr12:121125251 G>A maps to NM_014730.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:158310240 C>T maps to NM_001195432.1 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr3:158315948 G>A maps to NM_001195432.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:158314733 C>T maps to NM_001195432.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:158320654 C>T maps to NM_001195432.1 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:185637661 C>T maps to NM_024629.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:185652121 G>A maps to NM_024629.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:6859438 G>T maps to NM_005439.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:37048545 C>T maps to NM_000249.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:37090085 C>T maps to NM_000249.3 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:37090085 C>T maps to NM_000249.3 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:37045890 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:75513922 A>G maps to NM_001040108.1 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:75514684 A>C maps to NM_001040108.1 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:74729298 C>T maps to NM_152649.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:74729204 G>A maps to NM_152649.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:118376656 A>G maps to NM_001197104.1 Q3350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:118343827 C>T maps to NM_001197104.1 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:118374701 C>T maps to NM_001197104.1 R2699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:118374595 A>G maps to NM_001197104.1 S2663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr11:118343718 G>A maps to NM_001197104.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:118359441 T>C maps to NM_001197104.1 C1482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:118374581 C>T maps to NM_001197104.1 R2659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:118375925 T>C maps to NM_001197104.1 L3107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:118343988 T>C maps to NM_001197104.1 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:118374688 A>G maps to NM_001197104.1 S2694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:118343853 C>T maps to NM_001197104.1 D660D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:118352502 C>T maps to NM_001197104.1 N1236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118344801 C>T maps to NM_001197104.1 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118360944 C>T maps to NM_001197104.1 C1559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr11:118352736 G>A maps to NM_001197104.1 P1314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:49445986 G>A maps to NM_003482.3 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:49424717 G>A maps to NM_003482.3 D4543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:49435306 G>A maps to NM_003482.3 S2082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr12:49433848 G>A maps to NM_003482.3 P2568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr12:49424061 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:49444687 C>T maps to NM_003482.3 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:49421038 G>A maps to NM_003482.3 R4904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:49420205 C>A maps to NM_003482.3 G5181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr12:49425037 G>A maps to NM_003482.3 R4484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr12:49445716 A>C maps to NM_003482.3 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:49426525 G>A maps to NM_003482.3 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:49434349 G>A maps to NM_003482.3 R2401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:49434799 C>T maps to NM_003482.3 S2251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr12:49438224 C>A maps to NM_003482.3 E1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:49435087 C>T maps to NM_003482.3 S2155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:49447830 G>A maps to NM_003482.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:49436572 G>A maps to NM_003482.3 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr12:49424533 G>A maps to NM_003482.3 P4563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr12:49416539 G>A maps to NM_003482.3 L5391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr12:49427329 G>A maps to NM_003482.3 Q3720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr12:49425037 G>A maps to NM_003482.3 R4484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:49415897 G>A maps to NM_003482.3 A5483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:49438623 G>A maps to NM_003482.3 G1622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:49440498 G>A maps to NM_003482.3 S1437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:49443626 A>G maps to NM_003482.3 V1248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:151873335 G>A maps to ENST00000355193 Q3068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:151878748 G>A maps to ENST00000355193 R2066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:151878748 G>A maps to ENST00000355193 R2066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:151917680 G>A maps to ENST00000355193 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:151874712 G>A maps to ENST00000355193 R2609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:152027708 A>G maps to ENST00000355193 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:151917680 G>A maps to ENST00000355193 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr7:151878862 G>A maps to ENST00000355193 R2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr7:151893049 T>C maps to ENST00000355193 T1440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:151860313 G>A maps to ENST00000355193 Q3450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:151891594 A>G maps to ENST00000355193 S1479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr7:151859926 C>A maps to ENST00000355193 G3579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:151880165 G>A maps to ENST00000355193 Q1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:151866268 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr7:151927303 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:151970828 G>A maps to ENST00000355193 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:152007083 G>A maps to ENST00000355193 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr7:151884816 G>A maps to ENST00000355193 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:151879152 G>T maps to ENST00000355193 S1931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:151874709 G>A maps to ENST00000355193 R2610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:151841795 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:36212537 G>A maps to NM_014727.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:36223275 C>A maps to NM_014727.1 P1942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:36211881 C>T maps to NM_014727.1 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:36221487 C>T maps to NM_014727.1 C1749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:36223563 T>C maps to NM_014727.1 P2038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:36216188 C>T maps to NM_014727.1 G1199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr19:36218477 C>T maps to NM_014727.1 G1419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:36211208 C>A maps to NM_014727.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:36223431 G>A maps to NM_014727.1 A1994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr19:36214855 C>T maps to NM_014727.1 D1094D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:36221295 C>T maps to NM_014727.1 F1710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr19:36216526 G>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:36215888 G>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:36214077 C>T maps to NM_014727.1 H968H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:36229427 C>T maps to NM_014727.1 G2706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:36218422 G>A maps to NM_014727.1 W1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:36228110 G>A maps to NM_014727.1 Q2499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr19:36222960 C>T maps to NM_014727.1 R1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:36211137 C>T maps to NM_014727.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:104747107 G>A maps to NM_182931.2 T912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:104753200 G>A maps to NM_182931.2 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:104753083 C>A maps to NM_182931.2 P1627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:104707255 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:6216429 C>T maps to NM_005934.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:6222212 G>A maps to NM_005934.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:6230718 C>T maps to NM_005934.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:21959609 C>G maps to NM_004641.3 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:22022454 C>T maps to NM_004641.3 N826N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr1:151039753 C>A maps to NM_006818.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr9:20346482 G>A maps to NM_004529.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:20414330 G>A maps to NM_004529.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:20414369 G>A maps to NM_004529.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:20414300 G>A maps to NM_004529.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:20413988 C>T maps to NM_004529.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr9:20414330 G>A maps to NM_004529.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr6:168349017 C>T maps to ENST00000400822 Q1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:168265374 C>T maps to ENST00000400822 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:168352422 C>T maps to ENST00000400822 P1455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:168273010 C>T maps to ENST00000400822 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:168325764 A>G maps to ENST00000400822 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:168314925 C>T maps to ENST00000400822 R705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:36869017 G>A maps to NM_005937.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:36865785 C>T maps to NM_005937.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:36864112 T>C maps to NM_005937.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:36880977 C>T maps to NM_005937.3 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:36872881 G>A maps to NM_005937.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr17:36881036 G>A maps to NM_005937.3 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr17:36876053 C>T maps to NM_005937.3 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:49795006 C>T maps to NM_001507.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr13:49795273 C>T maps to NM_001507.1 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:238419297 C>T maps to NM_024101.5 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:2258498 G>A maps to NM_022372.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:2256621 G>A maps to NM_022372.4 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:2257279 C>T maps to NM_022372.4 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr17:40721265 G>A maps to NM_170607.2 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr12:122618124 C>T maps to NM_014938.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr12:122617977 T>G maps to NM_014938.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:122618496 C>T maps to NM_014938.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:73030507 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:73012007 G>A maps to NM_032951.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:83948955 C>T maps to NM_012213.2 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:83948685 G>A maps to NM_012213.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:146560419 G>A maps to NM_172250.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:109998867 G>A maps to NM_052845.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:110006572 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:150426630 G>A maps to NM_015702.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:53488652 T>C maps to NM_012329.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:53491523 A>G maps to NM_012329.2 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:53478859 T>A maps to NM_012329.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:4949601 G>A maps to NM_001100600.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:4947140 G>A maps to NM_001100600.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr3:154886413 C>T maps to NM_007289.2 H638H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr3:154802081 T>A maps to NM_007289.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:154862167 G>A maps to NM_007289.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:2526292 G>A maps to NM_033467.3 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:135047267 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135047291 C>T did not map to a codon.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr23:135049607 A>G did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:135049601 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:102650092 C>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr22:24122767 G>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:102742327 T>C maps to ENST00000326227 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:102738723 G>A maps to ENST00000326227 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:23315097 C>T maps to NM_004995.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6710-01A-11D-1882-08 chr14:23315133 C>A maps to NM_004995.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:23313027 C>T maps to NM_004995.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:23314567 C>T maps to NM_004995.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:23313911 A>G maps to NM_004995.2 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:23315088 C>T maps to NM_004995.2 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:58077493 T>C maps to NM_002428.2 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:58073832 C>T maps to NM_002428.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:58071452 C>A maps to NM_002428.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:58077213 G>A maps to NM_002428.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:89086857 G>A maps to NM_005941.4 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:89198805 G>A maps to NM_005941.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr8:89081739 G>A maps to ENST00000286611 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr8:89053874 T>A maps to NM_005941.4 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:132329950 C>T maps to NM_016155.4 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:132334581 C>T maps to NM_016155.4 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr12:132325351 C>T maps to NM_016155.4 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:132329674 C>T maps to NM_016155.4 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr12:132325375 C>T maps to NM_016155.4 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:132334515 G>A maps to NM_016155.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr12:56231057 G>T maps to NM_002429.4 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr16:55532321 C>T maps to NM_004530.4 N577N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:55518002 C>T maps to NM_004530.4 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:55513507 C>T maps to NM_004530.4 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:55519217 C>T maps to NM_004530.4 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:55525755 C>T maps to NM_004530.4 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr16:55516873 G>C maps to NM_004530.4 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:55518027 C>T maps to NM_004530.4 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:55522590 C>T maps to NM_004530.4 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:55519615 C>T maps to NM_004530.4 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr16:55513516 C>T maps to NM_004530.4 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr16:55523719 C>A maps to NM_004530.4 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:55516933 T>C maps to NM_004530.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:55513486 G>A maps to NM_004530.4 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr16:55522476 C>T maps to NM_004530.4 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:102482513 C>T maps to NM_004771.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr11:102496026 G>A maps to NM_004771.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr11:102482555 G>A maps to NM_004771.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr10:127461230 G>A maps to NM_147191.1 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:127462526 G>A maps to NM_147191.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:127462427 C>T maps to NM_147191.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr20:33842534 G>A maps to NM_006690.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:33862183 C>T maps to NM_006690.3 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr20:33862270 C>T maps to NM_006690.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr20:33842555 C>T maps to NM_006690.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:33851678 G>A maps to NM_006690.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:3100296 C>T maps to NM_022468.4 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr16:3100527 C>G maps to NM_022468.4 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:5012628 G>A maps to NM_021801.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr11:102563732 C>T maps to NM_022122.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:102567156 A>G maps to NM_022122.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:34106042 G>T maps to NM_024302.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:34095246 A>G did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:34100367 C>T maps to NM_024302.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:34105988 T>C maps to NM_024302.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr11:102713533 C>T maps to NM_002422.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr11:102395754 C>T maps to NM_002423.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:102585435 G>A maps to NM_002424.2 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:44639208 G>A maps to NM_004994.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:44639238 C>T maps to NM_004994.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:44644922 G>A maps to NM_004994.2 W680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr20:44639955 G>A did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr20:44642406 G>A maps to NM_004994.2 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:44641174 G>C maps to NM_004994.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:44642367 C>T maps to NM_004994.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:90856258 G>A maps to NM_007351.2 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:90849012 G>A maps to NM_007351.2 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:90816211 T>C maps to NM_007351.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr4:90816172 C>T maps to NM_007351.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:88703010 G>A maps to NM_024756.2 D510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:88703004 C>T maps to NM_024756.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:88703231 G>A maps to NM_024756.2 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:88705403 T>C maps to NM_024756.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:88717265 G>C maps to NM_024756.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:88702971 G>A maps to NM_024756.2 D523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:88703214 C>T maps to NM_024756.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:88702425 G>A maps to NM_024756.2 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:99223672 A>C maps to ENST00000422291 Y639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:28193408 C>T maps to NM_002430.2 V1041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:28195358 G>A maps to NM_002430.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:28194197 G>A maps to NM_002430.2 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr22:28193747 C>T maps to NM_002430.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr22:28193117 C>T maps to NM_002430.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:28194944 C>T maps to NM_002430.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:28193534 C>T maps to NM_002430.2 T999T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr1:158815415 A>C maps to NM_002432.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:158813828 G>T maps to NM_002432.1 G163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:56748710 T>C maps to NM_018365.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:2298236 C>T maps to NM_020310.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:156798300 G>A maps to NM_005515.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:1491524 G>A maps to NM_001172223.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr4:71844992 T>C maps to ENST00000396051 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:2078214 C>T maps to NM_130807.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:47078720 G>A maps to NM_145279.4 A143A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8687-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:47078942 C>T maps to NM_145279.4 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:198415088 G>A maps to NM_015387.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:198405142 T>C maps to NM_015387.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:198405142 T>A maps to NM_015387.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:33800025 G>A maps to NM_017947.2 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:33785067 C>A maps to NM_017947.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:33848582 T>C maps to NM_017947.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:33779930 G>A maps to NM_017947.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:33795822 C>T maps to NM_017947.2 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:33780188 G>A maps to NM_017947.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:39881118 C>T maps to ENST00000425303 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:39895296 G>T maps to ENST00000425303 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr6:39902072 G>T maps to ENST00000340692 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:49575693 C>T maps to NM_014484.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:49576278 C>T maps to NM_014484.3 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:49576678 T>C maps to NM_014484.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:49576278 C>T maps to NM_014484.3 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:49575846 G>A maps to NM_014484.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:49575759 G>A maps to NM_014484.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:223553066 G>A maps to NM_058165.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:75438571 G>A maps to NM_025098.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:75439012 A>C did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr7:100844060 G>A maps to NM_178176.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr7:100842084 C>T maps to NM_178176.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr7:100843710 C>G maps to NM_178176.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:74689114 G>A maps to NM_006302.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:74688479 G>A maps to NM_006302.2 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:74688755 G>A maps to NM_006302.2 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:49947985 C>T maps to NM_032355.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr3:49949400 G>A maps to NM_032355.3 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:77228319 G>A maps to NM_014940.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:77227597 G>A maps to NM_014940.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:77227570 G>A maps to NM_014940.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr16:77225411 G>A maps to NM_014940.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:62979233 T>C maps to ENST00000393630 H1621H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:62926341 G>T maps to ENST00000393630 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr12:62954268 A>T maps to ENST00000261188 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:62902071 G>T maps to ENST00000393630 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:62949835 T>C maps to ENST00000393630 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:62959810 G>A maps to ENST00000393630 P1399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr3:108677898 A>G maps to NM_014429.3 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr22:31345745 C>A maps to ENST00000397641 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr21:37710203 G>A maps to ENST00000290384 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:37741864 A>G maps to ENST00000290384 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr21:37741741 A>G maps to ENST00000290384 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr21:37709256 C>T maps to ENST00000290384 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:106185214 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:106185903 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:106236536 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:106184842 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:106185766 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:106236505 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr23:106199759 G>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:79170559 C>T maps to NM_206839.1 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr15:79186546 A>G maps to NM_206839.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:102931577 A>C did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:102931371 C>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:2303935 G>A maps to NM_024848.1 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:2290119 G>A maps to NM_024848.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:122107245 G>A maps to NM_173855.4 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:122097144 T>C maps to NM_173855.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:122107284 G>A maps to NM_173855.4 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:99377011 A>G maps to NM_001098831.1 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:124936901 C>T maps to NM_198469.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:124929124 C>T maps to NM_198469.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:124936901 C>T maps to NM_198469.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:57025620 C>T maps to NM_005372.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr8:57026166 C>T maps to NM_005372.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:57026166 C>T maps to NM_005372.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr8:57025797 C>A maps to NM_005372.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:57026082 G>A maps to NM_005372.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:220978446 T>C maps to NM_022746.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:134025639 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:134025601 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:14933800 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:14927023 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:14913458 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:14910987 A>C did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr1:113241042 G>A maps to NM_020963.3 K817K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:113240931 C>T maps to NM_020963.3 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:113241374 G>A maps to NM_020963.3 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:113239361 C>T maps to NM_020963.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:50530568 A>G maps to NM_018995.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr22:50582603 C>T maps to NM_018995.2 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:50563915 C>T maps to NM_018995.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:50591565 G>A maps to NM_018995.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:50528909 G>A maps to NM_001164105.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:50537978 C>T maps to NM_018995.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:132618384 C>T maps to NM_015529.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:132636880 T>C maps to NM_015529.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:132695859 A>G maps to NM_015529.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr6:132618967 T>C maps to NM_015529.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:13107092 G>A maps to ENST00000319217 D2028D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:13221385 T>C maps to ENST00000319217 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:13143470 G>A maps to ENST00000319217 A1278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:13190238 C>T maps to ENST00000319217 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:13168534 G>T maps to ENST00000319217 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:13188821 C>T maps to ENST00000319217 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:13176311 C>T maps to ENST00000319217 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:58979084 C>T maps to NM_001039396.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:58979453 A>G maps to NM_001039396.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr11:58979597 G>C maps to NM_001039396.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr11:58979846 A>C maps to NM_001039396.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr16:129485 G>A maps to NM_002434.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:71377060 A>G maps to NM_005791.2 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:71368363 T>G maps to NM_005791.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:71361860 A>G maps to NM_005791.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:82182416 G>A maps to NM_005792.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:20240590 C>T maps to ENST00000414242 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr13:20235929 C>T maps to ENST00000414242 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:20216316 C>T maps to ENST00000414242 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:123649914 C>A maps to NM_022782.2 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:43805795 A>C maps to NM_005373.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:43805155 A>G maps to NM_005373.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:43805672 C>A maps to NM_005373.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr17:56350796 G>A maps to ENST00000340482 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:56355356 G>A maps to ENST00000340482 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:56348169 G>T maps to ENST00000340482 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:154009925 C>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:154020456 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:154020487 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:154020079 C>T did not map to a codon.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr17:41959870 C>T maps to NM_005374.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr17:41955297 G>A maps to NM_005374.3 Y512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:41891391 G>A maps to ENST00000398393 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:41891391 G>A maps to ENST00000398393 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:41891580 G>A maps to ENST00000398393 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:41907102 C>T maps to ENST00000398393 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:41907448 G>A maps to ENST00000398393 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr17:41907135 C>T maps to ENST00000398393 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:41898339 C>T maps to ENST00000398393 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr17:41907403 C>T maps to ENST00000398393 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:41909259 C>T maps to ENST00000398393 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:202547562 G>A maps to NM_033066.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:202549796 C>T maps to NM_033066.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr2:202558644 T>G maps to NM_033066.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr14:67790528 G>A maps to NM_022474.2 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:24690172 C>T maps to ENST00000409253 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:28358713 G>A maps to NM_173496.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:28420596 A>G maps to NM_173496.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr10:28378672 G>A maps to NM_173496.3 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr10:28348657 T>A maps to NM_173496.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:28358699 C>T did not map to a codon.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr10:28420611 G>C maps to NM_173496.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:28345527 C>A maps to NM_173496.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:11884614 C>T maps to ENST00000344987 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr22:43831010 C>T maps to NM_001044370.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:30601839 C>T maps to NM_001584.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:17046080 T>C did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:17030056 C>T maps to NM_015134.2 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr16:15501818 A>G maps to NM_001128423.1 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:15501833 C>T maps to NM_001128423.1 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:18304192 C>A maps to NM_032683.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:118133654 A>G maps to NM_144765.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:118110973 A>T maps to NM_198275.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:118122994 T>G maps to NM_198275.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:118123002 G>A maps to NM_198275.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:181021587 C>T maps to NM_001531.2 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:181022772 G>T maps to NM_001531.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:181022742 C>G maps to NM_001531.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:181018257 G>A maps to NM_001531.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:33686876 A>G maps to NM_206898.1 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr6:84798908 C>T maps to NM_138409.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:138116241 C>T maps to NM_001085049.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:18138556 T>C maps to NM_002438.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:60743599 C>T maps to NM_006039.3 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:60767424 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:60741966 C>T maps to NM_006039.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:60757800 C>T maps to NM_006039.3 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr17:60742113 C>T maps to NM_006039.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr17:60765988 C>G maps to NM_006039.3 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:60742221 T>C maps to NM_006039.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:60759275 C>T maps to NM_006039.3 C927C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:60765720 G>A maps to NM_006039.3 Q1006Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:60767090 G>A maps to NM_006039.3 T1181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:60743867 C>T maps to NM_006039.3 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr17:60757797 C>T maps to NM_006039.3 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:60765666 C>T maps to NM_006039.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr17:60744154 C>G maps to NM_006039.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:94200986 G>A maps to NM_005591.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:94180538 A>G maps to NM_005591.3 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:216810364 A>G maps to NM_018000.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:216809617 C>A maps to NM_018000.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:216809668 G>A maps to NM_018000.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:216809612 C>T maps to NM_018000.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:216811831 C>T maps to NM_018000.2 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:216809714 A>G maps to NM_018000.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:216810376 G>A maps to NM_018000.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:68748125 T>C maps to NM_198923.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:68747522 C>T maps to NM_198923.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:3249825 C>T maps to ENST00000328215 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:3249354 G>A maps to ENST00000328215 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr11:3249927 G>A maps to ENST00000328215 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:3249837 G>A maps to ENST00000328215 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:3249855 G>A maps to ENST00000328215 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr11:68772960 C>A maps to NM_145015.4 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:18955509 G>A maps to NM_147199.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:18955383 C>T maps to NM_147199.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:18955404 A>G maps to NM_147199.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr11:18956196 G>A maps to NM_147199.3 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:19077583 G>A maps to NM_054030.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:18158907 C>A maps to NM_054031.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:18159639 C>T maps to NM_054031.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:18158958 G>A maps to NM_054031.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:18195606 C>T maps to NM_054032.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:18195720 G>C maps to NM_054032.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr11:18194814 C>T maps to NM_054032.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr11:18194988 C>T maps to NM_054032.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr11:18195432 G>A maps to NM_054032.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr11:18195399 G>A maps to NM_054032.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:13883013 C>A maps to NM_001031727.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:34964140 G>A maps to NM_024864.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr17:34958745 C>T maps to NM_024864.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:48331613 A>C maps to NM_001127176.1 T127T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-5721-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:79671730 T>A maps to NM_002949.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:79674254 C>T maps to NM_002949.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:160219094 A>T maps to NM_014161.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:75882353 T>C maps to NM_014763.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:43024151 G>A maps to NM_015950.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:43023643 G>A maps to NM_015950.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:43024070 A>C maps to NM_015950.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:43022173 A>G maps to NM_015950.3 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:68663993 G>A maps to NM_181514.1 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:419174 G>A maps to NM_006428.4 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:42972065 G>A maps to NM_031903.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:27997344 C>A maps to NM_004891.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:86433346 T>C maps to NM_016622.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr5:1798959 T>C maps to NM_032479.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:1798782 G>A maps to NM_032479.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr5:1798959 T>C maps to NM_032479.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:54666206 G>A maps to NM_016491.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:54671060 G>A maps to NM_016491.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:73895601 T>C maps to NM_032478.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:73897972 G>A maps to NM_032478.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr21:26979746 C>T maps to NM_080794.3 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:10368988 C>T maps to NM_146387.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr9:140446796 C>T maps to NM_032477.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr15:89008086 G>A maps to NM_022163.3 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:73555943 T>C maps to NM_016055.5 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:104160780 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:228294489 G>A maps to NM_181462.2 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:151733318 C>T maps to NM_031420.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr6:42185575 C>T maps to NM_018141.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:42176059 T>C maps to NM_018141.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:89020276 G>T maps to NM_022839.3 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:89010974 G>A maps to NM_022839.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:89020236 C>T maps to NM_022839.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr1:36921445 C>G maps to NM_031280.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr1:36929864 G>A maps to NM_031280.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:36921834 G>A maps to NM_031280.3 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:30587522 T>C maps to NM_014046.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:30590655 C>A maps to NM_014046.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr6:30587355 C>A maps to NM_014046.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:30593483 C>T maps to NM_014046.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:138395606 C>T maps to NM_016034.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr9:138395576 C>T maps to NM_016034.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:138395645 G>A maps to NM_016034.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:138395798 C>T maps to NM_016034.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:138395681 G>A maps to NM_016034.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:138393759 C>A maps to NM_016034.3 S80S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4184-01A-01D-1126-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-8361-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:55917297 T>C did not map to a codon.
Multiple mappings detected for codon TCGA-CG-5721-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:71524105 G>A maps to ENST00000513900 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:44811196 C>T maps to NM_016640.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr5:44809567 G>A maps to NM_016640.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:44811249 C>T maps to NM_016640.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr5:44809102 T>G maps to NM_016640.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:41323297 C>A maps to NM_005830.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:95766225 T>C maps to NM_031902.3 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:105713759 C>T maps to NM_182640.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:24418357 C>T maps to NM_020662.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:24412565 C>T maps to NM_020662.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:24403465 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:24403378 C>T maps to NM_020662.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr11:10673688 G>A maps to NM_001098579.1 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:10622465 A>T maps to NM_001098579.1 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:60231792 G>A maps to NM_152866.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:60559760 G>A maps to NM_206893.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr11:60565921 G>A maps to NM_206893.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr11:60559760 G>A maps to NM_206893.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr11:60558490 C>A maps to NM_206893.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:60274593 A>G maps to NM_017716.2 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr11:60274542 G>A maps to NM_017716.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:60296881 T>G maps to NM_001012417.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:60309994 C>T maps to NM_001012417.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr11:60285671 T>A maps to NM_001012417.2 L39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr11:60292678 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:60183916 C>A maps to NM_032597.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr11:60183028 T>C maps to NM_032597.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:60183280 A>G maps to NM_032597.3 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr11:60184012 C>T maps to NM_032597.3 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr11:60531283 G>A maps to NM_001098835.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:60531250 G>A maps to NM_001098835.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr11:60064784 G>A maps to NM_148975.1 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:60105315 C>T maps to NM_139249.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:60152694 T>C maps to NM_206939.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:72756092 C>T maps to NM_005098.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:72756293 C>T maps to NM_005098.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:72756074 G>A maps to NM_005098.3 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:72755897 G>A maps to NM_005098.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:17998309 C>T maps to NM_001105569.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr2:17998330 T>C maps to NM_001105569.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:17997958 T>G maps to NM_001105569.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:17998036 C>T maps to NM_001105569.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:17997940 G>A maps to NM_001105569.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:47705413 T>C maps to NM_000251.1 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:47641557 G>T did not map to a codon.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr2:47657027 T>G maps to NM_000251.1 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:80074640 G>A maps to NM_002439.3 W807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:80064740 C>T maps to NM_002439.3 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr5:79968172 A>T maps to NM_002439.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr1:76282160 G>T maps to NM_002440.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:31715179 C>A maps to ENST00000375742 C278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr6:31729611 G>A maps to ENST00000375742 E750E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:48026078 G>A maps to NM_000179.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:48026003 C>T maps to NM_000179.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr12:120784003 C>T maps to NM_002442.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr12:120784018 C>T maps to NM_002442.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr17:55334406 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr17:38282660 T>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:135870698 G>A maps to NM_018133.3 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:135870723 C>T maps to NM_018133.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:135870111 A>G maps to NM_018133.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr3:135870293 G>A maps to NM_018133.3 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr3:135871485 A>C maps to NM_018133.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:135870303 A>G maps to NM_018133.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:135871068 A>G maps to NM_018133.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr3:135870264 G>A maps to NM_018133.3 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:11783633 G>A did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr23:11786715 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:11778980 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:11778981 G>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:11779010 T>A did not map to a codon.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:11778527 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:11778585 C>T did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:11793169 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr23:11783876 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:234774826 C>T did not map to a codon.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr2:234775773 T>C did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:234774908 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr2:234775301 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr2:234775379 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:234774983 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:816648 T>C maps to NM_013404.4 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr16:815535 G>A maps to NM_013404.4 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr16:820287 G>A maps to NM_001025190.1 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:823248 G>A maps to NM_001025190.1 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:825479 C>T maps to NM_001025190.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr16:830766 G>A maps to NM_001025190.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:820110 C>G maps to NM_001025190.1 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:64951828 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:64957056 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:64887721 T>C did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:64947738 G>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:64959698 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:64936688 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr23:64957070 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:64949376 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:64959041 C>A did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr23:64949467 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:64955209 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr23:64949404 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr23:64936750 G>C did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:16026025 G>A maps to ENST00000445506 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:16026125 C>A maps to ENST00000445506 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:15978089 G>A maps to ENST00000445506 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:15978020 G>A maps to ENST00000445506 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:16007761 G>A maps to ENST00000445506 L337L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HF-7134-01A-11D-2053-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:15967674 A>G maps to ENST00000445506 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr8:16012653 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr8:16032693 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:15967635 G>T maps to ENST00000445506 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:10285671 C>T maps to NM_012331.3 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:10102701 T>G maps to NM_012331.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:65857047 C>T maps to NM_001031679.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:49724648 A>G maps to NM_020998.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr3:49722747 G>A maps to NM_020998.3 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:49723510 G>A maps to NM_020998.3 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HB-01A-12D-A25D-08 chr3:49723791 G>A maps to NM_020998.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:49721622 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:49929014 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:49936359 C>T maps to NM_002447.2 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:49936320 T>C maps to NM_002447.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr23:131208167 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:4864431 G>A maps to NM_002448.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr4:4864503 G>A maps to NM_002448.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:4864503 G>A maps to NM_002448.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:4864563 C>T maps to NM_002448.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:174156183 C>T maps to NM_002449.4 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr5:174156282 C>T maps to NM_002449.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:56693074 G>A maps to ENST00000394501 *63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr16:56700799 G>A maps to ENST00000379811 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:105927256 T>C maps to NM_004689.3 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:105930458 T>C maps to NM_004689.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:62361870 C>T maps to NM_004739.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:62362465 G>A maps to NM_004739.2 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr11:62365104 G>A maps to NM_004739.2 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:62361348 A>T maps to NM_004739.2 *669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:62362898 G>A maps to NM_004739.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr9:21854739 C>T maps to NM_002451.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:121466146 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:121463541 G>A maps to NM_022045.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:121514816 G>A maps to NM_022045.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr8:121500556 G>T maps to NM_022045.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:36946376 G>A maps to ENST00000373627 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:36946331 G>T maps to ENST00000373627 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:47656235 G>A maps to NM_014342.3 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:47640458 G>A maps to NM_014342.3 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:91503255 A>G maps to NM_006980.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:97270798 G>A maps to NM_015942.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:97251914 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:242039192 G>T maps to NM_182501.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr2:242035430 G>A maps to NM_182501.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:38304331 C>T maps to NM_005955.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:38281017 G>A maps to NM_005955.2 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:38304324 G>A maps to NM_005955.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:38305653 C>T maps to NM_005955.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr1:38323054 A>C maps to NM_005955.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:93581091 C>A maps to NM_007358.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:93599727 C>A maps to NM_007358.3 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:93583920 C>T maps to NM_007358.3 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:65308851 A>G maps to NM_139242.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr15:65319185 A>G maps to NM_139242.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:65295423 A>G maps to NM_139242.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr14:64894053 G>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:64908800 G>A maps to NM_005956.3 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr14:64891552 G>C maps to NM_005956.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr14:64916276 G>A maps to NM_005956.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:151281412 G>A maps to NM_015440.3 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:151270189 T>C maps to NM_015440.3 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:151331061 C>T maps to NM_015440.3 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:151336755 C>A maps to NM_015440.3 S838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr6:151266670 G>A maps to NM_015440.3 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:11861410 G>T maps to ENST00000376585 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:11860307 G>A maps to ENST00000376585 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:11861227 C>T maps to ENST00000376585 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:11851347 C>T maps to ENST00000376585 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:11854879 G>A maps to ENST00000376585 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:80181593 G>A maps to NM_006441.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:80181593 G>A maps to NM_006441.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:86575787 G>A maps to NM_001159377.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:86565928 C>T maps to NM_001159377.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:55490844 G>T maps to NM_002453.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:55464532 T>C maps to NM_002453.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:55490841 C>T maps to NM_002453.2 W51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:28014138 C>T maps to NM_152912.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:28014242 G>A maps to NM_152912.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:28014242 G>A maps to NM_152912.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:68475824 G>T maps to NM_004923.3 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:68517987 G>A maps to NM_004923.3 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:68506208 C>T maps to NM_004923.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:68483407 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:68517720 C>T maps to NM_004923.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:149814302 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:149814218 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:149809852 C>T did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:149787546 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:149818187 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:149818247 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:149809826 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:149901139 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:149931152 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:149931080 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:149905230 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:149905187 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:149912871 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr23:149905163 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:149901160 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:31247017 A>G maps to NM_017762.2 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:31233849 G>A maps to NM_017762.2 N719N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr15:31251155 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:31233828 G>A maps to NM_017762.2 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr1:149903216 G>A maps to NM_001145862.1 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:149903216 G>A maps to NM_001145862.1 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:32230243 T>C maps to NM_001040446.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr5:32229952 C>T maps to NM_001040446.1 W725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr3:9743655 G>A maps to NM_001077525.2 *651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr3:9712788 A>C maps to NM_001077525.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:9710416 G>A maps to NM_001077525.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:9711164 C>T maps to NM_001077525.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:31206223 C>T maps to NM_014967.4 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:31202889 C>A maps to NM_014967.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:31222834 C>T maps to NM_014967.4 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:31206261 C>T maps to NM_014967.4 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr15:31197144 C>A maps to NM_014967.4 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:95569392 G>T maps to NM_016156.5 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:95580893 C>T maps to NM_016156.5 W388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr11:95580876 C>G did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:95591780 G>A maps to NM_016156.5 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:95621343 G>A maps to NM_016156.5 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:95591763 A>G maps to NM_016156.5 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr11:95591780 G>A maps to NM_016156.5 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:30374968 C>T maps to NM_021090.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr22:30412614 T>C maps to NM_021090.3 C534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:30416737 C>T maps to NM_021090.3 R1030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:30405049 C>T maps to NM_021090.3 N351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:30415612 C>T maps to NM_021090.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr17:56572739 C>T maps to NM_004687.4 E921E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:56581217 C>T maps to NM_004687.4 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr17:56569161 C>T maps to NM_004687.4 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr17:56589813 G>A maps to NM_004687.4 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:56569035 T>C maps to NM_004687.4 T1192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr13:25825881 G>A maps to NM_004685.3 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:17157397 A>G maps to NM_004686.4 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:17198973 G>A maps to NM_004686.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:63579407 C>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:63555963 G>T did not map to a codon.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr23:63568643 A>G did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:63569938 G>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:63555962 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:63557212 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:11180275 C>T maps to NM_015458.3 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr8:11177306 C>A maps to NM_015458.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:187455685 C>T maps to NM_005958.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:187455570 G>A maps to NM_005958.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:187455634 C>T maps to NM_005958.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:187454959 C>T maps to NM_005958.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:187454959 C>T maps to NM_005958.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr4:187455406 G>A maps to NM_005958.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:187455361 G>T maps to NM_005958.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:187454869 A>G maps to NM_005958.3 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:92714706 G>A maps to NM_005959.3 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:92702911 C>T maps to NM_005959.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr11:92714700 C>T maps to NM_005959.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:11300579 G>A maps to NM_004958.3 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:11204706 G>A maps to NM_004958.3 Q1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:11184565 C>G maps to NM_004958.3 R2217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:11273587 C>T maps to NM_004958.3 T1051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:11291473 C>A maps to NM_004958.3 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:11303204 G>A maps to NM_004958.3 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr1:11181416 C>A maps to NM_004958.3 P2273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:11288787 G>A maps to NM_004958.3 F989F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:11181344 G>A maps to NM_004958.3 D2297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:11175525 C>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:11273587 C>T maps to NM_004958.3 T1051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:30822825 T>C maps to ENST00000439838 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:30611527 G>A maps to ENST00000358107 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:30615350 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:237049632 T>C maps to NM_000254.2 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:237015831 T>C maps to NM_000254.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:237026852 C>T maps to NM_000254.2 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:236987484 T>C maps to NM_000254.2 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:237016300 T>C maps to NM_000254.2 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:237026803 C>T maps to NM_000254.2 H785H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:236966833 C>T maps to NM_000254.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:237060402 G>A maps to NM_000254.2 K1232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr13:41797466 C>T maps to NM_004294.2 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:41834764 C>T maps to NM_004294.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr6:153311231 T>C did not map to a codon.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr6:153311052 C>A maps to NM_019041.5 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:153311146 C>T maps to NM_019041.5 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr16:70697993 C>T maps to NM_138383.2 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:70698347 G>A maps to NM_138383.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr16:70698104 G>A maps to NM_138383.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr16:70697912 C>T maps to NM_138383.2 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr4:100534215 T>C maps to ENST00000511045 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:100540225 T>C maps to ENST00000511045 Y798Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:100522852 T>C maps to ENST00000511045 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr8:17504589 T>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:17542010 G>A maps to NM_001001924.2 I888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:17510954 A>G maps to NM_001001924.2 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:17541950 A>G maps to NM_001001924.2 Y908Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:29598990 G>A maps to NM_001033602.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr13:29600628 C>A maps to NM_001033602.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:29600667 G>A maps to NM_001033602.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr13:29600661 T>C maps to NM_001033602.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:30077267 G>A maps to NM_001033602.2 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:29600664 C>A maps to NM_001033602.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:30062050 C>T maps to NM_001033602.2 T1148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr13:29608074 T>G maps to NM_001033602.2 Y763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:155178727 G>T maps to NM_002455.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:177202274 A>G maps to NM_006554.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr5:79285046 T>C maps to ENST00000512528 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:79279512 C>T maps to ENST00000512528 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:26586991 G>A maps to NM_001135091.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr11:26587339 A>G maps to NM_001135091.1 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:26586877 A>C maps to NM_001135091.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:9070330 C>T maps to NM_024690.2 A5705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:9090100 G>A maps to NM_024690.2 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:9075637 C>T maps to NM_024690.2 E3936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr19:9007842 A>C maps to NM_024690.2 G13127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:9047874 A>C maps to NM_024690.2 T11252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr19:9076651 A>G maps to NM_024690.2 T3598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:9084584 T>C maps to NM_024690.2 S2410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:9049227 C>T maps to NM_024690.2 A10801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:9008179 G>A maps to NM_024690.2 Y13124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:9046515 G>A maps to NM_024690.2 T11705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:9047430 T>A maps to NM_024690.2 V11400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr19:9056389 A>T maps to NM_024690.2 T10352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:9085172 A>G maps to NM_024690.2 N2214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:9063004 A>C maps to NM_024690.2 T8147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr19:9072190 T>G maps to NM_024690.2 T5085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr19:9058528 G>A maps to NM_024690.2 D9639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:9089933 G>A maps to NM_024690.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:9076900 A>G maps to NM_024690.2 H3515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:9082877 A>C maps to NM_024690.2 T2979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:9085751 A>G maps to NM_024690.2 S2021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:9070243 A>C maps to NM_024690.2 S5734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:9085238 A>C maps to NM_024690.2 V2192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:9060505 A>G maps to NM_024690.2 S8980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:9054250 C>G maps to NM_024690.2 S10457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr19:9063751 T>A maps to NM_024690.2 T7898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr19:9061336 A>C maps to NM_024690.2 T8703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:9057814 A>G maps to NM_024690.2 P9877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr19:9075508 A>C maps to NM_024690.2 S3979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:9073198 T>C maps to NM_024690.2 A4749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:9076651 A>G maps to NM_024690.2 T3598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr19:9017469 G>A maps to NM_024690.2 H12618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:9069064 T>C maps to NM_024690.2 S6127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9010989 G>A maps to NM_024690.2 S12976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9049698 G>T maps to NM_024690.2 I10644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9067438 G>A maps to NM_024690.2 I6669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9068734 A>C maps to NM_024690.2 T6237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9069873 C>A maps to NM_024690.2 E5858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr19:9087509 A>C maps to NM_024690.2 T1435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:9083879 C>T maps to NM_024690.2 P2645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr19:9070918 A>G maps to NM_024690.2 S5509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:9048507 C>T maps to NM_024690.2 V11041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr19:9015689 C>T maps to NM_024690.2 K12711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:9082931 G>T maps to NM_024690.2 T2961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:9060439 G>T maps to NM_024690.2 P9002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:9066127 G>T maps to NM_024690.2 T7106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:9072307 T>C maps to NM_024690.2 S5046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:9090341 C>T maps to NM_024690.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:9061717 G>A maps to NM_024690.2 F8576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:9077647 G>T maps to NM_024690.2 T3266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr19:9088916 A>T maps to NM_024690.2 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:9063742 T>C maps to NM_024690.2 A7901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr19:8994158 G>T maps to NM_024690.2 C13842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr19:9089843 C>T maps to NM_024690.2 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:9049047 G>A maps to NM_024690.2 S10861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:9091106 G>A maps to NM_024690.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:9026256 G>A maps to NM_024690.2 Y12243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:9072973 C>T maps to NM_024690.2 T4824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:9046899 C>T maps to NM_024690.2 W11577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr19:8976843 C>T maps to NM_024690.2 L14074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:9087353 A>G maps to NM_024690.2 A1487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:9085982 T>C maps to NM_024690.2 E1944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:9067749 A>G maps to NM_024690.2 L6566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr19:9075304 A>G maps to NM_024690.2 P4047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr19:9068980 G>A maps to NM_024690.2 I6155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr19:9018163 G>A maps to NM_024690.2 L12592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr19:9066001 T>C maps to NM_024690.2 V7148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:9069475 T>C maps to NM_024690.2 S5990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr19:9072871 T>C maps to NM_024690.2 T4858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:9070033 T>C maps to NM_024690.2 S5804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:9074872 T>G maps to NM_024690.2 S4191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr19:9071716 C>T maps to NM_024690.2 V5243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr19:9088382 G>A maps to NM_024690.2 G1144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr19:9073399 C>T maps to NM_024690.2 Q4682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr19:9066414 T>A maps to NM_024690.2 R7011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr19:9091604 C>T maps to NM_024690.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:9064773 C>A maps to NM_024690.2 E7558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:9068743 A>G maps to NM_024690.2 S6234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr19:9088844 A>C maps to NM_024690.2 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr19:9083303 C>A maps to NM_024690.2 L2837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:100682850 C>T maps to NM_001040105.1 D2718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:100686474 A>G maps to NM_001040105.1 V3926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr7:100685355 A>G maps to NM_001040105.1 Q3553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr7:100686765 T>G maps to NM_001040105.1 T4023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr7:100682328 T>C maps to NM_001040105.1 S2544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr7:100687002 C>G maps to NM_001040105.1 T4102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr7:100684302 T>G maps to NM_001040105.1 T3202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:100680228 A>T maps to NM_001040105.1 A1844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr7:100674399 G>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:100694939 G>A maps to NM_001040105.1 T4307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr7:100683864 G>A maps to NM_001040105.1 T3056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:100692246 G>A maps to NM_001040105.1 T4219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:100686858 G>A maps to NM_001040105.1 P4054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:100678206 G>A maps to NM_001040105.1 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:100684287 T>G maps to NM_001040105.1 T3197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr7:100685181 C>G maps to NM_001040105.1 T3495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr7:100686435 C>T maps to NM_001040105.1 A3913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr11:1090890 G>A maps to ENST00000441003 P1262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:1086051 G>A maps to ENST00000441003 T964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:1095794 C>T maps to ENST00000441003 R2102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr11:1093568 A>C maps to ENST00000441003 T1796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:1085790 C>T maps to ENST00000441003 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr11:1087572 C>T maps to ENST00000441003 C1108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr11:1093106 A>T maps to ENST00000441003 P1642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:1090842 C>T maps to ENST00000441003 N1246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:1085751 C>T maps to ENST00000441003 C891C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:1090914 C>A maps to ENST00000441003 T1270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:1093742 T>C maps to ENST00000441003 P1854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:1101019 C>T maps to ENST00000441003 C2473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr11:1093511 C>A maps to ENST00000441003 T1777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:1081790 C>A maps to ENST00000441003 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:1083286 G>A maps to ENST00000441003 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr11:1093046 T>C maps to ENST00000441003 T1622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:1081811 C>T maps to ENST00000441003 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr3:195451882 G>T maps to ENST00000447234 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr3:195451989 G>T maps to ENST00000447234 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr6:30955931 G>A maps to NM_001010909.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr3:195495954 G>A maps to NM_018406.5 S4489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:195492282 T>C maps to NM_018406.5 E4552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr3:195477790 G>A maps to NM_018406.5 I5280I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-4305-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:195497164 G>A maps to NM_018406.5 N4440N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:195481222 G>A maps to NM_018406.5 D5063D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:195474184 G>A maps to NM_018406.5 D5367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:195495990 G>A maps to NM_018406.5 D4477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:195486028 C>T maps to NM_018406.5 T4984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:1263878 G>A maps to ENST00000447027 T1926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:1262816 C>T maps to ENST00000447027 D1572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:1250469 C>A maps to ENST00000447027 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:1264268 T>C maps to ENST00000447027 T2056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:1265018 G>A maps to ENST00000447027 S2306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:1267502 G>A maps to ENST00000447027 T3134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:1267403 C>A maps to ENST00000447027 S3101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr11:1267073 G>A maps to ENST00000447027 G2991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:1266854 C>T maps to ENST00000447027 L2918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:1275370 C>A maps to ENST00000447027 T5092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr11:1268159 C>T maps to ENST00000447027 S3353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:1271225 G>A maps to ENST00000447027 T4375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr11:1274130 C>T maps to ENST00000447027 N5049N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr11:1253941 T>C maps to ENST00000447027 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:1278845 C>T maps to ENST00000447027 D5455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr11:1275469 G>A maps to ENST00000447027 T5125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:1264181 C>T maps to ENST00000447027 T2027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr11:1276096 C>G maps to ENST00000447027 T5220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:1258210 C>A maps to ENST00000447027 A1041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:1263617 C>T maps to ENST00000447027 P1839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:1272677 C>T maps to ENST00000447027 T4859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:1261420 C>T maps to ENST00000447027 T1265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:1253734 G>A maps to ENST00000447027 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:1268789 G>A maps to ENST00000447027 S3563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:1270970 C>G maps to ENST00000447027 T4290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:1270988 T>C maps to ENST00000447027 S4296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:1256348 C>A maps to ENST00000447027 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:1265114 C>T maps to ENST00000447027 G2338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr11:1272158 G>A maps to ENST00000447027 T4686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:1271489 G>A maps to ENST00000447027 T4463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:1261606 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:1262735 G>A maps to ENST00000447027 Q1545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:1265474 G>A maps to ENST00000447027 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr11:1263338 G>C maps to ENST00000447027 T1746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr11:1256377 C>T maps to ENST00000447027 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:1265150 C>T maps to ENST00000447027 A2350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:1267664 C>T maps to ENST00000447027 S3188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:1269785 C>T maps to ENST00000447027 S3895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:1264928 G>T maps to ENST00000447027 P2276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:1268804 G>A maps to ENST00000447027 T3568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:1278845 C>T maps to ENST00000447027 D5455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr11:1262687 C>T maps to ENST00000447027 D1529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:1018711 A>G maps to NM_005961.2 R1363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:1018684 T>C maps to NM_005961.2 P1372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:1027754 G>A maps to NM_005961.2 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:1026403 G>A maps to NM_005961.2 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:1025843 G>A maps to NM_005961.2 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr11:1016368 A>G maps to NM_005961.2 Y2144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:1031985 G>A maps to NM_005961.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:1017295 T>C maps to NM_005961.2 T1835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:1026074 G>A maps to NM_005961.2 Y871Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:1021245 G>A maps to NM_005961.2 F1186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:1017058 A>C maps to NM_005961.2 T1914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr11:1016416 G>C maps to NM_005961.2 S2128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr4:71346557 A>C maps to NM_152291.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:71347243 A>G maps to NM_152291.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:71347003 T>G maps to NM_152291.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr4:71347207 A>G maps to NM_152291.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:57741069 A>G maps to ENST00000431972 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr14:57741027 A>G maps to ENST00000431972 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:57747007 A>G maps to ENST00000431972 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr1:20827536 C>T maps to NM_024544.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:20827479 G>T maps to NM_024544.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:20827644 G>A maps to NM_024544.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:20827563 G>A maps to NM_024544.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:105450134 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:105451073 A>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:105450020 T>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:105449593 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr23:105450562 C>T did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr23:105450998 C>T did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:105450083 T>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:105450488 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:105451264 C>G did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:105450792 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:105450189 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:105450684 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:65632485 A>G did not map to a codon.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr9:113563099 C>T maps to ENST00000189978 Y820Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:113445032 C>A maps to ENST00000189978 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:113530123 C>T maps to ENST00000189978 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:113547893 G>A maps to ENST00000189978 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:49416613 A>G maps to NM_000255.3 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:49419393 C>A maps to NM_000255.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr6:49415469 C>T maps to NM_000255.3 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:45799171 G>A maps to NM_001128425.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr1:45798154 G>A maps to NM_001128425.1 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr1:45799207 C>T maps to NM_001128425.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:88725066 G>A maps to NM_002461.1 H44H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:110019268 C>T maps to NM_001114185.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:29853262 G>A maps to NM_017458.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr16:29853241 C>A maps to NM_017458.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:29847043 C>T maps to NM_017458.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:29848269 C>T maps to NM_017458.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr16:29857216 C>T maps to NM_017458.3 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:29845350 G>T maps to NM_017458.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr21:42817380 C>T maps to NM_001144925.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:42824609 C>T maps to NM_001144925.1 H524H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:42780120 A>G maps to NM_002463.1 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr21:42762584 C>T maps to NM_002463.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:42770828 G>A maps to NM_002463.1 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:70164408 C>T maps to NM_002357.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:70164404 C>T maps to NM_002357.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:70162561 T>C maps to NM_002357.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:70162549 C>T maps to NM_002357.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr4:2252844 C>T maps to NM_006454.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:111987986 G>A maps to NM_130439.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:111967673 G>A maps to NM_130439.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr23:3229244 G>A did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:3235404 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:3240640 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:3228468 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:3235645 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:3229208 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:3248156 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:3261859 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:3229041 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:3239356 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:3239945 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:3240583 G>T did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:3227889 C>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:3228136 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:3242752 C>T did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:3261860 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:3261859 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:3229370 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:3235195 G>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:3235706 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:3235850 G>A did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr23:3227993 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:3235237 C>A did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr23:3235213 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:3239544 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr23:3239827 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:3235294 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:3240107 C>T did not map to a codon.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr23:3238446 C>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:3228380 G>A did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:3228890 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:3248315 G>A did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr23:3239958 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:3227796 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:3228419 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:3239209 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:3228889 C>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:3241476 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:3235933 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:3240514 T>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:3240251 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr23:3235275 G>A did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr23:3229021 C>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:3235465 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:3261812 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:3240887 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:3239182 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:3240743 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr23:3235382 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr23:3241736 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:3241680 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:3227907 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:3238126 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:3242750 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:1289836 G>A maps to NM_032348.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:1290437 G>A maps to NM_032348.2 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:1289408 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:1290092 G>A maps to NM_032348.2 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:1290266 A>G maps to NM_032348.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:54377622 C>T maps to NM_001020818.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:54377199 C>T maps to NM_001020818.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:54377406 G>T maps to NM_001020818.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr6:135539111 C>A maps to NM_001130173.1 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr6:135517007 G>A maps to NM_001130173.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr6:135521252 C>T maps to NM_001130173.1 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4457518 C>A maps to NM_001105538.1 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr8:67492544 A>C maps to NM_001080416.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:67488262 T>C maps to NM_001080416.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:42310461 G>A maps to NM_002466.2 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr20:42343836 T>C maps to NM_002466.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:42328422 C>T maps to NM_002466.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:42331533 G>A maps to NM_002466.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:42315577 T>C maps to NM_002466.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:42320925 C>T maps to NM_002466.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr20:42344711 C>T maps to NM_002466.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr20:42331389 C>T maps to NM_002466.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:42328683 G>A maps to NM_002466.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:42338650 G>T maps to NM_002466.2 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:42328683 G>A maps to NM_002466.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr12:102010977 A>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:102041874 G>A maps to NM_002465.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr12:102069088 A>G maps to NM_002465.2 Q943Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:102069193 T>C maps to NM_002465.2 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:102046518 T>C maps to NM_002465.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr19:50958503 T>C maps to NM_004533.3 A718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr19:50958491 C>T maps to NM_004533.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:50954193 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:50951485 A>G maps to NM_004533.3 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:50939881 C>A maps to NM_004533.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:50957401 C>G maps to NM_004533.3 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr19:50949193 C>T maps to NM_004533.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:50961932 C>T maps to NM_004533.3 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr19:50961955 G>A maps to NM_004533.3 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:47363660 G>A maps to ENST00000399249 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:47371348 G>A maps to ENST00000399249 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr11:47354131 G>A maps to ENST00000399249 V1204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:47357491 C>T maps to ENST00000399249 R891R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:47364635 C>T maps to ENST00000399249 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:47365113 G>A maps to ENST00000399249 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:47372949 G>A maps to ENST00000399249 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:203139458 C>T maps to NM_004997.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:203144769 G>A maps to NM_004997.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:109849544 C>T maps to NM_001010985.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:128753089 C>T maps to NM_002467.4 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:128752801 G>A maps to NM_002467.4 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr13:77745687 A>T maps to NM_015057.4 S1911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:77807297 C>T maps to NM_015057.4 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr13:77780920 C>T maps to NM_015057.4 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:77652956 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:77780842 T>C maps to NM_015057.4 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:77779484 G>T maps to NM_015057.4 S1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:77807399 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr13:77732133 T>C maps to NM_015057.4 E2236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr13:77725075 C>A maps to NM_015057.4 V2308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr13:77755994 A>T maps to NM_015057.4 A1594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:77670607 G>A maps to NM_015057.4 R3265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:77672620 C>A maps to NM_015057.4 E2890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:77672480 G>A maps to NM_015057.4 C2936C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:77799623 G>A maps to NM_015057.4 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr13:77635847 G>A maps to NM_015057.4 D4284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:77651308 G>A maps to NM_015057.4 R3900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:48603285 G>A maps to NM_032133.4 W652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:40363564 G>A maps to NM_001033082.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:16082452 C>A maps to NM_005378.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:38182636 C>T maps to NM_001172567.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:38181460 G>A maps to NM_001172567.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr3:38181924 C>T maps to NM_001172567.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr15:48435170 G>T maps to NM_016132.3 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:69063583 G>T maps to NM_138768.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:81111207 G>A maps to NM_005593.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr12:81101581 A>G maps to NM_002469.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:81102714 C>T maps to NM_002469.2 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:81101719 C>T maps to NM_002469.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:10405119 C>A maps to NM_005963.3 E1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:10417428 G>A maps to NM_005963.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:10404982 G>A maps to NM_005963.3 S1092S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4280-01A-01D-1126-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:8409745 G>A maps to ENST00000360416 D1092D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8361-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:8445462 G>A maps to ENST00000360416 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:8408177 G>A maps to ENST00000360416 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:8404185 T>C maps to ENST00000360416 T1234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr17:8451697 T>C maps to ENST00000360416 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:8396255 C>T maps to ENST00000360416 A1432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:8452088 T>C maps to ENST00000360416 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr17:8422058 C>T maps to ENST00000360416 K798K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:15797970 G>A maps to NM_001040114.1 N1939N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:15815482 G>T maps to NM_001040114.1 A1465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:15818574 G>A maps to NM_001040114.1 Q1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:15820851 G>A maps to NM_001040114.1 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr16:15931923 C>A maps to NM_001040114.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:15811202 G>A maps to NM_001040114.1 A1773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:10248524 G>A maps to NM_003802.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr17:10216004 C>T maps to NM_003802.2 S1417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr17:10233732 C>G maps to NM_003802.2 R802R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:10258071 G>A maps to NM_003802.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr17:10243716 G>A maps to NM_003802.2 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:10214521 C>T maps to NM_003802.2 E1518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:10227374 C>T maps to NM_003802.2 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr17:10216578 G>A maps to NM_003802.2 A1359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:10227551 T>C maps to NM_003802.2 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:10216650 G>A maps to NM_003802.2 H1335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr17:10219279 G>A maps to NM_003802.2 D1267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:10209931 A>G maps to NM_003802.2 A1770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:50720888 C>T maps to NM_001145809.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:50735185 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:50779397 G>A maps to NM_001145809.1 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:50764739 G>A maps to NM_001145809.1 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:50764824 C>A maps to NM_001145809.1 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:50753884 C>T maps to NM_001145809.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:50774700 G>A maps to NM_001145809.1 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:108220599 G>A maps to NM_014981.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:108224572 T>C maps to NM_014981.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr3:108195276 G>A maps to NM_014981.1 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr3:108147526 C>A maps to NM_014981.1 E1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:108220693 G>A maps to NM_014981.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr17:10428136 G>A maps to NM_017534.5 N1636N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8078-01A-11D-2340-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-8081-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:10441020 G>A maps to ENST00000399342 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:10447415 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:10447415 C>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:10428367 A>G maps to NM_017534.5 H1559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:10428788 G>A maps to NM_017534.5 R1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr17:10426630 A>C maps to NM_017534.5 T1857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:10430070 G>A maps to NM_017534.5 H1344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:10428367 A>G maps to NM_017534.5 H1559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:10430317 T>C maps to NM_017534.5 R1309R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-A4GX-01A-12D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:10440996 G>A maps to ENST00000399342 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:10428247 G>T maps to NM_017534.5 I1599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:10431116 C>T maps to NM_017534.5 Q1273Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-R5-A804-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr17:10440987 G>A maps to ENST00000399342 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr17:10426499 C>T maps to NM_017534.5 T1860T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr17:10442656 T>A maps to NM_017534.5 V427V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-AA6F-01A-31D-A410-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr17:10426815 G>C maps to NM_017534.5 A1823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:10532946 G>T maps to NM_002470.2 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:10542987 C>T maps to NM_002470.2 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:10546232 C>T maps to NM_002470.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:10545554 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:10550505 C>T maps to NM_002470.2 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr17:10545980 G>A maps to NM_002470.2 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr17:10544003 C>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:10535237 G>A maps to NM_002470.2 A1684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:10549159 G>A maps to NM_002470.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:10543507 G>T maps to NM_002470.2 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:10538324 C>T maps to NM_002470.2 Q1396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:10541626 C>T maps to NM_002470.2 A1154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr17:10362659 G>A maps to NM_017533.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:10366494 C>T maps to NM_017533.2 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:10354171 A>G maps to NM_017533.2 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:10348334 C>T maps to NM_017533.2 A1808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:10346802 G>A maps to NM_017533.2 L1903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:10356186 T>C maps to NM_017533.2 K1058K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr17:10368833 G>A maps to NM_017533.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:10358319 G>A maps to NM_017533.2 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:10362627 G>A maps to NM_017533.2 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr17:10369948 G>T maps to NM_017533.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:10350533 C>A did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr14:23874325 G>A maps to NM_002471.3 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr14:23868195 G>T maps to NM_002471.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:23871974 G>A maps to NM_002471.3 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:23866188 G>A maps to NM_002471.3 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:23871980 G>A maps to NM_002471.3 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:23853809 G>A maps to NM_002471.3 A1802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr14:23866230 G>T maps to NM_002471.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:23869929 G>A maps to NM_002471.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:23862140 C>T maps to NM_002471.3 Q1077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr14:23872599 G>A maps to NM_002471.3 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:23869596 G>A maps to NM_002471.3 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:23858083 C>A maps to NM_002471.3 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr14:23873528 G>T maps to NM_002471.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:23857096 C>T maps to NM_002471.3 S1465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:23859421 C>T maps to NM_002471.3 A1192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:23873937 G>A maps to NM_002471.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:23858216 G>A maps to NM_002471.3 C1342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:23870076 G>A maps to NM_002471.3 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:23886744 T>C maps to NM_000257.2 A1440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:23891462 G>A maps to NM_000257.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr14:23899792 G>A maps to NM_000257.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:23885002 G>A maps to NM_000257.2 N1664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr14:23899792 G>A maps to NM_000257.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr14:23902764 G>A maps to NM_000257.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:23883075 G>A maps to NM_000257.2 S1894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:23884368 G>A maps to NM_000257.2 D1798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:23901998 G>T maps to NM_000257.2 Y117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:33582005 G>A maps to NM_020884.3 W876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr20:33585430 G>C maps to NM_020884.3 L1287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr20:33578611 C>T maps to NM_020884.3 N725N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:33576025 C>T maps to NM_020884.3 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:33568502 G>A maps to NM_020884.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr20:33575070 G>A maps to NM_020884.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:10315782 C>T maps to NM_002472.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:10304653 C>A maps to NM_002472.2 E1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:10300236 A>C maps to NM_002472.2 A1415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:10312470 C>T maps to NM_002472.2 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr17:10315971 G>A maps to NM_002472.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:10315824 C>T maps to NM_002472.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:10309611 T>C maps to NM_002472.2 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:10317532 G>A maps to NM_002472.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:10318674 G>A maps to NM_002472.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:10317532 G>A maps to NM_002472.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr17:10303961 A>C maps to NM_002472.2 T1160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr17:10323526 G>A maps to NM_002472.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:36708255 C>T maps to NM_002473.4 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:36692911 C>T maps to NM_002473.4 E1083E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:36693033 G>A maps to NM_002473.4 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:36718563 G>A maps to NM_002473.4 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:36684429 G>A maps to NM_002473.4 D1600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:36681701 A>G did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr22:36690197 G>T maps to NM_002473.4 V1259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:36680498 G>A maps to NM_002473.4 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:3254034 T>C maps to NM_006471.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr18:3253947 T>C maps to NM_006471.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:111352094 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:111356997 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:111358329 C>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:111348946 G>A maps to NM_000432.3 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr3:46899745 G>T maps to NM_000258.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr12:56552183 A>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:35176474 C>T maps to NM_006097.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:35176474 C>T maps to NM_006097.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:16143370 C>T maps to NM_013262.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr6:16143325 G>A maps to NM_013262.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:16130861 A>G maps to NM_013262.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:16146930 G>A maps to NM_013262.3 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr3:123359314 G>A maps to NM_053025.3 D1552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:123452834 C>T maps to NM_053025.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:123332965 C>A maps to NM_053025.3 E1911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:123401074 A>G maps to NM_053025.3 T1216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:123359179 C>T maps to NM_053025.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr3:123471319 G>T maps to NM_053025.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr3:123366072 C>T maps to NM_053025.3 E1539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr3:123366186 T>C maps to NM_053025.3 K1501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:123419632 C>T maps to NM_053025.3 Q894Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:30411334 C>T maps to NM_033118.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr20:30414608 C>T maps to NM_033118.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr20:30414608 C>T maps to NM_033118.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr20:30414686 C>T maps to NM_033118.3 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:46763517 G>A maps to NM_182493.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:2683359 A>G maps to NM_001012418.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:2675354 G>A maps to NM_001012418.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:2685573 G>A maps to NM_001012418.3 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:30387187 C>T maps to NM_013292.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:30387175 C>T maps to NM_013292.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:16673838 G>A maps to NM_012334.2 G1708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:16818204 G>A maps to NM_012334.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:16701392 G>A maps to NM_012334.2 N1037N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:16701575 G>A maps to NM_012334.2 C976C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr5:16671581 G>A maps to NM_012334.2 D1793D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr5:16671581 G>A maps to NM_012334.2 D1793D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr5:16694520 G>A maps to NM_012334.2 S1253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:16670844 C>T maps to NM_012334.2 R1891R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr5:16682100 G>A maps to NM_012334.2 I1356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:16701362 C>T maps to NM_012334.2 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr5:16675242 G>A maps to NM_012334.2 G1561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:16673853 C>A maps to NM_012334.2 T1703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:16818216 C>T maps to NM_012334.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:18039936 C>T maps to ENST00000205890 N1572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:18022182 G>A maps to ENST00000205890 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:18022482 C>T maps to ENST00000205890 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:18023040 C>T maps to ENST00000205890 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:18023034 C>T maps to ENST00000205890 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:18023436 G>A maps to ENST00000205890 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:18077132 G>A maps to ENST00000205890 S3463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:18023049 C>T maps to ENST00000205890 Y312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:18023409 C>T maps to ENST00000205890 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:18039026 G>A maps to ENST00000205890 T1495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:18051507 C>T maps to ENST00000205890 D2225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr17:18044112 G>A maps to ENST00000205890 L1791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:18022932 C>A maps to ENST00000205890 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:18034841 T>C maps to ENST00000205890 F1401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:18022482 C>T maps to ENST00000205890 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:18023439 C>T maps to ENST00000205890 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr17:18039939 G>A maps to ENST00000205890 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:18023436 G>A maps to ENST00000205890 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:18061118 C>T maps to ENST00000205890 Q2958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:18022704 C>T maps to ENST00000205890 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr17:18051477 G>A maps to ENST00000205890 A2215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:109496834 C>T maps to NM_015011.1 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:109535429 C>A maps to NM_015011.1 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr13:109779803 G>A maps to NM_015011.1 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr13:109475608 C>T maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:109831917 G>A maps to NM_015011.1 R1762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:109672093 A>G maps to NM_015011.1 E855E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr13:109617205 G>A maps to NM_015011.1 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:109793422 C>T maps to NM_015011.1 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:109753196 C>T maps to NM_015011.1 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:109496819 C>T maps to NM_015011.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:109777700 C>T maps to NM_015011.1 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr13:109475608 C>T maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr13:109793644 C>T maps to NM_015011.1 D1673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:109792753 C>T maps to NM_015011.1 P1376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr13:109779689 C>T maps to NM_015011.1 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr13:109379786 G>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:109793695 G>A maps to NM_015011.1 A1690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:109792876 G>A maps to NM_015011.1 G1417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:109779803 G>A maps to NM_015011.1 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:109379807 C>T maps to NM_015011.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:27447648 G>A maps to NM_078471.3 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:27442811 C>A maps to NM_078471.3 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:27438749 A>G maps to NM_078471.3 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr17:27493223 G>A maps to NM_078471.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:27446420 C>T maps to NM_078471.3 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:27493496 C>T maps to NM_078471.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:27446377 G>A maps to NM_078471.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:26422846 C>T maps to ENST00000407587 L2305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:26159196 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr22:26351272 C>T maps to ENST00000407587 A2035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr22:26173745 C>A maps to ENST00000407587 S691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr22:26193918 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr22:26224932 G>T maps to ENST00000407587 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:34883420 G>A maps to NM_001163735.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:34862383 G>A maps to NM_001163735.1 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:34883423 C>T maps to NM_001163735.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:34869253 C>T maps to NM_001033580.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:34856714 G>A maps to NM_001163735.1 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr17:34856763 C>T maps to NM_001163735.1 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr12:57437100 C>A maps to NM_005379.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:192265121 G>A maps to NM_001130158.1 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:192228908 C>T maps to NM_001130158.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr2:192194739 G>T maps to NM_001130158.1 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:1386932 G>A maps to NM_001080779.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:1395771 G>A maps to NM_001080779.1 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:1371156 G>A maps to NM_001080779.1 Q982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:1373489 C>T maps to NM_001080779.1 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:1386274 G>A maps to NM_001080779.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:1370577 C>T maps to NM_001080779.1 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:31075961 G>A maps to NM_015194.1 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:30821884 G>A maps to NM_015194.1 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:31092066 C>T maps to NM_015194.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:30965802 A>G maps to NM_015194.1 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr17:30986209 G>A maps to NM_015194.1 Y756Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr15:59548484 G>T maps to NM_004998.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr15:59523936 G>A maps to NM_004998.2 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:8618251 G>A maps to NM_012335.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:8612925 G>A maps to NM_012335.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:8619567 G>A maps to NM_012335.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:8612994 G>A maps to NM_012335.3 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:8609254 G>A maps to NM_012335.3 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:8609189 G>A maps to NM_012335.3 Y505Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:8620590 G>A maps to NM_012335.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr7:45005234 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:45006353 G>A maps to NM_033054.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:109845645 A>G maps to NM_001101421.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:109826649 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:109845667 C>T maps to NM_001101421.3 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr12:109845696 C>T maps to NM_001101421.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:109826582 C>T maps to NM_001101421.3 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:109839055 G>A maps to NM_001101421.3 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr12:109826621 C>A maps to NM_001101421.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:109874341 C>T maps to NM_001101421.3 Y714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:109843788 C>T maps to NM_001101421.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:26414414 A>G maps to NM_017433.4 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:26359254 T>C maps to NM_017433.4 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr10:26463194 G>A maps to NM_017433.4 R1334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:26455049 C>A maps to NM_017433.4 T1018T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr10:26463374 T>A maps to NM_017433.4 Y1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:26286158 G>A maps to NM_017433.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:26446277 C>T maps to NM_017433.4 Q945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr10:26482177 C>T maps to NM_017433.4 R1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:26500813 G>A maps to NM_017433.4 E1591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:26315377 T>C maps to NM_017433.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:26443676 C>T maps to NM_017433.4 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr10:26463102 G>T maps to NM_017433.4 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr2:171264298 A>G maps to NM_138995.3 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:171399448 C>T maps to NM_138995.3 C1203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:171399457 C>T maps to NM_138995.3 F1206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr2:171242769 T>G maps to NM_138995.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:171258105 C>T maps to NM_138995.3 D678D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:52680090 C>A maps to ENST00000358212 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:52688527 C>T maps to ENST00000358212 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:52662615 T>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:52606370 T>C maps to ENST00000358212 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr15:52664320 C>T maps to ENST00000358212 Q939Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr15:52622645 G>A maps to ENST00000358212 R1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:52609256 T>C maps to ENST00000358212 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:52699555 A>G maps to ENST00000358212 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:47511133 G>A maps to NM_001080467.2 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:47431167 C>T maps to NM_001080467.2 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr18:47363929 A>G maps to NM_001080467.2 L1699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:47479668 C>A maps to NM_001080467.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:47390530 G>A maps to NM_001080467.2 R1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:47402094 G>A maps to NM_001080467.2 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr18:47363929 A>G maps to NM_001080467.2 L1699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:52548868 G>A maps to NM_018728.3 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:52497303 G>A maps to NM_018728.3 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:52539150 G>A maps to NM_018728.3 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:52497186 G>A maps to NM_018728.3 N1565N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:76545674 T>C did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:76623783 G>A maps to ENST00000428345 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:76604946 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr6:76551088 T>C maps to ENST00000428345 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:76604977 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr6:76602398 G>T maps to ENST00000428345 A1033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:76924064 C>A maps to NM_000260.3 I2141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:76909567 C>T maps to NM_000260.3 I1490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:76916548 G>A maps to NM_000260.3 T1841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:76885961 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:128394475 C>T maps to ENST00000389524 C2080C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr2:128388867 G>A maps to ENST00000389524 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr2:128367091 G>A maps to ENST00000389524 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr15:72196296 T>C maps to ENST00000424560 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr15:72227775 T>A maps to ENST00000424560 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr15:72338408 G>A maps to ENST00000424560 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:17311595 C>T maps to NM_004145.3 N1507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:17213231 C>T maps to NM_004145.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr19:17298760 C>T maps to NM_004145.3 D865D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:17213186 C>T maps to NM_004145.3 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:17311595 C>T maps to NM_004145.3 N1507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:17308627 C>T maps to NM_004145.3 S1358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr19:17291786 C>T maps to NM_004145.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:17308624 G>A maps to NM_004145.3 T1357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17320506 C>T maps to NM_004145.3 R1913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:171605700 C>T maps to NM_000261.1 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:171605748 G>A maps to NM_000261.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:171621298 A>T maps to NM_000261.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:12656116 C>T maps to NM_001146312.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:12666429 A>G maps to NM_001146312.1 Q810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:12639604 C>T maps to NM_001146312.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:12656200 C>T maps to NM_001146312.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr17:12649276 C>A maps to NM_001146312.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:12655774 G>A maps to NM_001146312.1 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:12639544 G>A maps to NM_001146312.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:12639604 C>T maps to NM_001146312.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:17741379 C>T maps to NM_002478.4 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr11:17741343 G>A maps to NM_002478.4 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:17741355 C>T maps to NM_002478.4 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:17741818 C>T maps to NM_002478.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:17741550 C>T maps to NM_002478.4 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:17741490 C>T maps to NM_002478.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr10:95119648 G>A maps to NM_013451.3 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr10:95069866 G>A maps to NM_013451.3 I2019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:95079634 C>T maps to NM_013451.3 A1864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:203054893 G>A maps to NM_002479.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:203054834 C>T maps to NM_002479.4 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr18:3134757 C>T maps to NM_003803.3 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr18:3214999 C>T maps to NM_003803.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:3142041 G>A maps to NM_003803.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr18:3126752 T>C maps to NM_003803.3 V979V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:2024224 T>C maps to NM_003970.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr8:2092695 C>T maps to NM_003970.2 Q1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr8:2024314 G>A maps to NM_003970.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:2044087 C>A maps to NM_003970.2 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:2040279 C>T maps to NM_003970.2 Y645Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:2037898 C>G maps to NM_003970.2 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:2005502 C>A maps to NM_003970.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:2026950 C>T maps to NM_003970.2 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:2037976 G>A maps to NM_003970.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr8:2050518 C>T maps to NM_003970.2 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:2026940 G>A maps to NM_003970.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr8:2077169 G>A maps to NM_003970.2 Q1250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:2063870 G>A maps to NM_003970.2 Q1100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr8:2044180 G>A maps to NM_003970.2 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr8:2054065 A>G maps to NM_003970.2 Q923Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr8:2040208 C>T maps to NM_003970.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr8:2092796 C>T maps to NM_003970.2 D1430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:2005883 G>A maps to NM_003970.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:24421460 G>A maps to ENST00000330966 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:24419452 G>T maps to ENST00000330966 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:24421950 G>A maps to ENST00000330966 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:24413269 A>G maps to ENST00000330966 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:24401806 A>G did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:24416561 A>T maps to ENST00000330966 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:24385440 C>T maps to ENST00000330966 P1344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:24409197 T>C maps to ENST00000330966 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:69948774 G>A maps to NM_032578.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr10:69881983 A>G maps to NM_032578.2 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:46393880 T>C maps to NM_001012643.2 *400W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:46393901 G>A maps to NM_001012643.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:40204291 C>T maps to NM_015460.2 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr3:40085714 C>G maps to NM_015460.2 Y95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:40085750 C>T maps to NM_015460.2 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:40192664 C>T maps to NM_015460.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:40085744 C>T maps to NM_015460.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:59132820 G>T maps to NM_001085487.1 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:59154729 C>A maps to NM_001085487.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:59131249 A>G maps to NM_001085487.1 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31142180 G>A maps to NM_182958.2 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:47904070 G>A maps to NM_007067.4 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:47898712 G>A maps to NM_007067.4 W390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:47869285 C>T maps to NM_007067.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr17:47888905 A>G maps to NM_007067.4 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:41839430 G>A maps to NM_006766.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:41834757 T>C maps to NM_006766.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:41794924 G>A maps to NM_006766.3 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr8:41798800 G>A maps to NM_006766.3 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:41794881 T>G maps to NM_006766.3 R1082R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:41791414 G>A maps to NM_006766.3 G1441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:41794924 G>A maps to NM_006766.3 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:41791348 G>A maps to NM_006766.3 D1463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:41792385 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:76781835 G>A maps to NM_012330.2 E1073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:76790221 A>G maps to NM_012330.2 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:76789459 C>T maps to NM_012330.2 Y1626Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr10:76789438 C>T maps to NM_012330.2 V1619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:76735911 G>A maps to NM_012330.2 W606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:76784853 C>T maps to NM_012330.2 Q1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:76603124 G>A maps to NM_012330.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:76789459 C>A maps to NM_012330.2 Y1626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:76790791 C>T maps to NM_012330.2 Y2070Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:62839457 G>A maps to NM_004535.2 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:62848506 G>A maps to NM_004535.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr20:62838986 C>T maps to NM_004535.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:62837073 T>C maps to NM_004535.2 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:62837074 G>T maps to NM_004535.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr20:62848548 C>T maps to NM_004535.2 Y587Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:62839760 G>A maps to NM_004535.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:62871117 C>A maps to NM_004535.2 S1033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:62848431 C>T maps to NM_004535.2 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:62871234 C>T maps to NM_004535.2 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:1855432 G>A maps to ENST00000399161 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:1926085 G>A maps to ENST00000399161 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:1906930 G>A maps to ENST00000399161 Y651Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:1914025 C>T maps to ENST00000399161 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:1926340 C>T maps to ENST00000399161 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:1890321 G>T maps to ENST00000399161 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:1906993 C>T maps to ENST00000399161 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:1983513 C>T maps to ENST00000399161 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:1926427 C>T maps to ENST00000399161 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:1926820 G>A maps to ENST00000399161 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:1842994 C>T maps to ENST00000399161 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:59074413 C>T maps to NM_198055.1 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:59074761 T>C maps to NM_198055.1 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr16:48594879 G>A maps to NM_153029.3 C558C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:48595875 A>G maps to NM_153029.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:48596112 T>C maps to NM_153029.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr16:48594663 C>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr13:33017424 G>A maps to NM_033111.3 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr13:33016957 T>G maps to NM_033111.3 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:177548743 C>T maps to NM_015111.1 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:177548792 C>T maps to NM_015111.1 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:177546826 C>T maps to NM_015111.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr13:21306106 G>C maps to NM_174928.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:80246787 G>T maps to NM_032693.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:140262202 C>T maps to NM_057175.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:140264014 G>A maps to NM_057175.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:140306064 G>A maps to NM_057175.3 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:140275178 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:140264041 T>C maps to NM_057175.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:41894848 T>C maps to NM_024561.4 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:20013154 G>A maps to NM_016100.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:112513573 A>T maps to NM_024953.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr12:112481430 G>A maps to NM_024953.3 Q750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:112485517 G>A maps to NM_024953.3 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:112485517 G>A maps to NM_024953.3 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:112499108 C>T maps to NM_024953.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr12:112471036 C>G maps to NM_024953.3 P932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:112480909 G>A maps to NM_024953.3 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr14:57858400 T>A maps to NM_001011713.2 Y242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr14:57858355 C>A maps to NM_001011713.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:57858298 G>A maps to NM_001011713.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:63719909 C>T maps to NM_024771.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:63706575 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:113442283 G>A maps to NM_025146.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:89896481 G>A maps to NM_005467.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr11:89882276 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:89914786 G>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr11:89903285 G>T maps to NM_005467.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:64812883 C>T maps to ENST00000340252 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:64822015 A>G maps to ENST00000340252 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:175042055 C>A maps to NM_207015.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr3:175473203 T>C maps to NM_207015.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:174814793 C>T maps to NM_207015.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:174814907 C>T maps to NM_207015.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:57485291 C>T maps to NM_005967.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:57106629 C>A maps to NM_001113203.1 S2054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:57114974 T>C maps to NM_001113203.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:57113162 G>A maps to NM_001113203.1 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:57107320 C>T maps to NM_001113203.1 K1990K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:57110006 C>T maps to NM_001113203.1 A1769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:57111809 T>A maps to NM_001113203.1 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:57114911 T>C maps to NM_001113203.1 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:59668208 G>A maps to NM_199290.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr17:59667947 A>G maps to NM_199290.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:13246329 G>T maps to NM_052876.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:13246113 C>T maps to NM_052876.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:13248312 C>T maps to NM_052876.2 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr9:138908117 C>T maps to NM_144653.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:1687947 G>A maps to ENST00000344463 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:1685058 T>C maps to ENST00000344463 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:1696664 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:1696698 G>C maps to ENST00000344463 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:1685594 C>A maps to ENST00000344463 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:71201914 C>T maps to NM_018161.4 Y529Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:71202891 G>A maps to NM_018161.4 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:66852490 C>T maps to ENST00000359087 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:66844291 C>A maps to ENST00000359087 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:66858766 A>G maps to ENST00000359087 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr4:164087687 C>T maps to NM_138386.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:164069586 C>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:42464548 G>A maps to NM_000262.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:42463258 C>T maps to NM_000262.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:42463222 G>A maps to NM_000262.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:40695346 G>A maps to NM_000263.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:40695343 C>T maps to NM_000263.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:5083686 C>T maps to NM_016256.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:42082081 G>A maps to NM_153006.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:130825855 G>A maps to NM_197956.3 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:130829149 G>A maps to NM_197956.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:70308438 G>A maps to NM_004536.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:101733919 C>T maps to NM_052867.2 T1281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:101757278 C>A maps to NM_052867.2 G868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:101910796 C>T maps to NM_052867.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:101742313 C>T maps to NM_052867.2 A1091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:101755554 C>A maps to NM_052867.2 E1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:101797192 G>A maps to NM_052867.2 R632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr13:101726010 C>T maps to NM_052867.2 S1374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr13:101759836 C>T did not map to a codon.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr13:101936301 G>A maps to NM_052867.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:101759836 C>T did not map to a codon.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr13:101735456 A>G maps to NM_052867.2 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:101755585 T>C maps to NM_052867.2 K998K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr13:101747982 A>G maps to NM_052867.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr13:101717886 C>T maps to NM_052867.2 K1491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr13:101756693 A>G maps to NM_052867.2 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:101735207 T>G maps to NM_052867.2 V1239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr13:102029265 A>G did not map to a codon.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr13:101755543 G>A maps to NM_052867.2 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:101997641 C>A maps to NM_052867.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:101707700 G>A maps to NM_052867.2 T1721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:101707718 T>C maps to NM_052867.2 E1715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr13:101797193 C>A maps to NM_052867.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr12:7947570 C>T maps to NM_024865.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:46417621 C>T maps to NM_001029861.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:13988457 C>T maps to NM_001098622.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:76449857 C>T maps to NM_139207.2 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr12:76449895 C>A maps to NM_139207.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:72433874 G>A did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:72433469 G>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:72434187 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:72433252 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:72433984 A>C did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:72433059 T>G did not map to a codon.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:72433488 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:72433308 A>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:72433800 A>G did not map to a codon.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr23:72433513 A>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:72434172 G>A did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr23:72433042 T>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:72433766 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:72434173 G>T did not map to a codon.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr23:92926798 T>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:92927518 T>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:92927270 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:92928183 G>A did not map to a codon.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr23:92928029 A>G did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:92927240 T>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:92927973 C>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:92927390 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:92927069 C>T did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:92927837 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr23:92927364 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr23:92926798 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:92928198 G>A did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:92927343 C>T did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:92927705 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:2997296 G>A maps to ENST00000399624 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:89618767 G>A maps to NM_153757.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:47996223 G>A maps to NM_003827.2 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:102769196 A>C maps to ENST00000455523 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:102760246 C>A maps to ENST00000455523 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:10549068 G>A maps to NM_003826.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr8:144658645 C>T maps to ENST00000276844 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr8:144658638 G>A maps to ENST00000276844 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr8:144659013 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:144657423 C>T maps to ENST00000276844 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:50861860 G>A maps to NM_004851.1 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr19:50864331 G>A maps to NM_004851.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:50862330 G>A maps to NM_004851.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:50868803 T>C maps to NM_004851.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:80430461 G>A maps to ENST00000374611 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:780437 A>G maps to NM_022493.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr16:780984 C>T maps to NM_022493.1 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:780542 C>T maps to NM_022493.1 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr16:780494 C>T maps to NM_022493.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:784276 C>T maps to NM_022493.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr15:60734732 A>C maps to NM_024611.4 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr18:55270136 G>A maps to NM_004539.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:55274418 A>G maps to NM_004539.3 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr18:55274523 A>G maps to NM_004539.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:78285485 G>A maps to NM_024678.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:78176990 G>A maps to NM_024678.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:34163345 G>A maps to NM_024662.2 K931K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr16:3533573 C>T maps to NM_024845.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr8:18258346 T>C maps to NM_000015.2 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:18257857 C>T maps to NM_000015.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr8:18257993 C>T maps to NM_000015.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:18257854 T>C maps to NM_000015.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:50334958 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:73868653 C>T maps to NM_003960.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:2065739 A>G maps to ENST00000423729 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:72769712 A>G did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:72767907 G>A maps to NM_015654.3 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:201687703 C>T maps to ENST00000367296 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:201781715 C>T maps to ENST00000367296 L1716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:201779756 C>A maps to ENST00000367296 L1556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr1:201687643 C>T maps to ENST00000367296 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr1:201618002 C>T maps to ENST00000367296 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:201750153 A>C maps to ENST00000367296 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:20077453 G>A maps to ENST00000396087 K1617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:20066922 C>T maps to ENST00000396087 N1226N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:19955097 C>T maps to ENST00000396087 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:19961239 C>T maps to ENST00000396087 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:19955106 C>T maps to ENST00000396087 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr11:20113855 G>T maps to ENST00000396087 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:19735498 C>T maps to ENST00000396087 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:20112543 G>T maps to ENST00000396087 E1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:20112450 C>T maps to ENST00000396087 Q1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr11:20077342 C>T maps to ENST00000396087 S1580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:20005784 C>T maps to ENST00000396087 D943D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:19955142 C>T maps to ENST00000396087 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:20113819 C>T maps to ENST00000396087 S1966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:19901478 G>A maps to ENST00000396087 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:78400964 A>G maps to NM_014903.4 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr12:78334096 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:78513720 C>T maps to NM_014903.4 R1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr12:78569084 G>T did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr12:78443822 T>C maps to NM_014903.4 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:78225342 A>G maps to NM_014903.4 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr12:78443851 C>A maps to NM_014903.4 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:78444657 G>A maps to NM_014903.4 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:78540154 G>T maps to NM_014903.4 E1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:15614423 G>A maps to NM_015909.2 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:15694198 A>G maps to NM_015909.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:15676569 G>A maps to NM_015909.2 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr2:15615938 G>A maps to NM_015909.2 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr13:36241607 C>T maps to ENST00000400445 S2833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr13:36006530 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:36242654 A>C maps to ENST00000400445 R2917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:35733850 T>C maps to ENST00000400445 S1181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:36180561 G>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr13:35692530 T>C maps to ENST00000400445 D721D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr13:36242524 C>T maps to ENST00000400445 D2873D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:35782965 A>G maps to ENST00000400445 T1832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:35517238 G>A maps to ENST00000400445 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr13:36006492 T>G maps to ENST00000400445 T2089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:35517247 C>T maps to ENST00000400445 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:36125121 C>T maps to ENST00000400445 S2253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:35733236 A>T maps to ENST00000400445 K977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr13:36241641 C>T maps to ENST00000400445 R2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:35644127 T>C maps to ENST00000400445 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr13:36241641 C>T maps to ENST00000400445 R2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr13:35692560 G>A maps to ENST00000400445 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:204001464 A>G maps to NM_001114132.1 E1482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:204045235 G>A did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr2:204055112 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:19981834 C>T maps to NM_182744.2 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:90982767 G>A maps to NM_002485.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:90990515 T>C maps to NM_002485.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:90983457 C>T maps to NM_002485.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:16913542 A>G did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr1:16914254 C>T maps to NM_017940.3 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr1:16907957 G>A maps to NM_017940.3 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:16890674 G>A maps to NM_017940.3 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:16893782 A>G maps to NM_017940.3 C910C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:145325966 G>C maps to NM_001039703.4 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:148015780 G>A maps to ENST00000310701 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:148756509 G>A maps to ENST00000442702 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:21795286 G>A maps to NM_032264.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr1:21806542 G>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:41343440 C>T maps to NM_005899.3 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:41345125 C>A maps to NM_005899.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:41341639 G>A maps to NM_005899.3 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:102731524 G>A maps to NM_032041.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr8:102731641 G>A maps to NM_032041.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:102701587 C>T maps to NM_032041.2 P177P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8360-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:113102925 C>A maps to ENST00000316851 Y424*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8DT-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr21:22906921 G>T maps to NM_004540.2 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:22746310 G>A maps to NM_004540.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr21:22656514 G>T maps to NM_004540.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr21:22804467 G>A maps to NM_004540.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr21:22804560 G>A maps to NM_004540.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr21:22881275 C>T maps to NM_004540.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr21:22804503 G>A maps to NM_004540.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr21:22881187 T>A maps to NM_004540.2 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr21:22782719 T>A maps to NM_004540.2 L441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr21:22910226 T>C maps to NM_004540.2 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr21:22782726 T>C maps to NM_004540.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:22790889 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:19330021 G>A maps to NM_004386.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:19337826 C>T maps to NM_004386.2 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:19351409 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:19329853 C>T maps to NM_004386.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr19:19339179 G>A maps to NM_004386.2 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:19338120 C>A maps to NM_004386.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr12:6623968 G>A maps to NM_014865.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr12:6637164 C>A maps to NM_014865.3 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:6634801 G>A maps to NM_014865.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr12:6636066 C>T maps to NM_014865.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:134048792 C>T maps to NM_015261.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:134051037 G>A maps to NM_015261.2 C831C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:134022910 G>T maps to NM_015261.2 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:134050983 G>A maps to NM_015261.2 D849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:134037944 G>A maps to NM_015261.2 D1173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr11:134063916 G>T maps to NM_015261.2 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:97019988 C>T maps to NM_015341.3 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100423345 C>T maps to NM_002486.4 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:196666225 A>C maps to NM_007362.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:39690988 C>T maps to NM_001001414.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:36026732 G>A maps to NM_001014839.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:36026369 C>T maps to NM_001014839.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr1:36026174 G>C maps to NM_001014839.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:36026082 C>T maps to NM_001014839.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:74197372 C>T maps to NM_000265.4 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:74191683 C>T maps to NM_000265.4 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:74197384 C>T maps to NM_000265.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:183534899 C>T maps to NM_001127651.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:183538296 C>T maps to NM_001127651.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:183538296 C>T maps to NM_001127651.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:183559419 C>A maps to NM_001127651.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr22:37272121 G>T maps to NM_000631.4 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:37260992 A>G maps to NM_013416.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:136665097 A>G maps to NM_006153.4 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr3:136646966 C>T maps to NM_006153.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:106498309 C>T maps to NM_001004720.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:106497874 C>T maps to NM_001004720.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:106497811 C>T maps to NM_001004720.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:106498348 G>A maps to NM_001004720.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr2:106497823 G>A maps to NM_001004720.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:106498372 C>T maps to NM_001004720.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:183848064 C>T maps to NM_205842.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr2:183860434 G>A maps to NM_205842.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:183853876 G>A maps to NM_205842.1 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:183792930 A>G maps to NM_205842.1 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:183817965 T>C maps to NM_205842.1 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:183822240 A>G maps to NM_205842.1 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr2:183846104 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr2:183792843 C>G did not map to a codon.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr2:183818059 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:54930015 C>T maps to NM_005337.4 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:54902228 A>C maps to NM_005337.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr12:54932721 A>C maps to NM_005337.4 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr12:54910751 T>C maps to NM_005337.4 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:54893227 C>T maps to NM_005337.4 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:54925967 C>T maps to NM_005337.4 H932H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:54936432 C>A maps to NM_005337.4 A1116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:54902171 G>A did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr2:133542727 T>G maps to NM_207363.2 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:133489466 A>C maps to NM_207363.2 S1762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:133542364 C>T maps to NM_207363.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:133542087 G>A maps to NM_207363.2 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:133541593 C>T maps to NM_207363.2 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr2:133542676 G>T maps to NM_207363.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:133489397 G>A maps to NM_207363.2 S1785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr2:133540879 C>T maps to NM_207363.2 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr2:133547604 G>A maps to NM_207363.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:133539526 C>T maps to NM_207363.2 T1619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:133541937 G>A maps to NM_207363.2 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:133541059 A>G maps to NM_207363.2 N1108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:133542958 G>A maps to NM_207363.2 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:133483296 G>A maps to NM_207363.2 S1872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr2:133540638 T>A maps to NM_207363.2 R1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:133538705 G>A maps to NM_207363.2 I1656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:133542670 G>A maps to NM_207363.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:50190189 G>A maps to NM_001037806.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:48717232 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:232325258 T>C maps to NM_005381.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr2:232326383 G>A maps to NM_005381.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:232326263 G>A maps to NM_005381.2 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:24928021 C>T maps to NM_003743.4 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:24929853 C>T maps to NM_003743.4 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:24930501 G>T maps to NM_003743.4 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:24933897 G>A maps to NM_003743.4 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:24881611 G>A maps to NM_003743.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:24929664 A>C maps to NM_003743.4 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:71068295 T>C maps to NM_006540.2 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:71069387 G>T maps to NM_006540.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr8:71082535 T>G maps to NM_006540.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:71126173 C>A maps to NM_006540.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:71057030 A>G maps to NM_006540.2 N886N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:71071750 A>G maps to NM_006540.2 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr8:71078866 G>A maps to NM_006540.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:71071819 A>G maps to NM_006540.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:46264164 G>A maps to NM_181659.2 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:46267788 T>A maps to NM_181659.2 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:46265283 C>T maps to NM_181659.2 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr20:46268543 G>A maps to NM_181659.2 Q977Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:46265202 T>C maps to NM_181659.2 N691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:46279844 G>A maps to NM_181659.2 Q1257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:46251036 C>T maps to NM_181659.2 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:46265283 C>T maps to NM_181659.2 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr20:46254222 C>T maps to NM_181659.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:46268495 G>A maps to NM_181659.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:46279841 G>A maps to NM_181659.2 Q1256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr20:46279841 G>A maps to NM_181659.2 Q1256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:51580587 T>C maps to NM_001145260.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr10:51580945 C>T maps to NM_001145260.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:51585082 T>C maps to NM_001145260.1 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:44691316 C>T maps to NM_020967.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:44691343 C>A maps to NM_020967.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:33356267 T>C maps to NM_014071.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:33330812 G>A maps to NM_014071.2 Q1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:33331121 G>A maps to NM_014071.2 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:33345719 T>C maps to NM_014071.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr20:33345128 C>T maps to NM_014071.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:33345656 C>T maps to NM_014071.2 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:33330966 T>C maps to NM_014071.2 Q1031Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:33330510 T>C maps to NM_014071.2 Q1183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:33345769 G>A maps to NM_014071.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:33328371 C>T maps to NM_014071.2 P1896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:33303155 C>T maps to NM_014071.2 A2054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:33330513 C>T maps to NM_014071.2 Q1182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:33345722 C>T maps to NM_014071.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:126210196 C>T maps to NM_181782.4 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:16049687 A>G did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr17:16068475 C>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:15971387 G>A maps to ENST00000395857 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:16068427 C>T maps to ENST00000395857 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:15968181 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:16024444 G>A maps to ENST00000395857 N591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:16042374 A>G maps to ENST00000395857 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:16075114 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:16024503 G>A maps to ENST00000395857 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:15974751 G>T maps to ENST00000395857 R1391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:16041477 C>T maps to ENST00000395857 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:15989673 C>T maps to ENST00000395857 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:16024411 C>T maps to ENST00000395857 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:15983784 G>A maps to ENST00000395857 R1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr17:16004958 G>C maps to ENST00000395857 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:124857106 A>G maps to NM_006312.4 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:124968139 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:124835151 G>T maps to NM_006312.4 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:124827626 G>T maps to NM_006312.4 G1627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:124821386 C>T maps to NM_006312.4 P2016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr12:124832723 G>A maps to NM_006312.4 I1334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr12:124846807 G>A maps to NM_006312.4 D987D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:55420812 C>T maps to NM_004829.5 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:55420751 C>T maps to NM_004829.5 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:55417574 C>T maps to NM_004829.5 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:41309824 G>A maps to NM_004828.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr6:41309550 C>A maps to NM_004828.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:132988753 C>T maps to NM_014286.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:132980176 C>T maps to NM_014286.3 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr1:160326121 C>T maps to NM_015331.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:160319416 C>A maps to NM_015331.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr1:160327003 C>T maps to NM_015331.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:160326877 G>A maps to NM_015331.2 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr18:2595493 C>T maps to NM_006101.2 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:2577853 C>T maps to NM_006101.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:2575050 G>A maps to NM_006101.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr18:2578994 G>A maps to NM_006101.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:8350199 C>T maps to ENST00000402554 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:8358206 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:23931740 G>A maps to NM_002487.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:23931989 C>T maps to NM_002487.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr15:23932079 C>T maps to NM_002487.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:23932076 C>T maps to NM_002487.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:23932202 G>A maps to NM_002487.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:29561678 C>A maps to NM_138704.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:29561063 G>T maps to NM_138704.2 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:140108802 C>T maps to NM_001144026.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:140108240 C>T maps to NM_001144026.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:140108309 C>T maps to NM_001144026.1 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:140110804 C>T maps to NM_001144026.1 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:140110126 C>A maps to NM_001144026.1 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:134276799 G>T maps to NM_006096.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:134292507 G>T maps to NM_006096.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr14:21490643 C>A maps to NM_201537.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:21490025 T>C maps to NM_201537.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:35293700 G>A maps to ENST00000373803 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:35310929 G>A maps to ENST00000373803 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:35288784 G>A maps to ENST00000373803 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:149901097 G>A maps to NM_001543.4 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:149927850 C>T maps to NM_001543.4 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:149900962 G>A maps to NM_001543.4 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:149901259 C>T maps to NM_001543.4 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:149927859 G>A maps to NM_001543.4 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr5:149907685 C>T maps to NM_001543.4 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr5:149900872 C>T maps to NM_001543.4 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:75565361 G>A maps to NM_003635.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr10:75563057 T>C maps to NM_003635.3 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:119176866 G>T maps to NM_004784.2 *874Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:119163292 A>C maps to NM_004784.2 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:119154276 A>C maps to NM_004784.2 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:119158199 G>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:118975700 A>G maps to NM_004784.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:119145776 G>T maps to NM_004784.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:118975751 C>A maps to NM_004784.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:115998015 T>A maps to NM_022569.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:115891705 T>C maps to NM_022569.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:115773956 T>C maps to NM_022569.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:115997355 C>T maps to NM_022569.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:119007296 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:19638862 C>T maps to ENST00000450144 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:140027105 G>A maps to NM_002488.4 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:54610151 G>A maps to NM_004542.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr19:8376454 C>T maps to NM_005001.2 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:124906576 G>A maps to NM_014222.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:124914654 C>T maps to NM_014222.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr12:4796210 C>T maps to NM_005002.4 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr12:4763606 C>T maps to NM_005002.4 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:49059971 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:49059585 C>A maps to NM_199069.1 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr6:97344624 A>G maps to NM_014165.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:92583936 A>C maps to NM_004545.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:47001791 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:47003889 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:47003963 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:201950220 T>C maps to NM_002491.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:120315274 C>T maps to NM_004547.5 Y23Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr19:14677058 C>T maps to NM_004146.4 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:125559293 T>G maps to NM_005005.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:207009719 C>T maps to ENST00000455934 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:207008753 G>A maps to ENST00000455934 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:207003256 G>A maps to ENST00000455934 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:161180179 G>T did not map to a codon.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr11:47604019 G>A maps to NM_004551.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:47603971 C>T maps to NM_004551.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:1390982 G>A maps to NM_024407.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:1390982 G>A maps to NM_024407.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:67799756 T>C maps to NM_002496.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:67378678 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:67377009 G>A maps to NM_007103.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr21:44324108 G>A maps to NM_021075.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:152501055 T>G maps to NM_001164507.1 R2524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:152382734 G>A maps to NM_001164507.1 C7329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:152410410 G>A maps to NM_001164507.1 H6519H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:152472521 A>G maps to NM_001164507.1 A3761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:152496961 A>G maps to NM_001164507.1 D2864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:152496993 G>A maps to NM_001164507.1 L2854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr2:152486100 G>A maps to NM_001164507.1 D3261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:152427009 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:152500373 G>A maps to NM_001164507.1 S2638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:152411513 C>T maps to NM_001164507.1 T6453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr2:152385744 G>A maps to NM_001164507.1 D7238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:152352869 C>A maps to NM_001164507.1 E8136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:152382698 C>T maps to NM_001164507.1 A7341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:152411447 G>A maps to NM_001164507.1 I6475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:152432772 G>T maps to NM_001164507.1 I5600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:152474791 A>G maps to NM_001164507.1 N3691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:152563475 T>G maps to NM_001164507.1 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr2:152420118 C>G did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr2:152529050 G>A maps to NM_001164507.1 T1377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:152539238 G>A maps to NM_001164507.1 G960G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:152476093 G>A maps to NM_001164507.1 I3581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:152544187 G>A maps to NM_001164507.1 D825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr2:152396911 A>G maps to NM_001164507.1 V6946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr2:152521047 C>T maps to NM_001164507.1 K1806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:152394411 G>A maps to NM_001164507.1 R7026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr2:152554108 G>A maps to NM_001164507.1 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr2:152466519 T>G maps to NM_001164507.1 R4045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr2:152527728 G>A maps to NM_001164507.1 D1438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:152394745 C>A maps to NM_001164507.1 E6969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:152522804 A>C maps to NM_001164507.1 S1610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr10:21074771 G>A maps to ENST00000430741 N985N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:21147168 G>A maps to ENST00000430741 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:21177121 G>A maps to ENST00000430741 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr10:21139350 T>G maps to ENST00000430741 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:21108358 C>T maps to ENST00000430741 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr10:21076217 G>T maps to ENST00000430741 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr10:21101758 A>C maps to ENST00000430741 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr10:21104553 C>T maps to ENST00000430741 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:21141527 A>G maps to ENST00000430741 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr10:21117563 C>G did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr8:91940517 G>T maps to NM_022351.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr8:91929743 G>T maps to NM_022351.4 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr16:84030846 C>T maps to NM_019065.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr16:84027966 C>T maps to NM_019065.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:32248162 C>T maps to NM_031232.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:32248126 T>C maps to NM_031232.3 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr20:32248162 C>T maps to NM_031232.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:8245508 T>C maps to NM_015509.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:8248233 G>A maps to NM_015509.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:16767270 G>A maps to NM_018090.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:16775641 C>A maps to NM_018090.4 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:16774556 C>T maps to NM_018090.4 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:97337416 T>C maps to NM_001135175.1 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:97328923 G>A maps to NM_001135175.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr15:56208942 G>A maps to ENST00000508342 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:56140716 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:56122784 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:55919282 A>G maps to NM_001144967.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:56008368 C>T maps to NM_001144967.1 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:56001084 T>C maps to NM_001144967.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr18:55996337 G>A maps to NM_001144967.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr6:11191198 G>A maps to NM_006403.3 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:11190802 G>A maps to NM_006403.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr6:11190484 G>A maps to NM_006403.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:11193913 G>A maps to NM_006403.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr6:11191045 C>T maps to NM_006403.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr6:11190445 G>A maps to NM_006403.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:11192589 C>T maps to NM_006403.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:11191399 T>C maps to NM_006403.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:29879421 G>A maps to NM_021076.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr22:29886667 A>G maps to NM_021076.3 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr22:29885530 C>A maps to NM_021076.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr8:24811293 G>A maps to ENST00000221169 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr8:24813351 C>G maps to ENST00000221169 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:24813204 G>A maps to ENST00000221169 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:24811203 G>A maps to ENST00000221169 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:24813258 C>T maps to ENST00000221169 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:24813882 G>T maps to ENST00000221169 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:24771746 C>T maps to NM_005382.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:24773230 C>T maps to NM_005382.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:24771920 G>A maps to NM_005382.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:24772256 C>T maps to NM_005382.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:24771398 G>A maps to NM_005382.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr8:24774699 C>G maps to NM_005382.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr8:24771914 C>T maps to NM_005382.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr8:24772193 C>T maps to NM_005382.2 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:24771869 C>T maps to NM_005382.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:72748048 C>T maps to NM_173808.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:72076710 C>T maps to NM_173808.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:75644697 G>A maps to NM_024608.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:75646104 C>T maps to NM_024608.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr8:11643641 C>T maps to NM_145043.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:11637249 G>A maps to NM_145043.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:11637207 G>A maps to NM_145043.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:11637330 C>T maps to NM_145043.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:11643586 T>C maps to NM_145043.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr4:178256868 C>T maps to NM_018248.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:170345784 C>T maps to ENST00000507142 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:170400580 T>C maps to ENST00000507142 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:170428877 G>A maps to ENST00000507142 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:170322818 G>A maps to ENST00000507142 N1189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr4:170506563 G>T maps to ENST00000507142 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:170523228 T>C maps to ENST00000507142 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:27346259 G>A maps to ENST00000396636 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:27326329 C>T did not map to a codon.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr3:27326453 T>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:130947465 G>A maps to NM_024800.4 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:211842454 G>A maps to NM_002497.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:211847635 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr1:211847651 C>T maps to NM_002497.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:211836782 G>A maps to NM_002497.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:52745873 C>T maps to NM_003157.4 R815R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:52786313 G>T maps to NM_003157.4 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:52777457 C>T maps to NM_003157.4 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:52639734 C>T maps to NM_199289.1 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:52684695 T>C maps to NM_199289.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:52686484 A>G maps to NM_199289.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:127089653 C>T maps to NM_001166171.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:127101922 C>T maps to NM_001166171.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr9:127089677 T>C maps to NM_001166171.1 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:127113223 T>C maps to NM_001166171.1 *348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:198288606 T>G maps to NM_133494.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr1:198247155 C>T maps to NM_133494.2 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:27064894 C>A maps to NM_178170.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:27068462 C>T maps to NM_178170.2 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr17:27062000 C>T maps to NM_178170.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:27068434 C>T maps to NM_178170.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr14:75573235 C>T maps to NM_033116.4 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr9:140350864 T>C maps to NM_001130969.1 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr9:140343923 C>T maps to NM_001130969.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:140352210 G>A maps to NM_001130969.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:140352309 G>A maps to NM_001130969.1 P59P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-4305-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:20948909 T>G maps to NM_006157.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:20907077 T>C maps to NM_006157.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:21135210 C>T maps to NM_006157.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:21250983 C>T maps to NM_006157.3 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:20940855 G>A maps to NM_006157.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr11:20949920 A>G did not map to a codon.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr11:21135237 T>C maps to NM_006157.3 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr11:20940834 A>G maps to NM_006157.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:44915908 T>C maps to NM_001145107.1 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:44915857 G>A maps to NM_001145107.1 C750C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:45269071 C>T maps to NM_001145107.1 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:44926490 G>T maps to NM_001145107.1 C609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:212619245 C>T maps to NM_013349.4 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:73594971 C>T maps to NM_002499.3 L1441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:73542046 C>T maps to NM_002499.3 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr15:73580779 A>G maps to NM_002499.3 P1179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:73418761 T>C maps to NM_002499.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:73541997 G>T maps to NM_002499.3 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr15:73408891 C>T maps to NM_002499.3 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:73585743 C>A maps to NM_002499.3 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:73570469 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr15:73562760 G>A maps to NM_002499.3 W941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr15:73562535 C>T maps to NM_002499.3 R894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr1:156640712 G>C maps to NM_006617.1 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:156645009 G>A maps to NM_006617.1 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr1:156645072 G>A maps to NM_006617.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:156642652 C>A maps to NM_006617.1 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:156646945 G>A maps to NM_006617.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr1:156641840 A>T maps to NM_006617.1 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr1:156641692 G>A maps to NM_006617.1 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:5495289 T>C maps to NM_001047160.1 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:5498108 C>T maps to NM_001047160.1 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr10:5498108 C>T maps to NM_001047160.1 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:5498072 A>G maps to NM_001047160.1 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr18:70461449 C>A maps to NM_153181.2 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr18:70450954 G>A maps to NM_153181.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr18:70451125 A>G maps to NM_153181.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr18:70417352 G>A maps to NM_153181.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr18:70526078 G>A maps to NM_153181.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:70526083 G>T maps to NM_153181.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr18:70526205 A>G maps to NM_153181.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:47163218 G>A maps to NM_018092.3 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:47165898 G>A maps to NM_018092.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:31829887 C>T maps to NM_000434.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:31829854 G>A maps to NM_000434.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:233899562 G>A maps to NM_005383.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:233897494 G>A maps to NM_005383.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:233899484 C>T maps to NM_005383.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:233898989 G>A maps to NM_005383.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:233898911 G>T maps to NM_005383.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr11:74705695 T>C maps to NM_006656.5 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:74705644 G>A maps to NM_006656.5 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr10:105331526 G>A maps to NM_004210.4 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr10:105349313 C>A maps to NM_004210.4 C461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:105349957 C>T maps to NM_004210.4 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr20:44519207 G>C maps to NM_080749.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr20:44519400 C>T maps to NM_080749.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:182543446 G>A maps to NM_002500.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:182542663 C>T maps to NM_002500.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr2:182542846 G>A maps to NM_002500.2 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:182543539 G>T maps to NM_002500.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:182543032 C>T maps to NM_002500.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:182543575 C>T maps to NM_002500.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:182542720 C>T maps to NM_002500.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:37762189 G>T maps to NM_006160.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:37762006 G>A maps to NM_006160.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr12:55420234 T>G maps to NM_021191.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr12:55420234 T>G maps to NM_021191.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr12:55421021 C>T maps to NM_021191.2 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:31377946 G>A maps to NM_022728.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:134871158 G>C maps to NM_006161.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:134870906 G>A maps to NM_006161.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:113436382 T>C maps to NM_024019.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:113436100 G>C maps to NM_024019.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:113436262 G>A maps to NM_024019.2 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:71332526 G>A maps to NM_020999.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr17:29533377 C>T maps to NM_001042492.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr17:29685543 C>T maps to NM_001042492.2 Q2673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr17:29662039 C>T maps to NM_001042492.2 S1999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:29576056 G>T maps to NM_001042492.2 E1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:29559873 A>G maps to NM_001042492.2 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:29701122 C>T maps to NM_001042492.2 Q2824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:29552150 C>T maps to NM_001042492.2 Y628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:29497002 C>T maps to NM_001042492.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:29556374 G>A maps to NM_001042492.2 R914R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:29654701 A>G maps to NM_001042492.2 E1818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:29587385 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr17:29562681 C>A maps to NM_001042492.2 Y1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:30057231 C>A maps to NM_181832.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr1:204955198 T>C maps to ENST00000367172 D916D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:204948671 C>T maps to ENST00000367172 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:69727556 C>T maps to NM_138713.2 Q1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:69660351 T>C maps to NM_138713.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:69727102 C>A maps to NM_138713.2 T1125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:69729042 T>C maps to NM_138713.2 C1473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:69681373 C>T maps to NM_138713.2 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:69727813 G>A maps to NM_138713.2 S1362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr16:69727069 A>C maps to NM_138713.2 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:69726328 A>C maps to NM_138713.2 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:77211695 C>T maps to NM_172387.1 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr18:77171138 C>T maps to NM_172387.1 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:77170568 G>T maps to NM_172387.1 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:77171051 C>T maps to NM_172387.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr18:77246791 G>A maps to NM_172387.1 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:77211058 C>T maps to NM_172387.1 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr18:77246761 G>A maps to NM_172387.1 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr18:77208861 C>T maps to NM_172387.1 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:77246401 G>A maps to NM_172387.1 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:77193581 G>A maps to NM_172387.1 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:77246926 C>T maps to NM_172387.1 Y911Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:50048988 G>A maps to NM_012340.3 D779D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr20:50159029 G>A maps to NM_012340.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:50051836 A>G maps to NM_012340.3 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:50051779 G>A maps to NM_012340.3 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:28970421 G>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:68191770 G>A did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr14:24843059 G>A maps to NM_001136022.1 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:24843568 C>A maps to NM_001136022.1 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:54686820 G>A maps to NM_001136023.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:54686847 G>A maps to NM_001136023.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:54686658 G>T maps to NM_001136023.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:46135781 G>A maps to ENST00000362042 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr17:46128573 C>T maps to ENST00000362042 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr17:46128983 C>T maps to ENST00000362042 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:46128991 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:46136684 G>A maps to ENST00000362042 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr17:46133881 C>T maps to ENST00000362042 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:178098750 T>G maps to NM_006164.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr7:26224982 C>T maps to NM_004289.6 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr7:26224556 T>C maps to NM_004289.6 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr1:61872277 C>T maps to NM_001145512.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:61921002 G>A maps to NM_005595.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:14150262 C>T maps to ENST00000397581 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:14307363 G>A maps to ENST00000397581 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:3382065 G>A maps to ENST00000269778 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr19:3433552 C>T maps to ENST00000269778 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:94172248 T>C maps to NM_005384.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:94172524 G>A maps to NM_005384.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:13192650 G>A maps to ENST00000397661 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:13201131 C>T maps to ENST00000397661 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr19:13192536 G>A maps to ENST00000397661 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:103514651 T>C maps to NM_003998.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:103537598 C>T maps to NM_003998.3 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:104156719 A>G maps to NM_001077494.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:104161009 G>A maps to NM_001077494.1 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:104160087 G>T maps to NM_001077494.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:36380853 G>A maps to ENST00000352614 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:31526078 C>T maps to NM_005007.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145661145 T>C maps to NM_013432.4 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145665766 G>A maps to NM_013432.4 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr8:145661048 G>A maps to NM_013432.4 Q923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:145655793 G>A maps to NM_013432.4 G1312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:145661487 G>A maps to NM_013432.4 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:101574021 T>C maps to NM_031419.3 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr3:101574052 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:101572368 G>A maps to NM_031419.3 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:129740015 C>T maps to NM_006165.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:129754691 C>T maps to NM_006165.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:129739943 C>T maps to NM_006165.3 Q1017Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:129739946 G>A maps to NM_006165.3 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:129739601 G>A maps to NM_006165.3 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:129739493 T>C maps to NM_006165.3 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:129754772 C>T maps to NM_006165.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:34262503 C>A maps to NM_021100.4 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:34286423 A>G maps to NM_021100.4 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr20:34278406 G>A maps to NM_021100.4 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:33369963 C>T maps to NM_002504.4 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:33295420 C>T maps to NM_002504.4 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:33294991 G>A maps to NM_002504.4 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:33319096 C>T maps to NM_002504.4 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:33294676 G>A maps to NM_002504.4 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:33295159 A>C maps to NM_002504.4 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr4:47901012 A>T maps to NM_152995.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:47896255 G>A maps to NM_152995.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:23945485 C>T maps to NM_001042635.1 R195*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-4362-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:233785032 C>T maps to NM_019850.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr1:115829230 G>A maps to NM_002506.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:115829353 G>A maps to NM_002506.2 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:115829175 G>A maps to NM_002506.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:47583718 C>T maps to NM_002507.3 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:47583940 G>A maps to NM_002507.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:47589349 C>T maps to NM_002507.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr17:47590139 C>G maps to NM_002507.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:47583739 G>A maps to NM_002507.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr17:47583835 C>T maps to NM_002507.3 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:102632527 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr23:102632527 C>T did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr23:102632561 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:102632689 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:103870504 C>T maps to NM_139173.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:103827696 A>G maps to NM_139173.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:103870468 T>A maps to NM_139173.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr4:103912855 C>A maps to NM_139173.3 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:103870468 T>C maps to NM_139173.3 G109G. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:103911068 A>G does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr4:103853398 T>C maps to NM_139173.3 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:219941147 C>T maps to NM_024782.2 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:160340832 G>A maps to NM_005598.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:116380780 G>C maps to NM_005599.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:116380624 G>T maps to NM_005599.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:18122828 G>A maps to NM_198586.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:18122486 G>A maps to NM_198586.2 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:115661479 C>T maps to NM_198514.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:115639426 A>T maps to NM_198514.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:115664652 A>C maps to NM_198514.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:17746816 C>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:17705907 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:17744153 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:17744771 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:17745810 T>C did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr23:17745706 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:17742446 A>G did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:17750506 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:17743967 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:17744388 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:17745599 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr23:17744272 G>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:17739628 T>C did not map to a codon.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr23:17745825 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:17744538 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:17739684 C>T did not map to a codon.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr23:17743693 G>A did not map to a codon.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr23:17750498 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:17744830 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:17705866 T>C did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:71358768 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:71359621 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:71359173 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:71359789 C>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:71360036 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:71360087 T>C did not map to a codon.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr23:71359740 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:71358761 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:236154335 C>T maps to NM_002508.2 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:236189262 G>A maps to NM_002508.2 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:236201452 G>T maps to NM_002508.2 C412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:236143153 G>A maps to NM_002508.2 Y1159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:236144977 G>A maps to NM_002508.2 Q1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr1:236142364 C>T maps to NM_002508.2 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:236157044 C>T maps to NM_002508.2 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:236195818 G>A maps to NM_002508.2 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr14:52508985 C>T maps to NM_007361.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr14:52535484 G>A maps to NM_007361.3 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:52494042 G>A maps to NM_007361.3 N850N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:52520474 G>A maps to NM_007361.3 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:52507366 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:52535541 G>A maps to NM_007361.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:52535553 G>A maps to NM_007361.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr2:201768268 C>T maps to NM_001136039.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:51208343 C>A maps to NM_020921.3 E1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr14:51224806 G>A maps to NM_020921.3 Q981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:51243810 A>G maps to NM_020921.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr14:51224536 G>A maps to NM_020921.3 Q1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:675143 C>A maps to NM_016533.4 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr20:25459830 G>A maps to NM_025176.4 Y643Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:25507058 G>A maps to NM_025176.4 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:25457247 G>A maps to NM_025176.4 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:25456683 G>A maps to NM_025176.4 N1081N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr20:25484647 G>A maps to NM_025176.4 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:25439087 A>G maps to NM_025176.4 R1258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr20:25434181 G>A maps to NM_025176.4 R1352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr20:25456683 G>A maps to NM_025176.4 N1081N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:25498443 C>T maps to NM_025176.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:23049188 C>T maps to NM_144599.4 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:23049053 G>A maps to NM_144599.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:23049278 C>T maps to NM_144599.4 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr15:23006655 G>T maps to NM_030922.6 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:23014502 G>A maps to NM_030922.6 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr4:48037690 G>A maps to NM_207330.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:48027092 C>T maps to NM_207330.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:99248422 A>G maps to NM_024759.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:24746099 C>T maps to NM_020448.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:24776016 T>C maps to NM_020448.4 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:156899931 A>T maps to NM_001099287.1 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:156899808 C>T maps to NM_001099287.1 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:36976271 G>A maps to NM_133433.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:37022372 C>T maps to NM_133433.3 R1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr5:36984937 C>T maps to NM_133433.3 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:36985831 T>C maps to NM_133433.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:37059069 A>G maps to NM_133433.3 E2496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:37006670 C>A maps to NM_133433.3 Y1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:37020716 C>T maps to NM_133433.3 R1723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:37027459 G>T did not map to a codon.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr5:37020586 G>A maps to NM_133433.3 Q1679Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:37022158 C>T maps to NM_133433.3 R1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr5:37052623 C>T maps to NM_133433.3 R2407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:36985831 T>C maps to NM_133433.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:37000601 T>C maps to NM_133433.3 G1144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr5:37000673 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:36984874 G>A maps to NM_133433.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr5:37016205 T>G maps to NM_133433.3 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr5:37010242 A>G maps to NM_133433.3 A1492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr22:29956771 G>A maps to NM_003634.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr9:107513406 T>C maps to NM_015469.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:107535335 A>G maps to NM_018376.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:52491917 C>T maps to NM_007184.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:52522417 C>T maps to NM_007184.3 H970H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:52522195 G>A maps to NM_007184.3 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:52522234 G>A maps to NM_007184.3 W909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:52504924 T>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:52522495 C>T maps to NM_007184.3 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:52505857 C>A maps to NM_007184.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr3:52521667 C>T maps to NM_007184.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:52522246 G>A maps to NM_007184.3 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr3:52521724 C>T maps to NM_007184.3 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:52491935 T>C maps to NM_007184.3 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:52524131 G>A maps to NM_007184.3 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:100067662 A>C maps to NM_020202.4 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr3:100058730 C>T maps to NM_020202.4 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:100071246 G>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:124125393 C>T maps to NM_001040214.1 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:124979411 G>A maps to NM_001040214.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:119068455 C>T did not map to a codon.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr23:119077494 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:119068468 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:119077560 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr23:119064117 C>A did not map to a codon.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr23:119059333 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:119065933 T>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:28227238 G>A maps to NM_001007531.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:28227367 G>A maps to NM_001007531.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:28227418 G>A maps to NM_001007531.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr6:28227361 G>A maps to NM_001007531.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr6:28227547 G>A maps to NM_001007531.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr6:28227900 C>G maps to NM_001007531.1 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:50659406 C>T maps to NM_033119.3 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr16:50642254 C>T maps to NM_033119.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:50667160 A>G maps to NM_033119.3 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:1037965 G>A maps to NM_033120.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:51875206 G>T maps to NM_005601.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:23952391 C>A maps to NM_020345.3 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:45656239 C>T maps to NM_198478.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:45655846 G>A maps to NM_198478.3 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:45655516 G>A maps to NM_198478.3 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr19:45656073 G>A maps to NM_198478.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:118723341 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:118723330 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:118723880 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:118724033 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr23:118724854 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:118724534 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:118723957 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:118724649 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:42679031 C>T maps to NM_005385.3 D612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:42679754 C>T maps to NM_005385.3 C853C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:42680000 G>A maps to NM_005385.3 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:42674256 C>T maps to NM_005385.3 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:36987202 C>T maps to NM_001079668.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr14:36987175 G>A maps to NM_001079668.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:36988394 G>A maps to NM_001079668.2 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr14:36988385 C>T maps to NM_001079668.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr14:36986998 C>T maps to NM_001079668.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:21493106 G>A maps to NM_002509.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:21492692 C>T maps to NM_002509.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr20:21494271 G>A maps to NM_002509.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:21494211 C>T maps to NM_002509.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:21492937 G>A maps to NM_002509.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr20:21492734 G>A maps to NM_002509.2 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:21377058 T>C maps to NM_033176.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:172659582 G>A maps to NM_004387.3 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:172660159 G>A maps to NM_004387.3 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:172660042 G>A maps to NM_004387.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:172660102 C>T maps to NM_004387.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:172659802 G>A maps to NM_004387.3 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:172660141 C>T maps to NM_004387.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:37051464 G>A maps to NM_014360.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:23538895 T>C maps to NM_006167.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:13545771 T>C maps to NM_001189.3 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:85414654 G>A maps to NM_006168.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:85416929 C>T maps to NM_006168.2 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:134598437 G>A maps to NM_177400.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:134598810 C>T maps to NM_177400.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr10:134598810 C>T maps to NM_177400.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:134598861 G>A maps to NM_177400.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:33467010 G>T maps to NM_018096.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:173996753 T>C maps to NM_014932.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:173998564 A>G maps to NM_014932.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr3:173997320 C>A maps to NM_014932.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:173322504 G>A maps to NM_014932.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:70367984 T>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:70389753 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:70367839 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:70389592 C>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:70384071 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:70368013 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:70367957 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:70389594 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:70384061 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:70389349 G>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:70389195 G>A did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:70375089 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:70387059 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:70367786 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:70386935 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:70375088 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:70387071 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:5811197 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:5821796 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:5821510 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:5827246 C>T did not map to a codon.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr23:5821173 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:6069135 C>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:5947434 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:5821700 A>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:5811219 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:5821126 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:5821497 G>A did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr23:5821834 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:5821575 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:6069041 C>T did not map to a codon.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr23:5821800 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr23:6069106 G>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:5821128 G>A did not map to a codon.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr23:5811224 G>A did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:5810978 T>A did not map to a codon.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr23:5821347 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:5821155 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:6069147 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:6069401 A>C did not map to a codon.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr23:5811356 T>A did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:5821575 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:5827118 A>G did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr23:5811501 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:5821683 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:5810907 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:5821683 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:5821693 G>A did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:5811180 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:5821720 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr23:5811185 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:6069221 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr24:16952742 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr24:16953055 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr24:16941709 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr24:16952312 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr24:16941638 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:26518100 C>T maps to NM_016231.4 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr17:26518099 G>A maps to NM_016231.4 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:65105421 G>A maps to NM_020726.4 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr5:65073294 A>G maps to NM_020726.4 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:65118658 C>T maps to NM_020726.4 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:3614998 G>A maps to ENST00000448023 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr16:3614349 C>A maps to ENST00000448023 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr16:3613635 C>T maps to ENST00000448023 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr16:3614463 G>A maps to ENST00000448023 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:3614280 G>A maps to ENST00000448023 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:3602258 C>T maps to ENST00000448023 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:3614878 C>T maps to ENST00000448023 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:32476208 T>G maps to NM_021209.4 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:32476212 C>T maps to NM_021209.4 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr2:32449562 A>C maps to NM_021209.4 A1018A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:57054632 C>A maps to NM_032206.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:57092034 C>T maps to NM_032206.3 Q1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:57095557 C>T maps to NM_032206.3 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:57100497 G>T maps to NM_032206.3 E1432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:57110757 C>T maps to NM_032206.3 V1593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:57060175 C>T maps to NM_032206.3 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr16:57059472 C>T maps to NM_032206.3 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:5436263 G>A maps to NM_033004.3 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:5434014 G>A maps to NM_033004.3 F1102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:5418367 C>T maps to NM_033004.3 P1376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:5463093 G>A maps to NM_033004.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:5462047 C>T maps to NM_033004.3 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:5424951 G>A maps to NM_033004.3 A1225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr17:5442790 G>A maps to NM_033004.3 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:5456869 C>T maps to NM_033004.3 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:5485275 G>A maps to NM_033004.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:7982582 G>A maps to NM_176821.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:7982668 G>A maps to NM_176821.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr11:7982303 C>T maps to NM_176821.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:56321606 G>A maps to NM_145007.3 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:56303725 G>A maps to NM_145007.3 Y818Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:56321600 C>T maps to NM_145007.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr19:56329268 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:54297341 C>T maps to ENST00000391773 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:54314258 C>T maps to ENST00000391773 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:54297337 G>A maps to ENST00000391773 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr19:54304557 C>T maps to ENST00000391773 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:54313571 C>T maps to ENST00000391773 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr19:54313730 G>A maps to ENST00000391773 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:56407478 C>T maps to NM_176810.2 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:56423489 C>A maps to NM_176810.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:56443464 A>G maps to NM_176810.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:56413558 G>A maps to NM_176810.2 C877C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:56413492 G>A maps to NM_176810.2 H899H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:7065122 T>C maps to NM_176822.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr11:7064426 A>T maps to NM_176822.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr11:7064387 T>G maps to NM_176822.3 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr11:7064213 G>A maps to NM_176822.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:55508825 A>G maps to NM_017852.3 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:55481623 C>T maps to NM_017852.3 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr19:55494613 C>A maps to NM_017852.3 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:55481475 G>A maps to NM_017852.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:55494232 G>A maps to NM_017852.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr19:55494430 G>A maps to NM_017852.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:55493929 C>T maps to NM_017852.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:247599443 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:247582371 G>A maps to NM_004895.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:247588580 T>C maps to NM_004895.4 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:247599289 C>A maps to NM_004895.4 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:247588067 G>A maps to NM_004895.4 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr1:247588490 C>T maps to NM_004895.4 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:247582206 C>T maps to NM_004895.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:247588367 A>G maps to NM_004895.4 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:56369640 A>G maps to NM_134444.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr19:56369487 C>T maps to NM_134444.4 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr19:56369634 G>T maps to NM_134444.4 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr19:56369526 G>A maps to NM_134444.4 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:56369146 G>T maps to NM_134444.4 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:56370009 C>T maps to NM_134444.4 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:56369487 C>T maps to NM_134444.4 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:56538969 G>A maps to NM_153447.4 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr19:56539524 C>T maps to NM_153447.4 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:56515300 C>T maps to NM_153447.4 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:56539245 C>T maps to NM_153447.4 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr19:56569734 T>A maps to NM_153447.4 C1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:56549537 C>T maps to NM_153447.4 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:56538861 C>A maps to NM_153447.4 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr19:56539239 C>T maps to NM_153447.4 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:56538981 C>T maps to NM_153447.4 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:281194 C>T maps to NM_138329.1 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:280966 G>A maps to NM_138329.1 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:281296 C>T maps to NM_138329.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:278598 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr11:284630 G>A maps to NM_138329.1 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:55450707 G>A maps to ENST00000446217 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:55450872 G>A maps to ENST00000446217 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr19:55449461 C>A maps to ENST00000446217 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:55451097 G>A maps to ENST00000446217 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:55451376 G>A maps to ENST00000446217 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr19:55451652 G>A maps to ENST00000446217 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:55451583 G>A maps to ENST00000446217 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr19:55451628 C>T maps to ENST00000446217 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:55451643 G>A maps to ENST00000446217 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:55441970 G>T maps to ENST00000446217 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:55447771 C>T maps to ENST00000446217 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr19:55450892 G>A maps to ENST00000446217 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:55451652 G>T maps to ENST00000446217 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr19:55451655 G>A maps to ENST00000446217 H205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:55451247 C>T maps to ENST00000446217 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr19:56477710 G>A maps to NM_176811.2 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr19:56490858 G>A maps to NM_176811.2 A992A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:56465978 C>T maps to NM_176811.2 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:56477620 C>T maps to NM_176811.2 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:56466476 C>T maps to NM_176811.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:56243921 G>A maps to NM_176820.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:56243848 C>A maps to NM_176820.2 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr19:56235401 G>A maps to NM_176820.2 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr19:56241342 G>A maps to NM_176820.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:56226482 A>G maps to NM_176820.2 D813D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr19:56235422 G>A maps to NM_176820.2 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:56243837 G>A maps to NM_176820.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr11:119044605 G>A maps to NM_024618.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:119045328 T>C maps to NM_024618.2 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:119045475 G>A maps to NM_024618.2 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:119044209 G>A maps to NM_024618.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:142397168 G>A maps to NM_002511.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:142409702 C>T maps to NM_002511.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:142409696 C>T maps to NM_002511.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr6:142409654 C>T maps to NM_002511.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:160951188 A>G maps to ENST00000472947 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:160958886 C>T maps to ENST00000472947 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr3:160945112 C>A maps to ENST00000472947 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:160958925 C>T maps to ENST00000472947 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:160964131 C>T maps to ENST00000472947 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr16:449631 G>A maps to ENST00000382940 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:137464979 A>G maps to NM_003551.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr5:137454572 T>C maps to NM_003551.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr5:137451429 C>T maps to NM_003551.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:48336186 G>A maps to NM_005793.3 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:48336622 T>C maps to NM_005793.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:169292428 G>T maps to NM_013330.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:169267892 C>T maps to NM_013330.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr1:169200054 G>A maps to NM_013330.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:152139393 A>G maps to NM_004688.2 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:10032226 G>A maps to NM_022787.3 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:183259292 G>A maps to NM_015039.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:183255851 G>A maps to NM_015039.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:139279977 T>C maps to ENST00000296202 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr2:101099719 G>A maps to NM_001011717.1 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:43180413 G>A maps to NM_021079.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:43176869 C>T maps to NM_021079.3 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr4:56471504 C>T maps to NM_006681.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:56466695 A>C maps to NM_006681.2 L161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:232393578 G>A maps to NM_006056.4 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:151784473 G>A maps to NM_020167.4 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:151784173 G>A maps to NM_020167.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:151783946 A>G did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr5:151784461 C>T maps to NM_020167.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:114182862 C>T maps to NM_006169.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:114168791 C>T maps to NM_006169.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:114168763 C>T maps to NM_006169.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:114182907 C>T maps to NM_006169.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:43656830 C>T maps to NM_182977.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr5:43653151 C>T maps to NM_182977.2 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:43609362 C>A maps to NM_182977.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:43644364 T>C maps to NM_182977.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr5:43656014 T>G maps to NM_182977.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:69782982 C>T maps to NM_014062.1 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:886560 C>T maps to NM_015658.3 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:892321 A>C maps to NM_015658.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr1:891583 A>C maps to NM_015658.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:889245 C>T maps to NM_015658.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:96109867 A>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:96116928 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:96093999 G>T maps to NM_022451.9 Y779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:96117943 T>C maps to NM_022451.9 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:96117057 A>G maps to NM_022451.9 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:132632495 C>T maps to NM_024078.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:132635800 A>G did not map to a codon.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr12:132635871 C>T maps to NM_024078.1 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:30491121 G>A maps to NM_006092.2 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:30485815 A>G maps to NM_006092.2 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr7:30492159 C>T maps to NM_006092.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:30494837 G>A maps to NM_006092.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:30465313 G>A maps to NM_006092.2 N934N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:30491601 G>C maps to NM_006092.2 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:30492471 G>T maps to NM_006092.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:30492519 A>G maps to NM_006092.2 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:50733414 G>A maps to NM_022162.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr16:50750496 G>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:50746062 C>T maps to NM_022162.1 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr16:50744628 G>A maps to NM_022162.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:50741837 G>T maps to NM_022162.1 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr10:72192775 C>T maps to NM_018055.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:72195497 G>T maps to NM_018055.4 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:72195098 G>A maps to NM_018055.4 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:10729374 T>C maps to NM_024894.2 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:65720241 C>T maps to NM_015462.3 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr17:65717631 G>T maps to NM_015462.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:65722732 A>G maps to NM_015462.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:67208596 A>G maps to ENST00000432069 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:31709978 G>A maps to NM_003787.4 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:31599386 C>T maps to NM_003787.4 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:31599431 C>T maps to NM_003787.4 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr18:31685106 G>C maps to NM_003787.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr18:31538235 G>A maps to NM_003787.4 D401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr18:31432849 G>A maps to NM_003787.4 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr18:31709843 A>G maps to NM_003787.4 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr18:31599566 T>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:33466160 G>A maps to NM_022917.4 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr9:33466321 G>A maps to NM_022917.4 Y731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:33469526 G>A maps to NM_022917.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:33462739 T>C maps to NM_022917.4 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:33472010 A>G maps to NM_022917.4 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:33463911 G>A maps to NM_022917.4 Q971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:33464951 G>A maps to NM_022917.4 R902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr9:33463283 C>T maps to NM_022917.4 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:33469000 G>A maps to NM_022917.4 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:33469228 G>A maps to NM_022917.4 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:95077544 A>G maps to NM_017948.5 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:95076605 C>T maps to NM_017948.5 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:6585973 A>G maps to NM_024654.4 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:6586024 A>G maps to NM_024654.4 D666D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:6586027 C>T maps to NM_024654.4 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:103918965 A>G maps to ENST00000405356 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:156761818 T>A maps to NM_138400.1 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:156762297 C>T maps to NM_138400.1 N828N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:156762321 C>T maps to NM_138400.1 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:156762297 C>T maps to NM_138400.1 N828N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:14958557 A>G maps to ENST00000456867 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr16:14947461 G>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:16349608 C>T maps to ENST00000263012 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr16:16357001 C>T maps to ENST00000263012 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:70517704 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:70516762 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:70517749 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr23:70514184 C>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:70519794 C>A did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr12:6675950 A>G maps to ENST00000382421 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:6670216 C>G maps to ENST00000382421 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:6672656 G>A maps to ENST00000382421 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:2637469 C>T maps to NM_006392.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:203139834 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:203157520 C>T maps to NM_015934.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr12:117657957 G>C maps to ENST00000338101 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:117672424 C>T maps to ENST00000338101 P1094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:117664549 G>A maps to ENST00000338101 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:117768385 G>A maps to ENST00000338101 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:117685281 G>A maps to ENST00000338101 C932C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:117691545 G>A maps to ENST00000338101 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:117723131 G>A maps to ENST00000338101 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr12:117672460 G>A maps to ENST00000338101 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr12:117768787 T>A maps to ENST00000338101 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr12:117710312 C>T maps to ENST00000338101 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr12:117715774 G>T maps to ENST00000338101 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr12:117768757 C>A maps to ENST00000338101 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:117768789 C>A maps to ENST00000338101 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:117665431 G>A maps to ENST00000338101 Y1174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:117681123 G>A maps to ENST00000338101 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr1:162325083 C>T maps to NM_014697.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:162325130 C>T maps to NM_014697.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:162302875 C>T maps to NM_014697.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:162335234 G>A maps to NM_014697.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:26105982 G>T maps to NM_000625.4 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:26107890 G>A maps to NM_000625.4 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:26108172 A>G maps to NM_000625.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:26105781 C>T maps to NM_000625.4 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:26116641 C>T maps to NM_000625.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:26105952 G>A maps to NM_000625.4 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr17:26107839 G>A maps to NM_000625.4 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:26106006 G>A maps to NM_000625.4 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:169718512 G>A maps to NM_001171631.1 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:169707787 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:139407575 G>A maps to NM_017617.3 C788C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:139412320 G>A maps to NM_017617.3 Q442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:139391869 G>A maps to NM_017617.3 H2107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:139409853 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:139397685 C>T maps to NM_017617.3 A1705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:139412691 G>A maps to NM_017617.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:139396734 G>A maps to NM_017617.3 S1791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:139413178 G>A maps to NM_017617.3 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:139401050 C>T maps to NM_017617.3 K1314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:139400303 G>A maps to NM_017617.3 D1348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:139391776 C>T maps to NM_017617.3 P2138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:139412607 G>A maps to NM_017617.3 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr9:139410510 C>A maps to NM_017617.3 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr9:139397646 G>A maps to NM_017617.3 I1718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:139405213 C>T maps to NM_017617.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:139396206 G>A maps to NM_017617.3 R1877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr9:139399546 G>A maps to NM_017617.3 Y1532Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr9:139391806 C>T maps to NM_017617.3 P2128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr9:139410088 G>A maps to NM_017617.3 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:120458867 C>T maps to NM_024408.2 T2159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:120497754 G>A maps to NM_024408.2 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:120465331 C>T maps to NM_024408.2 T1643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:120480507 G>A maps to NM_024408.2 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr1:120539719 G>A maps to NM_024408.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:120462203 G>A maps to NM_024408.2 R1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:120484285 T>G maps to NM_024408.2 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:120510771 G>A maps to NM_024408.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:145273301 A>T maps to ENST00000454606 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:145273221 C>T maps to ENST00000454606 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:15281200 G>A maps to NM_000435.2 D1685D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:15302454 C>T maps to NM_000435.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:15271757 G>A maps to NM_000435.2 H2227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:15276887 G>A maps to NM_000435.2 L1793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:15311611 C>G maps to NM_000435.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:15302589 G>A maps to NM_000435.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:15271700 G>T maps to NM_000435.2 T2246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr19:15289980 G>A maps to NM_000435.2 C1191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:15300207 G>T maps to NM_000435.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr6:32169878 G>A maps to NM_004557.3 Y1243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:32187375 G>A maps to NM_004557.3 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr6:32164798 C>T maps to NM_004557.3 G1701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:32172013 G>A maps to NM_004557.3 D1006D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr6:32169917 G>A maps to NM_004557.3 H1230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr6:32172007 G>A maps to NM_004557.3 D1008D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:32187951 G>A maps to NM_004557.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:32169929 G>A maps to NM_004557.3 D1226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:32188989 G>A maps to NM_004557.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr17:79910989 G>A maps to NM_178493.5 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:79910970 G>A maps to NM_178493.5 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:79913387 C>A maps to NM_178493.5 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:79913388 G>A maps to NM_178493.5 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:120435302 C>T maps to NM_002514.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr8:120430439 T>C maps to NM_002514.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:120430322 C>T maps to NM_002514.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr8:120429130 C>T maps to NM_002514.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:120435321 G>T maps to NM_002514.3 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr14:26918124 C>T maps to ENST00000449198 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr14:26917992 T>C maps to ENST00000449198 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr14:26949248 C>A maps to ENST00000449198 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr14:26917188 A>G maps to ENST00000449198 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:26917656 A>G maps to ENST00000449198 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr14:26917394 A>G maps to ENST00000449198 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr19:46443435 G>A maps to NM_002516.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:100105261 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100104912 C>T did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:100106241 G>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:100117181 T>C did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr23:100125712 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr23:100104297 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:155743923 G>A maps to NM_015718.2 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:155761235 G>A maps to NM_015718.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:155776221 C>T maps to NM_015718.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:155743923 G>A maps to NM_015718.2 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:155764412 G>A maps to NM_015718.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:89075246 G>A maps to NM_016931.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr15:69335033 C>A maps to NM_024505.3 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr15:69339811 C>T maps to NM_024505.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr15:69327704 C>T maps to NM_024505.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:69325382 C>T maps to NM_024505.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:140325258 C>T maps to NM_006647.1 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:2030037 C>T maps to NM_172168.1 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr19:47542708 T>C maps to NM_002517.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:47524417 C>A maps to NM_002517.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:47548494 C>T maps to NM_002517.2 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr19:47543773 G>A maps to NM_002517.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr19:47542711 G>A maps to NM_002517.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:47548494 C>T maps to NM_002517.2 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:47542756 A>G maps to NM_002517.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:101591323 G>T maps to NM_002518.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:101549439 G>T maps to NM_002518.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:101612038 C>T maps to NM_002518.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr14:34269030 G>A maps to NM_001164749.1 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr14:34270056 G>A maps to NM_001164749.1 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:34269447 G>C maps to NM_001164749.1 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr14:33684529 C>A maps to NM_001164749.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:33684480 G>A maps to NM_001164749.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr14:34269603 C>T maps to NM_001164749.1 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66190620 C>T maps to NM_178864.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr11:66191452 C>T maps to NM_178864.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr11:66192583 G>A maps to NM_178864.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:66190304 G>A maps to NM_178864.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:66191380 G>A maps to NM_178864.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:66190221 C>T maps to NM_178864.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:108043646 C>T maps to NM_002519.2 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:53853441 C>T maps to NM_005285.3 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:53852655 G>A maps to NM_005285.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:53853399 C>T maps to NM_005285.3 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:53853312 G>A maps to NM_005285.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:62738070 G>A maps to NM_005286.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:62737266 G>A maps to NM_005286.2 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:21131672 A>G maps to NM_000271.4 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:21128007 A>G maps to NM_000271.4 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:44553054 C>T maps to NM_013389.2 R1357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:44579932 A>G maps to NM_013389.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:44555405 G>A maps to NM_013389.2 Y1291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:44578498 C>T maps to NM_013389.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr7:44555793 C>T maps to NM_013389.2 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:44556852 C>T maps to NM_013389.2 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr7:44579659 G>A maps to NM_013389.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:44579425 G>T maps to NM_013389.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:74947475 G>A maps to ENST00000434013 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:139935550 C>T maps to ENST00000371600 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:57290351 G>A maps to NM_024663.3 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr20:57268890 G>A maps to NM_024663.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:45663059 G>A maps to NM_006310.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr17:45668086 G>A maps to NM_006310.3 W367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr12:53900561 A>T maps to NM_003717.2 *114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:53901168 G>A maps to NM_003717.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:73012836 C>A maps to NM_004885.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:72897893 C>T maps to NM_004885.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:73003814 C>T maps to NM_004885.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr4:73013067 A>T maps to NM_004885.2 K370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr4:72897734 C>T maps to NM_004885.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:110901210 G>A maps to NM_000272.3 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr2:110927507 C>A maps to NM_000272.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:132403634 T>C maps to ENST00000393156 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr3:132416141 C>A maps to ENST00000393156 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:132403523 C>T maps to ENST00000393156 K1148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:132403628 G>A maps to ENST00000393156 D1113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr3:132440854 G>A maps to ENST00000393156 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:5924517 G>A maps to NM_015102.2 G1292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:6038350 C>T maps to NM_015102.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:5925293 G>T maps to NM_015102.2 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:5965732 C>T maps to NM_015102.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:5965470 G>T maps to NM_015102.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:36332671 A>G maps to NM_004646.3 C920C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:36342239 C>T maps to NM_004646.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr19:36322009 C>T maps to NM_004646.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:36341893 C>T maps to NM_004646.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:36333365 T>C maps to NM_004646.3 K807K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:36340034 C>T maps to NM_004646.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:36340037 C>T maps to NM_004646.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:182798040 T>G maps to NM_030769.1 *321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr17:79573782 C>T maps to NM_017921.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:170833402 G>A maps to NM_001037738.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:170818391 A>T maps to NM_002520.6 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:170827871 A>G maps to NM_002520.6 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:170818792 G>A maps to NM_002520.6 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:21892018 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:103543107 G>A maps to NM_006993.2 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:106848586 T>C did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr1:11907409 C>T maps to NM_006172.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:11907421 C>T maps to NM_006172.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr2:232790332 G>A maps to NM_024409.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:153658343 A>G maps to NM_000906.3 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr1:153661759 G>A maps to NM_000906.3 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:153659752 C>A maps to NM_000906.3 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:35800818 C>T maps to NM_003995.3 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:35799718 C>T maps to NM_003995.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr9:35800104 G>A maps to NM_003995.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:35801942 G>A maps to NM_003995.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr9:35792587 C>T maps to NM_003995.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr9:35799620 T>C maps to NM_003995.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:35792986 C>T maps to NM_003995.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:32783105 G>A maps to ENST00000265074 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr5:32780831 C>T maps to ENST00000265074 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:50385277 A>T maps to NM_006545.4 Y329*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-7707-01A-11D-2053-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-BR-8487-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:138811 C>T maps to ENST00000399953 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:142646 A>G maps to ENST00000399953 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:139732 G>A maps to ENST00000399953 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:138811 C>T maps to ENST00000399953 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr16:160566 C>T maps to ENST00000399953 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:34917720 G>A maps to NM_207173.1 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:34851404 C>A maps to NM_207172.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:73866029 C>T maps to NM_012428.3 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr15:73889459 G>A maps to NM_012428.3 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:73889392 G>A maps to NM_012428.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:78449518 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr7:98256550 C>A maps to NM_002523.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:25266465 G>A maps to NM_022150.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr4:156135405 G>A maps to NM_000910.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr4:156135405 G>A maps to NM_000910.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr4:156135769 T>C maps to NM_000910.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr4:156136044 T>G maps to NM_000910.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:164272057 T>C maps to NM_006174.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:164271916 G>A maps to NM_006174.2 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:30327193 G>A did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:30326664 C>T did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr23:30326859 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:30327189 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:30327181 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:30326324 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:30327280 C>G did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:27240395 C>T maps to NM_021969.2 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr1:27239981 T>C maps to NM_021969.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:38253489 G>A maps to NM_021724.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:38252041 G>T maps to NM_021724.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:24004096 G>A did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr3:23996232 T>C maps to NM_005126.4 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:23996118 C>A maps to NM_005126.4 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr3:23997558 C>T maps to NM_005126.4 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:24018880 G>T maps to NM_005126.4 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:50882013 G>A maps to NM_007121.4 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:50883101 C>T maps to NM_007121.4 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:47282095 C>T maps to NM_005693.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr12:100904823 G>A maps to ENST00000392986 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:100930826 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:100957257 C>T maps to ENST00000392986 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:100928722 G>A maps to ENST00000392986 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr12:100904823 G>A maps to ENST00000392986 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr3:119534624 C>T maps to NM_022002.2 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr3:119526186 C>T maps to NM_022002.2 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:161201197 T>C maps to NM_001077482.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:161202681 G>A maps to NM_001077482.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:161199655 G>A maps to NM_001077482.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:95422175 T>C maps to NM_003297.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:15057747 C>T maps to NM_003298.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:92923896 C>T maps to NM_005654.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:92923761 G>A maps to NM_005654.4 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:92923677 C>T maps to NM_005654.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:92923743 C>T maps to NM_005654.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr5:92929392 C>T maps to NM_005654.4 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:92923983 G>A maps to NM_005654.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:92924137 C>T maps to NM_005654.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:92929430 C>T maps to NM_005654.4 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:92923698 C>T maps to NM_005654.4 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:92929325 C>T maps to NM_005654.4 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:96875555 G>A maps to NM_021005.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:96880778 C>A maps to NM_021005.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:17343352 C>T maps to NM_005234.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:142780029 G>A maps to NM_001024094.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr5:142693629 C>A maps to NM_001024094.1 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr4:149041318 T>C maps to ENST00000511528 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:149035412 C>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:149356398 C>A maps to ENST00000511528 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:149356383 A>C maps to ENST00000511528 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:149357028 A>G maps to ENST00000511528 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:149115966 A>G maps to ENST00000511528 D652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:149357499 G>A maps to ENST00000511528 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr4:149357088 G>T maps to ENST00000511528 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr4:149357082 A>T maps to ENST00000511528 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:52448960 A>G maps to ENST00000360284 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:52450284 A>G maps to ENST00000360284 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr12:52448156 G>A maps to ENST00000360284 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:157182438 G>A maps to NM_006186.3 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:157185873 G>A maps to NM_006186.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr2:157186461 G>T maps to NM_006186.3 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:102590656 G>A maps to NM_173200.1 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr9:102590395 G>A maps to NM_173200.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:102590422 C>T maps to NM_173200.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:102590785 G>A maps to NM_173200.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:102595561 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:127255347 G>A maps to NM_004959.4 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:127262452 G>A maps to NM_004959.4 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:200143337 A>C maps to NM_205860.1 *542Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:127289151 G>A maps to NM_033334.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr9:127298386 T>C maps to NM_033334.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:115402722 G>A maps to ENST00000369358 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:115364628 G>T maps to ENST00000369358 P1330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:115380376 C>A maps to ENST00000369358 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:27662649 C>T maps to ENST00000379863 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:27662757 A>G maps to ENST00000379863 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:27664198 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:27663725 G>A maps to ENST00000379863 Q424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:27664013 C>T maps to ENST00000379863 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:144920920 A>G maps to NM_178564.3 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:144919464 C>T maps to NM_178564.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:144920884 G>A maps to NM_178564.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:144921093 G>A maps to NM_178564.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:107807441 T>C maps to ENST00000379032 T1130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:107818474 C>T maps to ENST00000379032 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:107807390 T>C maps to ENST00000379032 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:107872809 G>A maps to ENST00000379032 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:107824975 T>G maps to ENST00000379032 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:107832203 G>A maps to ENST00000379032 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:52343944 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:52263976 C>A maps to NM_002525.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr1:52280262 G>A maps to NM_002525.2 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:52272559 G>A maps to NM_002525.2 F740F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:52285520 G>A maps to NM_002525.2 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:52293531 C>T maps to NM_002525.2 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:52280255 A>T maps to NM_002525.2 L597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:129394885 C>T maps to ENST00000393231 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr8:32617750 C>T maps to NM_013956.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:32453466 G>A maps to NM_013956.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:32463103 A>G maps to NM_013956.3 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr8:32621860 G>T maps to NM_013956.3 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:32505415 G>A maps to NM_013959.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:32617801 C>T maps to NM_013956.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr8:32505535 G>A maps to NM_013959.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr8:32505682 T>G maps to NM_013959.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr8:32599535 G>T maps to ENST00000338921 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr8:32617810 T>C maps to NM_013956.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr8:32505364 T>G maps to NM_013959.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr5:139231208 G>A maps to NM_013982.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:139231223 G>A maps to NM_013982.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:139260468 G>A maps to NM_013982.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:139228158 C>T maps to NM_013982.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:83635494 C>A maps to ENST00000404547 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr10:84498377 G>A maps to ENST00000404547 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr10:83635659 G>A maps to ENST00000404547 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:84498344 C>T maps to ENST00000404547 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr10:84738723 C>A maps to ENST00000404547 C477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:84745201 C>A maps to ENST00000404547 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:84745309 G>A maps to ENST00000404547 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr10:84744955 C>T maps to ENST00000404547 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr10:84498332 G>T maps to ENST00000404547 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:124615535 C>T maps to NM_001126181.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr21:16338140 G>A maps to NM_003489.3 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr21:16338716 T>C maps to NM_003489.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr21:16340024 G>T maps to NM_003489.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:2939903 T>C maps to NM_031474.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:2943969 A>G maps to NM_031474.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:105153077 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:105178302 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:105153046 C>T did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:105142675 A>G did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:105193614 T>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:105142689 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:105178280 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:105179300 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:105197094 G>T did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:105153260 A>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:105152837 A>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:105181435 A>G did not map to a codon.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr23:105178263 A>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:105178288 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:105189886 C>T did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:105153077 A>G did not map to a codon.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr23:105197149 C>T did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:105153086 T>G did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:105132294 A>C did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:105189885 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:105137884 C>T did not map to a codon.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr23:105197130 A>G did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:105153030 G>T did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:105190450 A>C did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:105193680 T>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:105142689 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:105178265 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:105139512 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:105167186 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr23:105178288 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:105168814 A>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:6002701 C>T maps to NM_016588.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:33545354 G>A maps to NM_003873.5 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:33502475 C>T maps to NM_003873.5 W484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:33515118 G>A maps to NM_003873.5 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:33545348 G>A maps to NM_003873.5 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:206587397 C>T maps to NM_201266.1 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:206608101 G>A maps to NM_201266.1 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:206659484 C>T maps to NM_201266.1 Y833Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:206580994 G>A maps to NM_201266.1 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:334249 C>T maps to NM_024958.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:50463983 G>A maps to ENST00000404971 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:50724781 C>T maps to ENST00000404971 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:50779923 G>A maps to ENST00000404971 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:51254673 C>T maps to ENST00000404971 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr2:50850745 T>C maps to ENST00000404971 E313E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-7707-01A-11D-2053-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:50464106 A>G maps to ENST00000404971 P1162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr2:50573835 G>A maps to NM_138735.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:50280723 A>G maps to ENST00000404971 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:51255183 G>A maps to ENST00000404971 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:51253548 T>C maps to ENST00000404971 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:51255156 G>A maps to ENST00000404971 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:50464091 G>T maps to ENST00000404971 I1167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:50850556 G>T maps to ENST00000404971 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr2:50733717 G>C maps to ENST00000404971 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr2:50780157 T>A maps to ENST00000404971 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr2:50318608 C>T maps to ENST00000404971 K1230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr2:50779726 G>T maps to ENST00000404971 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr2:51255084 A>C maps to ENST00000404971 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr2:51254931 C>T maps to ENST00000404971 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:50464030 G>A maps to ENST00000404971 R1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:51255150 G>A maps to ENST00000404971 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr2:50724790 T>C maps to ENST00000404971 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:51254658 G>A maps to ENST00000404971 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:51255156 G>A maps to ENST00000404971 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr2:51254931 C>T maps to ENST00000404971 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:51254742 G>A maps to ENST00000404971 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:51254814 G>A maps to ENST00000404971 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr2:51254922 G>A maps to ENST00000404971 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr2:51254964 C>T maps to ENST00000404971 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:50464016 C>A maps to ENST00000404971 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:50780123 G>A maps to ENST00000404971 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr2:51254742 G>A maps to ENST00000404971 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:64428293 G>A maps to NM_015080.3 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:64374786 G>A maps to NM_015080.3 R1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr11:64416245 G>A maps to NM_015080.3 D1081D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr11:64480955 G>A maps to NM_015080.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:64434839 G>A maps to NM_015080.3 D560D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:64419615 G>A maps to NM_015080.3 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:64390422 G>A maps to NM_015080.3 A1325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:64427987 G>A maps to NM_015080.3 Y735Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:64390506 G>A maps to NM_015080.3 I1297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:64419046 C>T maps to NM_015080.3 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr11:64390362 G>A maps to NM_015080.3 S1345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:79270110 C>T maps to NM_004796.4 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:80164261 C>T maps to NM_004796.4 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr14:80328201 C>T maps to NM_004796.4 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:79175876 C>T maps to NM_004796.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:79181373 C>T maps to NM_004796.4 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:79434537 G>A maps to NM_004796.4 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:80328228 G>A maps to NM_004796.4 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr14:79746837 T>C maps to ENST00000440563 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr14:80328210 C>T maps to NM_004796.4 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:79432494 T>C maps to NM_004796.4 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:79432704 T>C maps to NM_004796.4 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:79181438 C>T maps to NM_004796.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:79181417 C>T maps to NM_004796.4 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:80328021 G>T maps to NM_004796.4 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:79433670 T>C maps to NM_004796.4 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:79933606 C>A maps to NM_004796.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:74066521 C>T maps to NM_014886.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:176673694 T>C maps to NM_022455.4 F1465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:176562871 C>T maps to NM_022455.4 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:176694614 C>T maps to NM_022455.4 C1733C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:176673787 A>G maps to NM_022455.4 P1496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:176638978 T>C maps to NM_022455.4 S1193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:176720830 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:152034373 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:152037482 T>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:152031180 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:152018924 T>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:152018834 C>A did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:152014935 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:152027359 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:152034496 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr17:44832735 G>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:44770369 T>G maps to NM_006178.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:1444987 T>C maps to ENST00000476071 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:1426390 G>A maps to ENST00000476071 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:59548041 G>A maps to NM_001144772.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:59506821 G>A maps to NM_001144772.1 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr8:59535980 A>T maps to NM_001144772.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:59502028 C>T maps to NM_001144772.1 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:59498295 G>A maps to NM_001144772.1 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:59502067 A>G maps to NM_001144772.1 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:59522162 C>T maps to NM_001144772.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:6600044 G>A maps to NM_017755.5 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:6604299 G>A maps to NM_017755.5 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:6611108 C>T maps to NM_017755.5 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:46826500 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:72722780 G>A maps to NM_148956.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:72717395 C>G maps to NM_001168347.1 *471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:72717598 T>C maps to NM_148956.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:72717908 C>T maps to NM_148956.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:72717441 T>G maps to NM_148956.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:72717830 G>A maps to NM_148956.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:18905143 G>T maps to NM_182543.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr4:40752721 C>G maps to NM_024677.4 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr4:40753001 C>T maps to NM_024677.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:40124849 A>G maps to NM_032526.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:40124987 A>G maps to NM_032526.1 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:40137680 C>T maps to NM_032526.1 Q10Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:40129044 G>T maps to NM_032526.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr1:40137638 G>A maps to NM_032526.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr2:18766139 C>T maps to ENST00000455492 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:18765854 G>A maps to ENST00000455492 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:33057164 G>A maps to NM_001002010.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:33066499 G>A maps to NM_001002010.1 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:33055401 G>A maps to NM_001002010.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr7:33102235 G>A maps to NM_001002010.1 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:52568609 C>T maps to NM_022908.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:52558683 G>T maps to NM_001134231.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:86181054 G>A maps to NM_002526.2 S221S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:17250221 C>T maps to ENST00000379552 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:17209921 C>T maps to ENST00000379552 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:17250218 G>A maps to ENST00000379552 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr16:15132043 A>G maps to NM_173474.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:15131996 A>T maps to NM_173474.2 L275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:5603724 G>A maps to NM_001102654.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr12:5603607 G>C maps to NM_001102654.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:5603607 G>C maps to NM_001102654.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:5603649 C>T maps to NM_001102654.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr12:5603685 G>A maps to NM_001102654.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:5603523 C>A maps to NM_001102654.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr16:2096246 C>T maps to NM_002528.5 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:132016334 C>T maps to NM_001144058.1 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr11:132177682 G>A maps to NM_001144058.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:132180069 G>A maps to NM_001144058.1 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:132177583 G>A maps to NM_001144058.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr17:8926511 C>T maps to NM_004822.2 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:2522139 G>A maps to NM_006181.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:49167959 G>A maps to NM_145807.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:107867346 G>A maps to NM_001113226.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:107691418 G>A maps to NM_001113226.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:108023365 C>A maps to NM_001113226.1 C508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:107867343 C>T maps to NM_001113226.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:107961229 G>A maps to NM_001113228.1 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:108023371 C>T maps to NM_001113226.1 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr1:107867164 C>T maps to NM_001113226.1 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:107937907 A>G maps to NM_001113226.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr1:107691252 G>A maps to NM_001113226.1 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:107979392 G>A maps to NM_001113226.1 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:135114554 C>T maps to NM_032536.2 C373C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:135073516 G>A maps to NM_032536.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:135114576 C>T maps to NM_032536.2 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:135116396 C>T maps to NM_032536.2 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5716-01A-21D-1800-08 chr9:135073843 G>A maps to NM_032536.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:135114620 C>T maps to NM_032536.2 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:135073570 C>T maps to NM_032536.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:135102325 C>T maps to NM_032536.2 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:135102358 C>A maps to NM_032536.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:135073750 C>A maps to NM_032536.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:135102292 C>T maps to NM_032536.2 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:156849015 G>A maps to NM_002529.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr1:156834522 C>T maps to NM_002529.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr1:156844187 G>A maps to NM_002529.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:87285818 C>T maps to NM_006180.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:87482167 C>T maps to NM_006180.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr15:88679769 G>A maps to NM_001012338.1 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:88679172 G>A maps to NM_001012338.1 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:88680683 G>A maps to NM_001012338.1 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr15:88476346 C>A maps to NM_001012338.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:88799237 G>A maps to NM_001012338.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr15:88680632 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:88669571 G>T maps to NM_001012338.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr20:61391603 C>A maps to NM_002531.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr20:61341128 C>T maps to NM_002531.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr20:61391603 C>A maps to NM_002531.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:61391411 C>T maps to NM_002531.2 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:61340657 G>A maps to NM_002531.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:11809757 G>A maps to NM_012344.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8210-01A-11D-2340-08 chr2:11802135 G>A maps to NM_012344.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:11798843 G>A maps to NM_012344.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:106480538 G>A maps to NM_014840.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr12:106464549 A>C did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr12:106461100 C>A maps to NM_014840.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:106532256 C>A maps to NM_014840.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr1:205273099 G>A maps to ENST00000441520 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr1:205277708 C>T maps to ENST00000441520 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:151049912 T>C maps to ENST00000355851 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:151053218 G>T maps to ENST00000355851 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:151052932 G>A maps to ENST00000355851 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:151057315 C>T maps to ENST00000355851 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:10846528 A>G maps to NM_002484.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:1836583 A>G maps to NM_012225.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr14:32315786 T>G maps to NM_025152.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:32295919 C>T maps to NM_025152.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:49409125 C>T maps to NM_006184.5 D120D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GX-01A-12D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr11:17323308 G>T maps to ENST00000458064 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:205688790 G>A maps to NM_022731.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:27269257 G>A maps to NM_006600.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr1:27272099 G>A maps to NM_006600.2 K289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:110308668 T>G maps to NM_032869.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:162887020 T>C maps to NM_145266.4 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr7:44425618 C>T maps to NM_015332.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:2290629 G>A maps to NM_198954.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:2284281 C>T maps to NM_198954.1 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:2284268 G>A maps to NM_198954.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:51075981 G>A did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:51076256 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:51076060 G>A did not map to a codon.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr23:51075840 A>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:51076038 G>A did not map to a codon.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr23:51076234 C>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:51239178 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:51238942 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:51239052 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr23:51238836 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:102891659 G>A maps to NM_031438.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:102895757 A>G maps to NM_031438.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:74879835 G>A maps to NM_015901.4 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:105642868 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:145587452 G>A maps to NM_001012758.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:145586678 C>T maps to NM_001012758.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:56485036 C>T maps to NM_007006.2 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:56473613 G>A maps to NM_007006.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:63994402 C>A maps to NM_032344.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:123818803 G>A maps to NM_007083.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:123814249 G>A maps to NM_007083.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:88375608 T>C did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:163310206 C>T maps to NM_145697.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:45563442 C>T maps to NM_012345.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr13:45523974 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:27614006 G>C maps to NM_020772.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:71725377 C>T maps to ENST00000393695 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:71725086 C>T maps to ENST00000393695 R1160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr11:71724062 G>A maps to ENST00000393695 R1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:71732292 G>A maps to ENST00000393695 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:71726676 A>G maps to ENST00000393695 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr11:71726699 G>A maps to ENST00000393695 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:71740258 A>G maps to ENST00000393695 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:71729315 C>T maps to ENST00000393695 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr11:71727045 G>A maps to ENST00000393695 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:73753989 A>C maps to NM_001005743.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:73743384 C>T maps to NM_001005743.1 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:41188831 G>A maps to NM_004756.3 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:69113182 A>G maps to NM_020401.2 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:69085851 C>A maps to NM_020401.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:69107563 T>C maps to NM_020401.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:69084527 T>C did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:229593998 G>C maps to NM_018230.2 Y963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:229635469 C>T maps to NM_018230.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr1:229601203 T>C maps to NM_018230.2 E754E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:229600369 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:17632902 T>C maps to ENST00000430136 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:17626216 A>G maps to ENST00000430136 G1272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:17626267 A>G maps to ENST00000430136 A1255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr6:17629624 A>C maps to ENST00000430136 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:17637581 G>A maps to ENST00000430136 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr5:37364385 T>C maps to NM_153485.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr5:37333693 C>T maps to NM_153485.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:37314389 C>T maps to NM_153485.1 Q782Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:37292070 C>T maps to NM_153485.1 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:47858455 G>A maps to NM_015231.1 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:47814390 G>A maps to NM_015231.1 R1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:47825037 A>T maps to NM_015231.1 C909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:47837093 G>A maps to NM_015231.1 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr9:131745577 G>A maps to NM_015354.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr9:131768030 T>C maps to NM_015354.1 N1615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:131715087 C>T maps to NM_015354.1 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:131761489 G>A maps to NM_015354.1 T1185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:131745253 G>A maps to NM_015354.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:131749906 G>T maps to NM_015354.1 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:131765223 C>T maps to NM_015354.1 F1422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:131768860 G>A maps to NM_015354.1 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:131768571 G>A maps to NM_015354.1 A1666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:135303204 C>T maps to NM_015135.2 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:135304190 G>A maps to NM_015135.2 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:135301988 T>C maps to NM_015135.2 N1228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:135269637 C>T maps to NM_015135.2 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:135333150 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:135286175 T>C maps to NM_015135.2 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr7:135304190 G>A maps to NM_015135.2 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr7:135303239 G>A maps to NM_015135.2 E1284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:135286255 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:13372049 T>C maps to NM_024923.2 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:13372082 A>G maps to NM_024923.2 V1329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:13381416 G>A maps to NM_024923.2 G1136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:13381470 G>A maps to NM_024923.2 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:13363105 C>T maps to NM_024923.2 P1715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:13370368 C>T maps to NM_024923.2 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:13461720 C>T maps to NM_024923.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:13383523 G>A maps to NM_024923.2 R1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:13401898 C>T maps to NM_024923.2 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:13417054 G>T maps to NM_024923.2 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr1:154127376 G>A maps to NM_207308.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:154030658 T>G maps to NM_207308.2 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:154027308 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:134022877 A>G maps to ENST00000451030 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:134027124 G>A maps to ENST00000451030 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:134049508 G>A maps to ENST00000451030 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:134021653 C>T maps to ENST00000451030 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr2:184023067 A>T maps to NM_138285.3 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:150067126 G>A maps to NM_198887.1 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr6:150048161 A>T maps to NM_198887.1 C362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:150063643 G>T maps to NM_198887.1 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:45564090 A>C maps to NM_007172.3 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr22:45577197 C>T maps to NM_007172.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr4:77065317 C>T maps to ENST00000458189 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:77053838 C>T maps to ENST00000458189 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:50412512 T>C maps to NM_012346.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:50411972 C>T maps to NM_012346.4 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:50411684 C>T maps to NM_012346.4 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr17:73231770 C>T maps to NM_024844.3 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:5322931 C>T maps to NM_002532.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:56864564 G>A maps to NM_014669.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:56782279 G>T maps to NM_014669.3 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:56862945 C>T maps to NM_014669.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:56875717 C>T maps to NM_014669.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:3720467 G>A maps to NM_016320.4 R1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr13:25882000 T>C maps to NM_014089.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:25911074 G>A maps to NM_014089.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:25895203 T>C maps to NM_014089.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr13:25899185 T>C maps to NM_014089.3 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:23239805 C>T maps to ENST00000413919 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr7:23240343 C>T maps to NM_007342.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:23239156 G>A maps to ENST00000413919 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:28549504 A>G maps to NM_001042483.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:118015302 A>G maps to NM_138459.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:118014203 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:41650446 T>C maps to NM_016359.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:41650389 C>T maps to NM_016359.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr15:41663820 A>T maps to NM_016359.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:67902271 A>G maps to NM_005796.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:224455819 G>A maps to NM_002533.2 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:224514115 C>T maps to NM_002533.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr19:16926139 A>T maps to ENST00000438489 *1565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:16918397 C>T maps to ENST00000438489 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:16918703 C>T maps to ENST00000438489 P1348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:16874646 G>A maps to ENST00000438489 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr11:62567922 C>T maps to NM_006362.4 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:101623732 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:101624959 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:101624640 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:101572351 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:101623722 T>G did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:102334517 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:102339720 C>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:102337225 T>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:102335076 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:102339743 A>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:101095487 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:101087248 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:101095512 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:101095824 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:101096039 C>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:101095861 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:708347 G>A maps to NM_022463.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:708452 G>A maps to NM_022463.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr9:91150519 C>T maps to NM_001161625.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:91150403 G>T maps to NM_001161625.1 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:8475381 G>A maps to NM_152745.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr7:8790739 T>C maps to NM_152745.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:139429148 G>A maps to NM_007226.2 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr2:139428995 A>G maps to NM_007226.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:47656634 T>C maps to NM_007225.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:108780201 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:108785799 A>G did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:108785789 A>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:24882593 C>T maps to NM_025081.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr14:24878880 T>G maps to NM_025081.2 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr14:24884515 C>A maps to NM_025081.2 A1187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:24884818 G>A maps to NM_025081.2 A1288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:24884818 G>A maps to NM_025081.2 A1288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:24884674 G>A maps to NM_025081.2 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr14:24885244 C>T maps to NM_025081.2 T1430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:24880345 C>A maps to NM_025081.2 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:24885562 C>A maps to NM_025081.2 V1536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:41333773 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:41334050 C>T did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:41333459 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:41333484 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:41333036 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:41333565 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:41333635 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:120082131 C>T maps to NM_178507.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:120097589 C>T maps to NM_178507.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr12:113346552 G>A maps to NM_001032409.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:113346441 C>G maps to NM_001032409.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:113346600 C>T maps to NM_001032409.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr12:113355546 T>A maps to NM_002534.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:113354352 C>T maps to NM_001032409.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:113354534 G>A maps to NM_001032409.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:113348937 C>T maps to NM_001032409.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr12:113354462 C>A maps to NM_001032409.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:113416559 A>G maps to NM_016817.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr12:113424901 C>T maps to NM_016817.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:113433245 T>C maps to NM_016817.2 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:113379523 G>A maps to NM_006187.2 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:113384576 G>A maps to NM_006187.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:113386826 C>T maps to NM_006187.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr12:121458497 T>A maps to NM_003733.2 K471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:121476747 G>A maps to NM_003733.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:121461816 G>A maps to NM_003733.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:126097147 C>T maps to NM_000274.3 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:126097427 C>T maps to NM_000274.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:64982607 G>A maps to ENST00000403937 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:105659879 G>A maps to NM_024928.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr9:138438673 G>A maps to NM_014582.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr9:138438064 C>T maps to NM_014582.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:136084559 C>T maps to NM_014581.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:228400305 C>T maps to NM_001098623.1 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:228467552 G>A maps to NM_001098623.1 E2476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:228509532 C>T maps to NM_001098623.1 S4997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:228401920 C>T maps to NM_001098623.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:228404717 C>T maps to NM_001098623.1 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:228547795 C>T maps to NM_052843.2 R6401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:228431127 C>T maps to NM_001098623.1 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:228468348 C>T maps to NM_001098623.1 G2683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:228523972 T>C did not map to a codon.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr1:228437777 G>A maps to NM_001098623.1 T1382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr1:228462137 C>T maps to NM_001098623.1 T1892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr1:228548383 C>T maps to NM_052843.2 F6597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:228495857 G>A maps to NM_001098623.1 T4171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:228506693 T>C maps to NM_001098623.1 R4747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:228511059 A>G maps to NM_001098623.1 Q5135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr1:228467904 G>A maps to NM_001098623.1 P2563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:228468438 C>T maps to NM_001098623.1 A2713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:228511095 C>T maps to NM_001098623.1 C5147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr1:228432099 G>A maps to NM_001098623.1 T1103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:228494755 G>A maps to NM_001098623.1 V4027V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:228496851 C>T maps to NM_001098623.1 G4264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:228434433 C>T maps to NM_001098623.1 G1321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr1:228474640 C>A maps to NM_001098623.1 R3149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr1:228404966 G>A maps to NM_001098623.1 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:228433237 C>T maps to NM_001098623.1 D1202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:228437897 C>T maps to NM_001098623.1 C1422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:228437903 C>T maps to NM_001098623.1 A1424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:228548353 C>A maps to NM_052843.2 T6587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:228466969 G>A maps to NM_001098623.1 V2407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:228504491 C>T maps to NM_001098623.1 S4456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:228495059 C>T maps to NM_001098623.1 A4098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:228444499 G>A maps to NM_001098623.1 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr1:228444583 C>T maps to NM_001098623.1 C1514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:228404780 G>A maps to NM_001098623.1 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:228464337 G>A maps to NM_001098623.1 S2136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:228468012 C>T maps to NM_001098623.1 N2599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:228444454 G>A maps to NM_001098623.1 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:228547975 C>T maps to NM_052843.2 G6461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:228550290 C>T maps to NM_001098623.1 R6226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:228462438 C>T maps to NM_001098623.1 G1950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:228402119 C>T maps to NM_001098623.1 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:228402695 C>T maps to NM_001098623.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:228412241 C>T maps to NM_001098623.1 C912C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:228433174 G>T maps to NM_001098623.1 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:228402650 G>A maps to NM_001098623.1 W560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:228509322 G>A maps to NM_001098623.1 V4927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:228462327 C>T maps to NM_001098623.1 G1913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:228464703 C>T maps to NM_001098623.1 C2187C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-A4H8-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr1:228437820 C>T maps to NM_001098623.1 R1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr1:228525643 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:228465464 C>T maps to NM_001098623.1 Y2255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:220421446 T>C did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:220420874 G>A maps to NM_015311.2 H1492H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:220434994 G>A maps to NM_015311.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:220435507 G>A maps to NM_015311.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:220419259 G>T maps to NM_015311.2 A1604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:220429979 G>A maps to NM_015311.2 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:220419340 T>C maps to NM_015311.2 V1577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:133053403 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:133041401 G>A maps to ENST00000262283 C564C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr8:133044143 T>G maps to ENST00000262283 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:28211896 C>T maps to NM_000275.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:28200317 C>A maps to NM_000275.2 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr15:28259939 G>T maps to NM_000275.2 Y342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr15:28196945 G>A maps to NM_000275.2 G645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:28235760 A>G maps to NM_000275.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:28090166 G>A maps to NM_000275.2 N790N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:28196963 G>C maps to NM_000275.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr15:28261278 C>G maps to NM_000275.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr4:48852082 C>T maps to NM_001168254.1 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr4:48851985 T>C maps to NM_001168254.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr7:5923595 G>A maps to NM_001097622.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:5922229 C>T maps to NM_001097622.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:97617762 G>A maps to NM_006188.3 N53N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:128696606 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:128718326 G>A did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:128703264 G>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:128724179 C>A did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:128695193 A>C did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:128723913 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:128703272 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:128723843 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:128710000 G>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr4:71068594 T>A maps to NM_017855.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:10581969 G>A maps to NM_002539.1 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:10582276 C>T maps to NM_002539.1 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:10582053 G>A maps to NM_002539.1 D305D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:103572811 G>A maps to NM_024410.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:103572952 C>T maps to NM_024410.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:131262533 A>T maps to NM_153435.1 *894C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr9:131256994 C>T maps to ENST00000372814 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr1:86826216 A>G maps to ENST00000370567 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:76017503 C>T maps to NM_175881.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr17:8243563 G>A maps to NM_153007.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:8243653 A>T maps to NM_153007.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:124029833 T>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:123514893 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:123517987 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:123539083 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:123556365 G>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:123517644 T>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:123526073 C>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:123517967 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:123785940 G>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:123518247 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:123556220 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:123631107 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:123663718 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:124028173 T>G did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:123615809 T>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:123775718 A>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:123775728 T>G did not map to a codon.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr23:124028193 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:123787482 G>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:123680889 A>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:123514831 G>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:123556187 A>G did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:123556373 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:123805640 C>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:123680874 A>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:123519751 T>C did not map to a codon.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr23:123525996 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:123517912 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:123538902 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:123657245 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:123870960 T>G did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:123657355 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:123539071 G>A did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:124030033 G>T did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:123554434 C>T did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr23:123540328 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:123779094 G>T did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr23:123540198 G>A did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:123554378 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:123839038 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:123517932 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:123657294 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:123695632 T>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:123540218 G>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:123775704 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:123556128 A>C did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:123637483 T>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:123615688 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:123654413 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:123526013 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:123785794 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:123554387 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:123519837 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:123657425 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:123838872 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:167674381 C>T maps to NM_001122679.1 A2137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:167674063 C>T maps to NM_001122679.1 F2031F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:167553834 C>T maps to NM_001122679.1 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:167379677 C>T maps to NM_001122679.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:167671460 C>T maps to NM_001122679.1 R1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:167674042 C>T maps to NM_001122679.1 Y2024Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:167689673 C>T maps to NM_001122679.1 G2719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr5:167420137 C>T maps to NM_001122679.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:167674741 C>T maps to NM_001122679.1 D2257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:167420176 G>A maps to NM_001122679.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:167545303 C>T maps to NM_001122679.1 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:167545432 C>A maps to NM_001122679.1 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr5:167517688 G>A maps to NM_001122679.1 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr4:183713738 G>T maps to NM_001080477.1 E1972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:183721041 G>A maps to NM_001080477.1 T2546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:183714661 A>G maps to NM_001080477.1 G2279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr4:183721188 C>T maps to NM_001080477.1 D2595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr4:183696161 G>A maps to NM_001080477.1 P1720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:183721398 G>A maps to NM_001080477.1 Q2665Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:183721416 C>T maps to NM_001080477.1 Y2671Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:183603165 C>T maps to NM_001080477.1 N678N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:183675539 A>G maps to NM_001080477.1 V1340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:183721188 C>T maps to NM_001080477.1 D2595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:183721332 C>T maps to NM_001080477.1 G2643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr4:183609478 C>T maps to NM_001080477.1 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr4:183714430 G>A maps to NM_001080477.1 T2202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:78440667 A>G maps to NM_001098816.2 S1053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:78412902 C>T maps to NM_001098816.2 E1585E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:78369150 G>A maps to NM_001098816.2 S2754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr11:78381503 C>T maps to NM_001098816.2 A1962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:78413445 A>C maps to NM_001098816.2 V1404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:78440646 C>T maps to NM_001098816.2 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr11:78413142 G>A maps to NM_001098816.2 L1505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:78423524 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:78369543 T>C maps to NM_001098816.2 G2623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr11:78387400 G>A maps to NM_001098816.2 A1764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:78369474 G>A maps to NM_001098816.2 N2646N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:78413244 G>A maps to NM_001098816.2 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:78380837 T>C maps to NM_001098816.2 G2184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:78399126 G>T maps to NM_001098816.2 A1744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:13785382 G>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:13786259 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:13764476 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:13753378 A>G did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:13753461 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:13785291 A>G did not map to a codon.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr23:13781865 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:13762569 A>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:13778669 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:13764537 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:13771504 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:44714123 C>T maps to ENST00000444676 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:44734126 C>T maps to ENST00000444676 Y555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:44736534 T>C maps to ENST00000444676 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:44737840 C>T maps to ENST00000444676 N818N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:44747287 C>T maps to ENST00000444676 Y983Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr7:44721434 C>T maps to ENST00000444676 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:44733483 C>A maps to ENST00000444676 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:44737840 C>T maps to ENST00000444676 N818N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:50959916 G>A maps to NM_018245.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:50954897 G>A maps to NM_018245.2 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr10:50955073 C>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:50955200 G>A maps to NM_018245.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:50945990 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr10:50944166 C>T maps to NM_018245.2 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr10:50955200 G>A maps to NM_018245.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:61444235 C>T maps to NM_007346.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:61444595 C>T maps to NM_007346.2 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:61441913 C>T maps to NM_007346.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:61443860 C>T maps to NM_007346.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:72011355 G>A maps to NM_024576.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:72006047 A>G maps to NM_024576.3 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:71998698 C>T maps to NM_024576.3 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:72011139 G>A maps to NM_024576.3 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:72006265 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:72003315 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr6:72011415 T>C maps to NM_024576.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:95152282 A>G maps to NM_033014.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:95165629 T>C maps to NM_033014.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:95152156 T>C maps to NM_033014.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:70779182 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:70757853 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:70787389 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:70783004 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:74692182 C>T maps to NM_152635.1 C513C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:74684342 C>T maps to NM_152635.1 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:74684030 A>G maps to NM_152635.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:74692257 G>A maps to NM_152635.1 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr9:138012011 C>T maps to NM_014279.4 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:138011369 T>A maps to NM_014279.4 Y250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:9965413 G>A maps to NM_058164.2 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:9968486 G>A maps to NM_058164.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:9967527 G>A maps to NM_058164.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:9965005 G>A maps to NM_058164.2 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:9965425 C>T maps to NM_058164.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:102270105 G>A maps to ENST00000338858 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:102290762 G>A maps to ENST00000338858 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:53624245 G>A maps to NM_006418.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr13:53624158 C>T maps to NM_006418.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:53602982 C>T maps to NM_006418.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr13:53624668 C>T maps to NM_006418.3 N432N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr13:53624272 G>A maps to NM_006418.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:7531211 G>T maps to NM_198474.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:127549518 T>C did not map to a codon.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr9:127566439 C>T maps to NM_182487.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:127561748 G>A maps to NM_182487.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:127549468 C>T maps to NM_182487.2 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:127570084 C>A maps to NM_182487.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:127549309 C>T maps to NM_182487.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:127549342 G>A maps to NM_182487.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:161953869 G>C maps to ENST00000451379 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:161969962 G>T maps to ENST00000451379 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:161989930 G>A maps to ENST00000451379 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:161953890 G>C maps to ENST00000451379 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:161969978 G>T maps to ENST00000451379 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:161954657 G>A maps to ENST00000451379 Y530Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:161989765 G>T maps to ENST00000451379 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:161967828 A>C maps to ENST00000451379 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:161953550 G>A maps to ENST00000451379 Q724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:161970058 G>A maps to ENST00000451379 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:114524258 T>C maps to NM_020190.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr21:34442983 C>T maps to NM_138983.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr21:34399406 G>A maps to NM_005806.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr21:34399313 G>A maps to NM_005806.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:137815190 C>T maps to NM_175747.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr12:10312523 A>G maps to NM_002543.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:10324631 A>G maps to NM_002543.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:95177489 C>A maps to NM_005014.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr9:95179786 T>C maps to NM_005014.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:29622152 G>T maps to NM_002544.4 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr15:53049844 G>A maps to NM_004498.1 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:53049964 G>A maps to NM_004498.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:53082075 G>A maps to NM_004498.1 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:55103631 C>T maps to NM_004852.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr18:55103658 C>T maps to NM_004852.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr6:74079494 G>A maps to NM_001080507.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:193361318 T>C maps to NM_130837.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:193343942 C>T maps to NM_130837.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:46032370 G>A maps to NM_001017989.2 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:46056951 G>A maps to NM_025136.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:46087971 C>T maps to NM_001017989.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:98105763 A>G maps to NM_033207.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:132812873 G>A maps to NM_002545.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr11:132290137 A>G maps to NM_002545.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:132399027 G>A maps to NM_002545.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr11:132290088 A>G maps to NM_002545.3 *346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:132527132 G>A maps to NM_002545.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:67333077 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:67502905 T>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:67430048 A>G did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:67273625 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:67293123 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:67412806 A>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:67272395 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:67273536 T>G did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:67339098 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:67412814 A>G did not map to a codon.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr23:67273625 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:67413749 T>C did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:67502907 C>A did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr23:67652721 G>A did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr8:145107480 G>A maps to ENST00000360660 R1058R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:145113479 C>T maps to ENST00000360660 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:145108222 C>T maps to ENST00000360660 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:145113452 G>A maps to ENST00000360660 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:145108141 G>A maps to ENST00000360660 D947D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:145112395 G>A maps to ENST00000360660 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:145110069 C>T maps to ENST00000360660 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:145106641 G>A maps to ENST00000360660 T1235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:145110769 G>A maps to ENST00000360660 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:145111051 G>A maps to ENST00000360660 N698N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:145109753 G>A maps to ENST00000360660 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153416151 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153416195 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153416330 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153416215 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153416360 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153420112 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153421956 C>A did not map to a codon.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr23:153420175 A>G did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:153421949 A>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:153421851 G>A did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:153416411 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:153416240 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:153418410 A>G did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:153490662 C>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:153461451 A>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:153453503 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:128415176 C>A maps to NM_001708.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:128415194 T>G maps to NM_001708.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr7:128412617 C>T maps to NM_001708.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:241803319 G>C maps to NM_014322.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:88416036 G>A maps to NM_001030015.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr10:88419066 C>T maps to NM_001030015.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:88423537 C>T maps to NM_001030015.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:47763079 C>T maps to ENST00000489301 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:29189407 C>T maps to NM_000911.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:29189494 T>C maps to NM_000911.3 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:54142294 G>A maps to NM_000912.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:54147469 G>A maps to NM_000912.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:54147652 T>G maps to NM_000912.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:54141918 G>A maps to NM_000912.3 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:54163405 C>T maps to NM_000912.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr8:54163480 G>A maps to NM_000912.3 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:54141880 G>A maps to NM_000912.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:62730103 C>T maps to NM_000913.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:62729785 G>A maps to NM_000913.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr20:62729271 G>A maps to NM_000913.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:62729725 C>T maps to NM_000913.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:62729409 G>A maps to NM_000913.3 T163T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D7-A4YT-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr20:62729905 G>A maps to NM_000913.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:154360915 C>T maps to NM_001145279.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:154360654 C>T maps to NM_001145279.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:154360690 C>T maps to NM_001145279.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:154412375 A>G maps to NM_001145279.1 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr6:154439829 G>T maps to NM_001145279.1 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr6:154360837 C>T maps to NM_001145279.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr6:154412399 T>C maps to NM_001145279.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:13169776 A>G maps to NM_021980.4 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:13174159 C>T maps to NM_021980.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:6891002 G>A maps to NM_001004460.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:6891023 A>G maps to NM_001004460.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:6891029 T>C maps to NM_001004460.1 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:7960148 T>G maps to NM_001003745.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:6898660 C>T maps to NM_207186.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr11:6898606 C>T maps to NM_207186.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:6898744 C>T maps to NM_207186.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:6867014 T>C maps to ENST00000379831 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:7949287 G>A maps to NM_001004461.1 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:55735780 A>G maps to NM_001005491.1 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:55735147 C>T maps to NM_001005491.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:55735738 G>A maps to NM_001005491.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr11:55735597 G>A maps to NM_001005491.1 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:29408112 C>T maps to NM_013941.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:29408586 C>T maps to NM_013941.2 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:29408577 G>A maps to NM_013941.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:29408112 C>T maps to NM_013941.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr14:22102167 C>T maps to NM_001005466.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr14:22102377 G>A maps to NM_001005466.1 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:123887009 C>T maps to NM_001004462.1 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:123886625 A>C maps to ENST00000375021 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr11:123886392 C>T maps to ENST00000375021 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:123886784 T>C maps to NM_001004462.1 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr11:123886647 T>C maps to NM_001004462.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:123886997 C>A maps to NM_001004462.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr11:123908817 A>C maps to NM_001004463.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:123909036 G>A maps to NM_001004463.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr11:123908973 G>A maps to NM_001004463.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr11:123909468 C>A maps to NM_001004463.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:123900388 G>A maps to NM_001004464.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:123900886 G>C maps to ENST00000375021 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:123900481 T>A maps to NM_001004464.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:123900388 G>A maps to NM_001004464.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:123900355 G>A maps to NM_001004464.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:123900376 C>T maps to NM_001004464.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:123901054 C>A maps to ENST00000375021 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr11:123900712 G>A maps to ENST00000375021 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr11:123901045 C>A maps to ENST00000375021 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr11:123894261 G>A maps to NM_001001953.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr11:123894204 T>A maps to NM_001001953.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:15918304 C>T maps to NM_013940.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:15918370 C>G maps to NM_013940.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:15918307 A>G maps to NM_013940.2 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr19:15839221 C>T maps to NM_013939.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15839023 G>A maps to NM_013939.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr19:15839755 C>T maps to NM_013939.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:15839068 C>T maps to NM_013939.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:15839275 C>T maps to NM_013939.2 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:15905397 C>T maps to NM_001004466.1 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15905628 C>T maps to NM_001004466.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:15905454 C>T maps to NM_001004466.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr1:159410368 C>G maps to NM_012351.2 S274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:159409817 A>C maps to NM_012351.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr1:159410408 C>G maps to NM_012351.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:159284422 C>T maps to NM_001004467.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:159284044 G>T maps to NM_001004467.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr1:159283837 G>A maps to NM_001004467.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:159284281 A>C maps to NM_001004467.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:159505638 A>G maps to NM_001004469.1 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:159505662 A>G maps to NM_001004469.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:158435959 T>C maps to NM_001004473.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:158435863 C>A maps to NM_001004473.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr1:158435500 G>A maps to NM_001004473.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:158436274 T>A maps to NM_001004473.1 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr1:158390236 C>A maps to NM_001004476.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:158390536 G>T maps to NM_001004476.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:57995828 G>A maps to NM_001004471.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:57995543 C>T maps to NM_001004471.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:57995678 G>A maps to NM_001004471.2 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:57996230 G>T maps to NM_001004471.2 Y39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:158450437 G>A maps to NM_001004472.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:123847891 G>A maps to NM_001004474.1 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr11:123848047 G>T maps to NM_001004474.1 C117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:158368815 A>C maps to NM_001004475.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:158368497 G>A maps to NM_001004475.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:158368797 A>G maps to NM_001004475.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:158368689 G>A maps to NM_001004475.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:59480553 G>A maps to NM_001005324.1 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:158549197 A>G maps to NM_001004477.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr1:158549419 C>T maps to NM_001004477.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:158548957 G>T maps to NM_001004477.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr1:158576891 T>C maps to NM_001004478.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:158576557 T>C maps to NM_001004478.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:158576644 C>T maps to NM_001004478.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr1:158576488 G>A maps to NM_001004478.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr1:158576977 T>C maps to NM_001004478.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr1:158576539 T>C maps to NM_001004478.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:158576881 C>T maps to NM_001004478.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr1:158576419 C>A maps to NM_001004478.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:158576476 T>C maps to NM_001004478.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:29394944 T>C maps to NM_013937.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:29394923 G>T maps to NM_013937.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:29395255 G>A maps to NM_013937.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr22:16449179 T>G maps to NM_001005239.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr22:16449738 A>T maps to NM_001005239.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:16449588 A>G maps to NM_001005239.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr14:19378048 T>A maps to NM_001013354.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr14:20711876 C>T maps to NM_001004479.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr14:20711735 T>G maps to NM_001004479.1 Y262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr14:20692368 G>A maps to NM_001004480.1 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:248005008 G>A maps to NM_001001959.1 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:248004661 G>A maps to NM_001001959.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:248005038 G>A maps to NM_001001959.1 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr1:248005090 G>T maps to NM_001001959.1 C36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:29364788 C>T maps to NM_013936.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:29342455 G>A maps to NM_030959.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr10:45799852 C>T maps to NM_001004297.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr10:45799786 G>A maps to NM_001004297.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:107367362 C>T maps to NM_001004481.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:107367620 G>T maps to NM_001004481.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:107298284 C>T maps to NM_001001961.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:107298416 A>G maps to NM_001001961.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr9:107289433 A>C maps to NM_001001919.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr9:107288533 T>C maps to NM_001001919.1 *319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:107288806 C>T maps to NM_001001919.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:107289040 A>G maps to NM_001001919.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr9:107289028 G>T maps to NM_001001919.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:107360980 G>T maps to NM_001004482.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:107361670 A>G maps to NM_001004482.1 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr9:107332408 T>G maps to NM_001004483.1 *321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr9:107331804 A>G maps to NM_001004483.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:107331744 G>T maps to NM_001004483.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr9:107379909 G>A maps to NM_001001956.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:107457073 C>A maps to NM_001004484.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr9:107457262 C>A maps to NM_001004484.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:107266758 G>A maps to NM_001004485.1 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr9:107267258 C>A maps to NM_001004485.1 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:247835485 C>T maps to NM_001005487.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr1:247835707 G>T maps to NM_001005487.1 C212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:130678358 C>T did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:130678948 G>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:130678545 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:130678803 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:35869831 G>A maps to NM_001004487.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:35869819 C>T maps to NM_001004487.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:35869822 C>T maps to NM_001004487.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:247978943 A>G maps to NM_001001966.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:247978698 G>C maps to NM_001001966.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr1:247978533 G>T maps to NM_001001966.1 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:248512651 C>T maps to NM_001001918.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:248845530 G>A maps to NM_001004734.1 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr1:248844939 C>T maps to NM_001004734.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:248845044 G>A maps to NM_001004734.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:29275413 A>G maps to NM_030946.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr17:3119804 T>C maps to NM_014565.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:3119157 C>T maps to NM_014565.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr17:3119768 T>G maps to NM_014565.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr17:3119042 G>T maps to NM_014565.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:3100940 G>A maps to NM_012352.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:3101154 T>C maps to NM_012352.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr9:125391408 A>G maps to NM_001004450.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:125391778 C>T maps to NM_001004450.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:247920970 T>C maps to NM_012353.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr1:247921687 T>G maps to NM_012353.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr1:247920982 G>A maps to NM_012353.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr1:247921585 C>A maps to NM_012353.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:2996176 C>T maps to NM_002548.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:2996176 C>T maps to NM_002548.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr17:3301638 C>T maps to NM_003553.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr17:3336883 G>A maps to NM_003554.1 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:3336204 C>A maps to NM_003554.1 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:3254533 C>T maps to NM_012360.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:3254620 C>T maps to NM_012360.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr16:3254893 T>G maps to NM_012360.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:3030349 G>A maps to ENST00000381953 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:3030644 G>A maps to ENST00000381953 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:3030731 C>T maps to ENST00000381953 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:15198124 G>A maps to NM_001004713.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr9:125239554 A>G maps to NM_001004451.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:125273592 G>A maps to NM_054107.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:125562730 A>G maps to NM_080859.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:125562751 G>A maps to NM_080859.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:125562772 C>T maps to NM_080859.1 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:125437935 T>C maps to NM_001005234.1 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:125512245 G>A maps to ENST00000373684 A76A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:125512574 A>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr9:125512557 C>G maps to ENST00000373684 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr19:9204307 T>C maps to ENST00000305465 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:125288708 A>G maps to ENST00000359439 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:125288840 G>A maps to ENST00000359439 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:125377433 C>T maps to NM_012364.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr11:57982413 G>A maps to NM_001004458.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:57982467 T>C maps to NM_001004458.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:57970843 G>A maps to NM_001004459.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr7:144015543 C>T maps to NM_001005287.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr7:143792958 C>T maps to NM_001004135.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:143826975 G>A maps to NM_001001659.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:143806950 C>A maps to NM_001005480.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:143771509 G>A maps to NM_001004488.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:143771746 G>A maps to NM_001004488.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:143956654 G>A maps to NM_001005328.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:143956181 G>T maps to NM_001005328.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr7:99474446 A>G maps to NM_001005276.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:99474305 G>A maps to NM_001005276.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr7:99473924 G>T maps to NM_001005276.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:99473840 A>G maps to NM_001005276.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:6807155 G>A maps to NM_001004489.2 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:6789861 G>A maps to NM_001004490.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:6789257 G>A maps to NM_001004490.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:6789714 T>C maps to NM_001004490.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr11:6789657 C>A maps to NM_001004490.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr1:248129100 C>A maps to NM_001004491.1 C156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:248129217 A>G maps to NM_001004491.1 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr1:248128932 C>T maps to NM_001004491.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:74800404 G>A maps to NM_001005285.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr1:247614816 G>T maps to NM_001004492.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:247614942 C>T maps to NM_001004492.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:247615028 G>A maps to NM_001004492.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:27879119 T>G maps to NM_033057.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:29054809 G>A maps to NM_001005226.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:29054461 T>C maps to NM_001005226.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:29054533 A>G maps to NM_001005226.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:27925083 G>A maps to NM_012367.1 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:3405967 C>T maps to NM_012368.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:3406836 C>T maps to NM_012368.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:247694925 C>T maps to NM_198074.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:6913395 G>A maps to NM_003700.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr11:6942564 T>C maps to NM_001004684.1 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:143657707 T>G maps to NM_012369.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:143657491 G>A maps to NM_012369.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:143632552 C>T maps to NM_001004685.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:143632954 T>C maps to NM_001004685.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr7:143633226 G>A maps to NM_001004685.1 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:247751876 G>A maps to NM_001001915.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr1:247752317 C>T maps to NM_001001915.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:247752050 C>A maps to NM_001001915.1 C130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:247752026 C>A maps to NM_001001915.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr1:247752494 T>C maps to NM_001001915.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:247769165 T>G maps to NM_001001914.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:247769369 T>C maps to NM_001001914.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:247769129 C>T maps to NM_001001914.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr1:247769165 T>C maps to NM_001001914.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:247768964 T>C maps to NM_001001914.1 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:247769552 T>G maps to NM_001001914.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr1:247769165 T>G maps to NM_001001914.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:29429648 T>C maps to NM_030883.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:29429650 G>A maps to NM_030883.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:29429656 G>A maps to NM_030883.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr6:29141693 G>A maps to NM_030905.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:248262814 C>T maps to NM_175911.2 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr1:248263420 C>A maps to NM_175911.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:248202141 T>C maps to NM_001004686.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:248202429 C>T maps to NM_001004686.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr1:248201727 T>C maps to NM_001004686.2 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:248202123 G>A maps to NM_001004686.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:248224726 T>G maps to NM_001004687.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:248224180 C>A maps to NM_001004687.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr1:248224726 T>C maps to NM_001004687.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:248224048 T>C maps to NM_001004687.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:248224852 C>T maps to NM_001004687.1 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr1:248224870 G>T maps to NM_001004687.1 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:248112582 C>T maps to NM_001001963.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:248112401 A>T maps to NM_001001963.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:248343832 T>G maps to NM_001004688.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:248366704 C>T maps to NM_001004689.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:248366509 C>G maps to NM_001004689.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:248367307 A>C maps to NM_001004689.1 *313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr1:248402820 A>G maps to NM_017504.1 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr1:248402430 C>T maps to NM_017504.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:248402973 C>T maps to NM_017504.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:248309378 T>C maps to NM_001004690.1 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:248308958 G>A maps to NM_001004690.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:248309018 T>C maps to NM_001004690.1 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr1:248309139 G>T maps to NM_001004690.1 G231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr1:248309087 C>A maps to NM_001004690.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:248308796 T>C maps to NM_001004690.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr1:248487714 A>G maps to NM_001004691.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr9:35957576 A>G maps to NM_019897.2 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:248569513 C>T maps to NM_030904.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:248570401 T>C maps to NM_030904.1 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr1:248569441 A>G maps to NM_030904.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:248756331 T>A maps to NM_001004693.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:248756418 A>G maps to NM_001004693.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:248756505 A>G maps to NM_001004693.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:248790057 A>G maps to NM_001001964.1 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr1:248457971 C>T maps to NM_001004692.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:248617018 G>T maps to NM_001004136.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:248616757 G>A maps to NM_001004136.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:248813393 A>G maps to NM_001001824.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr1:248637451 G>A maps to NM_001005495.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:248636890 C>T maps to NM_001005495.1 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr1:248437047 T>C maps to NM_001004695.1 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr1:248436999 G>T maps to NM_001004695.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr1:248737257 C>T maps to NM_001001821.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:248801983 C>T maps to NM_001001827.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:248525589 C>T maps to NM_001004696.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr1:248525067 C>G maps to NM_001004696.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:248550914 T>C maps to NM_001005471.1 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:248551073 C>A maps to NM_001005471.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr1:248551652 G>A maps to NM_001005471.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:248084483 G>A maps to NM_001005522.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr1:248084780 G>C maps to NM_001005522.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:180582007 T>C maps to NM_206880.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr5:180582043 G>A maps to NM_206880.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr6:29012625 T>C maps to NM_030903.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:29012664 A>C maps to NM_030903.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:248059481 C>T maps to NM_001001957.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:248059004 C>T maps to NM_001001957.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr1:248059820 A>G maps to NM_001001957.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr1:247654602 C>A maps to NM_001004698.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr1:247654884 C>T maps to NM_001004698.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr1:247654764 C>T maps to NM_001004698.2 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr5:180166563 G>A maps to NM_001001657.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr5:180166620 G>A maps to NM_001001657.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:8842178 C>T maps to NM_001004699.1 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr19:8841410 G>A maps to NM_001004699.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr19:8841851 C>G maps to NM_001004699.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:8842031 C>T maps to NM_001004699.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:3195642 G>A maps to ENST00000397187 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:3195188 G>A maps to ENST00000397187 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:3181296 C>T maps to NM_002551.3 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:3324784 C>T maps to NM_012373.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:55136188 T>A maps to NM_001005275.1 L277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:55135661 T>C maps to NM_001005275.1 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr11:55136270 T>G maps to NM_001005275.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:55136027 T>C maps to NM_001005275.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr11:55135536 T>C maps to NM_001005275.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr11:55111533 G>A maps to NM_001005274.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:55111356 T>C maps to NM_001005274.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:55110949 T>C maps to NM_001005274.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:48510550 C>A maps to NM_001005512.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr11:48510988 T>C maps to NM_001005512.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr11:48510688 G>T maps to NM_001005512.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr11:48510955 T>C maps to NM_001005512.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:51412116 T>C maps to NM_001005272.3 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr11:51411501 G>A maps to NM_001005272.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:51412263 C>A maps to NM_001005272.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:51412306 A>T maps to NM_001005272.3 L30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:51411678 G>A maps to NM_001005272.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr11:51412275 G>A maps to NM_001005272.3 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr11:51411521 T>G maps to NM_001005272.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr11:51412113 A>C maps to NM_001005272.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:48239198 C>T maps to NM_001005470.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr11:48238438 T>C maps to NM_001005470.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:48239218 A>T maps to NM_001005470.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr11:48239182 G>A maps to NM_001005470.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr11:55371380 G>A maps to NM_001004700.1 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:55371654 G>C maps to NM_001004700.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:50003317 A>G maps to NM_001005270.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr11:50003179 T>C maps to NM_001005270.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:50003326 G>T maps to NM_001005270.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:49974336 T>C maps to NM_001001955.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:49974072 C>A maps to NM_001001955.2 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr11:49974633 G>T maps to NM_001001955.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr11:49974147 C>A maps to NM_001001955.2 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:49974621 C>T maps to NM_001001955.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr11:49974090 A>C maps to NM_001001955.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr11:49974655 T>C maps to NM_001001955.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr11:55322127 T>C maps to NM_001001920.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:55322543 C>A maps to NM_001001920.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:55321976 C>G maps to NM_001001920.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr11:55322127 T>C maps to NM_001001920.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:55322516 T>C maps to NM_001001920.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr11:55322893 A>T maps to NM_001001920.1 *371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr11:55322127 T>C maps to NM_001001920.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:55321979 C>T maps to NM_001001920.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:55339887 C>T maps to NM_001004701.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:55340530 A>C maps to NM_001004701.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:48346743 G>A maps to NM_001004702.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr11:48346845 T>G maps to NM_001004702.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr11:48346845 T>C maps to NM_001004702.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr11:48346857 C>T maps to NM_001004702.1 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:51515844 T>C maps to NM_001004703.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:51516066 T>G maps to NM_001004703.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:51515505 T>C maps to NM_001004703.1 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr11:51515610 C>T maps to NM_001004703.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr11:55433004 C>T maps to NM_001004704.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:55433481 A>G maps to NM_001004704.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:55432731 T>C maps to NM_001004704.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr11:55432831 T>C maps to NM_001004704.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr11:55432831 T>C maps to NM_001004704.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr11:59245144 T>C maps to NM_001004705.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:59271509 C>T maps to NM_001004706.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:59271686 C>T maps to NM_001004706.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr11:59271452 C>T maps to NM_001004706.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:56247324 C>T maps to NM_001004707.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:56247045 A>C maps to NM_001004707.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:59224663 C>T maps to NM_001004708.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr11:59225149 G>A maps to NM_001004708.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:59282921 C>T maps to NM_001004711.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:59283284 A>G maps to NM_001004711.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:59283041 G>A maps to NM_001004711.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:22134093 C>A maps to NM_001001912.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr14:22133679 T>C maps to NM_001001912.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr15:102358634 T>C maps to NM_001001674.1 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr1:69494 C>T maps to NM_001005484.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr15:102346404 T>C maps to NM_001005326.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:102345981 G>A maps to NM_001005326.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:102346377 T>C maps to NM_001005326.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr15:102346285 C>T maps to NM_001005326.1 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:20404349 T>C maps to NM_001004063.2 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:20403941 G>A maps to NM_001004063.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr14:20404343 G>A maps to NM_001004063.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr14:20404280 C>T maps to NM_001004063.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr14:20404607 T>G maps to NM_001004063.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:20404205 T>C maps to NM_001004063.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:20502295 G>A maps to NM_001004714.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr14:20483283 A>G maps to NM_001004712.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr14:20483289 T>C maps to NM_001004712.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr14:20443856 A>G maps to NM_001005486.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr14:20586245 G>A maps to NM_001004715.1 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr14:20586501 T>C maps to NM_001004715.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:20344704 T>A maps to NM_001005501.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr14:20344476 C>T maps to NM_001005501.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr14:20345001 T>C maps to NM_001005501.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr14:20388905 C>T maps to NM_001005483.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr14:20388989 T>A maps to NM_001005483.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr14:20529030 A>T maps to NM_001004717.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr14:20529097 A>C maps to NM_001004717.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr14:20248624 C>A maps to NM_001005500.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:20248597 A>G maps to NM_001005500.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr15:22369459 A>G maps to NM_001004719.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:22369049 C>T maps to NM_001004719.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:20296293 T>G maps to NM_001004723.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr14:20296282 C>T maps to NM_001004723.1 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:20295660 C>T maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:20295915 C>T maps to NM_001004723.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr15:22382891 C>T maps to NM_001005241.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:22383014 C>A maps to NM_001005241.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:22383026 C>T maps to NM_001005241.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr15:22383053 G>A maps to NM_001005241.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr15:22382667 T>C maps to NM_001005241.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:20612316 C>T maps to NM_001004724.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr11:55405896 G>T maps to NM_001004124.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:20216006 C>T maps to NM_172194.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:20215645 T>C maps to NM_172194.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:48327839 G>A maps to NM_001004725.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:48327911 C>T maps to NM_001004725.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:55418832 T>C maps to NM_001004059.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr11:55419249 G>T maps to NM_001004059.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr11:55418591 C>A maps to NM_001004059.2 Y71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr11:48285906 G>T maps to NM_001004726.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:48285735 T>G maps to NM_001004726.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:4968090 C>T maps to NM_001005329.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:4967442 T>C maps to NM_001005329.1 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:4967643 A>G maps to NM_001005329.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr11:4928715 C>A maps to NM_001004749.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:5344588 T>C maps to NM_033180.4 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:5323053 G>A maps to NM_033179.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:5364321 C>A maps to NM_001005567.1 G145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr11:5364061 C>T maps to NM_001005567.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:5373204 A>G maps to NM_001004750.1 P156P. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr11:5373169 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr11:5373213 T>A maps to NM_001004750.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:4661385 C>T maps to NM_001004751.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr11:4661619 G>T maps to NM_001004751.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:4674676 A>T maps to NM_152430.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:4702989 C>A maps to NM_030774.3 G318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:4945548 G>A maps to NM_001005237.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:4944753 G>A maps to NM_001005237.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr11:4936527 A>G maps to NM_001005238.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:5461994 C>T maps to NM_001005288.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr11:5462105 T>C maps to NM_001005288.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:5474939 C>A maps to NM_001004754.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:5475614 C>A maps to NM_001004754.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:5020601 T>C maps to NM_001004755.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr11:5410660 C>T maps to NM_001004756.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:5411572 T>C maps to NM_001004756.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:5411260 A>G maps to NM_001004756.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:5443928 C>T maps to NM_001004757.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr11:5443928 C>T maps to NM_001004757.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr11:5444224 C>T maps to NM_001004757.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:4870018 G>C maps to NM_001004758.1 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:4870012 C>T maps to NM_001004758.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:4869841 T>C maps to NM_001004758.1 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:4870216 A>G maps to NM_001004758.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:4903764 C>T maps to NM_001004759.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr11:4904052 G>T maps to NM_001004759.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:5221891 A>G maps to NM_001004760.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:5173500 G>A maps to NM_012375.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:5142601 C>T maps to NM_001005222.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr11:5142384 G>A maps to NM_001005222.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:5153680 A>G maps to NM_001005160.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr11:5153614 G>A maps to NM_001005160.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:5153371 G>A maps to NM_001005160.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr11:6190926 G>A maps to NM_001004052.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr11:6190875 C>A maps to NM_001004052.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr11:5602825 C>T maps to NM_001005162.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:5510493 C>T maps to NM_001005163.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:5510802 T>A maps to NM_001005163.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:5509992 G>A maps to NM_001005163.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:5905953 T>C maps to NM_001005165.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr11:5905689 T>C maps to NM_001005165.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr11:5906082 C>T maps to NM_001005165.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:5906274 C>A maps to NM_001005165.1 C251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr11:5905962 T>G maps to NM_001005165.1 A147A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:5906191 C>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:5862839 A>G maps to ENST00000379946 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:5863112 G>A maps to ENST00000379946 N9N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr11:5862524 A>G maps to ENST00000379946 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:5878911 C>T maps to NM_001005168.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr11:5878171 A>C maps to NM_001005168.1 L254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:4615540 G>A maps to ENST00000450052 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:4608095 T>C maps to NM_001005170.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr11:5068261 C>A maps to NM_001001916.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:4511026 G>A maps to NM_001005171.2 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:4510534 G>A maps to NM_001005171.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:4470664 T>C maps to NM_001005172.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:4470694 T>A maps to NM_001005172.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:4470697 A>C maps to NM_001005172.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:4471033 G>A maps to NM_001005172.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr11:4471138 G>A maps to NM_001005172.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:6007638 A>G maps to NM_001005173.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr11:6008073 A>G maps to NM_001005173.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr11:6007356 G>A maps to NM_001005173.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr11:6007311 A>G maps to NM_001005173.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:6007737 A>G maps to NM_001005173.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:4567046 G>A maps to NM_001004137.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr11:5809860 A>T maps to NM_001001913.1 Y62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:5841885 T>C maps to NM_001005174.1 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr11:5776162 T>C maps to NM_001005175.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:5776933 T>C maps to NM_001005175.2 *322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr11:5799453 G>C maps to NM_001001922.2 Y137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:4825232 G>A maps to ENST00000380382 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:4825322 C>T maps to ENST00000380382 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:6220576 C>T maps to NM_001005178.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr11:6221178 C>A maps to NM_001005178.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:6048454 C>T maps to NM_001001917.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:5969244 C>T maps to NM_001003443.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:5968968 C>T maps to NM_001003443.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:6024036 C>T maps to NM_001005179.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:6023814 C>T maps to NM_001005179.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:59211504 G>T maps to NM_001004728.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:59211420 C>T maps to NM_001004728.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr3:97806522 T>G maps to NM_054106.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:56409174 A>G maps to NM_001002925.1 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:56409723 G>T maps to NM_001002925.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr11:56409732 G>T maps to NM_001002925.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr11:56431601 C>A maps to NM_001004730.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:56431886 G>T maps to NM_001004730.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:56431941 A>C maps to NM_001004730.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr11:56431541 T>A maps to NM_001004730.1 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:56431349 C>T maps to NM_001004730.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:56431496 C>A maps to NM_001004730.1 C112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:55798655 G>A maps to NM_001001921.1 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:21623788 G>T maps to NM_001004731.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr14:21623338 G>A maps to NM_001004731.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:58125978 A>G maps to NM_001005489.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:58126398 C>A maps to NM_001005489.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:58275209 C>T maps to NM_001005218.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:58275341 C>T maps to NM_001005218.1 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:58275020 T>C maps to NM_001005218.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:58170498 T>A maps to NM_001005469.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:125551852 G>A maps to NM_001001923.1 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:125551885 C>T maps to NM_001001923.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:125551336 C>T maps to NM_001001923.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:125551963 C>T maps to NM_001001923.1 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:125551447 C>T maps to NM_001001923.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:55541170 C>T maps to NM_001001967.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:55541716 T>G maps to NM_001001967.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:55541017 C>T maps to NM_001001967.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr11:55541186 A>T maps to NM_001001967.1 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr11:55541173 G>A maps to NM_001001967.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:55541551 A>G maps to NM_001001967.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr11:55606943 C>A maps to NM_001005496.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:55606613 C>T maps to NM_001005496.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:55606334 C>A maps to NM_001005496.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:55606706 A>G maps to NM_001005496.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr11:55606310 C>T maps to NM_001005496.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr11:55587671 T>G maps to ENST00000395203 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:55587821 C>T maps to ENST00000395203 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr11:55587683 T>G maps to ENST00000395203 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:55761390 A>C maps to NM_003697.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:55762041 C>T maps to NM_003697.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:55761558 A>G maps to NM_003697.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:55761381 C>T maps to NM_003697.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr3:97851634 T>C maps to NM_001005338.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:97851634 T>C maps to NM_001005338.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr3:97868964 T>C maps to NM_001005514.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr3:97869089 C>G maps to NM_001005514.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr3:97869147 A>T maps to NM_001005514.1 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr3:97868801 T>C maps to NM_001005514.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr3:97868726 A>C maps to NM_001005514.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:98001805 G>A maps to NM_001005482.1 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:98002163 C>T maps to NM_001005482.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:98002129 A>G maps to NM_001005482.1 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:98001799 A>G maps to NM_001005482.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:97983221 G>T maps to NM_001005479.1 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr3:97983781 C>T maps to NM_001005479.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:97983367 G>C maps to NM_001005479.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:55944902 A>G maps to NM_001005492.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:55944911 G>A maps to NM_001005492.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:55944929 G>A maps to NM_001005492.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:55944197 C>T maps to NM_001005492.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:55944531 G>T maps to NM_001005492.1 G147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:55944464 G>T maps to NM_001005492.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:55944473 G>T maps to NM_001005492.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr3:98189088 T>C maps to NM_001004736.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr3:98188572 A>C maps to NM_001004736.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr3:98073197 T>G maps to NM_001005517.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:98073326 C>T maps to NM_001005517.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:98073413 T>A maps to NM_001005517.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr11:55579430 T>C maps to NM_001004738.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:55579082 A>G maps to NM_001004738.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:55579769 G>T maps to NM_001004738.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr11:55595335 C>A maps to NM_001004739.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:56380423 G>A maps to NM_001004740.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:56380327 G>T maps to NM_001004740.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr11:56345185 T>C maps to NM_001004741.1 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:56344777 A>G maps to NM_001004741.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:56237823 A>G maps to NM_001004742.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr11:56258069 G>A maps to NM_001005282.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:56258402 A>G maps to NM_001005282.1 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:56258459 C>A maps to NM_001005282.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:56230297 C>A maps to NM_001004743.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:56230508 G>A maps to NM_001004743.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:56230190 G>A maps to NM_001004743.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:7817751 C>T maps to NM_153444.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr11:7817742 C>A maps to NM_153444.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:7818459 G>A maps to NM_153444.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:7847231 A>G maps to NM_153445.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr11:56184808 G>C maps to NM_001004744.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:56185039 G>T maps to NM_001004744.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr11:56043467 T>G maps to NM_001004745.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr11:56043950 T>G maps to NM_001004745.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr11:56043464 T>C maps to NM_001004745.1 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr11:55999992 G>A maps to NM_001004746.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr11:55999980 A>G maps to NM_001004746.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:56000058 A>G maps to NM_001004746.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr11:55999980 A>C maps to NM_001004746.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr11:55999980 A>C maps to NM_001004746.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr11:56020328 T>G maps to NM_001004747.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr11:56020076 T>C maps to NM_001004747.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:56020521 G>T maps to NM_001004747.1 G283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:56020328 T>G maps to NM_001004747.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr11:56019836 A>G maps to NM_001004747.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr6:29323303 G>A maps to NM_030876.5 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:55681485 A>G maps to NM_001001960.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:55681665 G>A maps to NM_001001960.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr11:55681964 A>G maps to NM_001001960.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr11:55681707 C>T maps to NM_001001960.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr11:6816801 G>T maps to NM_003696.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:240969018 G>A maps to NM_001005853.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:240969564 G>A maps to NM_001005853.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:240969840 A>G maps to NM_001005853.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr2:240969024 G>A maps to NM_001005853.1 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:240985381 G>A maps to NM_173351.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:240985162 G>A maps to NM_173351.1 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:240984766 G>A maps to NM_173351.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:240984625 C>T maps to NM_173351.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:55714598 A>C maps to NM_001005182.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:55715168 A>G maps to NM_001005182.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:55714988 G>A maps to NM_001005182.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:55714398 G>T maps to NM_001005182.1 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr12:55715063 T>G maps to NM_001005182.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:55846032 G>T maps to NM_054105.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr12:55846326 T>C maps to NM_054105.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:55726282 T>C maps to NM_054104.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr12:55725816 T>C maps to NM_054104.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr12:55945711 G>A maps to NM_001005494.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:55688542 C>T maps to NM_001005493.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr12:55688653 G>A maps to NM_001005493.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:55794671 C>T maps to NM_001005518.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:55794776 T>C maps to NM_001005518.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:55795199 A>G maps to NM_001005518.1 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:55886732 C>A maps to NM_001005519.1 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:55863403 A>G maps to NM_001005499.1 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr12:55641463 C>A maps to NM_001005490.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:55641091 A>G maps to NM_001005490.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:55641520 C>T maps to NM_001005490.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr12:55641925 C>A maps to NM_001005490.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:55820442 A>C maps to NM_001005183.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:247875373 G>A maps to NM_001005286.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:247875760 C>T maps to NM_001005286.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:158669992 A>G maps to NM_001005279.1 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr1:158670421 G>T maps to NM_001005279.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:158669932 C>T maps to NM_001005279.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr1:158669773 C>T maps to NM_001005279.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:158669860 G>A maps to NM_001005279.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:158670088 G>T maps to NM_001005279.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr1:158669692 C>T maps to NM_001005279.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:158687065 A>G maps to ENST00000368146 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:158687803 G>T maps to ENST00000368146 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr1:158687896 G>A maps to ENST00000368146 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr1:158687130 A>G maps to ENST00000368146 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:158724748 G>A maps to NM_001005184.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:158725630 G>A maps to NM_001005184.1 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:158724835 C>A maps to NM_001005184.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:158725381 A>G maps to NM_001005184.1 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr1:158724721 G>A maps to NM_001005184.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr1:158724853 G>T maps to NM_001005184.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr11:123676412 G>A maps to NM_001005325.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr11:123676811 G>A maps to NM_001005325.1 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:158735691 G>A maps to NM_001005185.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:158736445 T>C maps to NM_001005185.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:158736312 G>T maps to NM_001005185.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:158746981 A>T maps to NM_001005278.1 C148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr1:158746951 A>G maps to NM_001005278.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr1:158747262 G>A maps to NM_001005278.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr1:158746539 C>A maps to NM_001005278.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:158746933 G>T maps to NM_001005278.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:57798744 C>A maps to NM_001005186.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:21109463 A>G maps to NM_001001968.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:123814163 G>A maps to NM_001005187.1 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:123814251 G>A maps to NM_001005187.1 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:123814131 G>A maps to NM_001005187.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:123624521 A>C maps to NM_001005188.1 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr11:123624328 T>G maps to NM_001005188.1 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:123624937 G>A maps to NM_001005188.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr1:158517583 A>T maps to NM_001005189.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:158517115 T>G maps to NM_001005189.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr1:158517538 A>T maps to NM_001005189.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:14952341 G>A maps to NM_001005190.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:14991936 T>C maps to NM_030901.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:14991603 G>A maps to NM_030901.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:14991666 G>T maps to NM_030901.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:14910600 G>A maps to NM_198944.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:9297197 C>A maps to NM_175883.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:9296576 G>A maps to NM_175883.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:9296543 G>C maps to NM_175883.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr19:9297017 G>T maps to NM_175883.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9296765 C>T maps to NM_175883.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:9296684 C>T maps to NM_175883.2 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr19:9297112 C>G maps to NM_175883.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr19:9325460 G>C maps to NM_001005191.2 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:9324988 C>T maps to NM_001005191.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:9362174 C>T maps to NM_001079935.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr19:9361866 C>T maps to NM_001079935.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9226250 G>T maps to ENST00000293614 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:9213229 T>C maps to NM_001005193.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:9237176 G>A maps to NM_001001958.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:124440461 C>T maps to NM_001005194.1 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr11:124413457 C>A maps to NM_001005195.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:124413430 C>T maps to NM_001005195.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:124413367 G>A maps to NM_001005195.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr11:124412902 A>C maps to NM_001005195.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:124252939 C>T maps to NM_001005468.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr11:124252981 C>T maps to NM_001005468.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:124253125 G>A maps to NM_001005468.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr11:124253167 C>T maps to NM_001005468.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:124266482 C>T maps to NM_001005467.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr11:124266662 G>A maps to NM_001005467.1 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:124294518 A>G maps to NM_001005196.1 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr11:124294392 G>A maps to NM_001005196.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr11:124294714 G>C maps to NM_001005196.1 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:124310558 A>G maps to NM_012378.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:124180466 A>G maps to NM_001002917.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:124180455 G>A maps to NM_001002917.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr11:124180053 C>T maps to NM_001002917.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr11:124189171 T>G maps to NM_001002918.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr11:124189622 T>C maps to NM_001002918.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr11:123777191 T>A maps to NM_001005197.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:123777410 C>T maps to NM_001005197.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:123777974 C>A maps to NM_001005197.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:124135699 C>T maps to ENST00000341493 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:124134871 T>G maps to NM_001005198.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:56058387 G>A maps to NM_001005199.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:56058016 A>T maps to NM_001005199.1 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr11:56057754 T>G maps to NM_001005199.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:56057607 T>G maps to NM_001005199.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:56057977 G>T maps to NM_001005199.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr11:56057746 A>G maps to NM_001005199.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr11:56058004 G>A maps to NM_001005199.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr11:56058468 G>A maps to NM_001005199.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:55872940 C>T maps to NM_001005200.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:55872619 G>T maps to NM_001005200.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr11:55873033 C>T maps to NM_001005200.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:55889928 T>C maps to NM_001005201.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr11:55890576 T>C maps to NM_001005201.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:55890576 T>A maps to NM_001005201.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:55890546 A>G maps to NM_001005201.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr11:55890769 A>C maps to NM_001005201.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr11:55890033 T>C maps to NM_001005201.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr11:55890351 C>T maps to NM_001005201.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr11:55890390 T>G maps to NM_001005201.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:55861421 C>T maps to NM_001003750.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:55861385 A>G maps to NM_001003750.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:55860791 C>T maps to NM_001003750.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:56128399 A>G maps to NM_001005205.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:56128006 T>C maps to NM_001005205.1 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr11:55904987 G>T maps to NM_001004064.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr11:55904987 G>T maps to NM_001004064.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr11:55904630 A>C maps to NM_001004064.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr11:56113600 G>A maps to NM_001002907.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr11:56113543 G>C maps to NM_001002907.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:56086291 C>A maps to NM_001005202.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:55927378 G>A maps to NM_001004058.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:55926923 G>C maps to NM_001004058.2 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:48919914 C>A maps to NM_001005203.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:48921843 C>T maps to NM_001005203.2 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr7:142723589 C>T maps to NM_001001658.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:141619358 C>A maps to NM_001001656.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:56467958 C>T maps to NM_001013358.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:56468489 C>T maps to NM_001013358.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:56468147 C>T maps to NM_001013358.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr11:56468162 C>T maps to NM_001013358.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:56510840 A>G maps to NM_001005284.1 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr11:56510972 C>T maps to NM_001005284.1 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr11:56510657 G>A maps to NM_001005284.1 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr11:56510342 G>T maps to NM_001005284.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:57886595 A>G maps to NM_001005211.1 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:57886280 G>A maps to NM_001005211.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:57885992 G>T maps to NM_001005211.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:57886331 G>A maps to NM_001005211.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:57947125 C>T maps to NM_001005212.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:57947716 G>A maps to NM_001005212.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:57958079 T>C maps to NM_001005283.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr11:57958762 C>A maps to NM_001005283.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr11:57958183 G>A maps to NM_001005283.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:122079194 G>A maps to NM_032790.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:122079119 G>A maps to NM_032790.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:102086988 G>A maps to NM_032831.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:102087195 C>T maps to NM_032831.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr7:102079534 G>A maps to NM_032831.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:102087006 G>A maps to NM_032831.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr16:30964855 G>T maps to NM_152288.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:52851606 C>T maps to NM_004153.3 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:52849542 G>A maps to NM_004153.3 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:52850932 G>A maps to NM_004153.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:201791549 G>A maps to NM_006190.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:201784949 A>G maps to NM_006190.4 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr2:201822830 A>G maps to NM_006190.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:201784966 G>A maps to NM_006190.4 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr2:201796104 G>A maps to NM_006190.4 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:88315635 T>C maps to NM_181837.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr6:88317422 C>T maps to NM_181837.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr6:88376827 G>A maps to NM_181837.2 W709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr2:148715947 C>T maps to NM_181742.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr2:148701061 T>C maps to NM_181742.3 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:148733503 A>G maps to NM_181742.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:103844607 C>T maps to NM_002553.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:103808968 G>A maps to NM_002553.3 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:103835621 C>T maps to NM_002553.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr9:117087067 A>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:117087178 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:117093865 T>C maps to NM_000608.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:117092829 G>A maps to NM_000608.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:56214082 G>A maps to NM_014182.4 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:58109589 C>T maps to NM_006812.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr12:58087952 G>C maps to NM_006812.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr12:58109706 T>G maps to NM_006812.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:59368823 A>G maps to NM_002556.2 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:59345671 G>T maps to NM_002556.2 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:59369203 C>T maps to NM_002556.2 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:31266669 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:31091459 G>A maps to NM_030758.3 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:31285624 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:31725575 G>A maps to NM_017784.4 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:31871603 C>T maps to NM_017784.4 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:125271043 G>A maps to NM_022776.4 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:125266320 G>A maps to NM_022776.4 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:21819304 T>C maps to NM_080597.2 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr18:21759793 T>G maps to NM_080597.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:21757990 G>T maps to NM_080597.2 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:60856152 C>T maps to NM_144498.1 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr20:60859100 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:60854227 C>T maps to NM_144498.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:24903210 C>T maps to NM_015550.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:24839807 T>C maps to NM_015550.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:24874116 G>T maps to NM_015550.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr7:24905027 A>G maps to NM_015550.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr7:24905011 G>A maps to NM_015550.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:24874170 G>A maps to NM_015550.2 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:24849540 C>T maps to NM_015550.2 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr11:3114794 C>T maps to NM_020896.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:3111806 C>T maps to NM_020896.3 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:3140843 G>A maps to NM_020896.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:3140786 G>A maps to NM_020896.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:3115026 C>T maps to NM_020896.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:3125508 G>A maps to NM_020896.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr11:3114848 C>T maps to NM_020896.3 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:179214084 G>A maps to ENST00000392505 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:179247805 G>A maps to ENST00000392505 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179201134 G>A maps to ENST00000392505 S255S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8679-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:179201047 G>A maps to ENST00000392505 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr2:179197639 C>T maps to ENST00000392505 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr2:179197606 C>T maps to ENST00000392505 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:179197731 C>T maps to ENST00000392505 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:76778097 A>C maps to NM_020841.4 Y522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:52253121 C>T maps to ENST00000428468 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:36888481 T>C maps to ENST00000356637 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr14:20920249 T>C maps to NM_017807.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:190618641 C>A maps to NM_022353.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:83994313 C>T maps to NM_013370.3 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:90937492 T>C maps to NM_001126111.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr8:90937639 T>G maps to NM_001126111.1 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:90937018 G>A maps to NM_001126111.1 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:30662776 C>A maps to NM_020530.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:30660084 C>T maps to NM_020530.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:38884118 G>A maps to NM_003999.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:38925462 G>A maps to NM_003999.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:38869208 C>T maps to NM_003999.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:38876459 C>A maps to NM_003999.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:19552978 C>T maps to NM_145260.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr2:19552098 G>A maps to NM_145260.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:19552978 C>T maps to NM_145260.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr8:99961359 T>C maps to ENST00000457907 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr8:99961740 G>A maps to ENST00000457907 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:99961764 G>A maps to ENST00000457907 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:99962934 A>T maps to ENST00000457907 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr9:77703614 A>T maps to NM_012383.4 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:77755813 C>T maps to NM_012383.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:190930419 A>G maps to NM_198184.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:38240678 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr23:38226602 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:38271178 T>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:38262994 T>C did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr16:21698840 G>A maps to ENST00000286149 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:21690263 G>A maps to ENST00000286149 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr16:21716603 C>T maps to ENST00000286149 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr16:21716355 C>T maps to NM_170664.2 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:21698927 G>A maps to ENST00000286149 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:21763713 C>A maps to ENST00000286149 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:26684997 G>A maps to NM_194248.2 D1748D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:26684615 C>T maps to NM_194248.2 R1827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:26707418 G>A maps to NM_194248.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:26750773 C>T maps to NM_194248.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:26688845 G>A maps to NM_194248.2 I1533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:26690307 C>T maps to NM_194248.2 K1384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr2:26684573 G>A maps to NM_194248.2 D1841D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:26700602 G>A maps to NM_194248.2 N743N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:26688571 G>A maps to NM_194248.2 R1589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr2:26712164 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:26680949 G>A maps to ENST00000403946 Y1984Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:26741907 C>T maps to NM_194248.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr3:161221711 T>C maps to NM_001080440.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr4:4199435 G>A maps to NM_177998.1 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:4199698 G>A maps to NM_177998.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:4228314 G>A maps to NM_177998.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:4214665 C>A maps to NM_177998.1 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:72926833 C>T maps to NM_178160.2 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:72939796 C>T maps to NM_178233.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:72937881 C>T maps to NM_178233.1 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:72939781 C>T maps to NM_178233.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:72943356 C>T maps to NM_178233.1 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:16730618 T>G maps to NM_020157.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr20:16730656 T>C did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:16729075 G>A maps to NM_020157.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr5:76932915 G>A maps to NM_032109.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:63764867 G>A maps to ENST00000422031 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:63764652 C>T maps to ENST00000422031 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:94512114 G>A maps to NM_023112.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:94510328 C>T maps to NM_023112.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr14:94512105 G>A maps to NM_023112.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:146059220 A>G maps to ENST00000447906 D902D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:146059096 G>A maps to ENST00000447906 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:146064585 A>G maps to ENST00000447906 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:146059082 C>T maps to ENST00000447906 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:146058965 G>A maps to ENST00000447906 S987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:146077087 C>T maps to ENST00000447906 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:48781132 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:48791967 C>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:48792099 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:48783263 C>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:69283027 C>T did not map to a codon.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr23:69282671 A>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:69283210 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:69282414 G>A did not map to a codon.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr23:69282586 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:31819406 G>A maps to ENST00000382902 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:31776477 C>T maps to ENST00000382902 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr15:31822979 C>T maps to ENST00000382902 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:31851310 G>A maps to ENST00000382902 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:31776543 C>T maps to ENST00000382902 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:31822995 C>T maps to ENST00000382902 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr15:31795993 G>A maps to ENST00000382902 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:31862338 T>G maps to ENST00000382902 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:31776255 G>A maps to ENST00000382902 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:31818589 C>T maps to ENST00000382902 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:31776356 G>A maps to ENST00000382902 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:149916321 C>A maps to NM_020205.2 G656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:149931625 A>G maps to NM_020205.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr1:149916775 G>A maps to NM_020205.2 N504N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr2:63283144 G>A maps to NM_014562.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:63282961 G>A maps to NM_014562.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr14:57268587 A>C maps to NM_021728.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:57268653 A>G maps to NM_021728.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr17:1945947 G>A maps to NM_080822.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:29630379 T>C maps to NM_183378.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:29617461 G>A maps to NM_183378.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:29617590 T>C maps to NM_183378.2 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:7716408 G>T maps to NM_198185.2 C431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:7718030 A>T maps to NM_198185.2 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:111969182 G>A maps to ENST00000369728 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:111957787 G>A maps to ENST00000369728 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:18005393 C>T maps to NM_021220.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:23239725 G>A maps to NM_005015.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:41842865 A>T maps to NM_000436.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:41850185 C>T maps to NM_000436.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:41850185 C>T maps to NM_000436.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:41853523 T>A maps to NM_000436.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:41862804 A>G maps to NM_000436.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:40235970 G>A maps to NM_022120.1 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:40236753 G>A maps to NM_022120.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:42990344 G>A maps to NM_148962.4 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:42990173 G>A maps to NM_148962.4 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:97639035 C>T maps to NM_080818.3 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:16336470 G>A maps to NM_138381.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:107695428 T>C maps to NM_001198533.1 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr3:25833433 C>G maps to NM_017897.2 S308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:38292939 C>T maps to NM_005109.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:38287634 C>T maps to NM_005109.2 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:38263179 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr3:38278445 A>G maps to NM_005109.2 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:38291484 C>T maps to NM_005109.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:3053039 G>A maps to NM_000915.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:8808961 C>T maps to NM_000916.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:3807232 G>A maps to NM_002558.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:133197924 T>C maps to NM_170683.2 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr12:133196329 C>A maps to NM_170683.2 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:57114107 C>T maps to NM_002559.2 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:57135569 C>T maps to NM_002559.2 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:121670888 C>T maps to NM_002560.2 Y378Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:3599263 C>T maps to ENST00000435558 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:21377427 C>A maps to NM_005446.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr12:121622454 G>A maps to NM_002562.5 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:152553660 C>T maps to NM_002563.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:152554179 C>T maps to NM_002563.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr3:152554281 C>T maps to NM_002563.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr3:152554179 C>T maps to NM_002563.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:152553639 G>A maps to NM_002563.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:152554470 C>T maps to NM_002563.2 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:78216819 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:78216179 G>T did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr23:78216895 T>A did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:78216054 T>A did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:78216598 G>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:78216863 G>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:78216153 T>A did not map to a codon.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr23:78216283 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:78216536 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:78216845 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:78216197 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:78216570 T>C did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:78217007 A>T did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr3:151056201 G>C maps to NM_022788.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr3:151055928 G>A maps to NM_022788.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:151045838 C>T maps to NM_176894.2 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr3:151046345 G>A maps to NM_176894.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:151046204 G>A maps to NM_176894.2 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr3:150931957 G>A maps to NM_014879.3 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:150931732 T>C maps to NM_014879.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:72945326 C>T maps to NM_176071.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:72945612 C>T maps to NM_176071.1 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr11:72945521 C>A maps to NM_176071.1 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:72945323 C>T maps to NM_176071.1 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr11:72945734 C>T maps to NM_176071.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:69479031 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:69478727 C>A did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:69478800 C>G did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:69478800 C>G did not map to a codon.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr23:69478800 C>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:69478839 G>A did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:69478800 C>G did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:69478798 G>A did not map to a codon.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr23:69478800 C>G did not map to a codon.
Sequencing variant TCGA-FP-8209-01A-11D-2340-08 chr23:69478800 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:69478462 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:69478741 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:73008169 C>T maps to NM_004154.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:73008444 C>T maps to NM_004154.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:1584484 C>T did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr23:1585027 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1584390 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1585103 A>G did not map to a codon.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr23:1585139 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:1584881 C>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:1584879 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:1585025 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:1585128 T>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:1585332 C>T did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:1584750 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:1584491 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:1584731 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:1584732 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:74813220 G>A maps to NM_000917.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:74813169 C>T maps to NM_000917.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:131534589 C>T maps to NM_001142599.1 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr5:131539838 G>A maps to NM_001142599.1 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:74015429 A>G maps to NM_182904.3 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:74013509 A>G maps to NM_182904.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr11:74015450 G>A maps to NM_182904.3 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:74022611 C>T maps to NM_182904.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr17:79813047 G>C maps to NM_000918.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr17:79813367 C>T maps to NM_000918.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:49042449 C>T maps to NM_177938.2 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr12:56504999 G>A maps to NM_006191.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:73602176 T>C maps to NM_025155.1 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:43559189 C>T maps to NM_001124756.1 N354N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr20:43552830 C>T maps to NM_001124756.1 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:43552845 C>T maps to NM_001124756.1 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:43545431 C>T maps to NM_001124756.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr13:25671742 A>G maps to NM_030979.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr13:25670497 C>T maps to NM_030979.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:40038129 T>A maps to NM_001135653.1 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:90691228 T>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:90690584 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:90690987 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:90690638 C>T did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr23:90691562 T>A did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr23:90691625 T>C did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr23:90691444 G>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:90691721 C>A did not map to a codon.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr23:90690784 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr23:90690957 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:90691202 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:90691322 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:90691414 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:90690584 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:90690843 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr14:23792276 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:88931317 G>A maps to NM_001080487.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:163735932 G>T maps to NM_152410.2 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:20711338 G>A maps to ENST00000503585 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr4:20714514 T>A maps to ENST00000503585 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:66002811 C>T maps to NM_018026.2 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr14:105849214 G>A maps to ENST00000458164 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:105843115 G>A maps to ENST00000458164 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:105851249 G>A maps to ENST00000458164 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:34495113 G>A maps to NM_020804.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr6:34499469 C>T maps to NM_020804.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:34498085 A>G maps to NM_020804.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:43286997 G>A maps to NM_001184970.1 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:43275115 G>A maps to NM_001184970.1 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:43287078 G>A maps to NM_001184970.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr11:47199565 G>A maps to NM_016223.4 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:47202236 G>T maps to NM_016223.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:47202113 C>T maps to NM_016223.4 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr11:47202173 C>G maps to NM_016223.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:17565178 T>G maps to NM_013358.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N2-01A-12D-A364-08 chr1:17559357 T>A maps to NM_013358.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:17431555 G>A maps to NM_007365.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:17410240 G>A maps to NM_007365.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:17431552 C>T maps to NM_007365.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:17411113 G>A maps to NM_007365.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr1:17402247 C>A maps to NM_007365.2 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:17596767 C>T maps to NM_016233.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:17596815 G>A maps to NM_016233.2 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr1:17609471 T>A maps to NM_016233.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:17609501 T>C maps to NM_016233.2 H641H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:17586120 C>T maps to NM_016233.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:17657499 C>T maps to NM_012387.2 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:17690150 C>T maps to NM_012387.2 N631N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:39876978 G>A maps to NM_019088.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:39880925 G>T maps to NM_019088.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:39876873 C>T maps to NM_019088.2 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:39879316 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:39879430 C>T maps to NM_019088.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:2579900 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:2570369 G>T maps to NM_000430.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:26310480 G>A maps to NM_000437.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:81897169 A>G maps to NM_018440.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:81897571 G>A maps to NM_018440.3 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:81897147 C>A maps to NM_018440.3 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:81897283 A>G maps to NM_018440.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:81897571 G>A maps to NM_018440.3 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:81892717 T>C maps to NM_018440.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr8:81889065 C>A maps to NM_018440.3 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:81889021 G>T maps to NM_018440.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr8:81905432 G>A maps to NM_018440.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:49459348 A>G did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:49454057 G>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:55116966 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:55116485 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:55117853 A>G did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr23:49597159 G>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:55247074 A>G did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:103271263 T>G maps to NM_000277.1 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:57318171 G>A maps to NM_001079525.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:43556087 G>A maps to NM_006451.4 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr5:43536982 G>A maps to NM_006451.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:77091001 A>C maps to NM_001128620.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr11:77066711 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:196509565 C>T maps to NM_002577.4 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:196539088 G>A did not map to a codon.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr3:196534696 T>C maps to NM_002577.4 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:110406207 A>G did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:110435360 A>C did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:110435771 G>C did not map to a codon.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr23:110406247 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:110385347 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:110406809 T>G did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:110463598 A>T did not map to a codon.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr23:110391109 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:39669105 C>T maps to NM_005884.3 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:39664229 C>T maps to NM_005884.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:40565645 C>T maps to NM_020168.4 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:40568226 C>T maps to NM_020168.4 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:9546782 C>T maps to NM_177990.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr20:9546761 G>T maps to NM_177990.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:9561028 C>T maps to NM_177990.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:23637589 C>T maps to NM_024675.3 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:23641269 T>C maps to NM_024675.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:23632759 A>G maps to NM_024675.3 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr16:23647257 T>C maps to NM_024675.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:23641344 C>T maps to NM_024675.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:23614920 C>T maps to NM_024675.3 W1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr16:23640532 C>A maps to NM_024675.3 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:169812118 G>T maps to NM_001166108.1 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:169433122 G>A maps to NM_001166108.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:746585 C>T maps to NM_002579.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:746585 C>A maps to NM_002579.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr9:112705557 C>T maps to ENST00000413420 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:112686056 G>A maps to NM_007203.4 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:112705683 T>A maps to ENST00000448454 C407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:102237086 C>T maps to NM_000919.3 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:102237086 C>T maps to NM_000919.3 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:102249695 C>T maps to NM_000919.3 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:35547121 A>G maps to NM_015430.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr11:35454059 C>T maps to NM_015430.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr11:35496284 G>T maps to NM_015430.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr11:35492329 G>A maps to NM_015430.2 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:56716263 G>A maps to NM_001127460.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:56716263 G>A maps to NM_001127460.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:56712962 C>T maps to NM_001127460.2 V1095V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:56720444 T>C maps to NM_001127460.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr13:28862252 T>A maps to NM_175854.7 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:28862159 T>C maps to NM_175854.7 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:28866562 T>C maps to NM_175854.7 D856D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr13:28854576 C>T maps to NM_175854.7 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:28841298 T>C maps to NM_175854.7 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:28834651 C>T maps to NM_175854.7 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:28830624 T>C maps to NM_175854.7 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr10:91371721 C>A maps to NM_148977.1 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:91371451 C>T did not map to a codon.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr10:91353048 G>A maps to NM_148977.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:3899433 G>A maps to NM_153638.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:3897601 C>T maps to NM_153638.2 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:167995866 G>A maps to NM_024594.2 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:93912986 C>T maps to NM_015368.3 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr11:93913995 G>A maps to NM_015368.3 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr22:50615986 G>A maps to NM_052839.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:50615791 C>T maps to NM_052839.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr22:50615659 G>A maps to NM_052839.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:50615710 C>T maps to NM_052839.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:50615929 G>A maps to NM_052839.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:50616541 G>A maps to NM_052839.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:50615854 C>T maps to NM_052839.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr11:124482876 G>C maps to NM_052959.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr10:135203244 C>T maps to NM_152911.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:135195101 G>A maps to NM_152911.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:135195152 C>A maps to NM_152911.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:135193656 C>T maps to NM_152911.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:135204868 G>A maps to NM_152911.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:78936672 G>A did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr16:50258846 T>C maps to NM_001040284.2 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:50261812 C>T maps to NM_001040284.2 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:6751165 G>A maps to NM_006999.4 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:6753131 C>T maps to NM_006999.4 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:6746415 T>C maps to NM_006999.4 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:6739922 C>T maps to NM_006999.4 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:39600756 A>G maps to NM_001004318.2 *439W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:39589224 C>T maps to NM_001004318.2 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:39597684 C>T maps to NM_001004318.2 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:73721270 G>T maps to ENST00000427855 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:73718835 G>A maps to ENST00000427855 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:73717688 G>A maps to ENST00000427855 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:73721643 G>A maps to ENST00000427855 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:73718769 C>T maps to ENST00000427855 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:73718793 C>T maps to ENST00000427855 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:97002283 G>A maps to NM_032632.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:4901084 G>A maps to NM_020144.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr7:4900520 G>T maps to NM_020144.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:61020809 A>G maps to NM_022894.3 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:60983630 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:61021223 G>A maps to NM_022894.3 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:61019296 G>T maps to NM_022894.3 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:61021112 C>T maps to NM_022894.3 D592D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr9:118950312 G>C maps to NM_002581.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr9:118974065 G>A maps to NM_002581.3 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:119109444 C>T maps to NM_002581.3 G1307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr9:119115106 C>T maps to NM_002581.3 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:119130011 G>A maps to NM_002581.3 W1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:118950297 G>A maps to NM_002581.3 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr9:118950378 C>T maps to NM_002581.3 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr9:119115948 A>C maps to NM_002581.3 G1408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:118997788 T>C maps to NM_002581.3 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr9:119033624 C>T maps to NM_002581.3 D961D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr9:119106908 C>A maps to NM_002581.3 Y1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:118974188 C>G maps to NM_002581.3 Y632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:118950132 C>T maps to NM_002581.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:118974131 T>C maps to NM_002581.3 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr9:119097299 C>T maps to NM_002581.3 P1186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:118989724 A>G maps to NM_002581.3 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:118974015 C>T maps to NM_002581.3 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:119115090 C>T maps to NM_002581.3 L1357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:119130026 G>A maps to NM_002581.3 R1533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr9:118950132 C>T maps to NM_002581.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr1:176661332 C>T maps to NM_020318.2 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr1:176668365 C>T maps to NM_020318.2 H959H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr1:176563945 T>G maps to NM_020318.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr1:176668605 G>A maps to NM_020318.2 Q1039Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:176681095 A>G maps to NM_020318.2 K1259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:176640156 T>C maps to NM_020318.2 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:176563807 C>T maps to NM_020318.2 H356H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:176659456 C>T maps to NM_020318.2 T774T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr1:176526216 C>A maps to NM_020318.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr1:176709161 G>C maps to NM_020318.2 V1327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:176762726 C>T maps to NM_020318.2 P1684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr1:176679245 T>G maps to NM_020318.2 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:176564042 C>T maps to NM_020318.2 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:108615043 A>G maps to NM_005443.4 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:108575884 C>T maps to NM_005443.4 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:108622348 A>G maps to NM_005443.4 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr10:89504932 C>T maps to NM_001015880.1 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr10:89487101 G>A maps to NM_001015880.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr10:89487152 T>C maps to NM_001015880.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:79841731 T>C maps to NM_001040202.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr4:79860319 C>T maps to NM_001040202.1 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:79856322 C>T maps to NM_001040202.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:3021666 G>A maps to NM_152341.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr15:69696008 G>T maps to NM_017705.3 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr15:69677201 C>T maps to NM_017705.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:156213672 C>T maps to NM_024897.2 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:156214956 G>A maps to NM_024897.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:156214974 G>A maps to NM_024897.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr1:26189729 G>A maps to NM_178422.5 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:26189364 C>T maps to NM_178422.5 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:26189691 G>T maps to NM_178422.5 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:26189652 G>A maps to NM_178422.5 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:52268149 C>A maps to ENST00000361841 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:142681212 G>A maps to NM_198504.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:142681686 G>A maps to NM_198504.2 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:142681851 G>A maps to NM_198504.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:34759010 A>G did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:34558703 A>G maps to NM_019619.3 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:34620078 G>A maps to NM_019619.3 P936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:34667034 C>G did not map to a codon.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr10:34630664 A>G maps to NM_019619.3 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:34408641 G>A maps to NM_019619.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:34626307 C>A maps to NM_019619.3 G822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:205986629 C>A maps to ENST00000406610 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:205983710 C>T maps to ENST00000406610 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:206480188 C>T maps to ENST00000406610 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:205983663 C>T maps to ENST00000406610 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:205989105 C>T maps to ENST00000406610 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:205969157 G>A maps to ENST00000406610 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr2:206166296 C>G maps to ENST00000406610 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:67695811 C>T maps to NM_016948.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:49366778 C>T maps to NM_032521.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:49366958 G>A maps to NM_032521.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:49366211 T>C maps to NM_032521.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr20:49354416 T>C maps to NM_032521.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:49366646 A>G maps to NM_032521.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr18:77918109 G>A maps to NM_032510.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr18:77917986 C>T maps to NM_032510.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:77960806 C>T maps to NM_032510.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:77917965 G>A maps to NM_032510.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:161771139 G>A maps to NM_004562.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:161781144 G>A maps to NM_004562.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr6:162683734 T>C maps to NM_004562.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:161969976 A>T maps to NM_004562.2 L331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:161969939 C>T maps to NM_004562.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr6:162683734 T>C maps to NM_004562.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:161771163 G>A maps to NM_004562.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:161807879 C>T maps to NM_004562.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:8025394 C>T maps to NM_001123377.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:75937953 G>A maps to NM_015393.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:226555950 G>A maps to NM_001618.3 H742H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:226576443 G>A maps to NM_001618.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:226550839 T>C maps to NM_001618.3 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:226578277 C>T maps to NM_001618.3 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:226576413 C>T maps to NM_001618.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:226562028 T>G maps to NM_001618.3 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:226552831 G>A maps to NM_001618.3 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:226568874 G>A maps to NM_001618.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145059958 A>C maps to NM_032789.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr8:145058497 G>A maps to NM_032789.3 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:145051981 C>T maps to NM_032789.3 K916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:145059955 G>A maps to NM_032789.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:145059212 A>G maps to NM_032789.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:145052081 G>A maps to NM_032789.3 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:145059497 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:145057174 G>A maps to NM_032789.3 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:145051960 G>A maps to NM_032789.3 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:139741629 G>T maps to NM_022750.2 C332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:122419227 T>C maps to NM_017554.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:122418876 G>A maps to NM_017554.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:122422608 C>A maps to NM_017554.2 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:122419908 G>A maps to NM_017554.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr3:122354928 C>T maps to NM_001113523.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:122334583 T>C maps to NM_152615.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:122335916 T>C maps to NM_001113523.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:65559076 A>G maps to NM_017851.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:65555538 G>T maps to NM_017851.4 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:65555514 C>T maps to NM_017851.4 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:65551753 C>T maps to NM_017851.4 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:20825670 C>T maps to NM_005484.3 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:20822241 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:51978416 C>T maps to NM_001003931.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:51980201 C>T maps to NM_001003931.2 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr3:51980231 G>A maps to NM_001003931.2 W390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:51979624 C>T maps to NM_001003931.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:51980282 C>A maps to NM_001003931.2 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:25072361 T>C maps to NM_006437.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:25008670 G>A maps to NM_006437.3 C1536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:25030481 G>A maps to NM_006437.3 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:25009228 G>A maps to NM_006437.3 F1350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr13:25043206 G>A maps to NM_006437.3 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr13:25066689 G>A maps to NM_006437.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr15:72556893 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:50090764 G>C maps to ENST00000505697 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr5:50117138 T>C maps to ENST00000505697 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:50059055 G>A maps to ENST00000505697 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr5:50055475 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:50090968 T>C maps to ENST00000505697 H382H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:122247345 G>A maps to NM_031458.2 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:12530141 A>G maps to NM_018222.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr22:44514997 C>T maps to NM_001003828.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:44547379 G>A maps to NM_001003828.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:44585063 C>T maps to NM_001137606.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:150839573 A>C did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:150840246 A>C did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:150828295 C>T did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:150817161 T>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:150773195 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:150840970 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr23:150773160 T>G did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:150840246 A>C did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:150832639 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:150844590 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:150844473 A>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:150817163 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GJ-01A-11D-A25D-08 chr23:150840968 G>T did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:150789468 A>C did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:242065716 G>A maps to ENST00000358649 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:242075304 G>A maps to ENST00000358649 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:242066358 C>T maps to ENST00000358649 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:242065689 G>A maps to ENST00000358649 R880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:242066829 G>A maps to ENST00000358649 H500H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:242066673 T>C maps to ENST00000358649 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:242066643 A>G maps to ENST00000358649 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:242065998 G>A maps to ENST00000358649 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:242080004 T>C maps to ENST00000358649 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:242047654 A>G maps to ENST00000358649 F1205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:242065962 C>T maps to ENST00000358649 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:242054700 A>G did not map to a codon.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr2:242082441 C>T maps to ENST00000358649 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:242066346 C>T maps to ENST00000358649 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:59406603 T>C maps to NM_152716.2 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:59410350 A>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr11:59416969 A>G maps to NM_152716.2 Y566Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:59425038 T>C maps to NM_152716.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:59419060 G>A maps to NM_152716.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr22:31723044 G>A maps to NM_014323.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr22:31737552 G>A maps to NM_032051.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:31723053 G>A maps to NM_014323.2 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:31731680 G>A maps to NM_014323.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:31731680 G>A maps to NM_014323.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:21687490 C>T maps to NM_006192.3 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:21687259 C>T maps to NM_006192.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:21687523 G>A maps to NM_006192.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr20:21687616 G>C maps to NM_006192.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr20:21687580 C>T maps to NM_006192.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr20:21687400 C>T maps to NM_006192.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:21687220 C>T maps to NM_006192.3 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr20:21690005 G>A maps to NM_006192.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:102509533 G>A maps to NM_003987.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:223086049 C>T maps to NM_181459.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:223158931 G>A maps to NM_181459.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr2:223161735 G>T maps to NM_181459.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr2:223158907 G>A maps to NM_181459.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr7:127253103 C>T maps to NM_006193.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:36846849 C>T maps to NM_016734.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:36882019 C>T maps to NM_016734.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:31823240 T>C maps to NM_001604.4 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:31812408 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:31823108 G>A maps to NM_001604.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:31815287 T>C maps to NM_001604.4 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr11:31823144 C>A maps to NM_001604.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:31815214 G>A maps to NM_001604.4 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:19062343 C>T maps to NM_002584.2 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:19062319 C>T maps to NM_002584.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:19027169 C>T maps to NM_002584.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:19029645 C>T maps to NM_002584.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:114002047 G>A maps to NM_003466.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:37145596 G>A maps to NM_006194.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr14:37132196 C>T maps to NM_006194.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:37145482 G>A maps to NM_006194.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr14:37132489 C>A maps to NM_006194.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr14:37132438 G>A maps to NM_006194.3 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:154739610 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:154748931 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:154767561 A>G maps to NM_007349.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr10:70045123 C>T maps to NM_022129.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:70056652 G>A maps to NM_022129.3 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:70056044 T>C maps to NM_022129.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr10:70043948 G>C maps to NM_022129.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:52712519 G>A maps to ENST00000296302 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:52595942 G>T maps to ENST00000296302 G1376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr3:52613216 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr3:52702549 G>A maps to ENST00000296302 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:164815831 T>G maps to NM_002585.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr1:164761729 G>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:164761863 G>A maps to NM_002585.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:128723069 C>T maps to ENST00000373487 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:19681601 G>A maps to NM_025245.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:154919261 A>C maps to NM_020524.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:154926188 G>T maps to NM_020524.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66617873 G>A maps to NM_022172.2 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:66618280 G>A maps to NM_022172.2 G779G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:66638918 G>A maps to NM_022172.2 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:66618612 C>T maps to NM_022172.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:66620003 C>T maps to NM_022172.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:66633819 G>A maps to NM_022172.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr10:72644970 T>G maps to NM_000281.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:72645662 G>A maps to NM_000281.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:134246092 A>G maps to NM_032151.4 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:53849155 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:47360011 G>A maps to NM_020528.2 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:47359991 C>T maps to NM_020528.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:51995031 G>A maps to NM_033010.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:51992331 C>T maps to NM_033010.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:51993973 C>T maps to NM_033010.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:136048787 C>T maps to NM_001178014.1 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr5:141243651 G>T maps to NM_032420.2 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:141244950 G>A maps to NM_032420.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:141243885 G>A maps to NM_032420.2 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:141243672 G>A maps to NM_032420.2 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr5:141243882 C>T maps to NM_032420.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:141242841 G>A maps to NM_032420.2 S1018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:134073043 G>T maps to NM_032961.1 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:134072674 G>A maps to NM_032961.1 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:134084156 T>G maps to NM_032961.1 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:134073028 A>G maps to NM_032961.1 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr4:134073166 C>T maps to NM_032961.1 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:134073055 T>C maps to NM_032961.1 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr4:134071771 C>T maps to NM_032961.1 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr4:134084216 T>C maps to NM_032961.1 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr4:134072542 T>A maps to NM_032961.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:134073841 G>A maps to NM_032961.1 E849E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:134071387 C>T maps to NM_032961.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:134072896 G>A maps to NM_032961.1 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:134072269 A>G maps to NM_032961.1 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:134071393 C>T maps to NM_032961.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:134084226 C>T maps to NM_032961.1 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr4:134073625 G>A maps to NM_032961.1 A777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:134073361 C>T maps to NM_032961.1 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr4:134071537 C>T maps to NM_032961.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:134073076 G>A maps to NM_032961.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:134072932 G>A maps to NM_032961.1 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr4:134071387 C>T maps to NM_032961.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:134073814 C>T maps to NM_032961.1 C840C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:91133015 A>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:91133118 C>G did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:91132490 C>A did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:91131987 A>C did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:91133951 C>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:91873423 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:91137917 A>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:91873631 G>A did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr23:91131793 T>C did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:91131996 A>C did not map to a codon.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr23:91134130 A>C did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:91133642 G>T did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:91873739 G>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:91132509 T>C did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:91133202 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr23:91090689 T>G did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:91132324 T>C did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:91131987 A>G did not map to a codon.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr23:91133429 G>A did not map to a codon.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr23:91133208 C>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:91133387 G>T did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:91132784 G>T did not map to a codon.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr23:91873416 C>T did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr23:91133635 G>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:91456412 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:91132000 T>G did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:91090642 T>G did not map to a codon.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr23:91132495 G>C did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:91134256 C>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:91132395 C>T did not map to a codon.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr23:91132883 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:91090523 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:91132049 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr23:91873459 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:91133619 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:91873918 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:91134142 C>A did not map to a codon.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr23:91132450 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:91132395 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:91132728 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr23:91642800 G>C did not map to a codon.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr24:4925414 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr24:4925447 C>A did not map to a codon.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr24:4968064 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr24:4967201 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:4925116 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:4966921 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr24:4925360 A>C did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:141336021 A>G maps to NM_016580.2 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:141335043 G>A maps to NM_016580.2 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:141335703 G>A maps to NM_016580.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:141325308 G>T maps to NM_016580.2 P1064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:141335925 G>C maps to NM_016580.2 Y497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:55566536 A>G maps to ENST00000373965 P1619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:56077173 G>A maps to NM_001142763.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:55591247 C>T maps to NM_001142763.1 P1348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr10:55582244 A>G maps to NM_001142763.1 L1754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:55566761 G>A maps to ENST00000373965 N1544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr10:56424015 G>A maps to NM_001142763.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr10:56106145 A>G maps to NM_001142763.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr10:55755491 G>A maps to NM_001142763.1 R934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:55912942 G>A maps to NM_001142763.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:55582988 G>A maps to NM_001142763.1 D1506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr10:55581797 T>G maps to NM_001142763.1 V1903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:55581905 G>T maps to NM_001142763.1 S1867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr10:55582511 T>A maps to NM_001142763.1 S1665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:55698589 G>A maps to NM_001142763.1 R1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr10:56077045 A>T maps to NM_001142763.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr10:55587202 C>T maps to NM_001142763.1 P1444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr10:55780133 T>G maps to NM_001142763.1 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:55616945 T>C maps to NM_001142763.1 E1270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:55943275 C>T maps to NM_001142763.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr10:55912909 A>C maps to NM_001142763.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr10:56106124 C>T maps to NM_001142763.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:58208599 G>A maps to NM_001040429.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:58208794 G>A maps to NM_001040429.2 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:58207120 G>A maps to NM_001040429.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:58208647 G>A maps to NM_001040429.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:58207948 G>A maps to NM_001040429.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr13:58298908 C>T maps to NM_001040429.2 Y987Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:58207933 C>T maps to NM_001040429.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:58208011 G>A maps to NM_001040429.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:58208350 G>A maps to NM_001040429.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr13:58207390 C>T maps to NM_001040429.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:58299088 C>T maps to NM_001040429.2 C1047C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr13:58208086 G>A maps to NM_001040429.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr13:58298872 A>C maps to NM_001040429.2 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:58206889 C>A maps to NM_001040429.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:58208122 G>A maps to NM_001040429.2 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:58299161 T>C maps to NM_001040429.2 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr13:58208185 C>G maps to NM_001040429.2 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr13:58208608 C>T maps to NM_001040429.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr13:58299161 T>C maps to NM_001040429.2 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr13:58208320 T>C maps to NM_001040429.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr13:58208728 G>A maps to NM_001040429.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:58207579 C>T maps to NM_001040429.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr13:58207009 C>T maps to NM_001040429.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr13:58207243 C>T maps to NM_001040429.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr13:58298854 C>A maps to NM_001040429.2 Y969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:58208404 C>T maps to NM_001040429.2 D575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr4:138442508 C>A maps to NM_019035.3 E1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:138451729 A>G maps to NM_019035.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:138450911 C>T maps to NM_019035.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:138451388 G>A maps to NM_019035.3 C618C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr4:138452729 G>C maps to NM_019035.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:138451685 G>T maps to NM_019035.3 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr4:138451175 A>G maps to NM_019035.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr4:138452261 T>C maps to NM_019035.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:138452480 T>C maps to NM_019035.3 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr4:138452672 A>T maps to NM_019035.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:138442437 C>T maps to NM_019035.3 Q1051Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr4:138451619 G>A maps to NM_019035.3 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:138442539 C>T maps to NM_019035.3 P1017P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:99662948 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:99551448 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:99551343 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:99661922 T>C did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:99662239 G>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:99663535 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:99551739 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:99662843 G>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:99663155 C>T did not map to a codon.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr23:99662754 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:99551562 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:99662738 C>T did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr23:99551361 T>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:99663108 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:99663286 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:99662441 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:99662932 G>A did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:99662947 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:99662748 C>T did not map to a codon.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr23:99551590 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:99663302 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:99663155 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:99657661 G>A did not map to a codon.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr23:99661891 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:99551848 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:99662943 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:99551675 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:99662959 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr23:99661592 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:99551587 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:61986185 A>G maps to NM_022843.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:61986424 C>A maps to NM_022843.3 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr13:61987145 T>C maps to NM_022843.3 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr13:61988054 G>A maps to NM_022843.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr13:61987871 G>A maps to NM_022843.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:61987877 G>T maps to NM_022843.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr13:61985659 T>A maps to NM_022843.3 R858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr13:61987145 T>C maps to NM_022843.3 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:61985608 C>A maps to NM_022843.3 E875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:61986272 T>G maps to NM_022843.3 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:30723193 C>T maps to NM_001173523.1 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:30723160 C>T maps to NM_001173523.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:30723559 C>T maps to NM_001173523.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:53421056 C>T maps to NM_002590.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:53422040 C>T maps to NM_002590.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr13:53422115 C>T maps to NM_002590.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:53421737 G>A maps to NM_002590.2 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr13:53421449 G>A maps to NM_002590.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:53421515 G>A maps to NM_002590.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:53420984 G>A maps to NM_002590.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:53420525 G>A maps to NM_002590.2 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr13:53421998 G>A maps to NM_002590.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr13:53422474 G>A maps to NM_002590.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:53421149 C>T maps to NM_002590.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:53422175 C>T maps to NM_002590.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:53420186 C>T maps to NM_002590.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr13:53420276 G>A maps to NM_002590.2 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr13:53420186 C>A maps to NM_002590.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr13:53418817 G>A maps to NM_002590.2 V1030V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:67802392 G>A maps to NM_203487.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:67800538 T>C maps to NM_203487.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:67477737 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:67801411 T>G maps to NM_203487.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr13:66878825 T>C maps to NM_203487.2 A1225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:66878840 C>T maps to NM_203487.2 K1220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr13:67801678 T>C maps to NM_203487.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr13:67205372 A>C maps to NM_203487.2 T1103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:67800784 C>T maps to NM_203487.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr13:67205387 A>G maps to NM_203487.2 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr13:67801944 A>G maps to NM_203487.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:67477674 C>T maps to NM_203487.2 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr13:67800352 T>C maps to NM_203487.2 K740K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:67800274 C>T maps to NM_203487.2 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:67801804 T>C maps to NM_203487.2 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr13:67801359 T>G maps to NM_203487.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:67205360 G>A maps to NM_203487.2 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr13:66878786 T>G maps to NM_203487.2 *1238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140167728 G>A maps to NM_018900.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140166201 C>T maps to NM_018900.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140167455 G>A maps to NM_018900.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:140166075 G>A maps to NM_018900.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140166894 G>A maps to NM_018900.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140166396 G>A maps to NM_018900.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:140167326 G>A maps to NM_018900.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:140167302 G>A maps to NM_018900.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:140166567 C>T maps to NM_018900.2 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140166003 C>A maps to NM_018900.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140166588 C>T maps to NM_018900.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:140165991 C>A maps to NM_018900.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:140167239 C>T maps to NM_018900.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:140237828 G>A maps to NM_018901.2 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr5:140236730 C>T maps to NM_018901.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:140237714 C>G maps to NM_018901.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140237066 G>A maps to NM_018901.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr5:140237312 C>T maps to NM_018901.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr5:140235680 G>A maps to NM_018901.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr5:140237414 C>T maps to NM_018901.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:140237018 C>T maps to NM_018901.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140237300 C>T maps to NM_018901.2 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140237003 C>T maps to NM_018901.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr5:140236967 C>T maps to NM_018901.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr5:140237186 G>A maps to NM_018901.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140248963 C>T maps to NM_018902.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140249903 T>C maps to NM_018902.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140250709 G>A maps to NM_018902.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:140249248 G>A maps to NM_018902.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr5:140249980 G>A maps to NM_018902.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr5:140250856 G>A maps to NM_018902.3 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr5:140250841 G>A maps to NM_018902.3 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr5:140250586 G>A maps to NM_018902.3 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:140250121 G>A maps to NM_018902.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr5:140249917 C>T maps to NM_018902.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:140250610 G>A maps to NM_018902.3 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:140250523 G>A maps to NM_018902.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:140250553 C>T maps to NM_018902.3 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140249734 C>T maps to NM_018902.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:140257240 C>T maps to NM_018903.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140256547 G>A maps to NM_018903.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr5:140256418 G>A maps to NM_018903.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140256955 G>A maps to NM_018903.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr5:140255188 C>T maps to NM_018903.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:140256403 C>T maps to NM_018903.2 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr5:140257072 C>T maps to NM_018903.2 N672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:140256289 C>T maps to NM_018903.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr5:140256589 C>T maps to NM_018903.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:140255710 T>A maps to NM_018903.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:140256802 G>A maps to NM_018903.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr5:140256832 G>A maps to NM_018903.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:140256418 G>A maps to NM_018903.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:140257309 G>A maps to NM_018903.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140257216 G>A maps to NM_018903.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:140257288 C>T maps to NM_018903.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:140257111 C>T maps to NM_018903.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr5:140256802 G>A maps to NM_018903.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:140263604 G>A maps to NM_018904.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:140263514 C>T maps to NM_018904.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:140264042 C>T maps to NM_018904.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:140262137 G>A maps to NM_018904.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr5:140261954 C>T maps to NM_018904.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:140263298 G>A maps to NM_018904.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:140263503 C>T maps to NM_018904.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:140263535 C>T maps to NM_018904.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140261915 C>T maps to NM_018904.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140263418 G>A maps to NM_018904.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:140263715 G>A maps to NM_018904.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:140263419 T>C maps to NM_018904.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:140263983 T>C maps to NM_018904.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:140263586 C>T maps to NM_018904.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr5:140263568 C>T maps to NM_018904.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr5:140263898 G>A maps to NM_018904.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:140263262 G>A maps to NM_018904.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140263781 G>A maps to NM_018904.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140263148 G>A maps to NM_018904.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140263394 C>T maps to NM_018904.2 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140262152 G>A maps to NM_018904.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140263877 G>A maps to NM_018904.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:140263523 C>T maps to NM_018904.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr5:140263928 G>A maps to NM_018904.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:140174887 G>A maps to NM_018905.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140175844 G>A maps to NM_018905.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:140176156 C>T maps to NM_018905.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140176639 C>T maps to NM_018905.2 N697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:140176294 G>A maps to NM_018905.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:140175139 G>A maps to NM_018905.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:140176375 C>T maps to NM_018905.2 Y609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140174695 G>A maps to NM_018905.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140176039 G>A maps to NM_018905.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140176249 G>A maps to NM_018905.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:140181570 C>T maps to NM_018906.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:140181912 C>T maps to NM_018906.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:140182452 C>T maps to NM_018906.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr5:140180982 G>A maps to NM_018906.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140182254 C>A maps to NM_018906.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140182287 C>T maps to NM_018906.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr5:140183034 G>A maps to NM_018906.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:140182371 G>A maps to NM_018906.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr5:140182644 G>A maps to NM_018906.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:140182443 C>T maps to NM_018906.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:140180868 C>T maps to NM_018906.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr5:140181582 C>T maps to NM_018906.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:140182290 G>A maps to NM_018906.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:140182242 C>T maps to NM_018906.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:140180964 G>A maps to NM_018906.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140181615 G>A maps to NM_018906.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr5:140182626 C>T maps to NM_018906.2 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr5:140181069 C>T maps to NM_018906.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140188421 G>A maps to NM_018907.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:140188262 G>A maps to NM_018907.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:140188817 G>A maps to NM_018907.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140188484 T>C maps to NM_018907.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:140188685 C>T maps to NM_018907.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:140188298 G>A maps to NM_018907.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:140188298 G>A maps to NM_018907.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:140188622 C>T maps to NM_018907.2 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr5:140187212 G>A maps to NM_018907.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:140188559 G>A maps to NM_018907.2 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140187860 T>C maps to NM_018907.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr5:140188292 C>T maps to NM_018907.2 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr5:140188220 C>T maps to NM_018907.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:140188889 G>A maps to NM_018907.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr5:140188817 G>A maps to NM_018907.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140188394 C>T maps to NM_018907.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140188217 G>A maps to NM_018907.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr5:140188817 G>A maps to NM_018907.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140188208 G>A maps to NM_018907.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140201539 G>A maps to NM_018908.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:140202574 G>A maps to NM_018908.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140202808 G>A maps to NM_018908.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:140202835 G>A maps to NM_018908.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr5:140203411 C>T maps to NM_018908.2 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:140203225 C>T maps to NM_018908.2 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr5:140202817 C>T maps to NM_018908.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140201488 C>T maps to NM_018908.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140203027 C>T maps to NM_018908.2 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140203135 G>A maps to NM_018908.2 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140203210 G>A maps to NM_018908.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr5:140202805 C>T maps to NM_018908.2 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:140202784 G>A maps to NM_018908.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:140209646 G>A maps to NM_018909.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:140209208 C>T maps to NM_018909.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr5:140209208 C>T maps to NM_018909.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr5:140207975 G>A maps to NM_018909.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr5:140209169 G>T maps to NM_018909.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:140209847 G>A maps to NM_018909.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr5:140209730 C>T maps to NM_018909.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140208824 G>A maps to NM_018909.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr5:140207963 C>T maps to NM_018909.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140209127 G>A maps to NM_018909.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:140209766 C>T maps to NM_018909.2 N697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr5:140207888 C>T maps to NM_018909.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr5:140209733 C>T maps to NM_018909.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:140215575 C>T maps to NM_018910.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140215224 C>T maps to NM_018910.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140215332 C>T maps to NM_018910.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:140216232 G>A maps to NM_018910.2 R755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:140215887 G>A maps to NM_018910.2 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:140216061 G>T maps to NM_018910.2 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr5:140215212 C>T maps to NM_018910.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:140215587 G>T maps to NM_018910.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140221049 C>T maps to NM_018911.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:140221175 C>T maps to NM_018911.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr5:140222312 G>A maps to NM_018911.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:140223020 C>T maps to NM_018911.2 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:140221265 C>T maps to NM_018911.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:140221295 G>A maps to NM_018911.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:140222879 G>A maps to NM_018911.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr5:140221991 C>T maps to NM_018911.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:140222138 C>T maps to NM_018911.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr5:140222834 G>A maps to NM_018911.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr5:140222909 G>A maps to NM_018911.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:140221631 C>T maps to NM_018911.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140221046 G>C maps to NM_018911.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140222192 C>T maps to NM_018911.2 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr5:140222279 C>T maps to NM_018911.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140222183 C>T maps to NM_018911.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr5:140222588 C>T maps to NM_018911.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:140229615 G>A maps to NM_031857.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:140229690 G>A maps to NM_031857.1 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr5:140230059 G>A maps to NM_031857.1 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:140229441 G>A maps to NM_031857.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:140230116 G>A maps to NM_031857.1 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:140229417 C>T maps to NM_031857.1 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140229558 G>A maps to NM_031857.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr5:140230531 C>T maps to NM_014005.3 R818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:140230225 C>T maps to NM_031857.1 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:140229447 G>A maps to NM_031857.1 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140229804 C>T maps to NM_031857.1 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr5:140229702 C>T maps to NM_031857.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr5:140228895 C>T maps to NM_031857.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:140307317 C>T maps to NM_018898.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140307388 G>A maps to NM_018898.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr5:140307640 G>A maps to NM_018898.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:140306839 A>G maps to NM_018898.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140308327 G>A maps to NM_018898.3 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140307514 G>A maps to NM_018898.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr5:140308285 G>A maps to NM_018898.3 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140308684 C>A maps to NM_018898.3 C736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140347211 C>T maps to NM_018899.5 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:140346518 G>A maps to NM_018899.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:140346797 G>A maps to NM_018899.5 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr5:140348337 C>T maps to NM_018899.5 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140347895 G>A maps to NM_018899.5 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:140346614 C>T maps to NM_018899.5 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140347355 G>A maps to NM_018899.5 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140431397 C>T maps to NM_013340.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140433298 C>A maps to NM_013340.2 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:140431714 G>A maps to NM_013340.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr5:140432257 T>G maps to NM_013340.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:140431402 C>A maps to NM_013340.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140433151 C>T maps to NM_013340.2 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:140431351 C>T maps to NM_013340.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr5:140431195 C>T maps to NM_013340.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140432845 A>G maps to NM_013340.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr5:140433052 C>G maps to NM_013340.2 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr5:140431522 C>T maps to NM_013340.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:140574320 T>C maps to NM_018930.3 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:140573213 G>A maps to NM_018930.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140573027 C>A maps to NM_018930.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr5:140573465 C>T maps to NM_018930.3 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:140572676 C>T maps to NM_018930.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr5:140572541 C>G maps to NM_018930.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr5:140573399 C>T maps to NM_018930.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr5:140573732 C>T maps to NM_018930.3 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140573798 G>A maps to NM_018930.3 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:140573522 C>T maps to NM_018930.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:140574068 C>T maps to NM_018930.3 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:140581383 C>A maps to NM_018931.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:140581503 G>A maps to NM_018931.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:140581380 G>A maps to NM_018931.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:140581695 T>C maps to NM_018931.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140579518 G>T maps to NM_018931.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140581470 C>T maps to NM_018931.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr5:140581311 C>T maps to NM_018931.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr5:140581714 C>T maps to NM_018931.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:140581560 C>T maps to NM_018931.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:140581299 G>A maps to NM_018931.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:140581425 G>A maps to NM_018931.2 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:140580495 T>C maps to NM_018931.2 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140579772 C>A maps to NM_018931.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140590137 C>T maps to NM_018932.3 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:140590608 G>A maps to NM_018932.3 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:140590098 T>A maps to NM_018932.3 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr5:140588661 G>A maps to NM_018932.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr5:140590449 G>A maps to NM_018932.3 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140589744 C>T maps to NM_018932.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr5:140590323 C>T maps to NM_018932.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:140588828 T>A maps to NM_018932.3 L117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140589819 C>T maps to NM_018932.3 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:140589804 C>T maps to NM_018932.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:140589804 C>T maps to NM_018932.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140589777 C>T maps to NM_018932.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:140589393 A>G maps to NM_018932.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr5:140590074 C>T maps to NM_018932.3 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:140595728 G>A maps to NM_018933.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr5:140594777 G>A maps to NM_018933.2 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:140594823 G>T maps to NM_018933.2 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140595830 G>A maps to NM_018933.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140594771 G>A maps to NM_018933.2 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr5:140595077 C>T maps to NM_018933.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140594939 G>A maps to NM_018933.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr5:140595314 G>A maps to NM_018933.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:140593985 C>T maps to NM_018933.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:140595323 C>T maps to NM_018933.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr5:140595116 C>T maps to NM_018933.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140604672 C>T maps to NM_018934.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140605137 C>T maps to NM_018934.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:140604657 C>T maps to NM_018934.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr5:140604696 G>T maps to NM_018934.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:140603871 A>G maps to NM_018934.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140605164 G>A maps to NM_018934.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr5:140604639 C>T maps to NM_018934.2 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr5:140605365 G>A maps to NM_018934.2 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140605047 G>A maps to NM_018934.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr5:140603485 G>T maps to NM_018934.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr5:140625809 C>T maps to NM_018935.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:140627173 G>A maps to NM_018935.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140627137 C>T maps to NM_018935.2 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr5:140627002 G>A maps to NM_018935.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:140627302 G>A maps to NM_018935.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr5:140626262 C>T maps to NM_018935.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr5:140627110 C>T maps to NM_018935.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr5:140627047 C>T maps to NM_018935.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140563921 G>A maps to NM_020957.1 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:140563516 C>T maps to NM_020957.1 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140563825 G>A maps to NM_020957.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:140564257 C>T maps to NM_020957.1 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:140564125 C>T maps to NM_020957.1 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:140562719 T>C maps to NM_020957.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:140563825 G>A maps to NM_020957.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr5:140562739 G>A maps to NM_020957.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:140563639 C>T maps to NM_020957.1 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:140564110 C>T maps to NM_020957.1 H659H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140475264 T>C maps to NM_018936.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:140475354 G>T maps to NM_018936.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:140476008 C>T maps to NM_018936.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:140475705 C>T maps to NM_018936.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140476278 C>T maps to NM_018936.2 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:140474382 C>T maps to NM_018936.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:140476257 C>T maps to NM_018936.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140476536 G>A maps to NM_018936.2 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:140475678 C>A maps to NM_018936.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:140474400 C>T maps to NM_018936.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:140475273 G>A maps to NM_018936.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140476116 G>A maps to NM_018936.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140476692 C>T maps to NM_018936.2 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:140482029 C>T maps to NM_018937.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140481489 T>C maps to NM_018937.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:140482005 G>A maps to NM_018937.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr5:140480967 G>T maps to NM_018937.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:140480563 C>T maps to NM_018937.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140481018 C>T maps to NM_018937.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr5:140481366 C>T maps to NM_018937.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr5:140481828 C>T maps to NM_018937.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:140481105 T>G maps to NM_018937.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr5:140482077 C>T maps to NM_018937.2 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:140482389 G>A maps to NM_018937.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140482362 G>A maps to NM_018937.2 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:140481928 C>T maps to NM_018937.2 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140481822 C>T maps to NM_018937.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140481795 C>T maps to NM_018937.2 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:140503796 C>T maps to NM_018938.2 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:140503139 C>T maps to NM_018938.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:140503166 C>T maps to NM_018938.2 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr5:140501879 G>A maps to NM_018938.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140502261 C>T maps to NM_018938.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:140503475 C>T maps to NM_018938.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr5:140503130 G>A maps to NM_018938.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:140502923 C>T maps to NM_018938.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:140501699 C>T maps to NM_018938.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr5:140501696 G>A maps to NM_018938.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:140503286 G>A maps to NM_018938.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140503052 G>A maps to NM_018938.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140503442 C>T maps to NM_018938.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:140516377 C>A maps to NM_015669.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr5:140516110 C>T maps to NM_015669.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140515441 C>T maps to NM_015669.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:140515684 C>T maps to NM_015669.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:140516971 G>A maps to NM_015669.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:140516593 C>T maps to NM_015669.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:140516338 C>T maps to NM_015669.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr5:140516359 C>T maps to NM_015669.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:140516533 C>T maps to NM_015669.2 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr5:140517196 C>T maps to NM_015669.2 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr5:140517124 G>A maps to NM_015669.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:140516539 C>T maps to NM_015669.2 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140517106 G>A maps to NM_015669.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140515303 C>T maps to NM_015669.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:140517073 T>C maps to NM_015669.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:140516809 C>T maps to NM_015669.2 N598N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:140516696 C>T maps to NM_015669.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:140531172 C>T maps to NM_018939.2 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140531364 C>T maps to NM_018939.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:140530023 C>T maps to NM_018939.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr5:140530584 A>G maps to NM_018939.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr5:140530548 C>T maps to NM_018939.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140531448 G>A maps to NM_018939.2 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:140530203 C>T maps to NM_018939.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140531505 G>A maps to NM_018939.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140531247 C>T maps to NM_018939.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140531688 G>A maps to NM_018939.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140531394 C>T maps to NM_018939.2 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:140553417 G>T maps to NM_018940.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr5:140553744 C>T maps to NM_018940.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:140554635 C>T maps to NM_018940.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr5:140553576 C>T maps to NM_018940.2 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:140553939 G>A maps to NM_018940.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140553150 G>A maps to NM_018940.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr5:140554080 C>T maps to NM_018940.2 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:140553996 C>T maps to NM_018940.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr5:140554231 C>T maps to NM_018940.2 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:140553129 C>T maps to NM_018940.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:140554464 G>T maps to NM_018940.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:140554521 G>A maps to NM_018940.2 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr5:140554374 G>A maps to NM_018940.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:140554035 G>A maps to NM_018940.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr5:140554548 G>T maps to NM_018940.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:140553576 C>T maps to NM_018940.2 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:140552970 C>T maps to NM_018940.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:140554263 C>T maps to NM_018940.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr5:140554317 C>T maps to NM_018940.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140554194 C>T maps to NM_018940.2 D593D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr5:140553261 T>C maps to NM_018940.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:140559147 C>T maps to NM_019120.2 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:140559945 C>T maps to NM_019120.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140558613 C>T maps to NM_019120.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140559012 C>T maps to NM_019120.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr5:140559780 G>A maps to NM_019120.2 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr5:140559225 C>T maps to NM_019120.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr5:140559405 G>A maps to NM_019120.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr5:140558214 G>A maps to NM_019120.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140559921 A>G maps to NM_019120.2 K769K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr5:140558893 T>C maps to NM_019120.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr5:140559570 G>A maps to NM_019120.2 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:140559276 C>T maps to NM_019120.2 D554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:140559855 T>C maps to NM_019120.2 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140559447 G>A maps to NM_019120.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr5:140559000 C>T maps to NM_019120.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:140885040 C>T maps to NM_018915.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:140890547 T>C maps to NM_018915.2 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140711197 C>A maps to NM_018912.2 S316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:140890601 C>T maps to NM_018915.2 H887H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:140712161 G>A maps to NM_018912.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:140890601 C>T maps to NM_018915.2 H887H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:140712209 G>C maps to NM_018912.2 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140711012 C>T maps to NM_018912.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140712197 C>T maps to NM_018912.2 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:140710352 A>G maps to NM_018912.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:140711906 G>A maps to NM_018912.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr5:140712138 C>T maps to NM_018912.2 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:140794640 G>C maps to NM_018913.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr5:140794718 C>T maps to NM_018913.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140795117 C>T maps to NM_018913.2 N792N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:140794640 G>A maps to NM_018913.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr5:140793839 G>A maps to NM_018913.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr5:140792993 C>T maps to NM_018913.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140793359 C>T maps to NM_018913.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:140793317 C>T maps to NM_018913.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:140794640 G>A maps to NM_018913.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140794565 G>A maps to NM_018913.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140800890 C>T maps to NM_018914.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140802986 C>T maps to NM_018914.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:140800994 C>T maps to NM_018914.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr5:140803085 G>A maps to NM_018914.2 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr5:140802437 G>A maps to NM_018914.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:140802086 G>A maps to NM_018914.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:140801978 A>G maps to NM_018914.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:140801468 C>T maps to NM_018914.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:140801618 C>T maps to NM_018914.2 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:140801231 C>T maps to NM_018914.2 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140803022 C>T maps to NM_018914.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:140811627 G>A maps to NM_003735.2 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140810541 G>A maps to NM_003735.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140812002 G>A maps to NM_003735.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140811072 G>A maps to NM_003735.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:140812290 C>T maps to NM_003735.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140811975 G>C maps to NM_003735.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:140811195 A>G maps to NM_003735.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140812459 C>T maps to NM_003735.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:140811756 C>T maps to NM_003735.2 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr5:140812213 C>T maps to NM_003735.2 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140812557 C>T maps to NM_003735.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140810463 C>T maps to NM_003735.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:140811831 G>A maps to NM_003735.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:140810433 G>A maps to NM_003735.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:140812119 C>T maps to NM_003735.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140811072 G>A maps to NM_003735.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr5:140810886 C>T maps to NM_003735.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140810868 C>T maps to NM_003735.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:140719047 C>T maps to NM_018915.2 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:140720769 C>T maps to NM_018915.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140719386 A>G maps to NM_018915.2 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140720358 C>T maps to NM_018915.2 H607H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:140720763 C>T maps to NM_018915.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr5:140718567 C>A maps to NM_018915.2 C10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:140720427 A>G maps to NM_018915.2 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140719674 C>T maps to NM_018915.2 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr5:140720421 G>A maps to NM_018915.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:140720952 G>A maps to NM_018915.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140720820 G>A maps to NM_018915.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr5:140720682 G>A maps to NM_018915.2 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr5:140720448 G>A maps to NM_018915.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr5:140718669 C>T maps to NM_018915.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr5:140720292 C>T maps to NM_018915.2 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140719899 C>T maps to NM_018915.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:140724034 A>G maps to NM_018916.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:140724253 C>T maps to NM_018916.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr5:140724658 A>G maps to NM_018916.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140724814 G>A maps to NM_018916.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140725276 G>A maps to NM_018916.3 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140724589 A>G maps to NM_018916.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:140724817 G>A maps to NM_018916.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140725582 C>T maps to NM_018916.3 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:140725510 G>A maps to NM_018916.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:140725804 G>A maps to NM_018916.3 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:140725576 G>A maps to NM_018916.3 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr5:140725720 C>T maps to NM_018916.3 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140723815 G>A maps to NM_018916.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140725486 G>A maps to NM_018916.3 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr5:140724571 A>G maps to NM_018916.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr5:140734940 G>A maps to NM_018917.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140735027 G>A maps to NM_018917.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:140735324 C>T maps to NM_018917.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:140735156 A>G maps to NM_018917.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:140734979 G>A maps to NM_018917.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140736440 T>C maps to NM_018917.2 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:140746260 C>T maps to NM_018918.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr5:140744134 C>T maps to NM_018918.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:140745564 C>T maps to NM_018918.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140745879 C>T maps to NM_018918.2 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140744703 A>C maps to NM_018918.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:140745765 G>A maps to NM_018918.2 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:140743962 G>A maps to NM_018918.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:140744289 G>A maps to NM_018918.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:140744718 C>T maps to NM_018918.2 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:140744571 C>T maps to NM_018918.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:140754321 C>T maps to NM_018919.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:140754300 C>T maps to NM_018919.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr5:140754856 C>T maps to NM_018919.2 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr5:140753829 G>A maps to NM_018919.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140754084 C>T maps to NM_018919.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:140755359 C>T maps to NM_018919.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:140753736 G>A maps to NM_018919.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr5:140755557 C>T maps to NM_018919.2 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140753793 C>T maps to NM_018919.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:140755200 G>A maps to NM_018919.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr5:140755047 C>T maps to NM_018919.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140753887 C>T maps to NM_018919.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140755632 C>T maps to NM_018919.2 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:140755383 G>A maps to NM_018919.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr5:140755020 C>A maps to NM_018919.2 Y457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140762573 G>A maps to NM_018920.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140764595 A>G maps to NM_018920.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:140764118 C>T maps to NM_018920.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:140764748 G>A maps to NM_018920.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:140762726 G>A maps to NM_018920.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:140764700 G>T maps to NM_018920.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:140763254 G>A maps to NM_018920.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:140762927 A>G maps to NM_018920.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:140763129 C>T maps to NM_018920.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:140762852 C>T maps to NM_018920.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:140763023 C>T maps to NM_018920.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:140763803 C>T maps to NM_018920.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140772808 C>T maps to NM_032088.1 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr5:140772817 G>A maps to NM_032088.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:140772925 G>T maps to NM_032088.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:140773687 T>C maps to NM_032088.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:140774581 C>T maps to NM_032088.1 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140772596 C>T maps to NM_032088.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:140773888 G>A maps to NM_032088.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:140773114 G>A maps to NM_032088.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140772637 C>T maps to NM_032088.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr5:140773249 G>A maps to NM_032088.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140772577 C>T maps to NM_032088.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:140783913 C>T maps to NM_018921.2 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:140782827 G>A maps to NM_018921.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140782734 G>A maps to NM_018921.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:140783007 C>T maps to NM_018921.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:140784684 G>A maps to NM_018921.2 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140730669 C>A maps to NM_018922.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr5:140730589 G>T maps to NM_018922.2 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140731722 C>T maps to NM_018922.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:140730468 C>T maps to NM_018922.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr5:140731512 G>A maps to NM_018922.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140740019 C>T maps to NM_018923.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140739872 C>T maps to NM_018923.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr5:140741003 C>A maps to NM_018923.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140740781 G>A maps to NM_018923.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr5:140741306 C>T maps to NM_018923.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:140741225 C>T maps to NM_018923.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140739975 C>T maps to NM_018923.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr5:140740406 C>T maps to NM_018923.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr5:140752270 A>C maps to NM_018924.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140750425 A>G maps to NM_018924.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140751952 C>T maps to NM_018924.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:140751769 G>A maps to NM_018924.2 W603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr5:140751304 C>T maps to NM_018924.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140750431 G>A maps to NM_018924.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140752192 C>T maps to NM_018924.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:140768212 C>T maps to NM_003736.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:140768431 G>A maps to NM_003736.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140769649 C>T maps to NM_003736.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:140769247 C>T maps to NM_003736.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:140769352 C>T maps to NM_003736.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:140768794 G>A maps to NM_003736.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr5:140769436 C>T maps to NM_003736.2 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:140789385 G>A maps to NM_018926.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr5:140788956 T>G maps to NM_018926.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:140789058 G>A maps to NM_018926.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:140788104 T>C maps to NM_018926.2 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140789914 C>T maps to NM_018926.2 R716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:140788116 T>C maps to NM_018926.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:140789520 C>T maps to NM_018926.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr5:140789874 C>G maps to NM_018926.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr5:140788443 C>T maps to NM_018926.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:140799289 C>T maps to NM_018927.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:140799285 G>A maps to NM_018927.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr5:140798805 C>T maps to NM_018927.2 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr5:140798931 G>A maps to NM_018927.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:140798769 C>T maps to NM_018927.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:140799067 C>T maps to NM_018927.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140798892 C>G maps to NM_018927.2 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140799571 C>T maps to NM_018927.2 R716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:140856552 C>T maps to NM_002588.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:140856567 C>T maps to NM_002588.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:140857617 G>A maps to NM_002588.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:140856561 A>G maps to NM_002588.2 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:140856585 C>T maps to NM_002588.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:140855829 C>T maps to NM_002588.2 N49N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:140856978 C>T maps to NM_002588.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140857191 C>T maps to NM_002588.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:140867052 C>T maps to NM_018928.2 G771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:140864817 C>T maps to NM_018928.2 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140865297 C>T maps to NM_018928.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:140865447 C>T maps to NM_018928.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:140864925 C>T maps to NM_018928.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:140869616 C>T maps to NM_018929.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:82868585 G>A maps to NM_015885.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:82877631 C>T maps to NM_015885.3 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr11:82868551 C>G maps to NM_015885.3 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr11:82868591 C>T maps to NM_015885.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:82880340 G>A maps to NM_015885.3 Q988Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:82877042 G>A maps to NM_015885.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:82877373 C>T maps to NM_015885.3 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr11:82874884 G>A maps to NM_015885.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr11:82877702 G>A maps to NM_015885.3 W588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:82878522 C>T maps to NM_015885.3 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:36896592 G>A maps to NM_007144.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:731293 A>G maps to NM_006315.4 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:727561 C>T maps to NM_006315.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:93024259 C>T maps to NM_032373.3 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:93038066 C>T maps to NM_032373.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:93024277 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:93038066 C>T maps to NM_032373.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:105107191 T>C maps to NM_001011663.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:105093693 C>T maps to NM_001011663.1 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:113854824 G>A maps to ENST00000246505 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr13:113834470 C>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr20:44569533 G>A maps to NM_022104.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:44569551 G>A maps to NM_022104.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:44569461 G>A maps to NM_022104.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr20:44569763 G>A maps to NM_022104.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr20:56136535 A>G maps to NM_002591.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr20:56137797 G>A maps to NM_002591.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr20:56137806 A>G maps to NM_002591.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:24572962 A>G maps to NM_004563.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr14:24566313 C>T maps to NM_004563.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:24567462 G>A maps to NM_004563.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:24572734 C>T maps to NM_004563.2 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:24572734 C>T maps to NM_004563.2 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:82579727 G>A maps to NM_033026.5 S3392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:82580129 C>T maps to NM_033026.5 E3258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:82544740 C>T maps to NM_033026.5 K4187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:82763949 C>T maps to NM_033026.5 Q972Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:82764702 C>T maps to NM_033026.5 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:82595404 C>T maps to NM_033026.5 K1233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr7:82584625 T>C maps to NM_033026.5 Q1881Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:82763784 T>A maps to NM_033026.5 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr7:82545547 T>C maps to NM_033026.5 Q3918Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr7:82583157 T>A maps to NM_033026.5 K2371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr7:82451954 T>A maps to NM_033026.5 K4883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr7:82545562 A>G maps to NM_033026.5 T3913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:82545322 C>T maps to NM_033026.5 T3993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:82579562 C>T maps to NM_033026.5 T3447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr7:82582873 T>G maps to NM_033026.5 T2465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr7:82585192 A>C maps to NM_033026.5 Y1692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:82784066 C>T maps to NM_033026.5 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:82583830 T>C maps to NM_033026.5 V2146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:82578854 C>T maps to NM_033026.5 K3683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr7:82784906 T>C maps to NM_033026.5 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr7:82784786 A>G maps to NM_033026.5 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr7:82545484 T>C maps to NM_033026.5 Q3939Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr7:82764558 T>A maps to NM_033026.5 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:82583740 G>A maps to NM_033026.5 V2176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr7:82585561 A>C maps to NM_033026.5 A1569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr7:82582651 A>C maps to NM_033026.5 T2539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr7:82784813 A>C maps to NM_033026.5 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:82785095 G>A maps to NM_033026.5 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr7:82387932 G>A maps to NM_033026.5 V5129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr7:82545732 T>G maps to NM_033026.5 R3857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr7:82763849 C>A maps to NM_033026.5 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:82785656 C>T maps to NM_033026.5 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:82474763 C>T maps to NM_033026.5 Q4623Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr7:82585417 T>G maps to NM_033026.5 T1617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr7:82582531 A>C maps to NM_033026.5 T2579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr7:82583893 G>T maps to NM_033026.5 L2125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:82595269 G>A maps to NM_033026.5 G1278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr7:82474643 G>T maps to NM_033026.5 P4663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:17824575 G>A maps to NM_006197.3 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:17810588 C>T maps to NM_006197.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:17824623 G>A maps to NM_006197.3 Q1119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr8:17794816 C>T maps to NM_006197.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:17838264 G>T did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr6:150123406 G>A maps to NM_005389.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:150114764 C>T maps to NM_005389.2 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:62904613 C>T maps to NM_018257.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr20:62904871 G>A maps to NM_018257.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:62904847 G>A maps to NM_018257.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr21:47808671 C>T maps to NM_006031.5 D1160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:47863741 G>A maps to NM_006031.5 P3240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:47831962 G>A maps to NM_006031.5 P1992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr21:47786729 C>T maps to NM_006031.5 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr21:47754537 A>G maps to NM_006031.5 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr21:47786945 G>A maps to NM_006031.5 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr21:47851681 C>T maps to NM_006031.5 T2768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr21:47841989 G>A maps to NM_006031.5 P2377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr21:47836278 G>A maps to NM_006031.5 A2149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr21:47848451 G>T maps to NM_006031.5 L2546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:71462616 C>T maps to NM_014982.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:71435738 A>G maps to NM_014982.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:71555975 C>T maps to NM_014982.2 R1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:71479727 T>C maps to NM_014982.2 N935N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:71543055 C>T maps to NM_014982.2 R1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:233394560 G>T maps to NM_014801.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:233120165 G>A maps to NM_014801.3 R2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:233190016 G>A maps to NM_014801.3 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:233362999 G>A maps to NM_014801.3 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:233134035 G>A maps to NM_014801.3 Q1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr1:233335972 C>G maps to NM_014801.3 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr1:233190031 G>A maps to NM_014801.3 R1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:233136125 G>A maps to NM_014801.3 H1751H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:233160951 G>A maps to NM_014801.3 N1515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:233134087 C>T maps to NM_014801.3 P1900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:65386141 C>T maps to NM_032223.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:65403964 C>T maps to NM_032223.2 P1899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:65390988 C>T maps to NM_032223.2 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:65403106 G>A maps to NM_032223.2 A1764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:65391431 C>T maps to NM_032223.2 H848H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:100201579 A>G did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr7:100204068 C>A maps to NM_002593.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:142561846 A>G maps to NM_013363.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:142539758 G>A maps to NM_013363.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:7696661 A>G maps to NM_174895.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:95746543 G>A maps to NM_000439.4 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:95768713 A>G maps to NM_000439.4 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr5:95768635 C>T maps to NM_000439.4 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr5:95746489 G>A maps to NM_000439.4 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:17434529 C>T maps to NM_002594.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:17462675 C>T maps to NM_002594.2 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:17417498 C>T maps to NM_002594.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:17417440 C>T maps to NM_002594.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:17434595 C>T maps to NM_002594.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr20:17434529 C>T maps to NM_002594.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:1487274 G>A maps to NM_017573.3 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:1483413 G>A maps to NM_017573.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:1483746 G>A maps to NM_017573.3 Y431Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:1487262 C>T maps to NM_017573.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:1486875 G>A maps to NM_017573.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:1483746 G>A maps to NM_017573.3 Y431Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:1481799 G>A maps to NM_017573.3 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:78686646 C>T maps to NM_001190482.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:78686669 G>T maps to NM_001190482.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:78749045 C>T maps to NM_001190482.1 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr9:78711018 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:78773988 C>T maps to NM_001190482.1 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr11:117100482 G>A maps to NM_004716.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:55512209 C>A maps to NM_174936.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:55529118 C>A maps to NM_174936.3 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:53851105 C>T maps to NM_021213.3 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:70502204 G>A maps to NM_016297.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:70504481 T>C maps to NM_016297.3 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr2:70486654 C>T maps to NM_016297.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:148746954 C>T maps to NM_024028.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:148745579 C>A maps to NM_024028.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:24608150 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:24690691 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:24608228 A>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:24608250 G>A did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:24597469 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:24625970 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:24593349 T>C did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr23:24580206 A>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:79866755 G>A maps to NM_001184917.1 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:79866890 C>G maps to NM_001184917.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:99002517 G>A maps to NM_014891.6 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:242793371 C>T maps to NM_005018.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:242793326 G>T maps to NM_005018.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr10:105200311 G>T maps to NM_014976.1 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:105182763 G>A maps to NM_014976.1 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:105178355 C>T maps to NM_014976.1 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:105185262 C>T maps to NM_014976.1 R1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:105203691 C>T maps to NM_014976.1 N1715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr10:105172892 C>T maps to NM_014976.1 C333C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr10:105202142 T>C maps to NM_014976.1 A1627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:105198553 T>C maps to NM_014976.1 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:105203005 C>T maps to NM_014976.1 V1680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:105205158 T>C maps to NM_014976.1 H1823H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:105162906 C>T maps to NM_014976.1 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:105185247 C>T maps to NM_014976.1 R1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr10:105202181 C>T maps to NM_014976.1 A1640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:105178300 C>T maps to NM_014976.1 H672H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr10:105200537 C>T maps to NM_014976.1 D1496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr10:105158255 C>T maps to NM_014976.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:105184856 C>T maps to NM_014976.1 N960N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:5534982 A>G maps to NM_025239.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:170889179 C>T maps to NM_002598.3 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:112641195 C>T maps to NM_014456.4 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr5:311477 T>C maps to NM_013232.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:306813 C>T maps to NM_013232.3 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:33887073 C>T maps to NM_001162429.1 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:125582651 G>A maps to NM_005388.4 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:101192939 C>T maps to NM_024065.4 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:774113 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:165806269 C>T maps to NM_001130690.1 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr6:165895800 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:165895802 C>T maps to NM_001130690.1 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr6:165806200 C>T maps to NM_001130690.1 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:178879124 G>A maps to NM_016953.3 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:178879181 T>C maps to NM_016953.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:178879181 T>G maps to NM_016953.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr2:178769849 G>T maps to NM_016953.3 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr3:57542654 C>T maps to NM_177966.5 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:57543206 C>A maps to NM_177966.5 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:57545469 C>T maps to NM_177966.5 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:183129092 G>A maps to NM_005019.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:183095852 A>G maps to NM_005019.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:54966476 C>T maps to NM_000924.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:54963397 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:32109996 C>T maps to NM_001191057.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:31890295 G>A maps to NM_001191057.1 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:31890286 G>A maps to NM_001191057.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr7:31920358 C>G did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr7:31862789 C>T maps to NM_001191057.1 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:31855673 G>A maps to NM_001191057.1 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:31862789 C>T maps to NM_001191057.1 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr7:31920364 T>C maps to NM_001191057.1 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr7:31918790 C>T maps to NM_001191057.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr11:72295733 C>T maps to NM_002599.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:72295607 C>T maps to NM_002599.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:72295936 G>A maps to NM_002599.3 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:72385208 G>A maps to NM_002599.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:72288631 C>T maps to NM_002599.3 L874L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-4437-01A-01D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:72295355 C>T maps to NM_002599.3 E513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr11:72295691 G>A maps to NM_002599.3 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:72308581 C>T maps to NM_002599.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:72295733 C>T maps to NM_002599.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:20803458 T>C maps to NM_000921.3 D950D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:20766471 C>T maps to NM_000921.3 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr12:20523120 C>T maps to NM_000921.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:20799535 A>G maps to NM_000921.3 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:20766555 C>T maps to NM_000921.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr12:20523120 C>T maps to NM_000921.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr12:20833036 G>A maps to NM_000921.3 W1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr12:20787854 C>T maps to NM_000921.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr12:20833195 A>G maps to NM_000921.3 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:20774292 C>T maps to NM_000921.3 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:20782872 G>A maps to NM_000921.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:14856573 T>A maps to NM_000922.3 Y751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:14880773 C>T maps to NM_000922.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:14882858 C>T maps to NM_000922.3 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:14889179 T>C maps to NM_000922.3 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:10559811 C>T maps to NM_001111307.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr1:66821299 T>C maps to NM_001037341.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr1:66458720 A>G maps to NM_001037340.1 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:66831414 T>C maps to NM_001037341.1 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr1:66827322 A>C maps to NM_001037341.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:18321959 G>A maps to NM_000923.3 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:58270634 G>A maps to NM_001104631.1 C762C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:58287667 G>A maps to NM_001104631.1 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:144930751 T>C maps to NM_001002811.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:144922005 C>T maps to NM_014644.4 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:144867918 A>G did not map to a codon.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr1:144922017 T>C maps to NM_014644.4 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:144922548 G>C maps to NM_014644.4 L286L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8589-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:144923688 C>T did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr1:144906452 T>G maps to NM_014644.4 R802R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:144952197 T>C maps to NM_022359.5 *311W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:144994710 A>C maps to NM_014644.4 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr1:145075741 G>A maps to NM_022359.5 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:145015952 A>G maps to NM_001198832.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:145075751 C>T maps to NM_022359.5 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr1:144917552 A>G maps to NM_014644.4 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:120419776 G>A maps to NM_001083.3 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr4:120442087 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:120527967 G>A maps to NM_001083.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:120528265 A>G maps to NM_001083.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:149242739 G>A maps to NM_000440.2 Y816Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:149265934 C>T maps to NM_000440.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:149274814 G>A maps to NM_000440.2 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr4:628572 A>C maps to NM_000283.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:657602 C>T maps to NM_000283.3 H655H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:656380 C>T maps to NM_000283.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr4:629697 G>A maps to NM_000283.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:95394528 C>T maps to NM_006204.3 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:95381765 G>A maps to NM_006204.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:95381732 T>C maps to NM_006204.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:95422381 T>C maps to NM_006204.3 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr10:95400245 C>A maps to NM_006204.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr10:95422387 T>G maps to NM_006204.3 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr10:95399897 G>A maps to NM_006204.3 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:95399972 G>A maps to NM_006204.3 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:232597709 G>A maps to NM_002601.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:15130993 T>C maps to NM_006205.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr8:66635812 G>A maps to ENST00000401827 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr8:66659907 A>G maps to ENST00000401827 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:85658681 A>C maps to NM_002605.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:85660937 C>T maps to NM_002605.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:76704734 T>C maps to NM_003719.3 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:76707502 C>T maps to NM_003719.3 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:76700590 C>T maps to NM_003719.3 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:76709127 A>G maps to NM_003719.3 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr5:76704758 C>A maps to NM_003719.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr22:39621766 C>T maps to NM_002608.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:39621844 C>T maps to NM_002608.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:39627737 G>A maps to NM_002608.2 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:39627800 G>A maps to NM_002608.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr4:157771488 A>C maps to NM_016205.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr4:157732093 T>A maps to NM_016205.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:157684301 G>A maps to NM_016205.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:157693879 G>A maps to NM_016205.2 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:103866870 C>T maps to NM_025208.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr11:103870924 G>A maps to NM_025208.4 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:103866941 C>A maps to NM_025208.4 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:104034580 C>T maps to NM_025208.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:103866790 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:55139865 T>C maps to NM_006206.4 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:55138642 G>A maps to NM_006206.4 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:55139787 C>T maps to NM_006206.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:55140716 G>A maps to NM_006206.4 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:55131146 G>A maps to NM_006206.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:55133803 G>A maps to NM_006206.4 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:55127487 G>A maps to NM_006206.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:55146617 T>C maps to ENST00000507166 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:55156583 C>T maps to ENST00000507166 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:55155047 C>T maps to ENST00000507166 D679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr4:55127505 C>A maps to NM_006206.4 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:149513539 C>T maps to NM_002609.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:149498324 G>A maps to NM_002609.3 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:149506145 G>T maps to NM_002609.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr5:149500552 C>T maps to NM_002609.3 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:149501461 G>A maps to NM_002609.3 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:149515199 G>A maps to NM_002609.3 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:17486273 C>T maps to NM_006207.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:19372611 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:19375831 A>C did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr23:19372670 G>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:96761909 C>T maps to NM_005390.4 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:96761864 T>C maps to NM_005390.4 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr4:96761334 C>T maps to NM_005390.4 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr4:96761831 G>A maps to NM_005390.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr4:96762398 C>A maps to NM_005390.4 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr4:96762458 C>T maps to NM_005390.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:96761597 C>T maps to NM_005390.4 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr4:96761777 T>A maps to NM_005390.4 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr3:58419402 C>T maps to NM_000925.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:58417705 T>A maps to NM_000925.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:58416459 G>A maps to NM_000925.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:34988195 C>A maps to NM_003477.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:34988231 C>T maps to NM_003477.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:34991756 T>C maps to NM_003477.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:335550 C>T maps to NM_006849.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:335660 C>A maps to NM_006849.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:335353 C>T maps to NM_006849.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:335546 C>T maps to NM_006849.2 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr16:334906 C>T maps to NM_006849.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr7:148701056 G>A maps to NM_004911.4 D589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:148701188 G>A maps to NM_004911.4 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:10929976 G>A maps to ENST00000381611 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr2:10928836 T>C maps to ENST00000381611 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:20373874 G>A maps to NM_174924.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:20380897 G>A maps to NM_174924.1 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:20410547 G>A maps to NM_174924.1 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:173457700 C>T maps to ENST00000392571 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:173423515 G>T maps to ENST00000392571 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:48174907 C>T maps to NM_002611.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:48186067 C>T maps to NM_002611.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:24552100 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:24549779 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:24483603 C>T did not map to a codon.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr23:24517001 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:24523370 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:95224378 C>T maps to NM_002612.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr10:97023619 C>T did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr4:186423588 G>A maps to NM_014476.4 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:186423510 G>A maps to NM_014476.4 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:186435430 G>A maps to NM_014476.4 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:131607541 C>T maps to NM_003687.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr5:131607858 G>A maps to NM_003687.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:95506155 T>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:176916515 C>T maps to NM_005451.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:176916470 T>C maps to NM_005451.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr5:176911089 G>A maps to NM_005451.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:94934397 G>A maps to NM_001161778.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr8:94934856 C>T maps to NM_001161778.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr8:94935066 C>T maps to NM_001161778.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:13940906 G>A maps to ENST00000510906 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr1:13940883 C>T maps to NM_006474.4 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:70172859 C>T maps to NM_017990.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr16:70176522 A>G maps to NM_017990.3 E513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:70172926 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:39905807 G>A maps to NM_001100399.1 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr4:39910137 A>G maps to NM_001100399.1 H370H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:39864603 G>A maps to NM_001100399.1 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:33344392 C>T maps to ENST00000400481 G1253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:33258136 A>T maps to ENST00000400481 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:33344617 A>G maps to ENST00000400481 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:33222929 G>A maps to ENST00000400481 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:33225982 G>T maps to ENST00000400481 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:26998619 T>C maps to NM_014317.3 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:15112746 C>T maps to NM_015027.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr16:15122810 G>A maps to NM_015027.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:15129375 G>A maps to NM_015027.2 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr16:15100424 A>G maps to NM_015027.2 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:15129898 C>T maps to NM_015027.2 R712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr21:45168940 G>A maps to NM_003681.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr21:45163611 G>A maps to NM_003681.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:45163689 T>C did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:69509182 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:32098699 T>C maps to NM_178140.2 G2726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr5:32089721 C>T maps to NM_178140.2 R2056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:32088212 C>T maps to NM_178140.2 G1553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:32098573 C>T maps to NM_178140.2 H2684H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:32073989 C>T maps to NM_178140.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:32090738 C>T maps to NM_178140.2 R2395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:32048733 C>T maps to NM_178140.2 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:32058195 A>G maps to NM_178140.2 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:32087444 G>A maps to NM_178140.2 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:153068922 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:153069653 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153095696 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:153073994 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:153071026 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153069255 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153069305 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153069710 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:153073927 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:153071525 C>A did not map to a codon.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr23:153070156 C>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:153069624 C>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:153072790 C>T did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr23:153072791 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:153070217 G>A did not map to a codon.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr23:153072285 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153069908 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153070569 T>G did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr10:102778900 G>A maps to NM_001195263.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:102782102 G>A maps to NM_001195263.1 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:119078466 G>T maps to NM_173791.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:119044514 G>A maps to NM_173791.3 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:119043111 C>T maps to NM_173791.3 Q1044Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:119043330 T>C maps to NM_173791.3 T971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr10:119133925 G>A maps to NM_173791.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:119043936 G>A maps to NM_173791.3 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:119100537 C>T maps to NM_173791.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr16:21999998 G>A maps to ENST00000424898 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:22000061 G>A maps to ENST00000424898 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:145747081 C>G maps to NM_002614.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:145761218 G>A maps to NM_002614.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:73433391 G>A maps to NM_015009.1 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:73432974 C>T maps to NM_015009.1 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:73433388 G>A maps to NM_015009.1 D776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr3:73433106 G>A maps to NM_015009.1 H870H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:73433965 G>T maps to NM_015009.1 S584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:73433475 C>T maps to NM_015009.1 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr3:73433148 G>T maps to NM_015009.1 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:41967299 C>T maps to NM_001164595.1 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:41967250 G>A maps to NM_001164595.1 K890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr12:41831776 A>T maps to NM_013377.3 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:41582529 G>A maps to NM_001164595.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr12:41900358 T>A maps to NM_001164595.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:41967473 C>T maps to NM_001164595.1 R965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr12:41961638 T>C maps to NM_001164595.1 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr12:41900469 T>A maps to NM_001164595.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr12:41582775 G>A maps to NM_001164595.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr12:41900350 C>T maps to NM_001164595.1 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:160181414 C>T maps to ENST00000368075 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:156875184 T>C maps to NM_001080471.1 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:156877816 C>T maps to NM_001080471.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:22785140 C>T maps to NM_144962.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:4133937 G>A maps to NM_206836.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:4117628 T>C maps to NM_206836.2 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:4125507 G>A maps to NM_206836.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:4116152 G>A maps to NM_206836.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr2:216930155 G>A maps to NM_018441.5 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr1:32098237 G>A maps to NM_012392.3 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:94293283 G>A maps to NM_001172437.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:94293418 A>G maps to NM_001172437.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:94293700 G>A maps to NM_001172437.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:57335030 G>A maps to NM_006210.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr19:57327775 A>C maps to NM_006210.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:57327019 A>G maps to NM_006210.2 R930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:57327049 G>A maps to NM_006210.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr19:57328825 C>T maps to NM_006210.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr19:57327879 C>A maps to NM_006210.2 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:57325573 T>C maps to NM_006210.2 E1412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:57326968 A>G maps to NM_006210.2 N947N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr19:57327775 A>G maps to NM_006210.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:57326584 G>A maps to NM_006210.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr19:57325135 T>C maps to NM_006210.2 Q1558Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:56757152 G>A maps to NM_021255.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:56645118 G>A maps to NM_021255.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr14:56757011 C>T maps to NM_021255.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:56763565 C>T maps to NM_021255.2 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:66235676 C>T maps to NM_145065.2 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr11:66240869 C>T maps to NM_145065.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:66238784 C>T maps to NM_145065.2 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:66238781 G>A maps to NM_145065.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:66243211 G>A maps to NM_145065.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:66238752 C>T maps to NM_145065.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:66243481 C>T maps to NM_145065.2 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:52097316 A>G maps to NM_015946.4 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr5:52096551 C>G maps to NM_015946.4 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:4576293 C>T maps to ENST00000301396 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:4575195 C>T maps to ENST00000301396 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4575189 G>T maps to ENST00000301396 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:17480329 G>A maps to NM_148172.1 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:17415892 C>T maps to NM_148172.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:17415877 G>A maps to NM_148172.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:57354426 G>A maps to NM_001135690.1 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:33968992 G>A maps to NM_000285.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:33980957 G>A maps to NM_000285.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:33984234 G>A maps to NM_000285.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:8047099 C>T maps to NM_002616.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:8053325 C>T maps to NM_002616.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:239162215 G>A maps to NM_022817.2 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:239161702 C>T maps to NM_022817.2 S987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:239186493 C>T maps to NM_022817.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:239162197 C>T maps to NM_022817.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:7886759 A>G maps to ENST00000377532 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:7887863 C>T maps to ENST00000377532 Q959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr1:7863903 C>T maps to ENST00000377532 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:7863753 T>C maps to ENST00000377532 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:7863903 C>T maps to ENST00000377532 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:7887205 G>A maps to ENST00000377532 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr1:7887364 C>T maps to ENST00000377532 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:7887331 C>T maps to ENST00000377532 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:7887823 C>A maps to ENST00000377532 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:138428375 G>A maps to NM_022121.4 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr22:30977395 C>G did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr4:152638204 G>A maps to NM_004564.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:152637227 C>T maps to NM_004564.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:92146931 G>A maps to NM_000466.2 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:92146931 G>A maps to NM_000466.2 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:92122434 A>G maps to NM_000466.2 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:92147473 C>T maps to NM_000466.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:92119116 C>A maps to NM_000466.2 E1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:92143169 C>A maps to NM_000466.2 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:2338231 G>A maps to NM_153818.1 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:90226988 C>T maps to NM_003847.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:90227002 C>A maps to NM_003847.1 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr15:90226909 G>A maps to NM_003847.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:145522810 A>G maps to NM_003846.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:33904175 C>T maps to NM_000286.2 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:10690007 G>A maps to NM_004565.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:10690016 C>T maps to NM_004565.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:45936233 A>G maps to NM_057174.2 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:160252818 G>A maps to NM_002857.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:160251954 G>T maps to NM_002857.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr1:160252824 C>T maps to NM_002857.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr1:160253355 C>T maps to NM_002857.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:77895610 A>G maps to NM_001172087.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr22:18566232 T>C maps to NM_017929.5 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:143793295 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:7361759 T>C maps to NM_001131023.1 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:7361094 G>A maps to NM_001131023.1 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr12:7362388 G>A maps to NM_001131023.1 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:7362638 G>A maps to NM_001131023.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:179525469 G>A maps to NM_016559.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:179754368 G>A maps to NM_016559.1 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:179525580 C>T maps to NM_016559.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:179529622 C>A maps to NM_016559.1 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:42933449 G>A maps to NM_000287.3 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:42934035 G>A maps to NM_000287.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr6:42941747 G>A maps to NM_000287.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:137187846 T>C maps to NM_000288.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:137187763 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:137191047 G>A maps to NM_000288.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:74719623 C>T maps to NM_002620.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:8158377 C>T maps to NM_012393.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:8167097 G>A maps to NM_012393.2 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:8168253 C>T maps to NM_012393.2 C697C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:8158872 C>T maps to NM_012393.2 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:8161422 C>T maps to NM_012393.2 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:8161140 G>A maps to NM_012393.2 W364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:161071864 C>T maps to NM_012394.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:161072147 G>A maps to NM_012394.3 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:54986274 C>T did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:54987256 T>A did not map to a codon.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr23:54959865 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:54989722 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:54971959 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:54964063 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:54978348 G>A did not map to a codon.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr1:207243622 A>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:6262767 C>T maps to NM_004566.3 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:6261551 G>A maps to NM_004566.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr21:45741667 G>A maps to NM_002626.4 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr21:45732915 A>G maps to NM_002626.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:45736146 A>G maps to NM_002626.4 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:45741609 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:48534512 G>A maps to NM_001166686.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:48529150 C>A maps to NM_001166686.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:48534509 T>C maps to NM_001166686.1 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:3147694 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:3151611 C>T maps to NM_002627.3 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:3143640 C>T maps to NM_002627.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:3151611 C>T maps to NM_002627.3 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4849221 G>T maps to NM_005022.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr11:60975077 C>T maps to NM_001079807.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr11:60971080 C>T maps to NM_001079807.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr11:60975077 C>T maps to NM_001079807.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr11:61017152 C>T maps to ENST00000422676 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:61017281 C>T maps to ENST00000422676 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:44105023 G>A maps to NM_000290.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:44105053 C>T maps to NM_000290.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:77224637 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:77224948 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:77224556 A>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:77224578 T>C did not map to a codon.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr2:197708743 G>C maps to NM_024989.3 S798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr2:197757108 A>G maps to NM_024989.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:3838581 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:37829803 G>A maps to NM_033419.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr17:37829374 C>T maps to NM_033419.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:37830250 G>A maps to NM_033419.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:28269949 T>C maps to NM_032507.3 N773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr6:28270051 G>A maps to NM_032507.3 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr6:28265714 A>G maps to NM_032507.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:249212075 G>T maps to NM_170725.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:249211739 G>A maps to NM_170725.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:50723501 A>G maps to ENST00000515869 H1021H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:34395001 C>T maps to NM_152595.4 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:34396423 C>T maps to NM_152595.4 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:230492786 G>A maps to ENST00000321327 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:230492909 C>T maps to ENST00000321327 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:230492717 G>A maps to ENST00000321327 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:230468773 G>A maps to ENST00000321327 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr1:230472929 C>T maps to ENST00000321327 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:230486740 C>T maps to ENST00000321327 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:230492858 G>T maps to ENST00000321327 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:41711127 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:41712452 A>T maps to NM_002630.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:41710152 C>T maps to NM_002630.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr8:97797142 C>T maps to ENST00000325141 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr8:98078418 G>A maps to ENST00000325141 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr8:97797430 A>G maps to ENST00000325141 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr8:97797500 A>C maps to ENST00000325141 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:10477527 C>G maps to NM_002631.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr1:10479547 C>T maps to NM_002631.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:114573622 G>A maps to NM_005023.3 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:77372816 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:77369603 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:77381298 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:77359862 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:77378855 A>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:77380398 A>G did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:49754750 G>A maps to NM_138733.4 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:49753712 G>A maps to NM_138733.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:49754036 A>G maps to NM_138733.4 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:49754342 G>A maps to NM_138733.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr19:17631841 G>A maps to NM_012088.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:15587372 C>T maps to NM_052890.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:15580721 G>A maps to NM_052890.3 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:15582708 G>A maps to NM_052890.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr19:15582774 C>T maps to NM_052890.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:153279699 C>T maps to NM_052891.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr1:153303243 C>A maps to NM_020393.2 *374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr1:64100647 G>A maps to NM_002633.2 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:64120082 G>A maps to NM_002633.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:64120124 C>T maps to NM_002633.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:74058297 T>C maps to NM_173582.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:74085564 T>A maps to NM_173582.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr11:74047714 C>G maps to NM_173582.3 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:83891503 A>G maps to ENST00000416472 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:83888389 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:83900646 G>A maps to ENST00000416472 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr6:83889609 A>G maps to ENST00000416472 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:70993152 G>A maps to NM_021965.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:70993152 G>A maps to NM_021965.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:71094379 C>A maps to NM_021965.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr19:18474287 G>A maps to NM_017712.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:100996889 C>T did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr11:100912765 G>C maps to NM_000926.4 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr11:100999114 G>A maps to NM_000926.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr11:100999183 G>A maps to NM_000926.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:100998970 C>T maps to NM_000926.4 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:100933307 A>G maps to NM_000926.4 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:100998808 G>A maps to NM_000926.4 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:100999458 A>G maps to NM_000926.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:100999399 G>A maps to NM_000926.4 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr11:100920696 C>T maps to NM_000926.4 E817E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:118370567 T>C did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:118370533 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:118374361 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:118374396 A>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:13160485 C>T maps to NM_030948.1 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr6:144104378 G>T maps to NM_001100164.1 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:144086827 C>T maps to NM_001100164.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:144093508 C>T maps to NM_001100164.1 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:144086698 G>A maps to NM_001100164.1 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:58349435 C>T maps to NM_080672.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:58349363 C>T maps to NM_080672.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr20:58411615 G>A did not map to a codon.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr20:58318234 G>A maps to NM_080672.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:58349513 C>T maps to NM_080672.3 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr20:58411616 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:58349337 C>T maps to NM_080672.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:28802789 T>C maps to NM_023923.3 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:28819588 C>T maps to NM_023923.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:28819604 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:28818271 T>G maps to NM_023923.3 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:125939524 T>G maps to NM_032177.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:125939414 C>T maps to NM_032177.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr17:47486439 G>A maps to NM_002634.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:7079580 G>A maps to NM_001144831.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:9089849 C>T maps to ENST00000433083 R947R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:9083335 A>G maps to ENST00000433083 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:33840978 C>T maps to ENST00000419414 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:33836035 G>A maps to ENST00000419414 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:33836081 G>A maps to ENST00000419414 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:33820014 C>T maps to ENST00000419414 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:169831154 A>G maps to NM_024947.3 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:169863294 G>A maps to NM_024947.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:169890410 C>T maps to NM_024947.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:169867026 G>A maps to NM_024947.3 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:22117150 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:22051187 C>T did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:22244601 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:22196457 T>G did not map to a codon.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr23:22263518 C>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:22117221 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:22115093 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:22095681 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:22129610 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:22095707 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:22132626 T>C did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:22095739 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:22231057 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:33380150 G>A maps to NM_024165.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:33381853 C>G maps to NM_024165.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:33380520 G>A maps to NM_024165.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr13:50097358 G>T maps to NM_001040443.1 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr13:50095042 C>T maps to NM_001040443.1 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:50080831 C>T maps to NM_001040443.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr17:27233874 G>A maps to NM_001033561.1 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:27239794 G>A maps to NM_001033561.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr17:27240010 C>T maps to NM_001033561.1 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr17:27237334 C>T maps to NM_001033561.1 Q756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:27238238 G>A maps to NM_001033561.1 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:27240130 T>C maps to NM_001033561.1 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr17:27237292 C>T maps to NM_001033561.1 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:27233901 A>G maps to NM_001033561.1 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:6676919 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:6681474 C>T maps to NM_153812.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:11101629 T>C maps to ENST00000303905 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:11076292 A>C maps to ENST00000303905 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:11091325 A>G maps to ENST00000303905 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:11091406 G>T maps to ENST00000303905 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:133914472 C>T maps to ENST00000448712 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr5:133914283 G>A maps to ENST00000448712 W610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:133914937 T>C maps to ENST00000448712 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:133873697 C>T maps to ENST00000448712 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:46918267 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:46884162 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:46913961 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:46913988 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:46918474 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:46913629 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:129783139 G>A maps to NM_199320.2 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:129792672 T>C maps to NM_199320.2 H595H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:123620371 G>T maps to NM_015651.1 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:123636848 G>A maps to NM_015651.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:96415472 C>T maps to NM_005392.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:96428054 T>C maps to NM_005392.3 D675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr9:96438028 C>T maps to NM_005392.3 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:96437281 C>T maps to NM_005392.3 D900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:96429498 C>T maps to NM_005392.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr9:96425854 G>A maps to NM_005392.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:96422583 G>A maps to NM_005392.3 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr9:96408054 C>T maps to NM_005392.3 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:34435306 G>A maps to NM_016436.4 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:34526918 G>A maps to NM_016436.4 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:34451081 C>T maps to NM_016436.4 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:133806767 C>T maps to ENST00000395386 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr8:133811378 C>T maps to ENST00000395386 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:133854798 C>T maps to ENST00000395386 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:133856423 A>G maps to ENST00000395386 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr8:133827069 A>G maps to ENST00000395386 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:46001355 G>A maps to ENST00000257821 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:45991419 T>C maps to ENST00000257821 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:45992798 G>A maps to ENST00000257821 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:45987062 G>A maps to ENST00000257821 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr22:45312219 G>A maps to NM_138415.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:45279039 G>A maps to NM_138415.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr22:45312273 G>A maps to NM_138415.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr22:45312222 G>A maps to NM_138415.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr22:45312408 G>A maps to NM_138415.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:7139474 T>C maps to NM_024297.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr17:7140062 G>A maps to NM_024297.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr6:64422325 T>C maps to NM_015153.2 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:64395470 T>A maps to NM_015153.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:64422544 C>T maps to NM_015153.2 N1687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:64423102 A>G maps to NM_015153.2 S1873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:64410355 T>C maps to NM_015153.2 H1033H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:64413547 C>T maps to NM_015153.2 C1118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:41864624 G>A maps to NM_032758.3 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:133551318 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:133547613 A>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:133549152 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:54014279 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:54019238 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:54069131 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:54044102 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:54026319 C>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:53966871 T>A did not map to a codon.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr23:54020052 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:54022123 A>G did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:54043132 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:54037562 A>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:54028590 G>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:120278063 G>T maps to NM_006623.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:120263848 C>T maps to NM_006623.3 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr1:120263848 C>T maps to NM_006623.3 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:79695139 G>A maps to NM_017934.5 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:79700596 G>T maps to NM_017934.5 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:79752649 A>G maps to NM_017934.5 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:79656534 A>C maps to NM_017934.5 V1421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr6:79711670 G>A maps to NM_017934.5 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:79770252 C>T maps to NM_017934.5 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:79727094 A>G maps to NM_017934.5 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:79713473 G>A maps to NM_017934.5 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:79735264 C>T maps to NM_017934.5 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:71856205 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:71813008 G>A did not map to a codon.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr23:71800870 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:71801012 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:71829540 G>C did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr23:71864211 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:71932635 G>T did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:71830970 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:71800982 C>T did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr23:71895994 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:71846870 A>G did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:71932620 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:71873291 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:71933704 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr23:18972520 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:18927017 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:18912462 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:18961915 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:18924618 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:18938280 G>A did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:18926988 C>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:18949780 A>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:18969341 G>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:18912405 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:18913263 T>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:18912414 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:18912388 C>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:18954172 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:18923919 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:18925175 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:18958162 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:18912481 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:18919698 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:47674947 C>T maps to NM_000293.2 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:47730353 G>A maps to NM_000293.2 T986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:56149349 C>T maps to NM_006213.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:56150998 G>A maps to NM_006213.3 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr16:30768204 G>A maps to NM_000294.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr12:76424720 C>T maps to NM_007350.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:118512985 G>A maps to NM_015157.2 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:118516164 C>T maps to NM_015157.2 H1071H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:118499080 T>C maps to NM_015157.2 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:118509944 G>A maps to NM_015157.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:118514809 T>C maps to NM_015157.2 N1013N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:118527418 C>T maps to NM_015157.2 C1340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:118498951 G>A maps to NM_015157.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr3:111603421 G>A maps to NM_001134438.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8364-01A-11D-2340-08 chr3:111692579 C>T maps to NM_001134438.1 D1179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr3:111667810 G>A maps to NM_001134438.1 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr3:111659434 G>A maps to NM_001134438.1 Q780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:111693409 G>C maps to NM_001134438.1 *1254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:60645757 C>T maps to NM_194449.2 S1416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:60562360 A>G maps to NM_194449.2 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:60506063 T>C maps to NM_194449.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr18:60609076 G>A maps to NM_194449.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr18:60639815 C>T maps to NM_194449.2 D1210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:71712665 C>A maps to NM_015020.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:71683224 C>T maps to NM_015020.2 E1180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:71683920 G>A maps to NM_015020.2 C948C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:71715760 G>A maps to NM_015020.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:71736614 G>A maps to NM_015020.2 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr16:71736548 C>A maps to NM_015020.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:71701208 T>C maps to NM_015020.2 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:170557594 T>G maps to NM_001008489.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:170558161 A>G maps to NM_001008489.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr11:71954982 G>A maps to NM_005169.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:41748144 G>T maps to NM_003924.3 C208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:41747862 G>A maps to NM_003924.3 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:139743962 C>T maps to NM_014172.4 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr9:139744465 G>A maps to NM_014172.4 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:608884 C>T maps to ENST00000264555 H1143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:609247 C>T maps to ENST00000264555 S1264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr11:611719 C>T maps to ENST00000264555 R1631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:605237 G>A maps to ENST00000264555 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr11:608500 A>G maps to ENST00000264555 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:607393 G>A maps to ENST00000264555 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:596997 G>A maps to ENST00000264555 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:607381 T>C maps to ENST00000264555 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:608884 C>T maps to ENST00000264555 H1143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:609247 C>A maps to ENST00000264555 S1264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:114267507 G>A maps to NM_006608.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:114253066 G>A maps to NM_006608.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:114254719 A>G maps to NM_006608.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:77567103 T>C maps to ENST00000427986 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:77567055 C>T maps to ENST00000427986 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:77569912 T>A maps to ENST00000427986 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr7:77523311 T>G did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:77549655 C>T maps to ENST00000427986 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr10:13336442 G>T maps to NM_006214.3 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr9:131702968 C>T maps to NM_001100876.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:131703787 G>A maps to NM_001100876.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:131703841 G>A maps to NM_001100876.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:22079024 G>A maps to NM_014759.3 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr8:22084502 C>T maps to NM_014759.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:22079105 G>A maps to NM_014759.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:60996387 G>A maps to NM_032439.3 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr8:75757680 G>A maps to NM_015886.3 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr8:75756214 G>T did not map to a codon.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr8:75737621 A>G maps to NM_015886.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:36930861 C>A maps to NM_153370.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:36930810 T>C maps to NM_153370.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr6:36930863 C>G maps to NM_153370.2 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:25270821 T>C maps to NM_018323.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr22:21106009 C>A maps to NM_058004.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr22:21066896 G>A maps to NM_058004.2 C1835C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:21075681 G>A maps to NM_058004.2 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:21065105 G>A maps to NM_058004.2 L1930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:21153545 G>A maps to NM_058004.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr22:21107255 G>A maps to NM_058004.2 N916N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:151288915 A>C maps to NM_002651.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:68378711 C>T maps to NM_016166.1 H31H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:68438929 C>T maps to NM_016166.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:68479947 G>A maps to NM_016166.1 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:68438951 C>T maps to NM_016166.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:68378936 G>A maps to NM_016166.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:68466134 C>T maps to NM_016166.1 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:68445962 G>A maps to NM_016166.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr1:145584515 C>T maps to NM_006099.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:145578249 G>A maps to NM_006099.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:145584028 G>A maps to NM_006099.3 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:145581206 T>C maps to NM_006099.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:145579268 C>A maps to NM_006099.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:4033134 C>A maps to NM_015897.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:4037623 C>T maps to NM_015897.2 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:4028167 C>T maps to NM_015897.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:4037656 C>T maps to NM_015897.2 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:4037446 G>A maps to NM_015897.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:85689111 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:38470949 G>A maps to NM_012407.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:229890461 G>A maps to NM_017933.4 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:229890416 G>A maps to NM_017933.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:65111387 G>A maps to ENST00000333425 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:65112129 G>A maps to ENST00000333425 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:65110213 C>T maps to ENST00000333425 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:15349628 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:15349629 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:15349521 A>G did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:15349629 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:15349839 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:15342845 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:172411045 G>A maps to NM_153747.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr2:46815246 T>C maps to NM_173074.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:46808670 A>G maps to NM_002643.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:524278 G>A maps to NM_001127178.1 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:501309 C>T maps to NM_001127178.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr4:502757 C>T maps to NM_001127178.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:499697 C>T maps to NM_001127178.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr4:515678 G>C maps to NM_001127178.1 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:68060612 A>G maps to NM_004569.3 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:77587957 A>C did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:77635037 A>G maps to NM_005482.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:77629528 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:160000349 A>G maps to NM_145167.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:160001085 A>G maps to NM_145167.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:160001514 C>T maps to NM_145167.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:35089115 C>T maps to NM_032634.2 R1081R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:35095094 G>A maps to NM_032634.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:35091338 G>A maps to NM_032634.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:35095205 C>T maps to NM_032634.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:35091855 C>T maps to NM_032634.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:35095103 G>A maps to NM_032634.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:38439628 G>T maps to NM_153681.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:624232 G>A maps to NM_148920.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:624376 C>T maps to NM_148920.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr1:207112622 T>A maps to NM_002644.3 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:207107939 G>A maps to NM_002644.3 D510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:207107959 G>A maps to NM_002644.3 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:207112536 G>A maps to NM_002644.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr1:207105024 C>A maps to NM_002644.3 G711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:26883895 G>A maps to NM_033198.3 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr20:44045193 G>A maps to NM_015937.4 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:33222470 G>T maps to NM_080476.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:27121086 C>T maps to NM_017837.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:27117356 C>T maps to NM_017837.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr17:34894026 A>G maps to NM_178517.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:34893937 C>T maps to NM_178517.3 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:196454969 G>A maps to NM_001166304.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr3:196674282 C>T maps to NM_025163.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:196678827 C>T maps to NM_025163.2 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:196675209 C>T maps to NM_025163.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr3:196674045 C>T maps to NM_025163.2 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:49949870 G>A maps to NM_017916.2 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:98469666 G>A maps to NM_152309.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:98408508 C>T maps to NM_152309.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr10:98386588 C>T maps to NM_152309.2 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:98469728 C>A maps to NM_152309.2 G9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:98408568 C>T maps to NM_152309.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:98469321 A>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:17134210 C>T maps to NM_002645.2 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:17150965 A>G maps to NM_002645.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:17111326 C>T maps to NM_002645.2 E1673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:17190439 A>G maps to NM_002645.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:17177085 G>A maps to NM_002645.2 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr11:17156676 A>T maps to NM_002645.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:17115866 G>A maps to NM_002645.2 D1464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:17143868 A>C maps to NM_002645.2 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr11:17170211 A>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:204438318 C>T maps to NM_002646.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr1:204438204 C>T maps to NM_002646.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:204438815 G>T maps to NM_002646.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:18491428 C>T maps to NM_004570.4 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:18719881 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:18644488 C>T maps to NM_004570.4 H889H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:18793421 C>A maps to NM_004570.4 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr18:39570519 T>C did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr18:39575918 C>T maps to ENST00000398870 H284H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr18:39570431 C>T maps to ENST00000398870 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:178917658 A>G maps to NM_006218.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:178921492 A>G maps to NM_006218.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:178928347 G>T maps to NM_006218.2 G512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:138452200 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:138453547 T>G maps to NM_006219.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:138474614 A>G maps to NM_006219.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:9775946 C>T maps to ENST00000361110 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr1:9784135 C>T maps to ENST00000361110 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:9781279 C>T maps to ENST00000361110 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:9778765 C>A maps to ENST00000361110 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:9781258 C>T maps to ENST00000361110 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:106523538 C>A maps to NM_002649.2 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:106513319 T>C maps to NM_002649.2 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:106509610 C>T maps to NM_002649.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr7:106545597 C>T maps to NM_002649.2 N1025N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr7:106508824 C>T maps to NM_002649.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:106520076 T>C maps to NM_002649.2 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:106508512 C>T maps to NM_002649.2 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:106508551 C>A maps to NM_002649.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:106509445 C>T maps to NM_002649.2 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr5:67591120 C>T maps to ENST00000396611 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr5:67589662 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:67569269 G>A maps to ENST00000396611 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:67569822 C>T maps to ENST00000396611 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:67584575 C>T maps to NM_181524.1 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:18273012 G>A maps to NM_005027.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:18273009 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:18280055 G>A maps to NM_005027.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:18279571 G>A maps to NM_005027.2 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:18273782 C>T maps to NM_005027.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:18273782 C>T maps to NM_005027.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr1:46597555 C>T maps to NM_001114172.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:46531770 A>G maps to NM_001114172.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:130422672 G>A maps to NM_014602.2 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:130422667 A>G maps to NM_014602.2 I999I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:130463960 A>G maps to NM_014602.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:130447424 C>T maps to NM_014602.2 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:130398200 G>A maps to NM_014602.2 I1345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:130447381 A>G maps to NM_014602.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:130425789 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:130400352 T>G maps to NM_014602.2 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr17:8792136 C>A maps to NM_001142633.1 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:8794081 G>A maps to NM_001142633.1 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:8784051 T>C maps to NM_001142633.1 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr17:8791714 C>T maps to NM_001142633.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr17:8731506 C>T maps to NM_001010855.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr17:8706635 C>T maps to NM_001010855.2 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:8738637 C>T maps to NM_001010855.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:209198208 G>A maps to NM_015040.3 A1378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:209198112 T>C maps to NM_015040.3 Y1346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:209138323 C>T maps to NM_015040.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:209212721 C>T maps to NM_015040.3 T1783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:209204274 C>T maps to NM_015040.3 S1602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:209179075 G>A maps to NM_015040.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr2:209190438 T>A maps to NM_015040.3 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:209150474 T>C maps to NM_015040.3 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:209190915 C>T maps to NM_015040.3 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:99971836 C>T maps to NM_013439.2 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:99955940 C>T maps to ENST00000413850 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr7:99956990 C>T maps to ENST00000413850 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:99965001 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:99956505 G>A maps to ENST00000413850 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:37139028 C>G maps to ENST00000373507 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr6:37139028 C>G maps to ENST00000373507 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr6:37139028 C>G maps to ENST00000373507 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:37140781 G>A maps to ENST00000373507 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:37140776 C>T maps to ENST00000373507 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr6:37139028 C>G maps to ENST00000373507 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:48772562 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:9949265 G>A maps to NM_006221.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:71416694 T>A did not map to a codon.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr23:71401598 A>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:20971111 C>T maps to NM_032409.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:20964477 A>G maps to NM_032409.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:10623282 C>T maps to NM_017884.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:10690427 C>A maps to ENST00000354846 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr8:10683704 G>A maps to ENST00000354846 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:10677705 G>A maps to NM_017884.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:10623026 G>A maps to NM_017884.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:76942813 C>T maps to NM_017439.3 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:76940743 A>G maps to NM_017439.3 H832H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:76941474 A>G maps to NM_017439.3 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:77035408 G>A maps to NM_017439.3 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr17:36934601 C>T maps to NM_003559.4 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:36940537 T>C maps to NM_003559.4 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:57993208 C>T maps to NM_024779.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:151206962 T>C maps to NM_001135638.1 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:3648675 G>A maps to NM_012398.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:3653506 G>A maps to NM_012398.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:3638998 C>T maps to NM_012398.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:3644088 G>A maps to NM_012398.2 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:3653476 G>A maps to NM_012398.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:3633440 G>A maps to NM_012398.2 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:3651849 G>A maps to NM_012398.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:3656549 G>A maps to NM_012398.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:130687432 G>A maps to NM_001135219.1 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:130687441 T>C maps to NM_001135219.1 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:27371935 G>A maps to NM_016518.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:27380462 T>C maps to NM_016518.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:27380009 G>A maps to NM_016518.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr17:27382856 C>T maps to NM_016518.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:15474166 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:10728776 G>A maps to NM_001101387.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:32021759 G>A maps to NM_014338.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:28293786 A>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:65628317 C>T maps to NM_012417.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:67270087 G>A maps to NM_004910.2 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:67259512 G>A maps to NM_004910.2 S1242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:67264891 G>A maps to NM_004910.2 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:67267197 C>T maps to NM_004910.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:67259710 C>T maps to NM_004910.2 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:67261406 C>T maps to NM_004910.2 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:67266122 C>T maps to NM_004910.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:67266278 G>A maps to NM_004910.2 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:123481981 G>A maps to NM_020845.2 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:123471270 G>A maps to NM_020845.2 G1173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:123485613 C>T maps to NM_020845.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:123480009 T>C maps to NM_020845.2 Q660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:123472179 C>T maps to NM_020845.2 P1047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:123471069 G>A maps to NM_020845.2 D1213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:123498550 G>A maps to NM_020845.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:6387607 T>C maps to NM_031220.3 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:6381911 G>T maps to NM_031220.3 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr17:6376028 G>A maps to NM_031220.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr17:6374625 C>A maps to NM_031220.3 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:6380416 C>T maps to NM_031220.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:6377758 C>T maps to NM_031220.3 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:6381890 A>C maps to NM_031220.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:6374547 G>A maps to NM_031220.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:6377764 C>T maps to NM_031220.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr10:3197781 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:3180475 C>A maps to ENST00000380989 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:3207489 G>A maps to ENST00000380989 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:3182940 G>A maps to ENST00000380989 G904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:134364714 G>T maps to NM_002653.4 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:111539778 G>A maps to NM_153426.1 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:111553610 A>G maps to NM_153426.1 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:111553568 C>T maps to NM_153426.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:111554121 C>T maps to NM_153426.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:103990801 G>T maps to NM_005029.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr10:103990822 C>T maps to NM_005029.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:130842067 A>G maps to NM_004764.4 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:130855768 T>G maps to NM_004764.4 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr12:130841470 C>A maps to NM_004764.4 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr12:130856118 G>T maps to NM_004764.4 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:22210725 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:22172630 T>C maps to NM_001135721.1 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:22173816 C>T maps to NM_001135721.1 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr22:25151788 C>T maps to NM_001008496.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:25145381 A>G maps to NM_001008496.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:94328535 T>C maps to NM_152431.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr11:94337219 C>T maps to NM_152431.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:94353243 C>T maps to NM_152431.2 N792N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:94326703 G>A maps to NM_152431.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:68382184 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:68381383 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:68381998 G>T did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:68382959 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:68382234 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:68381907 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:68382734 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:68382055 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:108698723 C>A did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr5:108679917 T>C maps to NM_014819.4 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr16:2158762 C>T maps to NM_001009944.2 A2135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:2161267 T>C maps to NM_001009944.2 E1300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:2140033 G>A maps to NM_001009944.2 G4202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr16:2160622 G>A maps to NM_001009944.2 H1515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:2144015 T>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:2139988 G>A maps to NM_001009944.2 A4217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:2140588 G>A maps to NM_001009944.2 L4047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:2155907 G>A maps to NM_001009944.2 H2607H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:2164380 G>A maps to NM_001009944.2 F881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr16:2158939 C>T maps to NM_001009944.2 S2076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr16:2164359 C>T maps to NM_001009944.2 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:2147443 C>T maps to NM_001009944.2 P3427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:2152891 G>T maps to NM_001009944.2 C2957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr16:2159272 G>A maps to NM_001009944.2 I1965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:47842891 G>A maps to NM_138295.3 C2626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:47894796 G>A maps to NM_138295.3 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:47906160 G>A maps to NM_138295.3 Y1316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:47894628 C>T maps to NM_138295.3 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:47944042 G>T maps to NM_138295.3 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:47842891 G>A maps to NM_138295.3 C2626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:47898275 A>G maps to NM_138295.3 L1453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:47921654 T>C maps to NM_138295.3 G1098G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:47942043 G>A maps to NM_138295.3 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:47968828 C>T maps to NM_138295.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr7:47937791 C>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr7:47917176 C>T maps to NM_138295.3 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr7:47920383 C>T maps to NM_138295.3 V1154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:47925506 G>A maps to NM_138295.3 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:81253807 G>A maps to NM_052892.3 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:88986919 C>T maps to NM_000297.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:88989189 C>T maps to NM_000297.2 G833G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:88996023 C>T maps to NM_000297.2 D861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:102048786 C>A maps to NM_016112.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:102089764 G>A maps to NM_016112.2 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr10:102089752 T>C maps to NM_016112.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:137244596 A>G maps to ENST00000230643 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:42280471 C>T maps to NM_138370.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:42282159 G>T maps to NM_138370.2 G372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:42281306 C>T maps to NM_138370.2 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:42280398 G>A maps to NM_138370.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:46655301 C>T maps to NM_006071.1 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:46657155 C>A maps to NM_006071.1 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:46657386 T>C maps to NM_006071.1 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:46655211 A>G maps to NM_006071.1 D1336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr22:46656445 G>T maps to NM_006071.1 S925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr6:51484250 G>T maps to NM_138694.3 S3951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:51771121 G>A maps to NM_138694.3 G2233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:51882290 A>G maps to NM_138694.3 I1839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:51619588 C>T maps to NM_138694.3 R2930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr6:51512895 C>A maps to NM_138694.3 L3777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr6:51907858 T>A maps to NM_138694.3 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr6:51609228 T>C maps to NM_138694.3 V3370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr6:51907738 G>A maps to NM_138694.3 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr6:51524276 T>C maps to NM_138694.3 G3549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:51612918 C>T maps to NM_138694.3 V3165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:51524752 C>A maps to NM_138694.3 E3391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:51613338 G>A maps to NM_138694.3 G3025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:51524705 T>C maps to NM_138694.3 K3406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr6:51907735 G>A maps to NM_138694.3 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr6:51637555 A>C maps to NM_138694.3 A2862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:51524126 G>A maps to NM_138694.3 H3599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:51491807 A>G maps to NM_138694.3 T3924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:51613044 C>T maps to NM_138694.3 A3123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr6:51882287 G>A maps to NM_138694.3 C1840C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:51720693 C>T maps to NM_138694.3 L2636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:51889609 G>A maps to NM_138694.3 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:51893030 C>T maps to NM_138694.3 E1161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr8:110424510 G>A maps to ENST00000426474 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:110417312 A>C maps to ENST00000426474 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:110474073 C>T maps to ENST00000426474 C2440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr8:110478990 C>T maps to ENST00000426474 D2866D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:110439309 A>G maps to ENST00000426474 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:110477119 A>C maps to ENST00000426474 R2687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:110408346 C>T maps to ENST00000426474 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:110474094 A>G maps to ENST00000426474 V2447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:110441682 C>T maps to ENST00000426474 Q1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:110478936 G>A maps to ENST00000426474 A2848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr8:110487422 T>C maps to ENST00000426474 N2894N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr8:110477166 G>A maps to ENST00000426474 A2702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:79514052 C>T maps to NM_181839.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:123039071 T>C maps to ENST00000368446 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:43243337 C>T maps to NM_181805.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:155263246 C>T maps to ENST00000423816 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:155265009 C>T maps to ENST00000423816 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr1:155264448 C>G maps to ENST00000423816 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:155264040 A>G maps to ENST00000423816 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr1:155263038 G>A maps to ENST00000423816 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:155265485 C>T maps to ENST00000423816 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:155265284 G>A maps to ENST00000423816 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:155264505 G>A maps to ENST00000423816 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:155264508 G>A maps to ENST00000423816 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:72502687 G>A maps to ENST00000419739 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:72511432 C>T maps to ENST00000419739 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr15:72494883 G>A maps to NM_002654.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:72501131 C>T maps to ENST00000419739 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:72494844 G>T maps to NM_002654.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr15:72499083 C>T maps to ENST00000419739 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:72511393 G>A maps to ENST00000419739 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr15:72499497 T>C maps to ENST00000419739 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:3024374 C>T maps to NM_004203.4 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:3025407 C>A maps to NM_004203.4 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:3024407 G>A maps to NM_004203.4 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:14574679 C>T maps to NM_213560.1 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:14554387 G>A maps to NM_213560.1 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:14574679 C>T maps to NM_213560.1 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:14581439 C>T maps to NM_213560.1 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:14552041 C>T maps to NM_213560.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:14574685 G>A maps to NM_213560.1 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:14561787 C>T maps to NM_213560.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:14581059 G>A maps to NM_213560.1 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:89206690 G>A maps to NM_006256.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:89226052 T>C maps to NM_006256.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr1:89273384 A>T maps to NM_006256.2 K677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:89298758 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:89298836 C>T maps to NM_006256.2 F916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:89236100 C>T maps to NM_006256.2 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:89206690 G>A maps to NM_006256.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:131475830 C>T maps to NM_013355.3 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr9:131481963 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:125281698 C>T maps to NM_022062.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:125301168 G>T maps to NM_022062.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:125298985 T>C did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr11:125280210 A>G maps to NM_022062.2 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:201252934 G>A maps to NM_000299.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:201282595 G>A maps to NM_000299.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:201291194 C>T maps to NM_000299.3 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:201282302 G>T maps to NM_000299.3 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:32996206 G>A maps to NM_004572.3 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:33030838 G>A maps to NM_004572.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr12:32949047 G>A maps to NM_004572.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr12:32996161 G>A maps to NM_004572.3 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:32945631 G>A maps to NM_004572.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:33030913 C>T maps to NM_004572.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:32945631 G>A maps to NM_004572.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:32974415 G>A maps to NM_004572.3 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:32977077 G>A maps to NM_004572.3 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:396662 G>A maps to NM_007183.2 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:159526421 C>T maps to NM_003628.3 G973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:159523058 C>T maps to NM_003628.3 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:119325723 G>A maps to NM_015900.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:74695440 G>A maps to NM_032562.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr10:74714362 C>T maps to NM_032562.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:74701026 G>A maps to NM_032562.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:68289849 G>A maps to NM_012320.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr16:68289888 T>G maps to NM_012320.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr16:68293499 C>T maps to NM_012320.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:68293533 C>T maps to NM_012320.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:63365629 C>T maps to NM_001128203.1 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:20304961 C>T maps to NM_001161728.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:20302241 G>A maps to NM_001161728.1 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:20499362 G>A maps to NM_001105572.1 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr1:20490552 G>A maps to NM_001105572.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:20471084 C>A maps to NM_022819.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:31534344 G>A maps to NM_015715.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr22:31533771 C>T maps to NM_015715.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:186919834 T>C maps to NM_024420.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:48558273 G>A maps to NM_003706.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr15:42374529 G>A maps to NM_178034.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:42371821 C>A maps to NM_178034.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr15:42379563 C>T maps to NM_178034.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:42377687 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr15:42373789 G>A maps to NM_178034.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:42442819 G>A maps to ENST00000397272 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:20412714 C>T maps to NM_000929.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:38565403 G>T maps to NM_003560.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:38536070 G>A maps to NM_003560.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:46679256 C>T maps to NM_001168357.1 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:160832608 C>T maps to NM_007366.4 E855E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:160885388 C>T maps to NM_007366.4 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:160876694 G>A maps to NM_007366.4 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:26935203 A>G maps to NM_001031689.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr9:26906074 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:133700437 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:59814516 T>C maps to NM_173801.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:84026147 C>T maps to NM_001130715.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:84028969 G>A maps to NM_001130715.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:145477794 C>T maps to NM_001029869.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:145465116 G>A maps to NM_001029869.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:57079634 G>A maps to NM_002655.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:57080657 T>C maps to NM_002655.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:144263067 C>T maps to NM_001080951.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:30784818 G>A maps to NM_002657.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr20:30789768 A>T maps to NM_002657.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:30784581 C>T maps to NM_002657.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:42033525 G>A maps to NM_000930.3 D558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:75673764 C>T maps to NM_002658.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr19:44169537 C>G maps to NM_002659.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:44153260 A>G maps to NM_002659.2 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:44171771 G>A maps to NM_002659.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:28821627 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:28843196 G>A maps to NM_153021.4 W1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:14664528 G>A maps to NM_024829.5 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:14664193 C>A maps to NM_024829.5 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:14688686 C>T maps to NM_024829.5 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:113822727 G>A maps to NM_173542.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr12:113821936 A>T maps to NM_173542.3 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:8639247 G>A maps to NM_015192.2 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:8862336 C>T maps to NM_015192.2 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:8755366 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:8608942 C>T maps to NM_015192.2 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:40594732 G>A maps to NM_004573.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr15:40590079 G>A maps to NM_004573.2 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr15:40595515 G>A maps to NM_004573.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:40590823 G>A maps to NM_004573.2 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr15:40594696 G>A maps to NM_004573.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr15:40594684 C>T maps to NM_004573.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:64026011 C>T maps to NM_000932.2 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:64029068 C>T maps to NM_000932.2 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:64031187 C>T maps to NM_000932.2 N827N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:9454008 G>A maps to NM_001172646.1 E1164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:9438111 G>A maps to NM_001172646.1 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:9417771 C>T maps to NM_001172646.1 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:9360780 T>A maps to NM_001172646.1 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:38061760 C>T maps to NM_001130964.1 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:38051522 G>A maps to NM_001130964.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr17:43192474 G>T maps to NM_133373.3 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:219487416 A>G maps to ENST00000432688 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:219480483 C>T maps to ENST00000432688 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:219500574 G>T maps to ENST00000432688 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:95790895 A>G maps to ENST00000371380 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:96005832 C>T maps to ENST00000371380 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:96014706 T>A maps to ENST00000371380 L1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr10:96066441 C>T maps to ENST00000371380 R1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:95791573 C>T maps to ENST00000371380 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:95891941 A>G maps to ENST00000371380 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:95791015 G>A maps to ENST00000371380 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr10:95931102 C>T maps to ENST00000371380 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:95791855 G>A maps to ENST00000371380 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr10:96025642 C>T maps to ENST00000371380 I1403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr10:95987094 G>A maps to ENST00000371380 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:96005894 C>T maps to ENST00000371380 D871D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:95931102 C>T maps to ENST00000371380 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:96005981 C>T maps to ENST00000371380 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr10:96044672 A>G maps to ENST00000371380 A1662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:96064308 A>C maps to ENST00000371380 P1843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr10:96012128 C>A maps to ENST00000371380 G1051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:39800837 T>C maps to NM_002660.2 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:39791352 C>T maps to NM_002660.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:39792805 G>A maps to NM_002660.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:39801286 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:39795206 G>T maps to NM_002660.2 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr16:81914543 C>T maps to NM_002661.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:81973506 C>T maps to NM_002661.2 G1108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:81957091 T>C maps to NM_002661.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr16:81944244 C>T maps to NM_002661.2 R618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:81934351 G>A maps to NM_002661.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:81944172 C>T maps to NM_002661.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:81922783 G>A maps to NM_002661.2 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:81946264 C>T maps to NM_002661.2 D666D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:155203196 C>T maps to ENST00000340059 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:155301425 G>A maps to ENST00000340059 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:155199764 G>A maps to ENST00000340059 S1358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr3:155206449 A>G maps to ENST00000340059 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:155210592 C>T maps to ENST00000340059 K732K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:155200067 C>T maps to ENST00000340059 E1257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:155203277 G>A maps to ENST00000340059 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr3:155271896 C>T maps to ENST00000340059 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:155282899 C>T maps to ENST00000340059 T279T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-5717-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:155200526 A>G maps to ENST00000340059 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:155311884 G>A maps to ENST00000340059 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:198950793 T>C maps to NM_006226.3 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:198950523 T>C maps to NM_006226.3 C761C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr2:198950583 T>C maps to NM_006226.3 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:198950583 T>G maps to NM_006226.3 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:198950763 T>G maps to NM_006226.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr2:198949578 A>C maps to NM_006226.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:198949134 G>A maps to NM_006226.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:198966085 T>A did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr2:198949308 C>T maps to NM_006226.3 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr2:198953755 C>T maps to NM_006226.3 Q964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr2:198950583 T>G maps to NM_006226.3 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:209705 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:209791 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:215872 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:205516 T>C did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:200929 G>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:209707 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:205451 C>T did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:208207 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:215823 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:41382223 T>C maps to NM_001005473.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:171406483 C>T maps to NM_002662.3 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr3:171455826 G>A maps to NM_002662.3 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:171406525 T>C maps to NM_002662.3 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr3:171410121 C>T maps to NM_002662.3 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:171427480 G>A maps to NM_002662.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr3:171330093 G>T maps to NM_002662.3 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr3:171427372 G>A maps to NM_002662.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:4722428 G>T maps to NM_002663.3 G742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:4718005 G>A maps to NM_002663.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr17:4720036 C>T maps to NM_002663.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:4721857 G>T maps to NM_002663.3 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:40877624 C>T maps to NM_012268.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40872395 G>A maps to NM_012268.2 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr14:105398405 C>T maps to NM_138790.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr1:242383295 C>T maps to NM_152666.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:242511408 G>A maps to NM_152666.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:242271008 C>T maps to NM_152666.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr1:242253407 A>G maps to NM_152666.2 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:17106257 G>A maps to NM_178836.3 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:17109596 C>A maps to NM_178836.3 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:144993245 G>A maps to NM_201380.2 G3718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:144998441 C>T maps to NM_201380.2 A2022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145000980 C>A maps to NM_201380.2 E1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr8:144997652 C>T maps to NM_201380.2 R2285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:144991544 C>A maps to NM_201380.2 T4285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:144995507 G>A maps to NM_201380.2 D2964D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:144993911 G>A maps to NM_201380.2 G3496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:145002108 C>T maps to NM_201380.2 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr8:145049471 C>G maps to NM_000445.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:144996041 C>T maps to NM_201380.2 L2786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:145011330 A>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:145004448 A>G maps to NM_201380.2 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:144993941 C>T maps to NM_201380.2 T3486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:144990788 G>A maps to NM_201380.2 P4537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:144992276 G>A maps to NM_201380.2 D4041D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr8:145009468 G>A maps to NM_201380.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:144998486 C>T maps to NM_201380.2 A2007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr8:145002132 G>A maps to NM_201380.2 R1233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:144993437 C>T maps to NM_201380.2 T3654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:144995198 C>T maps to NM_201380.2 S3067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:144992276 G>A maps to NM_201380.2 D4041D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:144994802 G>T maps to NM_201380.2 A3199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:144999421 G>A maps to NM_201380.2 R1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:144990830 G>C maps to NM_201380.2 R4523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:144990746 G>A maps to NM_201380.2 R4551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:144997253 C>T maps to NM_201380.2 A2418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:144993398 G>A maps to NM_201380.2 C3667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:144998017 G>A maps to NM_201380.2 R2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:145006332 G>A maps to NM_201380.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:144995246 G>A maps to NM_201380.2 F3051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:144995572 G>A maps to NM_201380.2 L2943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:144997127 C>T maps to NM_201380.2 T2460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:144990674 A>G maps to NM_201380.2 P4575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:144993785 G>A maps to NM_201380.2 P3538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:144992351 G>A maps to NM_201380.2 D4016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:144995198 C>T maps to NM_201380.2 S3067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:145003292 G>A maps to NM_201380.2 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:144990707 G>A maps to NM_201380.2 D4564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:144992714 G>A maps to NM_201380.2 H3895H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr8:145003955 G>A maps to NM_201380.2 H1064H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:68607593 T>C maps to NM_002664.2 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:67862132 C>T maps to NM_016445.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:67864540 G>A maps to NM_016445.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:124186519 G>A maps to NM_021622.4 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:124159890 G>A maps to NM_021622.4 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:124172488 T>C maps to NM_021622.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr10:124183743 T>A maps to NM_021622.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:38809829 G>T maps to NM_021623.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:38810882 T>G maps to NM_021623.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:38793534 T>C maps to NM_021623.1 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:179350389 T>G maps to NM_019091.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:179355474 A>C maps to NM_019091.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr19:49364711 G>T maps to NM_020904.2 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:19498774 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:19475255 C>T maps to ENST00000429027 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:19427791 T>C maps to ENST00000429027 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:19436369 A>G maps to ENST00000429027 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:204226500 G>A maps to ENST00000367191 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr1:204197878 G>A maps to ENST00000367191 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:204197346 G>A maps to ENST00000367191 N985N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr1:204198208 A>G maps to ENST00000367191 H889H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:204197241 G>A maps to ENST00000367191 T1020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:204228663 C>T maps to ENST00000367191 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:16816141 G>A maps to ENST00000448080 R880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:16837792 G>A maps to ENST00000448080 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:16892680 A>G maps to ENST00000448080 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:16812598 G>A maps to ENST00000448080 R966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:30094481 G>A did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr12:45567962 G>A maps to ENST00000256692 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:45567968 G>T maps to ENST00000256692 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:73364058 G>A maps to NM_021200.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:73372523 G>A maps to NM_021200.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:131890527 T>C maps to ENST00000409158 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:131890539 G>A maps to ENST00000409158 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:30164922 C>T maps to ENST00000436066 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:30165558 G>C maps to ENST00000436066 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr19:30165081 G>A maps to ENST00000436066 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:30164799 G>T maps to ENST00000436066 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:30165132 C>T maps to ENST00000436066 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr19:30164943 C>T maps to ENST00000436066 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:96166568 A>G maps to NM_024613.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:151130347 G>A maps to NM_001029884.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:151152439 G>A maps to NM_001029884.1 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:151161753 C>T maps to NM_001029884.1 L1294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:151055032 C>T maps to NM_001029884.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr6:151130380 G>A maps to NM_001029884.1 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:151153342 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:151161743 G>A maps to NM_001029884.1 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:151151938 G>A maps to NM_001029884.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:151152244 T>C maps to NM_001029884.1 Y666Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:151153325 G>T maps to NM_001029884.1 G1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:39912907 C>T maps to NM_022835.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:65208052 G>A maps to ENST00000394691 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:65209940 C>T maps to ENST00000394691 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr14:65210267 A>G maps to ENST00000394691 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:65197814 T>C maps to ENST00000394691 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr14:65194600 A>T maps to ENST00000394691 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:65194558 C>T maps to ENST00000394691 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr14:65207761 G>A maps to ENST00000394691 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr14:65207905 A>G maps to ENST00000394691 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:67318713 G>A maps to NM_001129729.1 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:67316180 A>G maps to NM_001129729.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:162052 C>T maps to NM_052909.3 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:156322 C>T maps to NM_052909.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:171405 C>T maps to NM_052909.3 Y943Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:182313 G>A maps to NM_052909.3 W1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr5:140748 G>A maps to NM_052909.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr5:161980 G>A maps to NM_052909.3 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:169523 C>T maps to NM_052909.3 Y826Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr5:169622 C>T maps to NM_052909.3 H859H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:6533155 G>A maps to NM_198681.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:6534149 G>A maps to NM_198681.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:6556576 G>A maps to NM_198681.2 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:6422806 C>T maps to NM_001144856.1 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:6435694 C>A maps to NM_001144856.1 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:6421412 A>C maps to NM_001144856.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:6425052 C>T maps to NM_001144856.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:6427574 C>T maps to NM_001144856.1 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:6424298 C>T maps to NM_001144856.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr12:6436698 G>A maps to NM_001144856.1 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr12:93150130 A>T maps to NM_001004330.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:68028744 G>A maps to NM_020715.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:68047725 A>G maps to NM_020715.2 T1085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:43958647 C>T maps to NM_172069.3 H950H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:43958704 C>T maps to NM_172069.3 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:43973085 C>T maps to NM_172069.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:43991503 G>A maps to NM_172069.3 K1432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr2:43927176 G>A maps to NM_172069.3 W360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:40828491 G>A maps to NM_024927.4 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:40822024 G>A maps to NM_024927.4 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:43531399 G>A maps to NM_014798.2 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:43552854 G>A maps to NM_014798.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr17:43531124 C>T maps to NM_014798.2 W698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr1:16059104 A>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:208841407 G>A maps to NM_001080475.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:150123099 A>G did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:150131588 C>T maps to ENST00000443480 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:150131687 G>A maps to ENST00000443480 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr15:65153689 G>A maps to NM_025201.4 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:65157156 G>A maps to NM_025201.4 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:161152220 G>A maps to NM_000301.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:161152265 T>C did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr6:161143542 T>C maps to NM_000301.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr6:161158021 A>G maps to NM_000301.3 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:161139413 C>T maps to NM_000301.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:19116263 A>G maps to NM_001122.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:4859940 C>T maps to NM_005817.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:4859922 G>A maps to NM_005817.4 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:4504479 G>A maps to NM_001080400.1 G1355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr19:4511991 C>T maps to NM_001080400.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:4512042 G>A maps to NM_001080400.1 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:4511670 G>A maps to NM_001080400.1 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:4511361 G>A maps to NM_001080400.1 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr19:4504698 G>A maps to NM_001080400.1 A1282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:4523794 C>T maps to NM_001013706.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:23695279 C>T maps to NM_005030.3 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:23690462 C>T maps to NM_005030.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr16:23691500 C>T maps to NM_005030.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:23692259 C>T maps to NM_005030.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:23698842 C>T maps to NM_005030.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:23700568 C>T maps to NM_005030.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr16:23700571 T>A maps to NM_005030.3 C428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr20:21227215 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:57751520 A>G maps to NM_006622.2 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:45270161 G>T maps to NM_004073.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:128819591 A>G did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr4:128807157 C>T maps to NM_014264.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:128817955 T>C maps to NM_014264.4 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:12012686 C>T maps to ENST00000376369 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr7:100859522 C>T maps to NM_001084.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:100859468 C>T maps to NM_001084.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr7:100859254 C>T maps to NM_001084.4 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:100853725 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:100855869 G>A maps to NM_001084.4 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:103031928 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:103041610 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:103041610 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:103041548 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:103045490 G>A did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr23:49029562 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:155467034 G>T maps to NM_002669.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:114877714 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:114869330 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:114881875 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:146254324 A>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:146251311 C>T maps to NM_021105.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr3:146173070 T>C maps to ENST00000497985 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:7296193 G>A maps to NM_020360.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr3:146307508 G>A maps to NM_001085420.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:44533613 C>T maps to NM_006227.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:31825663 A>G maps to NM_130852.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:31829265 T>G maps to NM_130852.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:17476376 G>A maps to NM_031310.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:17476310 C>T maps to NM_031310.1 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:17487776 G>A maps to NM_031310.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:17476388 T>C maps to NM_031310.1 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17476718 G>A maps to NM_031310.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:37243860 C>T maps to NM_020405.4 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:37226123 C>T maps to NM_020405.4 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:37234199 G>T maps to NM_020405.4 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr10:20466335 A>G maps to NM_032812.7 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:20453413 A>G maps to NM_032812.7 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:20290848 T>C maps to NM_032812.7 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr10:20465938 A>C maps to NM_032812.7 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:20432314 C>T maps to NM_032812.7 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:20465997 G>A maps to NM_032812.7 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr10:20500612 T>C maps to NM_032812.7 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:20290821 G>A maps to NM_032812.7 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:20290770 G>A maps to NM_032812.7 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:126708524 G>A maps to NM_032242.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:126733355 G>A maps to NM_032242.3 T880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:126710240 T>C maps to NM_032242.3 D403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:126724973 G>A maps to NM_032242.3 K650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:126748299 G>A maps to NM_032242.3 S1597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:126736386 C>T maps to NM_032242.3 N1132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr3:126736734 G>A maps to NM_032242.3 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:126710303 G>A maps to NM_032242.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:126732870 C>T maps to NM_032242.3 Y774Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:126723973 C>T maps to NM_032242.3 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr3:126751403 C>T maps to NM_032242.3 Y1802Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:126707618 C>T maps to NM_032242.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:126707945 G>A maps to NM_032242.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:126724051 C>T maps to NM_032242.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:126724066 G>A maps to NM_032242.3 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:126736665 T>C maps to NM_032242.3 C1197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:126730889 G>A maps to NM_032242.3 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr3:126749099 G>A maps to NM_032242.3 K1692K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:126733583 C>A maps to NM_032242.3 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:126730835 C>T maps to NM_032242.3 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr3:126708020 C>T maps to NM_032242.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:126749159 G>A maps to NM_032242.3 P1712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:126735455 C>T maps to NM_032242.3 N1037N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr3:126723997 C>T maps to NM_032242.3 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:126707726 G>A maps to NM_032242.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:208269411 G>A maps to NM_025179.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:208216455 G>A maps to NM_025179.3 R1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:208202362 G>A maps to NM_025179.3 N1750N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:208390883 G>T maps to NM_025179.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr1:208201479 G>C maps to NM_025179.3 L1821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr1:208390682 G>A maps to NM_025179.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:208390709 C>A maps to NM_025179.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:208217991 G>A maps to NM_025179.3 G1245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:208225673 G>A maps to NM_025179.3 Y997Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr1:208266214 G>T maps to NM_025179.3 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:153689069 T>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:153697253 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153689601 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153698128 T>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:153689696 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153696425 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153699467 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:153696163 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:153699944 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:153694979 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153690581 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153693556 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153689623 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:153688858 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:153693145 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:153698446 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153688929 A>G did not map to a codon.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr23:153691737 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:153694126 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:153693429 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:153691781 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr23:153698477 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:153689683 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:153691739 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:153688787 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:153694758 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:153692761 C>T did not map to a codon.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr23:153690648 A>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:131866286 G>A maps to NM_020911.1 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:131864545 A>G maps to NM_020911.1 I1258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:131895800 C>T maps to NM_020911.1 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:131895836 C>T maps to NM_020911.1 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:131883350 A>C maps to NM_020911.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:132192891 C>T maps to NM_020911.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:131910963 G>A maps to NM_020911.1 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:132193356 C>T maps to NM_020911.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:131825491 G>A maps to NM_020911.1 D1768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:131908288 G>A maps to NM_020911.1 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr7:132192666 C>T maps to NM_020911.1 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:131817884 G>T maps to NM_020911.1 R1838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:131859623 G>A maps to NM_020911.1 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr7:131908333 A>G maps to NM_020911.1 H683H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:48461165 C>T maps to NM_001130082.1 T843T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:48451703 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:48461321 C>T maps to NM_001130082.1 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:48462705 G>A maps to NM_001130082.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:48464341 A>C maps to NM_001130082.1 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:48451442 G>T maps to NM_001130082.1 P1883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:48464990 C>A maps to NM_001130082.1 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:50716154 C>T maps to NM_012401.2 R1687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr22:50726197 C>T maps to NM_012401.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:50716355 G>A maps to NM_012401.2 F1658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:50719832 G>A maps to NM_012401.2 I1206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr22:50717048 G>A maps to NM_012401.2 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:50718431 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:50728800 C>T maps to NM_012401.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr22:50715102 C>T maps to NM_012401.2 Q1764Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:50718979 C>T maps to NM_012401.2 T1371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr22:50722305 G>A maps to NM_012401.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:50728806 C>T maps to NM_012401.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:153043006 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:153040419 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153042772 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:153036431 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153037094 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:153038719 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153039724 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:153033729 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:153040510 C>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:153043731 A>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:153042360 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr23:153036950 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr23:153037378 C>T did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:153036317 C>T did not map to a codon.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr23:153044075 T>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153043052 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr23:153040182 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:153040501 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:153039390 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153034425 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153036253 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:94631564 C>A maps to NM_005761.1 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:94580154 A>T maps to NM_005761.1 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:94648662 C>T maps to NM_005761.1 D994D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:94563011 C>T maps to NM_005761.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr12:94603462 C>T maps to NM_005761.1 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr12:94673282 C>T maps to NM_005761.1 N1211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr12:94562996 A>T maps to NM_005761.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:94654558 C>T maps to NM_005761.1 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:94543550 G>A maps to NM_005761.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:94620455 C>T maps to NM_005761.1 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:94676090 C>T maps to NM_005761.1 R1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr12:94543037 G>A maps to NM_005761.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:129292567 C>T maps to NM_015103.2 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:129324660 C>T maps to NM_015103.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:129289881 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:129324786 G>A maps to NM_015103.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:205814521 T>C maps to NM_152491.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:205814497 G>A maps to NM_152491.4 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:205797810 G>T maps to NM_152491.4 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:89871855 G>A maps to NM_001010853.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:89862776 C>A maps to NM_001010853.1 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:56234598 T>C maps to NM_020182.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:56227273 G>A maps to NM_020182.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:156206135 G>A maps to NM_007221.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:72173265 T>C maps to NM_031293.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:72153906 G>A maps to NM_031293.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr16:72198812 C>A maps to NM_031293.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr15:74327682 C>T maps to NM_033239.2 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:74315213 G>A maps to NM_033238.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:74337043 C>T maps to NM_033238.2 Q782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:74327977 C>T maps to NM_033239.2 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr15:74290634 C>T maps to NM_033238.2 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr15:74290463 G>A maps to NM_033238.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:41980049 G>A maps to NM_002676.2 I129I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr22:41980019 C>T maps to NM_002676.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr16:8941585 C>T maps to NM_000303.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:15134392 C>T maps to NM_000304.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr17:15142791 A>C maps to NM_000304.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr9:139309091 G>A maps to NM_015160.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr9:139305140 G>C maps to NM_015160.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:139317613 C>T maps to NM_015160.1 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:102948085 C>T maps to NM_004279.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:102940680 T>G maps to NM_004279.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:190719032 T>C maps to NM_000534.4 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:190732551 C>T maps to NM_000534.4 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr2:190738366 G>C maps to NM_000534.4 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:6029581 G>A maps to NM_000535.5 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:6026898 A>C maps to NM_000535.5 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:6037036 A>C maps to NM_000535.5 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:6017320 C>T maps to NM_000535.5 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:154897633 G>A maps to NM_006556.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:154898953 C>T maps to NM_006556.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:154897700 G>A maps to NM_006556.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:152938066 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:152937032 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:152938108 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr19:50367301 G>A maps to NM_007254.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:50365980 C>T maps to NM_007254.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:50365309 G>A maps to NM_007254.3 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:160240342 C>A maps to NM_173516.1 Y486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:160227083 A>G maps to NM_173516.1 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:160239670 G>A maps to NM_173516.1 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:118306821 C>T maps to NM_000936.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr10:118320981 A>G did not map to a codon.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr10:118315527 G>A maps to NM_000936.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:118320018 G>A maps to NM_000936.2 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:118307976 C>T maps to NM_000936.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr10:118315515 T>C maps to NM_000936.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:118354249 C>T maps to NM_006229.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:118380486 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:118383523 C>T maps to NM_005396.4 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:118404542 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:118215274 C>T maps to NM_001011709.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:118228694 A>G did not map to a codon.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr14:74179979 A>G maps to NM_006029.4 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:74180117 G>A maps to NM_006029.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:26365704 C>T maps to NM_007257.5 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:152226189 G>A did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr23:152226072 C>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:152226567 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:152226634 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:152226464 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:152226686 A>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:152159454 C>T did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:152159297 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:152158875 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:152158826 G>A did not map to a codon.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr23:152159383 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:152159298 G>A did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:152159885 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:46973944 G>A maps to NM_018215.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr19:46973368 C>T maps to NM_018215.3 A308A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4280-01A-01D-1126-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:46998568 G>A maps to NM_020709.1 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr19:46997108 C>T maps to NM_020709.1 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr19:46998641 C>T maps to NM_020709.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr19:46997201 C>T maps to NM_020709.1 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:46997774 C>T maps to NM_020709.1 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:46997816 C>T maps to NM_020709.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:39650998 C>T maps to NM_002687.3 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:39650887 G>T maps to NM_002687.3 G659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:39648326 T>C maps to NM_002687.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:39649827 G>A maps to NM_002687.3 A305A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-5733-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr14:20942679 C>A maps to NM_000270.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:36274153 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:36274132 C>T maps to ENST00000457797 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:824013 C>T maps to NM_020376.3 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr11:822473 G>A maps to NM_020376.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:44330511 A>G maps to NM_025225.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:7870100 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:7889821 T>C did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:7880118 T>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:44287021 G>A maps to ENST00000216177 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr22:44287127 C>T maps to ENST00000216177 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr22:44287075 G>A maps to ENST00000216177 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:7619867 C>T maps to NM_001166111.1 T918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr19:7623880 A>G maps to NM_001166111.1 V1191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:7619849 C>T maps to NM_001166111.1 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:7614887 C>T maps to NM_001166111.1 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:7614945 C>T maps to NM_001166111.1 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:140400149 G>A maps to NM_001098537.1 H463H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:140416105 G>T maps to NM_001098537.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr9:140437936 G>A maps to NM_001098537.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:140437936 G>A maps to NM_001098537.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr9:140435143 G>A maps to NM_001098537.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:140358899 C>T maps to NM_001098537.1 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:140437252 C>T maps to NM_001098537.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr9:140357909 G>A maps to NM_001098537.1 D1100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:140392657 C>T maps to NM_001098537.1 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:108143061 G>A maps to NM_015723.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr2:55872549 A>G maps to NM_033109.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:55870543 C>T maps to NM_033109.3 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:55920811 C>G maps to NM_033109.3 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr2:55907853 T>C maps to NM_033109.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:55908053 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:89790696 C>A maps to NM_006813.2 Y28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:89793716 G>A maps to NM_006813.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr3:52179895 G>A maps to NM_015426.4 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:89864188 C>T maps to NM_172240.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr1:53544288 C>T maps to NM_153703.4 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:53544372 C>T maps to NM_153703.4 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:14047183 G>A maps to NM_024825.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:127379770 C>T maps to NM_015720.2 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:127379824 C>T maps to NM_015720.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:127379707 C>T maps to NM_015720.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:127358265 C>T maps to NM_015720.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr3:127381087 C>A maps to NM_015720.2 C380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr23:84586034 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:84562198 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:30803241 G>A maps to NM_015352.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:46687542 G>A maps to NM_133635.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr21:46705827 G>A maps to NM_133635.4 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:46687473 G>A maps to NM_015227.4 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr21:46705686 G>A maps to NM_133635.4 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:166819123 C>T maps to NM_017542.3 H436H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:166815886 C>T maps to NM_017542.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr1:151396573 G>A maps to NM_015100.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:151378717 C>T maps to NM_015100.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:151378309 G>T maps to NM_015100.3 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr1:151380595 A>C maps to NM_015100.3 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:151378411 C>T maps to NM_015100.3 E1033E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:151378393 G>A maps to NM_015100.3 R1039R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:24742542 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:24732688 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:24759544 T>C did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:24757523 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:24751893 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:24751915 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:24750564 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:24833130 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:24745947 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:24760163 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:24734569 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:50905146 C>T maps to ENST00000391817 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:50905603 C>T maps to ENST00000391817 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr19:50912856 C>T maps to ENST00000391817 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:50905561 C>T maps to ENST00000391817 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:50916997 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:50906823 G>A maps to ENST00000391817 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr7:44157561 G>A maps to NM_006230.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr7:44155368 A>C maps to NM_006230.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:44161616 A>G maps to NM_006230.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:74315764 C>T maps to NM_006591.1 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:26680010 G>T maps to NM_015584.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:26676189 T>G did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:42998020 A>G maps to ENST00000415122 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:43010845 C>T maps to ENST00000415122 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:133244942 C>A maps to ENST00000455752 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:133256787 C>T maps to ENST00000455752 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr12:133233757 C>T maps to ENST00000455752 K1185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:133254217 G>A maps to ENST00000455752 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr12:133237569 G>A maps to ENST00000455752 D1018D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:133219827 G>A maps to ENST00000455752 S1514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:133201396 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:133210850 T>C maps to ENST00000455752 L1978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:133257270 G>A maps to ENST00000455752 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:133256633 T>C did not map to a codon.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr12:133209265 C>G maps to ENST00000455752 A2043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:133220110 G>A maps to ENST00000455752 G1445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:133256108 G>A maps to ENST00000455752 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr12:133248883 G>A maps to ENST00000455752 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:50131377 A>G maps to NM_002692.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:116171947 T>C maps to NM_017443.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:75187274 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:89870443 A>G maps to NM_002693.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:89864449 G>A maps to NM_002693.2 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr15:89862218 G>C maps to NM_002693.2 T1072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:89876835 C>T maps to NM_002693.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:89860718 G>A maps to NM_002693.2 V1177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr15:89872247 G>A maps to NM_002693.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr15:89868907 C>A maps to NM_002693.2 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:89867080 A>G maps to NM_002693.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:62486954 G>A maps to NM_007215.3 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr6:43571748 G>C did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr6:43582080 G>A maps to NM_006502.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr18:51820305 C>A maps to NM_007195.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:51820608 G>A maps to NM_007195.2 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:51820531 G>T maps to NM_007195.2 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr18:51820215 G>A maps to NM_007195.2 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:74892827 A>G maps to NM_016218.2 E770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:74877074 C>T maps to NM_016218.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:74892278 C>T maps to NM_016218.2 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr10:103340083 G>A maps to NM_013274.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:103344631 A>G maps to NM_013274.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:103340083 G>A maps to NM_013274.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:103339388 G>A maps to NM_013274.3 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:44112895 G>A maps to NM_013284.2 N493N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:44113277 G>A maps to NM_013284.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:2210190 C>T maps to NM_181808.2 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:121248489 A>G maps to ENST00000393672 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:121228491 T>C maps to ENST00000393672 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:121248524 G>A maps to ENST00000393672 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:121230874 G>A maps to ENST00000393672 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:121158853 A>C maps to ENST00000393672 P2594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:121229066 A>G maps to ENST00000393672 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:121207934 C>T maps to ENST00000393672 Q1417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr3:121151767 A>G maps to ENST00000393672 V2689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:121200436 G>A maps to ENST00000393672 Q2201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:121258409 T>C maps to ENST00000393672 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:121260234 G>T maps to ENST00000393672 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr3:121258316 G>A maps to ENST00000393672 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:121207127 A>G maps to ENST00000393672 C1686C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:121263571 A>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:121179016 A>G maps to ENST00000393672 H2480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:121212533 C>T maps to ENST00000393672 W907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr2:86308049 C>T maps to NM_015425.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr2:86276113 G>A maps to NM_015425.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr2:86315779 G>A maps to NM_015425.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:86272455 G>A maps to NM_015425.3 R972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:86305044 G>A maps to NM_015425.3 Y439Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:86267633 C>T maps to NM_015425.3 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:86281306 G>A maps to NM_015425.3 R722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:113331266 C>T maps to NM_019014.4 D800D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:113332741 A>G maps to NM_019014.4 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:113315656 A>G maps to NM_019014.4 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr2:113322006 C>T maps to NM_019014.4 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:113304623 G>A maps to NM_019014.4 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:43488474 C>A maps to NM_203290.1 C256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:28240012 C>T maps to NM_152705.1 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:37489338 C>A maps to NM_022490.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:7405936 C>T maps to NM_000937.4 Y891Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:7406983 G>A maps to NM_000937.4 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:7399665 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:7417069 G>A maps to NM_000937.4 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:7416808 A>G maps to NM_000937.4 S1742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:7400198 A>G maps to NM_000937.4 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:7402383 C>T maps to NM_000937.4 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:7416577 G>A maps to NM_000937.4 S1665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:57889685 C>T maps to NM_000938.1 G902G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:57865856 T>C maps to NM_000938.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:57503153 G>A maps to NM_032940.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr16:57503204 G>A maps to NM_032940.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr16:57504919 G>A maps to NM_032940.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:1094044 C>T maps to NM_002695.3 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:1090942 C>T maps to NM_002695.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr22:38363643 C>T maps to NM_021974.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr22:38352791 C>T maps to ENST00000407936 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr22:38355391 C>T maps to ENST00000407936 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:36604658 A>G maps to NM_006233.4 *126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:102114855 G>A maps to ENST00000393794 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:102116677 A>G maps to ENST00000393794 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:79750814 C>T maps to NM_007055.3 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:79789144 C>T maps to NM_007055.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr10:79784759 T>C maps to NM_007055.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:79759816 C>T maps to NM_007055.3 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr10:79737271 G>A maps to NM_007055.3 F1379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:106821126 T>C maps to NM_018082.5 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr12:106895166 A>T maps to NM_018082.5 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:106770228 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:106857279 T>C maps to NM_018082.5 Y865Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:106853056 T>G maps to NM_018082.5 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:106827563 A>G maps to NM_018082.5 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr1:145606348 T>G maps to NM_006468.6 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:145608659 C>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:145606364 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:145608467 G>A maps to NM_006468.6 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:22105427 C>T maps to NM_001722.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:22105998 C>T maps to NM_001722.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:22106823 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:22320325 C>T maps to NM_018119.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:22320298 A>G maps to NM_018119.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:22328528 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:145457968 T>C maps to NM_032305.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:620436 G>A maps to NM_005035.3 C897C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr19:621654 C>T maps to NM_005035.3 Q681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:621360 C>T maps to NM_005035.3 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:621150 C>T maps to NM_005035.3 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:72413408 G>A maps to ENST00000434423 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:72413633 G>A maps to ENST00000434423 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:72413423 G>A maps to ENST00000434423 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:72412826 C>T maps to ENST00000434423 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr7:72416236 T>G maps to ENST00000434423 V1214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:72412619 G>A maps to ENST00000434423 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:72413372 G>A maps to ENST00000434423 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:72400634 C>T maps to ENST00000434423 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr7:72413624 C>T maps to ENST00000434423 G1031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N0-01A-12D-A364-08 chr7:72412550 C>A maps to ENST00000434423 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:75053845 T>C maps to ENST00000257665 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:75052145 G>A maps to ENST00000257665 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:75068444 T>C maps to ENST00000257665 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:75051083 G>A maps to ENST00000257665 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr7:53103738 T>A maps to NM_182595.3 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr7:53104089 C>A maps to NM_182595.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:53103708 C>A maps to NM_182595.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:53103492 G>A maps to NM_182595.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr7:53103906 G>A maps to NM_182595.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:53104179 G>A maps to NM_182595.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:53103951 G>A maps to NM_182595.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr2:25387530 G>A maps to NM_001035256.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:25384366 C>T maps to NM_001035256.1 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:46658843 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr1:46657846 G>A maps to ENST00000371986 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr1:46660273 C>T maps to ENST00000371986 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:134379613 A>T maps to NM_007171.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:134384332 T>C maps to NM_007171.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr9:134397513 G>T maps to NM_007171.3 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr14:77751347 G>A maps to NM_013382.5 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:77751305 A>G maps to NM_013382.5 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:76254924 T>C maps to NM_012230.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:76254974 G>A maps to NM_012230.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:94944661 A>C maps to NM_000446.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr7:94928392 G>A maps to NM_000446.5 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:94991694 A>G maps to NM_000940.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:95025596 C>G maps to NM_000940.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr7:94989404 C>T maps to NM_000940.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:94991718 A>G maps to NM_000940.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr8:99148886 A>T maps to NM_015029.2 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:99158812 C>T maps to NM_015029.2 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:99149118 G>A maps to NM_015029.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:99170030 C>T maps to NM_015029.2 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:99168418 T>C maps to NM_015029.2 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:99139935 G>T maps to NM_015029.2 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr19:30101335 C>T maps to NM_006627.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr12:121018990 G>A maps to NM_015918.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:119379243 G>A maps to NM_022135.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:119379219 C>T maps to NM_022135.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr3:119367119 G>A maps to NM_022135.2 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:119367155 A>G maps to NM_022135.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:105609532 C>T maps to NM_022361.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:75608861 C>T maps to NM_000941.2 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:75609805 G>A maps to NM_000941.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48371052 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:48368301 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:48372713 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:48374499 G>A did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:48372642 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:48374498 C>T did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr13:38154094 C>T maps to NM_006475.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:38158193 C>T maps to NM_006475.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:38148745 C>T maps to NM_006475.2 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:38153249 A>G maps to NM_006475.2 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:38164610 C>T maps to NM_006475.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:38160399 C>T maps to NM_006475.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:38166276 A>G maps to NM_006475.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr13:38171385 G>T maps to NM_006475.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:124467345 T>C maps to NM_015450.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:43173621 T>C maps to NM_001005365.2 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr8:43197364 T>C maps to NM_001005365.2 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr8:43173684 T>C maps to NM_001005365.2 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr8:43171052 A>G maps to NM_001005365.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr18:14542857 G>A maps to ENST00000444806 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr18:14543139 C>T maps to ENST00000444806 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:14534928 A>C maps to ENST00000444806 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr18:14542809 G>A maps to ENST00000444806 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr18:14537967 T>C maps to ENST00000444806 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr21:14982926 C>T maps to NM_174981.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:131976328 C>T maps to NM_001083538.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr2:132021445 C>T maps to NM_001083538.1 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:131976088 C>T maps to NM_001083538.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:131976376 C>T maps to NM_001083538.1 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:131976385 A>C maps to NM_001083538.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr2:131976469 C>T maps to NM_001083538.1 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:132021901 C>T maps to NM_001083538.1 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr2:132010510 C>T maps to NM_001083538.1 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr2:130832596 G>A maps to NM_001099771.2 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:130832164 C>T maps to NM_001099771.2 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr2:130832926 A>G maps to NM_001099771.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr2:130877734 G>A maps to NM_001099771.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:19553814 C>A maps to NM_001005356.2 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:19574316 G>A maps to NM_001005356.2 Q458Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr14:19553748 G>A maps to NM_001005356.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:19573113 A>G maps to NM_001005356.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr22:16287789 G>A maps to NM_001136213.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:16287789 G>A maps to NM_001136213.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:16266972 A>G maps to NM_001136213.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr14:19990583 T>C maps to ENST00000439503 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:87322590 C>T maps to NM_001122757.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:87313465 A>G maps to NM_001122757.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:167365536 C>T maps to NM_002697.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:120169100 T>C did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr11:120168981 C>T maps to NM_014352.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr11:120180198 G>A maps to NM_014352.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:120175764 A>T maps to NM_014352.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr11:120168971 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:38512178 G>T maps to NM_002699.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:38512160 G>A maps to NM_002699.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:38511578 C>T maps to NM_002699.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:99283840 C>T maps to NM_005604.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr6:99284011 C>T maps to NM_005604.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:99282811 C>T maps to NM_005604.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:99283522 G>A maps to NM_005604.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:105473461 C>T maps to NM_006236.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:105472297 T>C maps to NM_006236.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:105472921 G>A maps to NM_006236.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:82764201 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:82764298 C>T did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:82764036 C>T did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:82764196 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:82763841 G>A did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:82763584 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:82764003 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:82763851 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:82764007 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:82763699 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:82763571 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:82764265 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:82763849 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr23:82763691 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:79175909 G>A maps to NM_006237.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr13:79175861 C>T maps to NM_006237.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr13:79175618 G>A maps to NM_006237.3 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:79175960 G>A maps to NM_006237.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:79175720 G>A maps to NM_006237.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr13:79175785 C>A maps to NM_006237.3 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:79175909 G>A maps to NM_006237.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:79177341 C>T maps to NM_006237.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:79177392 C>T maps to NM_006237.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr13:79175717 C>T maps to NM_006237.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr4:147561614 C>T maps to NM_004575.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:147560459 C>T maps to NM_004575.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr4:147561785 C>T maps to NM_004575.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr4:147561239 G>A maps to NM_004575.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr4:147561668 C>T maps to NM_004575.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:145719367 G>A maps to NM_002700.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:145719217 C>A maps to NM_002700.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr5:145719208 G>A maps to NM_002700.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:145719619 G>A maps to NM_002700.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:31132536 T>C maps to NM_002701.4 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:31133734 G>A maps to NM_002701.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr8:128428896 C>T maps to NM_001159542.1 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:128428413 C>T maps to NM_001159542.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:128428446 G>A maps to NM_001159542.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:93076992 G>A maps to NM_153216.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:93076927 C>T maps to NM_153216.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:93077152 C>T maps to NM_153216.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:51589896 G>A maps to NM_002702.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:39125533 T>C maps to NM_007252.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:39472695 G>A maps to NM_007252.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:39500290 G>A maps to NM_007252.3 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr7:39247127 A>G maps to NM_007252.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:71977566 C>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:10221525 C>T maps to NM_001040664.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:10220615 G>A maps to NM_001040664.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr19:10221460 G>T maps to NM_001040664.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr5:54763899 G>A maps to NM_176895.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:57002626 C>T maps to NM_003713.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:57002668 G>A maps to NM_003713.4 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:122348992 G>A maps to NM_001030059.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:122348836 C>T maps to NM_001030059.1 I213I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8368-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:4662416 C>T maps to NM_203453.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:4662737 G>A maps to NM_203453.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:134165479 C>G maps to NM_032728.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr9:134165438 C>A maps to NM_032728.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr22:46611218 G>T maps to NM_001001928.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:46614281 C>T maps to NM_001001928.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:46628026 G>A maps to NM_001001928.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:46631048 C>T maps to NM_001001928.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:35392428 G>A maps to NM_006238.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:12421296 C>A maps to NM_015869.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr4:23815665 C>T maps to NM_013261.3 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr4:23814435 G>C maps to NM_013261.3 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:23831130 A>G maps to NM_013261.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr4:23816031 G>C maps to NM_013261.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr4:23815805 G>A maps to NM_013261.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:23830128 G>A maps to NM_013261.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:149206303 C>T maps to NM_133263.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:149212460 C>T maps to NM_133263.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:149215998 C>T maps to NM_133263.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:57269248 T>C maps to NM_002703.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr4:57301584 G>C maps to NM_002703.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:57272696 A>G maps to NM_002703.3 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:57262800 G>A maps to NM_002703.3 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:74853697 A>G maps to NM_002704.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr4:74853295 G>A maps to NM_002704.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr4:74853742 C>G maps to NM_002704.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:74853682 C>T maps to NM_002704.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:62153072 G>A maps to ENST00000370177 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:18824563 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:18836179 C>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:18768030 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr23:18843908 C>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:76785640 G>A maps to NM_006239.2 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:76805795 C>A maps to NM_006239.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:76793200 G>A maps to NM_006239.2 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:76797688 C>T maps to NM_006239.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:76805841 T>A maps to NM_006239.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr12:81732995 C>T maps to NM_003625.2 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:81839400 G>T maps to NM_003625.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:82147943 C>A maps to NM_003625.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:81741407 C>T maps to NM_003625.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:49632104 C>T maps to NM_003660.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:49631307 C>T maps to NM_003660.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:49637337 C>T maps to NM_003660.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:49651342 C>T maps to NM_003660.2 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:49643052 G>A maps to NM_003660.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:27842019 C>T maps to NM_003622.3 R857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:27813820 C>T maps to NM_003622.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:7670466 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:42745850 A>G maps to NM_016488.6 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:42836452 A>G maps to NM_016488.6 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr1:143767464 G>A maps to NM_001123068.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:143767740 A>G maps to NM_001123068.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:143767650 G>A maps to NM_001123068.1 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:143767620 C>T maps to NM_001123068.1 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr15:64449049 C>T maps to NM_000942.4 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:159630905 A>G maps to NM_005038.2 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:159644353 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr1:40208961 C>T maps to NM_006112.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:81113510 C>T maps to NM_005729.3 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:170493493 C>T maps to NM_004792.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:36839500 T>A maps to NM_016059.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr22:22035654 G>A maps to NM_148175.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:149842223 C>T maps to NM_139126.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr14:50074336 C>T maps to NM_152329.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr14:50074221 A>G maps to NM_152329.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr15:43827564 G>A maps to NM_001130858.2 H1203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:102508908 T>C maps to ENST00000451606 C779C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:102509633 A>G maps to ENST00000451606 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:102482312 T>C maps to ENST00000451606 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:102465388 T>C maps to ENST00000451606 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr5:102490449 G>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:4933783 C>T maps to NM_002705.4 R1624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:4940784 G>A maps to NM_002705.4 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:4935286 G>A maps to NM_002705.4 D1123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:4944523 C>T maps to NM_002705.4 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:4933849 C>T maps to NM_002705.4 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:4934125 G>A maps to NM_002705.4 G1510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:4934377 C>T maps to NM_002705.4 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr16:4935103 C>T maps to NM_002705.4 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:60758132 C>T maps to NM_177952.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:44428872 C>T maps to NM_002706.4 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:58740867 A>G maps to NM_003620.3 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:58740888 C>T maps to NM_003620.3 H598H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr17:58740466 C>T maps to NM_003620.3 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:56833468 C>T maps to NM_014906.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:57057737 C>A maps to NM_014906.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:57050269 G>A maps to NM_014906.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:57049543 C>T maps to NM_014906.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr22:22277734 G>A maps to NM_014634.3 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:22300338 G>A maps to NM_014634.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr22:22287942 C>T maps to NM_014634.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:22285569 G>A maps to NM_014634.3 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:22277608 C>T maps to NM_014634.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:63195793 G>A maps to NM_020700.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:160786869 T>C maps to NM_139245.2 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:160679655 C>T maps to NM_139245.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:160783284 C>T maps to NM_139245.2 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr19:46003792 A>G maps to NM_001080401.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:73950294 C>T maps to NM_016147.1 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:161136993 G>A maps to NM_001122764.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:67166584 C>T maps to NM_001008709.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:67166077 C>T maps to NM_001008709.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:29016802 C>T maps to NM_002709.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:29022153 G>A maps to NM_002709.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:30569737 G>A maps to NM_002714.2 H896H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:30569866 G>A maps to NM_002714.2 H853H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:30572226 T>C maps to NM_002714.2 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr6:30570079 G>T maps to NM_002714.2 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:30577693 C>A maps to NM_002714.2 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:30570115 G>A maps to NM_002714.2 H770H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:30576684 A>T maps to NM_002714.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:30572187 C>T maps to NM_002714.2 W401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:80328666 T>C maps to NM_001143885.1 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr12:80214566 T>A maps to NM_001143885.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:202464773 A>G maps to ENST00000367270 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr1:202544207 C>T maps to ENST00000367270 R981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:202318224 T>G maps to ENST00000367270 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:55614868 C>T maps to NM_017607.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:45901549 C>T maps to NM_001142502.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr19:45895560 C>T maps to NM_001142502.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:45899881 G>A maps to NM_001142502.1 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:45895248 G>T maps to NM_001142502.1 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:45885874 G>A maps to NM_001142502.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:45895173 C>T maps to NM_001142502.1 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:45899632 C>T maps to NM_001142502.1 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:38742040 G>A maps to NM_033256.1 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:64012399 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:145724399 G>A maps to NM_032902.5 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr8:145722582 C>T maps to NM_032902.5 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr20:37529250 G>A maps to NM_015568.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:37536790 C>T maps to NM_015568.2 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:37536483 C>T maps to NM_015568.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:37531368 G>A maps to NM_015568.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:37546808 C>T maps to NM_015568.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:54974787 T>C maps to NM_006741.3 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:182928519 T>C did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr2:182850872 C>T maps to ENST00000280295 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:195245830 C>T maps to NM_006241.4 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:113519373 C>T maps to NM_002711.3 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:113518901 T>A maps to NM_002711.3 K749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr7:113558763 C>T maps to NM_002711.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:113519937 T>C maps to NM_002711.3 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:113518178 C>A maps to NM_002711.3 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr7:113519430 G>T maps to NM_002711.3 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr7:113519478 T>C maps to NM_002711.3 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr7:113519985 A>G maps to NM_002711.3 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:8998666 C>T maps to NM_024607.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr10:93389973 A>G maps to NM_005398.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr20:58514446 C>T maps to NM_006242.3 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:58514122 G>A maps to NM_006242.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:58514314 G>A maps to NM_006242.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:58514221 G>A maps to NM_006242.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:58514194 G>A maps to NM_006242.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:58514299 G>A maps to NM_006242.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:49137886 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:49143387 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:49127053 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:49127203 C>T did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:49127036 C>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:49138499 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:49143292 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:49143410 T>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:49142649 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:49142793 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:49127022 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:242089963 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:242102697 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:28165313 T>C maps to NM_014110.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:94827659 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:94855331 C>T maps to NM_001166160.1 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr7:94539578 C>T maps to NM_001166160.1 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:94740587 C>A maps to NM_001166160.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr7:94540214 C>T maps to NM_001166160.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:94539568 T>C maps to NM_001166160.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:94881151 G>C maps to NM_001166160.1 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:133536738 C>T maps to NM_002715.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:52714619 G>A maps to NM_014225.5 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:52719048 G>A maps to NM_014225.5 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr19:52722957 G>T maps to NM_014225.5 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:111618735 A>G maps to NM_181699.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:111612775 C>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:111597739 A>G maps to NM_181699.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:111631751 A>G maps to NM_181699.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:26227791 C>T maps to NM_001177591.1 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:26218506 T>C maps to NM_001177591.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:26151189 G>T maps to NM_001177591.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:146077584 C>T maps to ENST00000394414 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:146070774 G>A maps to ENST00000394414 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:146030224 G>A maps to ENST00000394414 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:146435238 C>T maps to ENST00000394414 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:146257586 G>A maps to ENST00000394414 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:6349591 C>T maps to NM_181876.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:6380272 G>A maps to NM_181876.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:6325118 C>T maps to NM_181876.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr4:6331023 G>A maps to NM_181876.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:6325190 G>A maps to NM_181876.2 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:6380227 A>G maps to NM_181876.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:133758886 C>T maps to ENST00000455566 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr10:133757519 C>T maps to ENST00000455566 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:135721356 G>A maps to NM_002718.4 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:135721302 C>A maps to NM_002718.4 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:135863920 C>A maps to NM_002718.4 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IZ-01A-32D-A25D-08 chr3:135722101 C>T maps to NM_002718.4 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:135720390 C>T maps to NM_002718.4 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:306399 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:306334 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:299552 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:299578 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:302118 C>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:306302 C>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:295140 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:322219 C>T did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:295131 T>C did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:306358 A>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:299351 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:306251 G>A did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:295131 T>C did not map to a codon.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr23:299397 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:301586 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:306381 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:299361 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:322256 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:299442 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:302618 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:301653 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:306380 C>G did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr14:35554855 C>T maps to NM_017917.2 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:131897122 G>T maps to NM_178001.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:131885368 C>T maps to NM_178001.2 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr9:131893898 G>A maps to NM_178001.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:212515579 T>C maps to NM_006243.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:212506873 T>C maps to NM_006243.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:212519207 C>T maps to NM_006243.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr11:64694200 C>T maps to NM_006244.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:64697971 C>T maps to NM_006244.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:102349640 A>G maps to NM_002719.3 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:102368057 G>T maps to NM_002719.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:102391578 C>T maps to NM_002719.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:102376001 C>T maps to NM_002719.3 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:42975936 A>G did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr14:63848862 C>T maps to ENST00000422769 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:63842768 C>T maps to ENST00000422769 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:63851160 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:63851208 G>A maps to ENST00000422769 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:101947155 G>A maps to NM_000944.4 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:101947155 G>A maps to NM_000944.4 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:101947155 G>A maps to NM_000944.4 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr4:102117122 G>C maps to NM_000944.4 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:101961639 T>A maps to NM_000944.4 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr4:101947176 C>A maps to NM_000944.4 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:75231342 A>G maps to NM_001142353.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:75238306 G>A maps to NM_001142353.1 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:75234730 T>A maps to NM_001142353.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:22355519 C>T maps to ENST00000397775 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr9:104356918 C>T maps to NM_147180.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:30096002 C>T maps to NM_002720.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:30096283 G>A maps to NM_002720.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr18:9595143 C>T maps to NM_001042388.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:9562040 G>A maps to NM_001042388.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:73108187 T>C maps to NM_174907.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:94674875 G>A maps to NM_058237.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr14:94674855 C>T maps to NM_058237.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:46888084 C>A maps to NM_006247.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:127920586 A>G maps to NM_001123355.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:127911966 C>T maps to NM_001123355.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:127923149 A>G maps to NM_001123355.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:244855309 A>G maps to NM_016076.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:41999260 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:103899332 C>T maps to NM_015062.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:103908402 A>G maps to NM_015062.3 S1523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:103908179 G>A maps to NM_015062.3 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:103899080 G>A maps to NM_015062.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:40546146 G>A maps to ENST00000372783 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:40558101 A>G maps to ENST00000372783 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:40557019 C>T maps to ENST00000372783 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:32130709 G>T maps to NM_138717.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr6:32125621 C>A maps to NM_138717.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:64881888 G>T maps to NM_015342.2 G560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:64883132 A>G maps to NM_015342.2 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:64867671 T>C maps to NM_015342.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:64865506 G>A maps to NM_015342.2 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr10:47087070 G>A maps to NM_005972.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:47087133 G>A maps to NM_005972.4 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:47087581 C>T maps to NM_005972.4 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:47087070 G>A maps to NM_005972.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:48759705 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:48759691 C>T did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:48759271 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:48758489 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:48760017 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:48759530 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr18:77679326 G>A maps to NM_025078.4 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:77679290 G>A maps to NM_025078.4 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr18:77664149 G>A maps to NM_025078.4 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:11312070 C>T maps to NM_152391.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:48931587 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:8563851 G>A maps to NM_032152.4 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:8555240 G>A maps to NM_032152.4 Y652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:8556024 A>G maps to NM_032152.4 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:8563986 G>A maps to NM_032152.4 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr22:22892266 C>T maps to NM_206954.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:22892499 G>A maps to NM_206954.1 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr22:22890845 C>T maps to NM_206954.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr22:22891013 C>T maps to NM_206954.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:12853639 G>A maps to NM_023013.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr1:12854439 A>C maps to NM_023013.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:12853597 T>C maps to NM_023013.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:12853477 G>T maps to NM_023013.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:12954966 G>T maps to NM_001039361.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr1:12954418 G>A maps to NM_001039361.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr1:12885132 T>C maps to NM_001146344.1 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:12884955 A>G maps to NM_001146344.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr1:12887515 C>T maps to NM_001146344.1 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr1:12884982 C>T maps to NM_001146344.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr1:12837237 G>A maps to NM_001080830.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:12835826 G>A maps to NM_001080830.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:13669153 A>G maps to ENST00000334600 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:13695902 G>T maps to NM_001099850.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:12920126 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:12920007 G>T maps to NM_023014.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:12920108 C>T maps to NM_023014.1 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:12920127 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:12921075 G>A maps to NM_023014.1 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:12939376 T>C maps to ENST00000376192 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:12941802 G>A maps to ENST00000376192 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:12943041 C>T maps to NM_001009611.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:12939841 C>T maps to ENST00000376192 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:12980058 T>C maps to NM_001012277.1 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:12979761 C>T maps to NM_001012277.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:11506765 G>A maps to NM_005039.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:11546744 A>G maps to NM_006248.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr12:11546375 A>C maps to NM_006248.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr12:11546744 A>C maps to NM_006248.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr12:11545865 A>G maps to NM_006248.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:11546300 A>G maps to NM_006248.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:11421600 A>G maps to NM_006249.4 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:11461555 C>A maps to NM_002723.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:11461618 C>A maps to NM_002723.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:11461618 C>A maps to NM_002723.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:91517403 G>A maps to NM_003981.2 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:91524788 G>A maps to NM_003981.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:156737592 T>C maps to NM_005973.4 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:156737934 T>C maps to NM_005973.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:156737937 A>C maps to NM_005973.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:82560970 G>A maps to NM_199418.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:82549487 G>T maps to NM_199418.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr6:106553507 G>A maps to NM_001198.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:106555297 C>T maps to NM_001198.3 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr6:106547386 T>C maps to NM_001198.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:129817094 C>T maps to NM_020228.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:129788547 G>A maps to NM_020228.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:129814884 C>T maps to NM_020228.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:133542070 C>A maps to NM_021619.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:100062100 C>T maps to ENST00000359773 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:100061350 G>A maps to ENST00000359773 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:100062154 G>A maps to ENST00000359773 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr6:100060990 C>T maps to ENST00000359773 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr8:70981814 C>T maps to NM_024504.2 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:70980554 G>A maps to NM_024504.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr8:70981819 C>A maps to NM_024504.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr8:70970952 G>A maps to NM_024504.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr8:70981762 C>A maps to NM_024504.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N0-01A-12D-A364-08 chr8:70967555 G>T maps to NM_024504.2 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr21:43241430 G>A maps to NM_022115.3 N1050N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr21:43256664 G>A maps to NM_022115.3 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr21:43221453 C>T maps to NM_022115.3 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:43230569 G>A maps to NM_022115.3 C1230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr21:43277344 G>A maps to NM_022115.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr21:43246336 G>A maps to NM_022115.3 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr21:43221519 C>T maps to NM_022115.3 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:3342750 T>C maps to NM_022114.3 N1082N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:3347516 C>T maps to NM_022114.3 D1122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:3319547 C>T maps to NM_022114.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:3322153 C>T maps to NM_022114.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:3328974 C>A maps to NM_022114.3 Y738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:3328728 G>A maps to NM_022114.3 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr1:3334447 G>A maps to NM_022114.3 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr1:3322072 C>T maps to NM_022114.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:3348571 G>A maps to NM_022114.3 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:3342702 C>T maps to NM_022114.3 D1066D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:3328338 G>A maps to NM_022114.3 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:3328983 G>A maps to NM_022114.3 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:3328749 C>T maps to NM_022114.3 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr1:3319508 C>T maps to NM_022114.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:3322162 C>T maps to NM_022114.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr1:3350341 G>A maps to NM_022114.3 E1266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:3329103 C>T maps to NM_022114.3 D781D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:14059378 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:14108309 A>G maps to NM_012231.4 K1340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:14108483 A>T maps to NM_012231.4 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:14108801 T>C maps to NM_012231.4 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:14108435 C>T maps to NM_012231.4 G1382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:14108081 T>C maps to NM_012231.4 D1264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr1:14142939 G>A maps to NM_012231.4 A1685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr1:14108600 C>T maps to NM_012231.4 N1437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:14108435 C>T maps to NM_012231.4 G1382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:14057565 G>A maps to NM_012231.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:14109218 G>A maps to NM_012231.4 E1643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:108128238 C>T maps to NM_012406.3 K718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:108147776 T>C maps to NM_012406.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:108145795 A>G maps to NM_012406.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:121732557 A>G maps to NM_018699.2 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr16:90128556 A>G maps to NM_001098173.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:81123473 T>C maps to NM_001099403.1 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:81123122 C>A maps to NM_001099403.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:81123200 C>T maps to NM_001099403.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:81124481 C>T maps to NM_001099403.1 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:81123233 C>G maps to NM_001099403.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:23509189 G>A maps to NM_020227.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr5:23521173 G>T maps to NM_020227.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr5:23509700 A>T maps to NM_020227.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr5:23522494 G>A maps to NM_020227.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr5:23522455 A>T maps to NM_020227.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr5:23526711 T>C maps to NM_020227.2 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr5:23526954 G>C maps to NM_020227.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:23527495 C>T maps to NM_020227.2 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:23509150 T>C maps to NM_020227.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:23526447 A>G maps to NM_020227.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr5:23521168 T>A maps to NM_020227.2 L130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:45977023 C>A maps to NM_181697.1 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:12911022 G>A maps to NM_005809.4 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:12907918 C>T maps to NM_005809.4 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:23685737 C>A did not map to a codon.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr23:23697384 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:23697292 C>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:64088155 G>A maps to NM_012094.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:64088504 G>A maps to NM_012094.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:27357253 A>G maps to NM_013388.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:145199531 G>A maps to NM_182960.2 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:203452401 T>C maps to NM_201348.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:105736745 A>G maps to NM_002726.4 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:105781354 A>G maps to NM_002726.4 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:105736670 G>A maps to NM_002726.4 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:44586850 G>A maps to NM_001171603.1 Q2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr20:47269999 G>A maps to NM_020820.3 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:69021846 T>C maps to NM_024870.2 C1045C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:69005937 T>C maps to NM_024870.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr8:69002884 A>T maps to NM_024870.2 K729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:68993074 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:69033267 C>T maps to NM_024870.2 I1236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr8:69069611 T>C maps to NM_024870.2 F1429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr8:68995527 T>A maps to NM_024870.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr8:69005937 T>C maps to NM_024870.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr8:69020558 G>A maps to NM_024870.2 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:68956787 G>A maps to NM_024870.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:69069573 G>T maps to NM_024870.2 G1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr8:69050687 A>C maps to NM_024870.2 A1341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr8:69104586 C>T maps to NM_024870.2 N1477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr8:69002904 C>T maps to NM_024870.2 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr8:69046291 A>T did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr8:69069557 A>T maps to NM_024870.2 A1411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:68992786 A>G maps to NM_024870.2 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr8:68965374 G>A maps to NM_024870.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr8:68864658 C>T maps to NM_024870.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:68930130 T>C maps to NM_024870.2 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr8:68930086 T>C maps to NM_024870.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr8:69028131 T>C maps to NM_024870.2 S1097S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:69017370 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:69058477 G>T maps to NM_024870.2 R1374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:69129887 C>T maps to NM_024870.2 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:72358861 G>A maps to NM_005041.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr10:72360439 G>T maps to NM_005041.4 C73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:72358761 G>A maps to NM_005041.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:57147020 G>A maps to NM_006093.3 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:186280648 A>T maps to NM_005807.3 G1238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:186273297 T>G maps to NM_005807.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:186278204 T>C maps to NM_005807.3 V1118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr1:186276026 T>C maps to NM_005807.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:186274032 G>T maps to NM_005807.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr13:28562669 C>T maps to NM_001105577.1 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:62200153 C>T maps to NM_001037335.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:62196898 G>A maps to NM_001037335.2 D1092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:62194855 G>A maps to NM_001037335.2 Y1773Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:62196229 G>T maps to NM_001037335.2 T1315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr20:62191323 C>A maps to NM_001037335.2 V2594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:62192701 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:62195761 G>A maps to NM_001037335.2 A1471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr20:62194513 G>A maps to NM_001037335.2 L1887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:62203576 G>T maps to NM_001037335.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr20:62203720 G>A maps to NM_001037335.2 A6A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr20:62196806 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:62195545 G>A maps to NM_001037335.2 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:62198205 G>A maps to NM_001037335.2 H835H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:42858776 C>T maps to NM_153026.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:42853838 G>A maps to NM_153026.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr12:42858712 A>G maps to NM_153026.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:42853619 A>G maps to NM_153026.2 I829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:42854129 G>A maps to NM_153026.2 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr12:42853841 G>A maps to NM_153026.2 Y755Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr12:42866210 G>T maps to NM_153026.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:64084972 G>A maps to NM_198859.3 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr3:64139011 C>T maps to NM_198859.3 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:64085233 G>A maps to NM_198859.3 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:64133070 C>T maps to NM_198859.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:64184457 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:64145666 G>A maps to NM_198859.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:64139007 G>A maps to NM_198859.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:49034430 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:49036123 T>C did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:49032335 G>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:49032440 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:49032320 T>C did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:49040235 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr6:41754857 C>T maps to NM_013397.5 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:57128006 T>C maps to NM_000946.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:57135216 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:57472419 C>A maps to NM_000947.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:57372343 C>T maps to NM_000947.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:57512698 T>G maps to NM_000947.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr6:57512656 A>G maps to NM_000947.2 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:57159507 T>C maps to NM_006252.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:57169679 C>T maps to NM_006252.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:14217672 G>A maps to NM_002730.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:14211687 G>C maps to NM_002730.3 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:84679840 A>G maps to NM_182948.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:84610151 T>C maps to NM_182948.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:84649797 C>T maps to NM_182948.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr9:71628450 G>A maps to NM_002732.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:71628957 G>A maps to NM_002732.3 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:71628546 G>T maps to NM_002732.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:49399286 G>A maps to NM_002733.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:49399286 G>A maps to NM_002733.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:49406894 T>C did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr7:151261253 A>C maps to NM_016203.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:151372718 G>A maps to NM_016203.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:151265921 G>A maps to NM_016203.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:219689019 T>C maps to NM_017431.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr2:219694946 G>A maps to NM_017431.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:219695072 G>A maps to NM_017431.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:219688556 G>A maps to NM_017431.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:66526418 T>C maps to NM_212472.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:66511557 C>T maps to NM_212472.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:66511560 C>T maps to NM_212472.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr7:720222 G>A maps to NM_002735.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr7:716894 G>C maps to NM_002735.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:751061 G>A maps to NM_002735.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr7:751067 G>A maps to NM_002735.2 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:48789702 G>A maps to NM_004157.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:48789612 G>T maps to NM_004157.2 C359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:106786830 C>T maps to NM_002736.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:106791469 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:64685128 C>T maps to NM_002737.2 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:64770154 C>T maps to NM_002737.2 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:64800154 A>G maps to NM_002737.2 *673W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr16:24192203 G>A maps to NM_002738.6 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:24192143 T>C maps to NM_002738.6 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr16:24192164 C>T maps to NM_002738.6 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr16:24104113 A>C maps to NM_002738.6 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:24046761 G>A maps to NM_002738.6 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr3:53220185 C>T maps to NM_212539.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:53212510 C>T maps to NM_212539.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:46378313 C>T maps to NM_005400.2 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:46228615 C>T maps to NM_005400.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr2:46411944 C>T maps to NM_005400.2 D713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:46234619 C>T maps to NM_005400.2 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:54394973 T>C maps to NM_002739.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:54401691 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:54409675 C>T maps to NM_002739.3 R624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:62014541 A>T maps to NM_006255.3 K615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:61923898 C>T maps to NM_006255.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:61857989 C>T maps to NM_006255.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:61858001 T>C maps to NM_006255.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:169999696 T>C maps to NM_002740.5 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:6553147 G>A maps to NM_006257.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:6498722 G>A maps to NM_006257.2 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:6552974 G>A maps to NM_006257.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr10:6520989 C>T maps to NM_006257.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:6533723 G>A maps to NM_006257.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:6557031 G>A maps to NM_006257.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:11548909 G>A maps to ENST00000436195 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr19:11556202 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:11558288 T>C maps to ENST00000436195 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:2103589 G>A maps to NM_002744.4 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:2077500 C>T maps to NM_002744.4 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr14:30093428 T>A maps to NM_002742.2 K612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:30047478 A>G did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr14:30068244 A>G maps to NM_002742.2 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr14:30095726 T>C maps to NM_002742.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:30066889 G>A maps to NM_002742.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:30095687 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:47177800 C>T maps to ENST00000449438 A882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:47177929 C>T maps to ENST00000449438 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:47177818 G>A maps to ENST00000449438 H876H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:47181701 G>A maps to ENST00000449438 N763N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:37516633 T>C maps to NM_005813.3 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:37543448 A>C maps to NM_005813.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:37513365 G>A maps to NM_005813.3 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:48772315 A>G maps to NM_006904.6 G2020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr8:48697800 G>A maps to NM_006904.6 N3659N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:48809838 G>A maps to NM_006904.6 S1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr8:48848298 A>G maps to NM_006904.6 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:48825008 C>T maps to NM_006904.6 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr8:48800143 G>A maps to NM_006904.6 S1511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr8:48809799 T>C maps to NM_006904.6 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr8:48743231 G>A maps to NM_006904.6 H2776H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr8:48772213 G>A maps to NM_006904.6 S2054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr8:48733369 G>A maps to NM_006904.6 Y3081Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:48697725 G>T maps to NM_006904.6 P3684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:48746910 C>T maps to NM_006904.6 P2665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:48740749 T>C maps to NM_006904.6 P2851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:48761848 C>T maps to NM_006904.6 V2381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:48774942 T>C maps to NM_006904.6 K1969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:48817530 T>C maps to NM_006904.6 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:48744482 C>T maps to NM_006904.6 A2718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr8:48740854 C>T maps to NM_006904.6 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:48743174 G>A maps to NM_006904.6 A2795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr8:48734314 T>C maps to NM_006904.6 T2986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr8:48711777 A>G maps to NM_006904.6 N3429N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:48749057 G>A maps to NM_006904.6 R2597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:52913010 T>C maps to NM_001098512.1 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:53227558 T>C maps to NM_001098512.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr10:53893599 G>T maps to NM_001098512.1 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr10:54040663 C>T maps to NM_001098512.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:82096097 A>G maps to NM_006259.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:82063968 A>G maps to NM_006259.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr4:82013549 A>T maps to NM_006259.1 L728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr4:82061718 G>T maps to NM_006259.1 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr2:179301023 A>T maps to NM_003690.4 L211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:179300870 C>T did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr7:102065545 C>A maps to NM_024653.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:102045104 C>T maps to NM_024653.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:3592807 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:3573187 A>G did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:3573439 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:3573211 A>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:3592694 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:22290518 G>A maps to ENST00000397199 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:22290528 A>G maps to ENST00000397199 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:22297193 C>T maps to ENST00000397199 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr6:22294766 G>A maps to ENST00000397199 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:22290498 A>G maps to ENST00000397199 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr6:22294694 G>A maps to ENST00000397199 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr10:120353796 G>A maps to NM_004248.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:35066131 A>G maps to NM_000949.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr5:35084584 G>A maps to NM_000949.4 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:50189895 G>A maps to NM_001536.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:50189958 C>T maps to NM_001536.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr19:50189486 C>T maps to NM_001536.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:50191499 T>C maps to NM_001536.3 *372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr21:48063466 C>T maps to NM_206962.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr21:48081792 C>T maps to NM_206962.1 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:48068532 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr21:48078787 G>A maps to NM_206962.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:20424473 C>T maps to NM_005788.3 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:23393382 G>A maps to NM_006109.3 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:23397732 G>A maps to NM_006109.3 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:68373744 T>C maps to NM_019023.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:68381544 C>T maps to NM_019023.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:68373280 C>T maps to NM_019023.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:3701424 G>A maps to NM_019854.3 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:3649830 C>T maps to NM_019854.3 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:3649864 G>T maps to NM_019854.3 G57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:4705394 C>T maps to NM_012409.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr20:4705529 C>T maps to NM_012409.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:4680429 G>A maps to NM_001080123.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:4680402 C>T maps to NM_001080123.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:4680114 G>A maps to NM_001080123.1 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:4680519 C>T maps to NM_001080123.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr17:27031230 C>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:27031395 G>T maps to ENST00000415329 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr20:33764013 C>T maps to NM_006404.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:33764235 G>A maps to NM_006404.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:33764528 G>A maps to NM_006404.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr22:18907071 G>A maps to NM_016335.4 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:36304126 A>G maps to NM_021232.1 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:36304051 G>A maps to NM_021232.1 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:110996680 C>T maps to NM_032414.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr2:68882617 T>G maps to NM_138964.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr2:68882419 G>A maps to NM_138964.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:68873255 C>T maps to NM_138964.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr20:5294673 G>A maps to NM_144773.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:15994011 A>G maps to NM_006017.2 H590H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:16020140 C>T maps to NM_006017.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:95947019 A>G maps to NM_144707.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:95952595 G>A maps to NM_144707.2 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:95952568 C>T maps to NM_144707.2 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr2:95953960 G>C maps to NM_144707.2 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:177419841 G>A maps to NM_006261.4 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:177419898 C>T maps to NM_006261.4 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:93624913 A>G maps to NM_000313.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:93619651 A>G maps to NM_000313.3 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:93593130 A>G maps to NM_000313.3 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr3:93596036 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:93605254 C>T maps to NM_000313.3 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:93692539 C>T maps to NM_000313.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:37632908 C>T maps to NM_007198.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:37633535 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:214171116 C>T maps to NM_002763.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:214170993 G>T maps to NM_002763.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:214170541 C>T maps to NM_002763.3 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr1:214170480 A>G maps to NM_002763.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:214171308 G>A maps to NM_002763.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr14:75321888 C>T maps to ENST00000445876 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:113826334 G>A maps to ENST00000342783 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:113812985 C>T maps to ENST00000342783 C4C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:60666066 T>C maps to NM_014502.4 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:60670960 C>T maps to NM_014502.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:150316963 C>T maps to NM_004698.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:54626915 C>T maps to NM_015629.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:54625257 C>T maps to NM_015629.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:54627954 C>T maps to NM_015629.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:54621675 G>A maps to NM_015629.3 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:109238367 G>A maps to NM_018061.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:116041259 C>T maps to NM_004697.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr9:116041255 C>T maps to NM_004697.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:116053804 G>A maps to NM_004697.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:153529039 C>A maps to ENST00000410080 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:153514438 T>C maps to ENST00000410080 K952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:153526808 A>G maps to ENST00000410080 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:153519622 G>A maps to ENST00000410080 R782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:153519622 G>A maps to ENST00000410080 R782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr12:50028896 G>T maps to NM_001031698.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:4060796 C>T maps to NM_003913.4 R991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:4041056 C>T maps to NM_003913.4 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr6:4032189 G>T maps to NM_003913.4 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:4037684 C>T maps to NM_003913.4 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:62657326 C>T maps to NM_012469.3 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr20:62630982 C>G maps to NM_012469.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr20:62657326 C>T maps to NM_012469.3 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:62664240 G>T maps to NM_012469.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:1576731 G>A maps to NM_006445.3 F1192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:1585244 C>T maps to NM_006445.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr17:1562829 G>A maps to NM_006445.3 D1653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr17:1579328 G>A maps to NM_006445.3 Q858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:1559715 G>A maps to NM_006445.3 D1921D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:49689012 C>T maps to ENST00000451891 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:49689975 G>A maps to ENST00000451891 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:49689231 C>T maps to ENST00000451891 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:42666206 C>T maps to NM_000322.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:106888485 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:106888570 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:106890851 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:12838800 T>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:12809647 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:12837741 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:12840908 G>A did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr17:74328422 G>A maps to NM_002766.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr17:74309055 C>T maps to NM_002766.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:50118248 G>A maps to NM_020719.1 R1669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:50123624 G>A maps to NM_020719.1 G1838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:50124782 C>T maps to NM_020719.1 D1875D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:50098299 A>G maps to NM_020719.1 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:50128755 G>A maps to NM_020719.1 Q2001Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:50099901 G>A maps to NM_020719.1 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:50098866 C>T maps to NM_020719.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:50099457 G>A maps to NM_020719.1 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:50128210 G>A maps to NM_020719.1 T1944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:50128791 G>A maps to NM_020719.1 P2013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:50099556 C>A maps to NM_020719.1 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:50102911 T>C maps to NM_020719.1 G1354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:50098053 G>T maps to NM_020719.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr19:50128133 G>T maps to NM_020719.1 E1919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:30663119 G>A maps to NM_024031.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:30666358 A>G maps to NM_024031.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:30666361 A>G maps to NM_024031.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr16:30663254 G>A maps to NM_024031.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:46030459 G>T maps to NM_024320.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr5:120022262 T>A maps to NM_016644.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr5:120021908 G>T maps to NM_016644.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:120021788 T>C maps to NM_016644.1 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr6:166721312 G>C maps to NM_175922.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:166721231 C>T maps to NM_175922.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:240981391 G>A maps to NM_001080835.1 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:5784044 G>A maps to NM_001134316.1 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:138724624 G>A maps to NM_001134659.1 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr3:138724597 G>A maps to NM_001134659.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:138724462 G>A maps to NM_001134659.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:138724708 G>A maps to NM_001134659.1 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr3:138739149 C>T maps to NM_001013650.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:138739077 G>A maps to NM_001013650.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:138739116 G>A maps to NM_001013650.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:138739335 C>T maps to NM_001013650.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr3:138738789 G>A maps to NM_001013650.2 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:138738759 C>T maps to NM_001013650.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:138738768 G>A maps to NM_001013650.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:138739176 G>A maps to NM_001013650.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr16:855738 G>A maps to NM_001013638.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:857485 G>A maps to NM_001013638.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:30529872 G>A maps to NM_025263.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:45110469 G>T did not map to a codon.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr11:36422779 C>T maps to NM_001160167.1 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:150869253 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:150869405 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:150869500 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:150869230 G>A did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr23:150869096 C>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:32117079 G>A maps to NM_030651.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:29825670 G>A maps to NM_145239.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr16:29825053 C>A maps to NM_145239.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr3:9990794 C>T maps to NM_207351.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:170688907 C>T maps to NM_022716.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:132482978 C>T maps to NM_016307.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:142460322 C>T maps to ENST00000486171 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:119237470 G>A maps to NM_003619.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:119216199 G>A maps to NM_003619.3 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr6:27215754 C>T maps to NM_005865.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:2906204 G>A maps to NM_022119.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:2905626 G>C maps to NM_022119.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:2764111 C>T maps to NM_031948.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:2763682 C>T maps to NM_031948.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:2764171 C>T maps to NM_031948.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:2763682 C>T maps to NM_031948.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:33797976 C>T maps to NM_007343.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr9:33798517 T>G maps to NM_007343.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:84233969 C>T maps to NM_153362.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:84233364 G>T maps to NM_153362.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:84233648 T>C maps to NM_153362.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:31152916 G>A maps to NM_173502.3 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr16:31157136 G>A maps to NM_173502.3 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:31152923 G>A maps to NM_173502.3 G589G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4G8-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:228003896 C>T maps to NM_183062.2 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr1:228033681 G>T maps to NM_183062.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:228003896 C>T maps to NM_183062.2 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:46783905 T>C maps to ENST00000331814 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:46784040 A>G maps to ENST00000331814 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:46754420 C>T maps to NM_013270.4 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:46754420 C>T maps to NM_013270.4 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:31099136 G>A maps to NM_001039503.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:31095542 C>T maps to NM_001039503.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:31096299 C>T maps to NM_001039503.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:58324963 C>T maps to NM_001080492.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:58320086 G>A maps to NM_001080492.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:58324951 C>T maps to NM_001080492.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:58314268 C>T maps to NM_001080492.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:58318532 G>A maps to NM_001080492.1 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:58327705 C>T maps to NM_001080492.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr8:10396038 C>T maps to NM_198464.3 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:10396279 T>C maps to NM_198464.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31143845 G>A maps to NM_002773.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:25226285 G>A maps to NM_020200.5 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:55930812 G>A maps to NM_173814.4 R796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:55974622 A>T maps to NM_173814.4 C205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:55971644 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:56032669 C>A maps to NM_173814.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:151006688 A>G maps to NM_021222.1 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:151001398 C>T maps to NM_021222.1 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr9:79441532 G>A maps to NM_015225.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:79325824 A>T maps to NM_015225.2 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr9:79323162 C>A maps to NM_015225.2 E1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr9:79325467 T>C maps to NM_015225.2 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr19:40901569 G>A maps to NM_181882.2 R897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:40900052 G>A maps to NM_181882.2 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:40901222 G>A maps to NM_181882.2 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:40899950 C>T maps to NM_181882.2 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40902632 C>T maps to NM_181882.2 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr19:40902917 A>T maps to NM_181882.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:73594248 C>T maps to ENST00000373120 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:80942969 T>C maps to ENST00000421149 C336C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:80932597 C>T maps to ENST00000421149 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:80919649 G>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:143763435 C>A maps to ENST00000301258 C86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:104176759 G>A maps to NM_002779.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr10:104173947 C>A maps to NM_002779.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:104173923 A>G maps to NM_002779.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr5:139189336 G>T maps to NM_032289.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:139217238 G>A maps to NM_032289.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:139216515 G>A maps to NM_032289.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:18666262 A>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:18432747 G>A maps to ENST00000440756 N845N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:18729716 C>T maps to ENST00000440756 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:18393318 C>T maps to ENST00000440756 K1028K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6803-01A-11D-1882-08 chr2:113955400 G>A maps to NM_012455.2 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr2:113943469 A>G maps to NM_012455.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr2:113950927 G>A maps to NM_012455.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr1:227073247 G>A maps to ENST00000391872 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:227076544 C>A maps to ENST00000391872 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:227079048 C>T maps to ENST00000391872 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:227075860 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:227073322 C>T maps to ENST00000391872 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr19:36237374 A>T maps to NM_172341.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:43382305 G>A maps to NM_006905.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:43519386 G>T maps to ENST00000306308 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:43519328 G>A maps to ENST00000306308 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:43529017 G>A maps to ENST00000306308 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr19:43514193 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:43528980 G>A maps to ENST00000306308 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:43579692 C>T maps to NM_031246.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:43585324 G>A maps to ENST00000449000 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr19:43242981 C>T maps to NM_021016.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:43233449 C>T maps to NM_021016.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:43243065 T>C maps to NM_021016.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:43244503 C>T maps to NM_021016.3 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:43236966 G>A maps to NM_021016.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr19:43709646 G>A maps to ENST00000449000 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:43699425 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr19:43680241 A>G maps to ENST00000270059 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:43680088 G>T maps to ENST00000270059 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:43411248 C>T maps to NM_002782.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr19:43421879 C>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:43259304 G>A maps to NM_182707.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr19:43258560 G>A maps to NM_182707.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:43258707 T>C maps to NM_182707.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr19:43268239 A>G maps to NM_182707.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:43258695 G>A maps to NM_182707.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:43258531 G>T maps to NM_182707.2 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:43772053 G>A maps to NM_002784.3 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr16:67942864 G>A maps to NM_006742.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr16:67943233 C>T maps to NM_006742.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:67942750 C>T maps to NM_006742.2 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr8:87076472 G>T maps to ENST00000276616 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:87060711 C>T maps to ENST00000276616 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:87076598 G>T maps to ENST00000276616 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr8:87081686 G>A maps to ENST00000276616 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:42957427 A>G maps to NM_002787.4 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:42962943 A>G maps to NM_002787.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr15:78834912 T>C maps to NM_002789.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr18:23759076 A>C maps to NM_144662.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:23731933 A>G maps to NM_144662.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:23758900 A>G maps to NM_144662.2 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:67968707 G>T maps to NM_002801.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:67968746 G>A maps to NM_002801.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:23511562 C>T maps to NM_001099780.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr14:23511988 C>T maps to NM_001099780.1 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr14:23512057 C>T maps to NM_001099780.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:36074952 C>T maps to NM_002794.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:36074952 C>T maps to NM_002794.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:151372167 G>A maps to NM_002796.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:151372477 C>A maps to NM_002796.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:151373272 C>T maps to NM_002796.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:4701656 G>A maps to NM_002798.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr17:4701675 C>T maps to NM_002798.1 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4700756 T>C maps to NM_002798.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr6:32810758 A>G maps to NM_148919.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:32823979 A>G maps to NM_002800.4 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:103004630 C>T maps to NM_002803.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:103004702 G>A maps to NM_002803.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:47445734 C>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:40480658 C>A maps to NM_006503.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:40485986 G>A maps to NM_006503.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:40480512 G>A maps to NM_006503.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:40485977 C>T maps to NM_006503.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:61907506 T>A maps to NM_002805.5 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr17:61908691 C>T maps to NM_002805.5 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr14:53194223 C>T maps to NM_002806.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr2:231931789 A>T maps to NM_002807.3 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:107331058 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:107331216 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:107332014 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:30796050 C>T maps to NM_002815.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:65343309 G>T maps to NM_002816.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:251577 A>G maps to NM_002817.3 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:184025727 C>T maps to NM_002808.3 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:184020205 T>C maps to NM_002808.3 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:184020535 C>T maps to NM_002808.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:38151522 G>A maps to NM_002809.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:38142880 G>A maps to NM_002809.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:123595604 G>T maps to NM_005047.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:123586805 G>T maps to NM_005047.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:63999232 G>A maps to ENST00000492933 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:74339300 C>T maps to NM_002811.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:74338253 A>T maps to NM_002811.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr19:38873942 G>A maps to NM_002812.4 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:24607278 C>T maps to NM_176783.1 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:54125108 A>T maps to NM_014614.2 I1168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:54117288 A>T maps to NM_014614.2 I1416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:54114543 C>T maps to NM_014614.2 S1527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:54125071 A>G maps to NM_014614.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:54122182 C>T maps to NM_014614.2 E1291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:54127127 C>T maps to NM_014614.2 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:54159000 A>G maps to NM_014614.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:1106262 C>T maps to NM_006814.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:1143791 G>A maps to NM_006814.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr21:40550510 G>A maps to NM_003720.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:12724554 C>T maps to NM_020232.4 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr18:12718568 C>T maps to NM_020232.4 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:31097423 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:20279894 A>G maps to NM_001042414.1 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:20277377 A>G maps to NM_001042414.1 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:56088812 G>A maps to NM_004577.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:56087372 G>C maps to NM_004577.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:6375770 G>A maps to NM_004158.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:124746901 G>A maps to NM_153336.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:43577771 G>A maps to NM_024430.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:43578805 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:28477205 G>A maps to NM_001164721.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:72347171 T>C maps to NM_001099666.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:807900 C>T maps to NM_002819.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:97272006 C>T maps to ENST00000370197 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:99022444 G>A maps to NM_001198879.1 D619D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:99022488 G>A maps to NM_001198879.1 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:71638850 C>T maps to NM_024754.3 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:86355070 G>A maps to NM_017952.5 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:86352156 A>G maps to NM_017952.5 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:86361964 C>T maps to NM_017952.5 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr2:86364654 C>T maps to NM_017952.5 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:86352129 C>T maps to NM_017952.5 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:86352117 A>G maps to NM_017952.5 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:98229518 C>T maps to NM_000264.3 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:98209421 C>A maps to NM_000264.3 T1372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr9:98232137 G>A maps to NM_000264.3 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr9:98220420 G>A maps to NM_000264.3 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:98268779 G>A maps to NM_000264.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr9:98268845 C>T maps to NM_000264.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr9:98231284 C>T maps to NM_000264.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:98241347 T>C maps to NM_000264.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:98241298 G>A maps to NM_000264.3 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:98215806 C>T maps to NM_000264.3 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:98239082 G>A maps to NM_000264.3 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:98238402 G>A maps to NM_000264.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:98209301 G>A maps to NM_000264.3 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr1:45293194 G>A maps to NM_003738.4 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr1:45288224 G>A maps to NM_003738.4 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr1:45293538 C>A maps to NM_003738.4 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:45292982 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:23397937 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:23397937 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:23412228 G>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:23411549 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:23410725 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:23411675 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:23353223 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:23411870 A>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:23398121 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:23397822 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:23411640 G>T did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:23411255 T>C did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr23:23411149 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:23411236 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:23411096 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:11580745 C>T maps to NM_020780.1 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:11580780 C>T maps to NM_020780.1 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr1:11561885 C>T maps to NM_020780.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:11580780 C>T maps to NM_020780.1 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:11561861 G>A maps to NM_020780.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:11579854 C>T maps to NM_020780.1 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:11591740 C>T maps to NM_020780.1 Q1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:27702399 C>T maps to NM_001034842.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr10:27703149 C>T maps to NM_001034842.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:27702414 G>A maps to NM_001034842.3 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr10:27687304 G>C maps to NM_001034842.3 S741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:27702567 G>A maps to NM_001034842.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr10:27702993 C>T maps to NM_001034842.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:27702627 G>A maps to NM_001034842.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:27702477 G>A maps to NM_001034842.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr10:27702138 G>A maps to NM_001034842.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr10:27703026 C>T maps to NM_001034842.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:27702138 G>A maps to NM_001034842.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:27702996 C>T maps to NM_001034842.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr10:27702477 G>A maps to NM_001034842.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:97299344 C>T maps to NM_014754.1 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr8:97318781 G>A maps to NM_014754.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:97321796 T>C maps to NM_014754.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr8:97274447 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr8:97311961 G>A maps to NM_014754.1 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:479106 C>T maps to NM_030783.1 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:489432 G>A maps to NM_030783.1 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:490557 C>T maps to NM_030783.1 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:490497 C>T maps to NM_030783.1 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:89717712 G>A maps to NM_000314.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr10:89653867 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:89685302 G>A maps to NM_000314.4 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:89653807 G>T maps to NM_000314.4 G36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr10:89624285 A>G maps to NM_000314.4 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr10:89653800 T>C maps to NM_000314.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr10:89711873 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:16528541 A>T maps to NM_030664.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:16528557 C>T maps to NM_030664.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:16553254 G>A maps to NM_030664.3 *350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:16528577 C>T maps to NM_030664.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr10:23482703 G>T maps to NM_178161.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr10:23481521 C>T maps to NM_178161.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr10:23481530 C>T maps to NM_178161.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:52735330 C>T maps to NM_000953.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:52735101 G>A maps to NM_000953.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr14:52741453 C>T maps to NM_000953.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr14:52734888 G>A maps to NM_000953.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr9:139872101 G>A maps to ENST00000224167 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:52781391 A>G maps to NM_000956.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr1:71418610 G>T maps to NM_198718.1 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr1:71478122 G>A maps to ENST00000354608 H314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:71513119 G>A maps to ENST00000354608 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:71512897 C>T maps to ENST00000354608 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:71512648 G>A maps to ENST00000354608 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:71418601 T>C maps to NM_198718.1 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr1:71512620 G>A maps to ENST00000354608 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:40691942 A>G maps to NM_000958.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:40681631 G>A maps to NM_000958.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:130889771 C>T maps to NM_025072.5 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:130885322 C>T maps to NM_025072.5 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:57081780 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:78959084 C>T maps to NM_000959.3 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr1:78958622 G>A maps to NM_000959.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr1:117491913 C>T maps to NM_020440.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:117509773 C>T maps to NM_020440.2 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr1:117516893 C>T maps to NM_020440.2 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:117484637 C>T maps to NM_020440.2 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:47127182 G>T maps to NM_000960.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:47124716 G>T maps to NM_000960.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr20:48156224 C>T maps to NM_000961.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:48156224 C>T maps to NM_000961.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr20:48127700 G>A maps to NM_000961.3 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr9:114325439 C>G maps to NM_001146108.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:125140214 C>A maps to NM_000962.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:125145861 G>A maps to NM_000962.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:125152625 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:125140229 C>T maps to NM_000962.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:125145786 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:186645043 G>A maps to NM_000963.2 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:186645622 G>A maps to NM_000963.2 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:46943317 C>T maps to NM_000316.2 N393N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-5718-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:209315474 G>A maps to NM_005048.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:209308073 C>T maps to NM_005048.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:209271803 T>C maps to NM_005048.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:209308073 C>T maps to NM_005048.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:209302277 T>C maps to NM_005048.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:28122391 C>T maps to ENST00000354417 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:28116398 G>A maps to ENST00000354417 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:28116576 C>T maps to ENST00000354417 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:141712785 T>C maps to NM_005607.4 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:141753358 G>A maps to NM_005607.4 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:141771261 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:141749152 G>A maps to NM_005607.4 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:27297937 C>T maps to NM_004103.3 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:27300490 C>T maps to NM_004103.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:27301751 G>A maps to NM_004103.3 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:27287639 A>G maps to NM_004103.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:62162143 G>A maps to NM_005975.2 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr20:62164955 G>A maps to NM_005975.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr20:62165513 G>A maps to NM_005975.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:43110014 G>A maps to NM_002821.3 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr6:43096748 G>A maps to NM_002821.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:43098288 G>A maps to NM_002821.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:136938211 G>A maps to NM_002825.5 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:136936034 G>A maps to NM_002825.5 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:136939672 G>T maps to NM_002825.5 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:50361196 C>T maps to NM_017432.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr19:50358106 C>T maps to NM_017432.3 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:50360332 C>T maps to NM_017432.3 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:50357700 T>C maps to NM_017432.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:32377334 A>G maps to NM_080391.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:142441116 G>A maps to NM_032611.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:142432426 G>A maps to NM_032611.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr8:142437148 C>T maps to NM_032611.1 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:96860858 C>T maps to ENST00000434261 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:96847620 G>A maps to ENST00000434261 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:96859909 G>A maps to ENST00000434261 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:96846961 G>A maps to ENST00000434261 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr9:96864033 G>A did not map to a codon.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr9:96857665 G>T maps to ENST00000434261 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:96859942 C>T maps to ENST00000434261 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:17636318 A>G maps to NM_014241.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr9:21007085 C>A maps to NM_001010915.3 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:47593159 T>G maps to NM_175732.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:49196317 C>T maps to NM_002827.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:49184936 C>T maps to NM_002827.2 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:112924295 G>A maps to ENST00000392596 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:112926846 C>T maps to ENST00000392596 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr12:112915737 G>A maps to ENST00000392596 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:112915820 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:77256456 C>T maps to NM_002835.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:77221536 A>G maps to NM_002835.3 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:87680176 T>C maps to NM_080685.2 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:87685813 G>A maps to NM_080685.2 K1362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr4:87724934 G>A maps to NM_080685.2 T2198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:87637690 C>T maps to NM_080685.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:87622547 T>G maps to NM_080685.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:87637690 C>T maps to NM_080685.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr4:87724880 C>T maps to NM_080685.2 N2180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr4:87687619 G>T maps to NM_080685.2 E1432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:87690962 C>T maps to NM_080685.2 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:87672209 T>C maps to NM_080685.2 S1033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:87696413 C>T maps to NM_080685.2 R1872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:87671684 C>T maps to NM_080685.2 R905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:87684103 C>T maps to NM_080685.2 Q1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:87735667 A>G maps to NM_080685.2 E2479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:214557901 G>A maps to NM_005401.4 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:214575075 A>G maps to NM_005401.4 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:214557589 C>T maps to NM_005401.4 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:214557226 C>T maps to NM_005401.4 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr1:214557343 A>G maps to NM_005401.4 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:214576290 C>T maps to NM_005401.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:214638038 C>T maps to NM_005401.4 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:214638020 T>C maps to NM_005401.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:214585029 A>C maps to NM_005401.4 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:131130795 A>G maps to NM_014369.3 *461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr14:88945668 C>T maps to NM_007039.3 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr14:88945665 G>A maps to NM_007039.3 D703D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:88935292 C>T maps to NM_007039.3 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:88946025 G>A maps to NM_007039.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr14:88946484 G>A maps to NM_007039.3 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:114401659 A>G maps to NM_015967.5 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:47449864 C>T maps to NM_015466.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:47454596 G>A maps to NM_015466.2 G1611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:47454674 A>G maps to NM_015466.2 *1637W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:47449945 C>T maps to NM_015466.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:47449900 C>T maps to NM_015466.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr3:47451046 C>T maps to NM_015466.2 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:47447463 G>A maps to NM_015466.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:112144724 G>A maps to NM_002829.3 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:112207535 C>T maps to NM_002829.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:112216794 G>A maps to NM_002829.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:112200416 G>A maps to NM_002829.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:112166751 G>A maps to NM_002829.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:112207522 G>A maps to NM_002829.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:112172544 G>A maps to NM_002829.3 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:112219456 T>C maps to NM_002829.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:18750528 G>A maps to NM_032781.3 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:18750570 G>A maps to NM_032781.3 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:18764949 G>A maps to NM_032781.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:18763930 G>A maps to NM_032781.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr11:18751349 G>A maps to NM_032781.3 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr12:7065607 C>T maps to ENST00000416215 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:7066905 C>T maps to ENST00000416215 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:7069347 C>T maps to ENST00000416215 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:202126900 G>A maps to ENST00000309017 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:202128485 G>A maps to ENST00000309017 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:75798029 A>T maps to NM_002833.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr20:2988066 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:3001962 C>T maps to NM_002836.3 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:3007385 A>G maps to NM_002836.3 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:3016503 C>T maps to NM_002836.3 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:70964914 G>A maps to NM_001109754.1 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:70948991 G>A maps to NM_001109754.1 S1697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:70925841 A>G maps to NM_001109754.1 L2159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:70960485 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr12:70954514 G>A maps to NM_001109754.1 Y1456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:70946687 G>A maps to NM_001109754.1 A1752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr12:71002846 A>G did not map to a codon.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr12:70990048 C>T maps to NM_001109754.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr12:70990069 C>T maps to NM_001109754.1 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:70948991 G>A maps to NM_001109754.1 S1697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:198687370 G>A maps to ENST00000271610 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:198682088 A>T maps to ENST00000271610 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:198711489 A>G maps to ENST00000271610 Q897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:198711110 T>C maps to ENST00000271610 N839N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:198711489 A>G maps to ENST00000271610 Q897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr1:198676005 A>T maps to ENST00000271610 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:198701675 C>T maps to ENST00000271610 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr1:198719668 G>T maps to ENST00000271610 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:198668765 G>A maps to ENST00000271610 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:198711038 G>A maps to ENST00000271610 Q815Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:198700746 T>C maps to ENST00000271610 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr1:198719704 A>C maps to ENST00000271610 R1053R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr1:198685919 G>A maps to ENST00000271610 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:198678921 C>T maps to ENST00000271610 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:8518268 C>T maps to NM_002839.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:8319959 G>A maps to NM_002839.3 G1847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:8484204 A>G maps to NM_002839.3 R1109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:8521487 G>A maps to NM_002839.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr9:8404617 A>G maps to NM_002839.3 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr9:8521481 G>A maps to NM_002839.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr9:8518229 C>T maps to NM_002839.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr9:8500769 A>G maps to NM_002839.3 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr9:8341953 G>T maps to NM_002839.3 C1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr9:8341910 T>A maps to NM_002839.3 K1577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr9:8499814 G>A maps to NM_002839.3 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr9:8389279 T>C maps to NM_002839.3 Q1446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr9:8636818 G>A maps to NM_002839.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:8449837 C>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:129870412 C>T maps to NM_006504.4 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:129847930 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:44054459 C>T maps to NM_002840.3 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:44035351 C>T maps to NM_002840.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:62253085 T>C maps to NM_002841.3 Y886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:62253472 G>A maps to NM_002841.3 T951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:62118331 C>T maps to NM_002841.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:62180830 G>A maps to NM_002841.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:62253139 C>T maps to NM_002841.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:55715342 G>A maps to NM_002842.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:55718171 T>C maps to NM_002842.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:55697343 A>G maps to NM_002842.3 C929C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr19:55708572 G>A maps to NM_002842.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr11:48171646 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:48166632 C>T maps to NM_002843.3 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:48149350 C>T maps to NM_002843.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:48188901 T>C maps to NM_002843.3 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:48149416 G>A maps to NM_002843.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr11:48177351 G>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:48152047 C>T maps to NM_002843.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr11:48166371 C>T maps to NM_002843.3 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:128388768 C>T maps to ENST00000368210 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:128561239 G>A maps to ENST00000368210 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:128318066 G>A maps to ENST00000368210 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:128388792 C>T maps to ENST00000368210 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:128410835 A>G maps to ENST00000368210 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:128399980 T>C maps to ENST00000368210 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr6:128326279 C>A maps to ENST00000368210 E815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:128297890 G>A maps to ENST00000368210 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr6:128643429 T>G maps to ENST00000368210 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:128298172 G>A maps to ENST00000368210 I1264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:128298085 G>A maps to ENST00000368210 N1293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:128294226 G>A maps to ENST00000368210 V1421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:128297890 G>A maps to ENST00000368210 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr6:128505686 C>T maps to ENST00000368210 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr18:8076537 A>G maps to NM_001105244.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:8343454 G>A maps to NM_001105244.1 R997R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:8069783 C>T maps to NM_001105244.1 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:7567872 G>A maps to NM_001105244.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr18:8394509 C>T maps to NM_001105244.1 I1415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr18:8380325 C>T maps to NM_001105244.1 T1273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr18:8076562 G>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr18:8085806 C>T maps to NM_001105244.1 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:220162660 G>A maps to NM_002846.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:220162722 G>A maps to NM_002846.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr2:220162660 G>A maps to NM_002846.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:220164966 C>T maps to NM_002846.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:157985113 G>A maps to NM_002847.3 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:157985111 T>A maps to NM_002847.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:157926631 A>G maps to NM_002847.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:157903531 G>A maps to NM_002847.3 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr7:157931127 G>A maps to NM_002847.3 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr7:157874020 G>A maps to NM_002847.3 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr7:157959935 C>T maps to NM_002847.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr7:157414081 G>A maps to NM_002847.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr7:157874062 G>A maps to NM_002847.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:157387998 G>A maps to NM_002847.3 H809H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:158109559 G>A maps to NM_002847.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:157414138 G>A maps to NM_002847.3 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:157369462 C>A maps to NM_002847.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:157959758 G>A maps to NM_002847.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:15652374 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:15704533 T>C maps to NM_030667.1 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:71050593 T>A maps to NM_002849.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:71078008 C>A maps to NM_002849.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:71056291 G>A maps to NM_002849.2 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:71094955 G>A maps to NM_002849.2 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr12:71158528 G>A maps to NM_002849.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:5222820 C>T maps to NM_002850.3 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:5238969 G>A maps to NM_002850.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:5225735 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:5225783 G>A maps to NM_002850.3 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:5240269 C>T maps to NM_002850.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:5210704 C>A maps to NM_002850.3 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr19:5221117 C>T maps to NM_002850.3 W1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:5212257 G>A maps to NM_002850.3 A1591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr19:5265159 A>G maps to NM_002850.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:5244017 C>A maps to NM_002850.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:5231327 G>A maps to NM_002850.3 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:5258115 A>G maps to NM_002850.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:5208285 C>T maps to NM_002850.3 E1868E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:5220165 C>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:5239008 G>A maps to NM_002850.3 Y590Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:5207964 G>A maps to NM_002850.3 R1916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:5221060 G>A maps to NM_002850.3 D1135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:5214613 C>T maps to NM_002850.3 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:5258088 C>T maps to NM_002850.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:5245976 G>A maps to NM_002850.3 C266C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:41400119 G>A maps to ENST00000373198 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:40735470 G>A maps to ENST00000373198 C1137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:40743942 G>A maps to ENST00000373198 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:40864896 T>G maps to ENST00000373198 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr20:40713353 G>A maps to ENST00000373198 D1390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:40980778 G>A maps to ENST00000373198 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr20:40864896 T>G maps to ENST00000373198 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr20:40864896 T>G maps to ENST00000373198 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr20:40714430 G>A maps to ENST00000373198 F1325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr20:41306530 G>A maps to ENST00000373198 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:40713353 G>A maps to ENST00000373198 D1390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr20:40790012 G>T maps to ENST00000373198 Y909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:40911165 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:41408873 G>A maps to ENST00000373198 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr20:41100954 G>A maps to ENST00000373198 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:40877442 A>G maps to ENST00000373198 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:41408897 G>A maps to ENST00000373198 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:41419957 G>A maps to ENST00000373198 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:40713419 C>T maps to ENST00000373198 T1368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:40730847 G>A maps to ENST00000373198 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:40790156 G>A maps to ENST00000373198 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr20:40727174 G>A maps to ENST00000373198 A1266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:29585825 T>C maps to NM_005704.4 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:29611287 C>A maps to NM_005704.4 S742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:29630478 G>A maps to NM_005704.4 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:29644432 C>T maps to NM_005704.4 D1239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:29647291 C>A maps to NM_005704.4 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr1:29644432 C>T maps to NM_005704.4 D1239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:29581829 C>T maps to NM_005704.4 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:29641883 C>T maps to NM_005704.4 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:29586015 C>T maps to NM_005704.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr1:29639110 G>A maps to NM_005704.4 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:121651001 A>G maps to NM_002851.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:121694042 G>A maps to NM_002851.2 W2111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:121651646 C>T maps to NM_002851.2 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr7:121651970 T>C maps to NM_002851.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:121652618 A>C maps to NM_002851.2 S1173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr7:121653683 T>C maps to NM_002851.2 S1528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:121651781 T>C maps to NM_002851.2 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:121651136 T>C maps to NM_002851.2 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:121650656 T>A maps to NM_002851.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr7:121623785 C>T maps to NM_002851.2 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:121616873 T>C maps to NM_002851.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:121653641 G>A maps to NM_002851.2 K1514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr17:40556836 G>A maps to NM_012232.5 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:40557268 C>T maps to NM_012232.5 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr17:40557229 G>A maps to NM_012232.5 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:57775294 A>G maps to ENST00000409433 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:159849800 T>G maps to NM_004219.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:159855660 A>G maps to NM_004219.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr21:46281075 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:157155332 G>A maps to NM_002852.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr16:1538405 G>A maps to NM_001013658.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr16:1537352 G>T maps to NM_001013658.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:1537872 C>T maps to NM_001013658.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr16:1536493 G>A maps to NM_001013658.1 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr8:144899112 G>A maps to NM_078480.1 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:31479865 C>T maps to ENST00000373741 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr1:31414061 T>A maps to ENST00000373741 K1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:20511271 G>A maps to ENST00000361078 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:20511424 C>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:20453705 G>T maps to ENST00000361078 C982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:20451432 C>T maps to ENST00000361078 K1038K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:20483137 T>C maps to ENST00000361078 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:20508338 A>T maps to ENST00000361078 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:20511425 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:20463158 G>A maps to ENST00000361078 R674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:139494689 T>C maps to NM_005859.4 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:44924584 G>A maps to NM_033224.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:44924608 G>A maps to NM_033224.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:30889509 C>T maps to NM_013357.2 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:132426071 C>T maps to NM_025215.5 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:132426053 G>A maps to NM_025215.5 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr2:61188646 T>C maps to NM_144709.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:61188655 T>C maps to NM_144709.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:61236033 A>G maps to NM_144709.2 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr2:61238962 A>G maps to NM_144709.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:125763721 C>T maps to NM_031307.3 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:105148755 C>T maps to NM_019042.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:105135656 G>T maps to NM_019042.3 C258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:105111184 G>A maps to NM_019042.3 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:44148199 T>C maps to NM_031292.3 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:44130312 G>A maps to NM_031292.3 H532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:44136257 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:1244908 C>T maps to NM_153339.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:99818218 C>T maps to NM_024070.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:119547870 G>A maps to NM_002855.4 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:119535675 G>A maps to NM_002855.4 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:119549296 G>A maps to NM_002855.4 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:119549158 G>A maps to NM_002855.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:119549182 G>A maps to NM_002855.4 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:119535981 G>A maps to NM_002855.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:161044095 G>A maps to NM_030916.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:161049560 G>A maps to NM_030916.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:161043524 C>T maps to NM_030916.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:161044461 G>A maps to NM_030916.2 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:161044470 G>A maps to NM_030916.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:108105907 C>T maps to NM_007062.1 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr21:45535690 A>G maps to NM_005049.2 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:45548014 G>A maps to NM_005049.2 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:45540347 C>T maps to NM_005049.2 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:45544526 C>T maps to NM_005049.2 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:159507739 C>T maps to NM_052927.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:159520770 G>A maps to NM_001130864.1 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:134219344 G>A maps to NM_138499.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:134219557 C>T maps to NM_138499.3 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:134218324 G>A maps to NM_138499.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr10:134219455 C>T maps to NM_138499.3 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:134218972 G>A maps to NM_138499.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:134218924 C>T maps to NM_138499.3 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr2:1653280 G>A maps to NM_012293.1 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr2:1652392 G>A maps to NM_012293.1 Y1053Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:1647272 G>T maps to NM_012293.1 I1273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:1652617 G>T maps to NM_012293.1 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:1639281 A>G maps to NM_012293.1 L1406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:1639245 G>A maps to NM_012293.1 A1418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:1647287 C>T maps to NM_012293.1 T1268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:1652185 G>A maps to NM_012293.1 F1122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:1680705 G>A maps to NM_012293.1 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr2:1648499 G>A maps to NM_012293.1 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:1652212 G>T maps to NM_012293.1 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:1652557 A>G maps to NM_012293.1 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr2:1653316 G>A maps to NM_012293.1 D745D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:1652680 C>T maps to NM_012293.1 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:1648402 G>A maps to NM_012293.1 R1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:1652518 G>A maps to NM_012293.1 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:1652161 C>T maps to NM_012293.1 V1130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:1652752 G>A maps to NM_012293.1 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr2:1653280 G>T maps to NM_012293.1 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:1652326 C>T maps to NM_012293.1 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr8:52321636 G>A maps to NM_144651.4 H849H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:52321633 G>A maps to NM_144651.4 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:52366262 G>A maps to NM_144651.4 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:52252188 C>A maps to NM_144651.4 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr8:52321906 G>A maps to NM_144651.4 D759D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:52322008 C>T maps to NM_144651.4 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr8:52321768 G>A maps to NM_144651.4 H805H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:52321690 C>T maps to NM_144651.4 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:52384838 C>T maps to NM_144651.4 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:52384841 C>T maps to NM_144651.4 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:52323921 C>T maps to NM_144651.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:58380795 C>T maps to NM_017771.3 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:58376324 G>A maps to NM_017771.3 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:133281218 C>T maps to NM_018663.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:32298426 G>A maps to NM_007238.4 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:32298461 G>A maps to NM_007238.4 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:120660798 G>A maps to NM_001080855.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr16:31213513 G>A maps to NM_013258.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:31212944 C>T maps to NM_013258.4 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:79894021 G>A maps to ENST00000432920 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:79893245 G>A maps to ENST00000432920 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:226109704 G>A maps to NM_013328.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:144688645 G>A maps to NM_023078.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:144688645 G>A maps to NM_023078.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:144688309 G>A maps to NM_023078.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:31228271 C>T maps to NM_152901.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:191179226 T>C maps to NM_001083308.1 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:25261592 C>T maps to NM_002862.3 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:25257946 G>A maps to NM_002862.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:25258995 C>T maps to NM_002862.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr20:25261745 G>T maps to NM_002862.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:25277133 G>A maps to NM_002862.3 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:25239955 C>T maps to NM_002862.3 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr14:51383824 T>G did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr14:51383389 A>G maps to NM_002863.4 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr14:51401875 C>A maps to NM_002863.4 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:51382635 C>T maps to NM_002863.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:51376806 T>C maps to NM_002863.4 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr14:51383678 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:64521043 C>T maps to NM_005609.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:64518008 A>G maps to NM_005609.2 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:55838475 C>T maps to NM_015617.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr15:55841185 A>G maps to NM_015617.1 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:154932142 C>T maps to NM_138300.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:154931980 T>C maps to NM_138300.3 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:158914699 C>T maps to NM_152501.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:158911817 C>T maps to NM_152501.3 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:21614990 C>T maps to NM_024854.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:21602534 G>A maps to NM_024854.3 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:21605064 C>T maps to NM_024854.3 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:21620440 G>A maps to NM_024854.3 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr10:100150464 G>A maps to NM_032709.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr10:100154954 A>G maps to NM_032709.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:100167413 T>G did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:100155182 G>A maps to NM_032709.2 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:100146993 T>C maps to NM_032709.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:100147053 G>A maps to NM_032709.2 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:9318693 G>A maps to NM_002864.2 R738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:9301588 A>G maps to NM_002864.2 D1476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:9318784 T>G maps to NM_002864.2 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr12:9317803 G>A maps to NM_002864.2 Y806Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr12:9345297 G>T maps to NM_002864.2 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:3146841 T>C maps to NM_014731.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:3145153 C>T maps to NM_014731.2 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:3147674 G>T maps to NM_014731.2 A45A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr20:3147761 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr20:3145774 G>T maps to NM_014731.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr3:49139686 A>C maps to NM_005051.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr6:163899840 T>A maps to ENST00000361752 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:37594391 G>A maps to NM_012413.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:37586937 C>T maps to NM_012413.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:46198750 C>A maps to NM_017659.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr19:46195969 C>G maps to NM_017659.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:46206207 G>A maps to NM_017659.3 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:133769183 C>T maps to NM_198180.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:122257979 C>T maps to NM_198179.2 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:122250696 G>A maps to NM_198179.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:49114336 C>T maps to NM_198880.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:49084643 C>T maps to NM_198880.1 Q458Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:49094840 C>T maps to NM_198880.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr3:49094327 C>T maps to NM_198880.1 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:49084634 T>C maps to NM_198880.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:49083908 A>G maps to NM_198880.1 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:74300519 C>T maps to NM_032134.1 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:74278022 C>T maps to NM_032134.1 R1229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:74289676 G>A maps to NM_032134.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:74289745 T>C maps to NM_032134.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:74287392 G>A maps to NM_032134.1 R973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:74288686 C>T maps to NM_032134.1 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:32953932 G>T maps to NM_001076786.1 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:32953670 G>A maps to NM_001076786.1 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:32956106 A>G maps to NM_001076786.1 Q972Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:32976959 T>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:180155211 G>A maps to NM_002826.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:180165496 C>T maps to NM_002826.4 D523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:180165598 T>C maps to NM_002826.4 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:180163399 C>T maps to NM_002826.4 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:139113733 G>A maps to NM_181701.3 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr9:139100597 G>C maps to NM_181701.3 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:139100960 C>T maps to NM_181701.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:10823276 C>T maps to NM_031209.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr19:10812360 C>G maps to NM_031209.2 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:113798904 G>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:113795747 G>A maps to ENST00000485050 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:136389318 G>T maps to ENST00000409606 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:136473118 G>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:57674224 T>C maps to ENST00000438036 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:57660559 C>T maps to ENST00000438036 Q747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr20:42973988 G>A maps to NM_178491.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:42973913 A>G maps to NM_178491.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr2:26350777 C>T maps to NM_016131.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:8468312 G>A maps to NM_004218.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:37730003 C>T maps to NM_001002814.2 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:37729769 G>A maps to NM_001002814.2 D850D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:37730468 G>A maps to NM_001002814.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:37729778 G>A maps to NM_001002814.2 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr8:37730603 G>A maps to NM_001002814.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr8:37756944 G>C maps to NM_001002814.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:119798814 T>C maps to ENST00000369199 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:511441 C>T maps to NM_014700.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr16:539000 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:511423 C>T maps to NM_014700.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:29848366 G>A maps to NM_032932.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr17:29855753 C>T maps to NM_032932.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:29854862 G>A maps to NM_032932.3 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:29857480 C>T maps to NM_032932.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:29761109 C>T maps to NM_032932.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr2:73316187 G>C maps to NM_015470.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr2:73303282 G>A maps to NM_015470.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr18:8633207 A>G maps to NM_001025300.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:8638256 T>C maps to NM_001025300.2 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr11:66039635 G>A maps to NM_030981.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr13:111176518 G>T maps to NM_017817.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr13:111213749 G>A maps to NM_017817.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:56918854 A>G maps to NM_020673.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr20:56928594 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:56929304 A>G maps to NM_020673.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:56929277 C>T maps to NM_020673.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr6:57075033 G>A maps to NM_016277.3 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr5:176730060 G>A maps to NM_130781.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:156035831 C>T maps to NM_020387.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:55497749 C>T maps to NM_183235.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:52556536 C>T maps to NM_004163.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:13481135 C>T maps to NM_004249.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:21936839 G>A maps to NM_032846.3 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr14:21944702 G>A maps to NM_032846.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:82693313 G>A maps to NM_014488.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:146865141 C>T maps to NM_006834.3 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:129318541 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:129318512 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:129306238 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:129318300 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:129318569 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr4:140375543 G>T maps to NM_031296.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr17:27043057 G>T maps to NM_001144943.1 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:27041918 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:27042857 C>A maps to NM_001144943.1 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:27041903 C>A maps to NM_001144943.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:27043057 G>T maps to NM_001144943.1 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr12:120535068 G>A maps to NM_006861.6 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:23503093 C>T maps to NM_004914.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr11:107832830 T>C maps to NM_017516.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:107799500 G>A maps to NM_017516.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr11:107832701 A>T maps to NM_017516.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:154490448 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:154490315 G>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:154493485 C>T did not map to a codon.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr23:154493545 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:154490501 G>A did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:18313418 G>A maps to NM_002866.4 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr19:18311171 G>A maps to NM_002866.4 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:18313397 G>A maps to NM_002866.4 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:18311162 C>T maps to NM_002866.4 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:18309615 G>A maps to NM_002866.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:52385786 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:58120961 C>T maps to NM_138453.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:57913585 A>G maps to NM_138453.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:58147174 C>T maps to NM_138453.2 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:58021939 C>T maps to NM_138453.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:11447928 G>A maps to NM_004283.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:11446375 G>A maps to NM_004283.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:11446213 G>A maps to NM_004283.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:135848569 T>C maps to NM_001172435.1 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:135870726 G>A maps to NM_001172435.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:135848569 T>C maps to NM_001172435.1 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:135926269 G>A maps to NM_001172435.1 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:220345284 C>T maps to ENST00000358951 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:220363813 A>G maps to ENST00000358951 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:220324706 T>C maps to ENST00000358951 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr1:220366600 A>G maps to ENST00000358951 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:220356237 T>C maps to ENST00000358951 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:220369672 T>C maps to ENST00000358951 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:61672091 C>T maps to NM_013401.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:61675531 C>T maps to NM_013401.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:70149410 T>C maps to NM_175623.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:102755663 G>A did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:102755053 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:102755235 A>G did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:102755045 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:102754894 T>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:102192885 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:102192724 A>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:677597 G>A maps to NM_021168.4 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:69502189 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:69503871 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:128813921 C>T maps to ENST00000418265 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:128840317 G>A maps to NM_198490.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:229422272 T>C maps to NM_004578.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:229438687 C>T maps to NM_004578.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr1:229438702 C>T maps to NM_004578.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr3:20017627 C>T maps to NM_004162.4 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:133557072 G>A maps to NM_016577.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:133558432 C>T maps to NM_016577.3 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:133553464 C>T maps to NM_016577.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr3:133553467 C>A maps to NM_016577.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr3:133583486 C>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:130738405 T>C maps to NM_032144.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:130738413 G>A maps to NM_032144.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr19:16243038 G>A maps to NM_005370.4 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:63551863 C>T maps to NM_016530.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:13726918 T>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:103080450 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:103080411 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:103080512 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:5250182 G>A maps to NM_004703.4 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:5238640 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr17:5264576 C>T maps to NM_004703.4 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:5264840 G>A maps to NM_004703.4 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:28925565 C>T maps to NM_024816.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:28931232 G>A maps to NM_024816.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:28919998 C>T maps to NM_024816.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:127982923 C>T maps to NM_005833.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr9:127990210 A>G maps to NM_005833.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:127975682 C>T maps to NM_005833.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:125758388 C>A maps to NM_012197.3 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr9:125863927 T>A maps to NM_012197.3 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:125758823 T>C maps to NM_012197.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr9:125748608 C>G maps to NM_012197.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:174671282 T>C maps to NM_014857.3 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:174606592 A>T maps to NM_014857.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:174188348 T>G maps to NM_014857.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:24738721 G>A maps to NM_182836.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:24737782 G>A maps to NM_182836.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:24738900 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:24740153 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:76259893 A>G maps to NM_004582.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:76256991 T>C maps to NM_004582.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr1:76257945 T>A maps to NM_004582.2 C220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr1:202850309 G>A maps to NM_002871.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr2:114399636 C>T maps to ENST00000409875 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:51214268 G>A maps to NM_001130923.1 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:100958510 A>G maps to NM_022777.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:6442040 C>T maps to NM_018890.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:6442040 C>T maps to NM_018890.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:79991662 G>A maps to NM_005052.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:50386087 G>C maps to NM_013277.3 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:50399109 G>A maps to NM_013277.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:50410413 G>A maps to NM_013277.3 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:50410413 G>A maps to NM_013277.3 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:68687698 A>T maps to NM_133339.1 K361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:68687757 A>G maps to NM_133339.1 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:8983300 C>A maps to NM_020165.3 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:9000664 C>T maps to NM_020165.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:117859878 G>A maps to NM_006265.2 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:117866579 C>T maps to NM_006265.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr19:13059067 G>A maps to NM_005053.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:131953825 C>T maps to NM_005732.3 R1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:131931337 C>T maps to NM_005732.3 C681C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:131939123 T>C maps to NM_005732.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:4654959 T>A maps to NM_001130862.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:17697057 T>C maps to NM_001099218.2 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:17697216 A>G maps to NM_001099218.2 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:17699598 G>T maps to NM_001099218.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:17697945 T>C maps to NM_001099218.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:17696565 A>G maps to NM_001099218.2 N1039N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:17698683 T>C maps to NM_001099218.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr2:17697693 C>T maps to NM_001099218.2 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr17:56772407 C>T maps to NM_058216.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr17:33428243 C>T maps to NM_002878.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:1025612 C>T maps to NM_134424.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:1025528 C>T maps to NM_134424.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:1038989 G>A maps to NM_134424.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:1036390 A>G maps to NM_134424.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:1034618 G>A maps to NM_134424.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:95470610 G>A maps to NM_012415.2 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:46726526 C>T maps to NM_003579.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:51664312 C>T maps to NM_015106.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr12:110943578 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr12:110957713 C>T maps to NM_152442.3 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:4871776 C>T maps to NM_018059.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:4856941 G>A maps to NM_018059.4 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:4855940 C>T maps to NM_018059.4 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:4841380 C>A maps to NM_018059.4 G915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:4856878 A>G maps to NM_018059.4 Y573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr7:4841614 G>A maps to NM_018059.4 H837H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr20:55942075 C>T maps to NM_001015885.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr20:55949844 C>T maps to NM_001015885.1 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:55948535 G>A maps to NM_001015885.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:150210619 A>G maps to NM_139165.1 H162H. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:150211122 T>C does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr6:150210685 G>A maps to NM_139165.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:150210637 G>T maps to NM_139165.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:12632427 T>G maps to ENST00000415519 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:12626628 G>A maps to ENST00000415519 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:12660190 C>T maps to ENST00000415519 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:36595309 G>A maps to NM_000448.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:36596056 G>A maps to NM_000448.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:36597478 C>T maps to NM_000448.2 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr11:36595300 T>G maps to NM_000448.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr11:36596998 G>C maps to NM_000448.2 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:36596863 G>A maps to NM_000448.2 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:155108810 G>T maps to NM_018845.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:155108816 C>T maps to NM_018845.3 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr11:36615565 C>T maps to NM_000536.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:102695910 C>T maps to NM_014226.1 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:102695952 T>C maps to NM_014226.1 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:17698481 C>T maps to ENST00000395776 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:17700168 A>T maps to ENST00000395776 K1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:17698551 G>T maps to ENST00000395776 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:17700155 C>T maps to ENST00000395776 P1298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:17700539 C>T maps to ENST00000395776 T1426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:17701058 G>A maps to ENST00000395776 V1599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:17699660 A>G maps to ENST00000395776 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:17697947 C>T maps to ENST00000395776 D562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:17699711 C>A maps to ENST00000395776 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:34824013 C>T maps to NM_001145521.1 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:34814722 G>A maps to NM_001145521.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr5:34811166 C>A maps to NM_001145521.1 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:34823884 C>T maps to NM_001145521.1 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:34823323 C>T maps to NM_001145521.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:34821835 G>A did not map to a codon.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr23:17819535 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:17818800 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:17819374 C>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:17818710 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:17818710 C>T did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr18:9530857 G>A maps to NM_006788.3 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr18:9535907 C>T maps to NM_006788.3 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:36194348 G>A maps to NM_194301.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:36147153 G>A maps to ENST00000258840 G1083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:36096543 C>T maps to NM_194301.2 Q1697Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GU-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr20:20621417 G>A maps to NM_020343.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr20:37144918 G>A maps to NM_020336.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:37121577 A>G maps to NM_020336.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:135982603 C>T maps to NM_006266.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr9:135978248 C>T maps to NM_006266.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:135982537 G>A maps to NM_006266.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:135974123 G>A maps to NM_006266.2 N865N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:135978615 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:129740005 T>C maps to NM_014636.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr9:129981047 A>G maps to NM_014636.2 *558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:178854242 C>T maps to NM_152663.3 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:178861407 C>T maps to NM_152663.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:178745913 C>T maps to NM_152663.3 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:32660017 C>A maps to NM_016732.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:32660005 C>T maps to NM_016732.1 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:32664876 C>T maps to NM_016732.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:85799873 C>T maps to NM_001100391.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:45216980 C>T maps to NM_005856.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:67763352 C>T maps to NM_020850.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:67763896 G>A maps to NM_020850.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:67763280 G>C maps to NM_020850.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:67763601 A>G maps to NM_020850.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:67768879 C>T maps to NM_020850.1 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:67771936 A>G maps to NM_020850.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:170346618 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:109382685 A>G maps to NM_006267.4 G1897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:109380501 T>C maps to NM_006267.4 G1169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:109388155 G>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:109374883 T>C maps to NM_006267.4 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:109380975 A>G maps to NM_006267.4 T1327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:109382508 A>G maps to NM_006267.4 G1838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:109381657 C>T maps to NM_006267.4 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:109347833 G>A maps to NM_006267.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:109382946 T>C maps to NM_006267.4 G1984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:109367741 T>C maps to NM_006267.4 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:109381509 G>A maps to NM_006267.4 P1505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:109379766 G>A maps to NM_006267.4 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr2:109384038 A>G maps to NM_006267.4 Q2348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:5917973 T>C maps to NM_007322.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:5923222 C>T maps to NM_007322.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:36257607 C>T maps to NM_001161429.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:6012697 G>T maps to NM_012416.2 T970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:6015586 T>C maps to NM_012416.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr9:6012436 C>T maps to NM_012416.2 E1057E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:13634705 G>A maps to NM_005493.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr6:13644913 G>A maps to NM_005493.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:13644898 C>T maps to NM_005493.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:41645452 A>G maps to NM_002883.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr22:41676937 A>G maps to NM_002883.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:41676982 C>T maps to NM_002883.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:41650491 G>A maps to NM_002883.2 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:41650404 T>C maps to NM_002883.2 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:8192689 G>A maps to NM_016492.4 W103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:112247109 T>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:21926079 C>T maps to NM_001145658.1 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:21937953 G>A maps to NM_001145658.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:21929358 C>T maps to NM_001145658.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:21938055 G>A maps to NM_001145658.1 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:2901576 G>A maps to NM_015085.4 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:2867363 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:2923871 C>T maps to NM_015085.4 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:99313169 C>T maps to NM_001100426.1 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:99300201 T>C maps to NM_001100426.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:98116605 C>T maps to NM_021033.6 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:131348296 A>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:131351263 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:131348327 A>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:134459790 C>T maps to NM_198679.1 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:134501509 G>A maps to NM_198679.1 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:160260431 T>C maps to NM_014247.2 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:160268151 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:48132502 T>C maps to NM_001098531.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:173852993 C>T maps to NM_007023.3 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:173891822 T>A maps to NM_007023.3 Y798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:173782535 C>T maps to NM_007023.3 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr2:173894948 C>T maps to NM_007023.3 N872N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:22206737 C>T maps to ENST00000344041 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:22176550 T>G maps to ENST00000344041 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:130764880 G>A maps to ENST00000514667 D1548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:130846112 G>A maps to ENST00000514667 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr5:130828378 G>A maps to ENST00000514667 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:130782199 G>A maps to ENST00000514667 Q1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:204304284 G>A maps to ENST00000374493 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr2:204354396 G>A maps to ENST00000374493 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:204305380 C>T maps to ENST00000374493 Q896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr2:204334976 A>G maps to ENST00000374493 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:204320200 G>A maps to ENST00000374493 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:47470378 C>T maps to NM_005055.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:38499006 G>T maps to NM_001024809.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:38487580 G>A maps to NM_001145301.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:38511644 T>C maps to NM_001145301.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:25637959 A>G maps to NM_000965.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr3:25611285 T>G maps to NM_000965.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr12:53607424 C>T maps to NM_000966.4 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr12:53621230 G>A maps to NM_000966.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:63313628 G>A maps to NM_004585.3 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:167929051 A>G maps to NM_002887.3 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:88239290 G>A maps to NM_020320.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:88228427 G>A maps to NM_020320.3 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:86659207 T>C maps to NM_002890.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:86629107 C>T maps to NM_002890.1 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:86674343 C>T maps to NM_002890.1 Q826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr5:86629107 C>T maps to NM_002890.1 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr5:86672328 C>T maps to NM_002890.1 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr3:141305574 C>T maps to ENST00000452898 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:141295905 C>T maps to ENST00000452898 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:141327407 C>T maps to ENST00000452898 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:141292020 T>C maps to ENST00000452898 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:141289864 C>T maps to ENST00000452898 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr13:114780805 C>T maps to ENST00000389544 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr13:114762185 C>T maps to ENST00000389544 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:114781735 G>A maps to ENST00000389544 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:114762032 C>T maps to ENST00000389544 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:114751162 G>A maps to ENST00000389544 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:114773058 C>T maps to ENST00000389544 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:113545987 G>A maps to NM_001193520.1 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:113541992 C>T maps to NM_001193520.1 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:113543653 C>T maps to NM_001193520.1 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr12:113543593 C>T maps to NM_001193520.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:113542070 G>A maps to NM_001193520.1 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr1:178414759 C>T maps to ENST00000263528 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:178414798 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:178427091 C>T maps to ENST00000263528 Q878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:178411821 C>T maps to ENST00000263528 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:178412039 G>A maps to ENST00000263528 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:17399357 G>A maps to NM_016084.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:35947712 C>T maps to NM_014310.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:85607892 A>T maps to NM_152573.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:85677650 C>T maps to NM_152573.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:85613287 A>G maps to NM_152573.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:43692442 C>T maps to ENST00000374459 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr4:82355018 G>A maps to NM_152545.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:82355837 A>G maps to NM_152545.1 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:179564615 G>A maps to NM_175062.3 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:179565046 T>C maps to NM_175062.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr5:179529123 G>A maps to NM_175062.3 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:179555580 T>C maps to NM_175062.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:179529138 A>C maps to NM_175062.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:79382810 G>A maps to NM_002891.4 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:79356790 G>A maps to NM_002891.4 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:79288102 C>T maps to NM_002891.4 T1018T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr15:79356826 G>T maps to NM_002891.4 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr15:79284094 G>C maps to NM_002891.4 A1039A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:79317733 G>A maps to NM_002891.4 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:79296390 T>C maps to NM_002891.4 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:79323836 G>A maps to NM_002891.4 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:79296444 G>A maps to NM_002891.4 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:80521543 G>A maps to NM_006909.1 T1223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:80382665 T>C maps to NM_006909.1 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:80381688 A>G maps to NM_006909.1 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:80363868 T>C maps to NM_006909.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:80382674 C>T maps to NM_006909.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:80497153 C>T maps to NM_006909.1 F933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:80513293 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:80513293 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr5:80369247 C>T maps to NM_006909.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr5:80497153 C>T maps to NM_006909.1 F933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:38811573 T>C did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:38786606 C>T maps to NM_005739.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr15:38786939 A>T maps to NM_005739.3 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr15:38811508 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:64504343 G>T maps to ENST00000320253 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:64508433 G>A maps to ENST00000320253 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:64507149 C>T maps to ENST00000320253 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr2:33747138 T>C maps to NM_170672.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:38910888 G>A maps to ENST00000405332 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:49227758 G>A maps to NM_017805.2 G793G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr17:34068086 C>T maps to NM_033315.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:34068170 C>T maps to NM_033315.3 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:34068068 A>G maps to NM_033315.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr13:27847279 C>T maps to NM_206827.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:53728802 C>T maps to NM_023940.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:53728733 G>A maps to NM_023940.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:50368023 G>A maps to NM_170714.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:4771162 C>T maps to NM_014737.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:65085253 C>T maps to NM_178169.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:74442416 C>T maps to NM_201431.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr12:26217558 C>T maps to NM_001164747.1 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:26217572 G>A maps to NM_001164747.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr12:26217701 G>T maps to NM_001164747.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:86198791 A>G maps to NM_005447.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr12:86199379 G>A maps to NM_005447.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:10428997 G>A maps to NM_133452.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:65272887 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:65247061 G>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:65296656 C>T maps to ENST00000294428 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr18:56939700 C>T maps to NM_013435.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:48955537 C>T maps to NM_000321.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:48936982 C>T maps to NM_000321.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr13:48919317 C>G maps to NM_000321.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:53569952 T>A maps to NM_014781.4 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:53568773 G>A maps to NM_014781.4 Y1205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:53596198 C>T maps to NM_014781.4 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:53569169 T>C maps to NM_014781.4 E1073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:5097397 C>T maps to NM_021163.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:5104754 A>G maps to NM_021163.3 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:5103476 A>G maps to NM_021163.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:205066018 G>C maps to NM_005057.3 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:205069380 C>T maps to NM_005057.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:24578544 A>T maps to NM_006910.4 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:24581094 G>A maps to NM_006910.4 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr16:24581589 G>A maps to NM_006910.4 R1193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:24578676 T>C maps to NM_006910.4 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr16:24582620 G>T maps to NM_006910.4 E1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:24578826 G>T did not map to a codon.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr23:16870201 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:16870946 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:16870925 G>A did not map to a codon.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr23:16870930 T>G did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:16876865 G>A did not map to a codon.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr23:16876897 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:16871810 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr23:16887281 A>C did not map to a codon.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr18:20529655 C>A maps to ENST00000360790 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:18477805 A>C maps to NM_006606.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:409611 C>T maps to NM_031229.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:409196 C>T maps to NM_031229.2 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:400113 T>C did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr20:402812 G>A maps to NM_031229.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:409695 C>A maps to NM_031229.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:28065936 C>A maps to NM_022128.1 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:28081320 C>T maps to NM_022128.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:35635936 A>G maps to NM_002895.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr20:35663899 A>G maps to NM_002895.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:35661169 A>G maps to NM_002895.2 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr20:35632269 C>G did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:53488588 T>C maps to NM_005611.3 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:53504298 T>C maps to NM_005611.3 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:53493430 G>A maps to NM_005611.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:53524073 A>C maps to NM_005611.3 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:47044602 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:47045754 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:47045525 A>G did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:47030563 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:47044481 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47041357 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47044456 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:47040963 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:47030547 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:47044526 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:47028857 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:47038779 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:47030578 G>T did not map to a codon.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr23:47030584 T>G did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr21:15599580 G>A maps to NM_144770.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:34241966 A>G maps to NM_001198838.1 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:34242788 T>C maps to NM_001198838.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:34240844 G>A maps to NM_001198838.1 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:34241113 C>A maps to NM_001198838.1 G711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:34241147 A>G maps to NM_001198838.1 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr20:34243148 G>A maps to NM_001198838.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:94746561 G>A maps to NM_203390.2 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:94747360 A>G maps to NM_203390.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:94746565 C>T maps to NM_203390.2 W691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:94746631 C>T maps to NM_203390.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:94746310 C>T maps to NM_203390.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:94745758 A>G maps to NM_203390.2 N960N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr8:94746334 T>C maps to NM_203390.2 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr8:94746348 T>G maps to NM_203390.2 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66393065 G>A maps to NM_006328.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:110883025 C>T maps to NM_022768.4 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:110883439 G>A maps to NM_022768.4 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:110884618 T>C maps to NM_022768.4 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:110884270 C>A maps to NM_022768.4 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:51430881 C>T maps to NM_013286.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr3:51430425 G>A maps to NM_013286.4 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:155153802 T>C maps to NM_014892.3 P1030P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:155114028 T>C maps to NM_014892.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:155114111 T>C did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:155141393 G>A maps to NM_014892.3 W573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:155095206 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:155136914 C>T maps to NM_014892.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr6:155153259 A>T maps to NM_014892.3 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:125009819 G>A maps to NM_033117.3 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:125009819 G>A maps to NM_033117.3 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:114364872 C>A maps to NM_016196.3 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:114296673 G>A maps to NM_016196.3 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:114397938 G>A maps to NM_016196.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr12:114395628 C>T maps to NM_016196.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:114352802 G>T maps to NM_016196.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:150075216 T>C maps to NM_018047.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr14:73572629 G>A maps to NM_021239.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr14:73577558 G>A maps to NM_021239.2 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr13:79940816 G>A maps to ENST00000438737 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:145631337 G>A maps to NM_018989.1 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:127964663 C>T maps to NM_018077.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:127955003 G>A maps to NM_018077.2 Q620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:127958072 G>A maps to NM_018077.2 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr23:48433595 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:48434785 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:155473529 G>A maps to NM_053043.2 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:66411053 C>T maps to NM_001198845.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66411053 C>A maps to NM_001198845.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:66411374 A>T maps to NM_001198845.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:66410969 C>T maps to NM_001198845.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:66407487 T>C maps to NM_002896.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:106312574 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:106331798 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:106358697 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr23:106358655 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:106358656 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:36124837 C>T maps to NM_024321.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:36124821 C>T maps to NM_024321.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:238726138 G>T maps to NM_001080504.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:178977344 C>T maps to ENST00000456670 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:178982856 C>T maps to ENST00000456670 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr4:155719398 T>C maps to NM_144979.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:155720282 T>C maps to NM_144979.3 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr4:155720606 T>C maps to NM_144979.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:40440532 G>A maps to NM_001098634.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:40440328 G>A maps to NM_001098634.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr4:40428121 G>A maps to NM_001098634.1 N527N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr4:40438456 C>T did not map to a codon.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr4:40439968 C>T maps to NM_001098634.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:40440379 G>A maps to NM_001098634.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:66436472 C>T maps to NM_031492.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:66436178 G>A maps to NM_031492.2 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:66436259 T>C maps to NM_031492.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr3:50148181 C>G maps to NM_005778.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:50106122 C>T maps to NM_005777.2 Q982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:50005641 C>T maps to NM_005777.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:36140244 C>T maps to ENST00000338644 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:36140272 G>A maps to NM_001082578.1 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:161349808 C>T maps to NM_016836.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr2:161174692 C>T maps to NM_016836.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:161141507 G>A maps to NM_016836.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:161223761 G>A maps to NM_016836.3 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:161135064 G>A maps to NM_016836.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:56962789 C>T maps to NM_002898.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:56956202 A>G maps to NM_002898.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:29925681 A>G maps to NM_001003793.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:29910398 C>T maps to NM_001003793.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:135956573 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:135961489 G>A did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:135960229 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:135958812 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:135956552 A>T did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:135957301 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:129546423 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:129546772 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:129546424 G>A did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:129545433 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:129546412 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:129546641 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:89449291 G>T maps to NM_019610.5 S73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr1:89448732 G>T maps to NM_019610.5 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:89448606 C>T maps to NM_019610.5 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:7111247 G>A maps to NM_014469.4 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:7111247 G>A maps to NM_014469.4 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:7111337 T>C maps to NM_014469.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr11:7111073 C>T maps to NM_014469.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:7111028 C>T maps to NM_014469.4 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:7111247 G>A maps to NM_014469.4 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:7111133 C>T maps to NM_014469.4 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr11:7110410 C>T maps to NM_014469.4 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr11:7111052 G>A maps to NM_014469.4 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr3:139236483 G>A maps to NM_002899.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:139173609 G>A maps to NM_004164.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:48389188 T>C maps to NM_002900.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:48382207 C>T maps to NM_002900.2 T1147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr10:48390214 G>A maps to NM_002900.2 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr10:48388252 G>A maps to NM_002900.2 G875G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr10:48390460 C>T maps to NM_002900.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr10:48389992 C>T maps to NM_002900.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:48390034 G>A maps to NM_002900.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:48388657 G>A maps to NM_002900.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:7280856 G>A maps to NM_031491.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:26407806 C>T maps to NM_005349.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:26431566 C>T maps to NM_005349.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr4:26431566 C>T maps to NM_005349.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:26426077 G>A maps to NM_005349.2 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:26431566 C>T maps to NM_005349.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:26430437 A>C maps to NM_005349.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:26364238 G>A maps to NM_203284.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr4:26407802 T>G maps to NM_005349.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:43940865 C>T maps to NM_014276.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:43945394 C>T maps to NM_014276.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:30402080 G>A maps to NM_001008712.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:65040632 G>A maps to NM_194272.1 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr15:65041331 G>A maps to NM_194272.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:41360109 G>T maps to NM_014248.3 G73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:173912740 T>G maps to NM_172071.2 R992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:173953745 C>T maps to NM_172071.2 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:173934065 C>T maps to NM_172071.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:173950009 C>T maps to NM_172071.2 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:173915727 T>C maps to NM_172071.2 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:125627677 G>A maps to NM_001100588.1 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:125618009 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr13:50125517 T>C maps to NM_018191.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:50108307 G>A maps to NM_018191.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:49084817 A>G maps to NM_001268.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr13:49089852 A>G maps to NM_001268.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:49084762 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr13:49076917 A>G maps to NM_001268.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr13:49084828 G>A maps to NM_001268.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:28864476 C>T maps to NM_001048194.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:28862497 C>T maps to NM_001048194.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:28856392 C>T maps to NM_001048194.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:28863316 T>C maps to NM_001048194.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:17743116 G>A maps to NM_018715.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:17747225 A>G maps to NM_018715.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91504965 C>A maps to NM_033544.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:66613484 G>A maps to NM_005133.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:4793105 G>A maps to NM_005772.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:32119956 T>C maps to NM_002901.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr11:32118797 C>T maps to NM_002901.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:77236172 T>C maps to ENST00000320963 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:103187411 A>G maps to NM_015156.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr14:103180948 C>T maps to NM_015156.2 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:63681569 G>A maps to NM_173587.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:63680356 T>A maps to NM_173587.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:211486763 A>G did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:211486764 G>C did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:167653174 G>A maps to NM_052862.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr1:167666868 A>C maps to NM_052862.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:9808170 G>A maps to NM_002903.2 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:9808263 G>A maps to NM_002903.2 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:9801417 G>A maps to NM_002903.2 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:211654645 G>A maps to NM_183059.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:211652455 G>A maps to NM_183059.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:31924610 T>C maps to ENST00000375425 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr14:68159191 A>G maps to NM_016026.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:68157058 G>A maps to NM_016026.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:55568078 C>T maps to NM_001145971.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:55556594 C>T maps to NM_001145971.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:55559832 G>T maps to NM_001145971.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:55570576 C>T maps to NM_001145971.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:18737023 G>A maps to ENST00000444297 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr12:57351063 C>T maps to NM_003708.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:56118265 A>C maps to NM_002905.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr19:10129584 G>A maps to NM_015725.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:34251626 A>G maps to NM_145654.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:34251607 C>A maps to NM_145654.3 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:110128523 A>C maps to ENST00000405097 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:24642218 C>T maps to NM_005132.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:24641957 C>T maps to NM_005132.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:36117104 C>T maps to NM_021111.2 H728H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:36122900 T>C maps to NM_021111.2 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr9:36083482 C>T maps to NM_021111.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:36109987 C>T maps to NM_021111.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:21628510 C>T maps to NM_032941.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:21628711 A>G maps to NM_032941.2 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr12:21627836 C>A maps to NM_032941.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr12:21644546 T>C maps to NM_032941.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:21624485 G>A maps to NM_032941.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:145742064 C>T maps to ENST00000428558 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr17:73625285 G>A maps to NM_004259.5 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:73626706 G>A maps to NM_004259.5 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:73627304 G>A maps to NM_004259.5 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:86481833 G>A maps to NM_022912.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:137781023 A>G maps to ENST00000378339 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr5:137781274 G>A maps to ENST00000378339 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:137780981 C>T maps to ENST00000378339 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr8:21997517 A>C maps to NM_025232.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:21996020 C>T maps to NM_025232.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:21997009 C>T maps to NM_025232.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:112222850 C>T maps to NM_005669.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:79314000 G>T maps to NM_006507.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:120341117 A>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:61144152 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:61145338 T>C maps to NM_002908.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:61118863 G>A maps to NM_002908.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:65429464 C>T maps to NM_021975.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:65429434 A>G maps to NM_021975.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:65425908 A>G maps to NM_021975.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:65422381 G>A maps to NM_021975.3 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:65422376 G>T maps to NM_021975.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:65426294 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:45525309 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:45528940 C>T maps to ENST00000221452 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:45515293 G>A maps to ENST00000221452 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:45515293 G>A maps to ENST00000221452 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:45515422 G>A maps to ENST00000221452 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr19:45515503 C>T maps to ENST00000221452 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:37651072 C>T maps to NM_001085399.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:37636636 G>A maps to NM_001085399.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:37636678 C>T maps to NM_001085399.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr4:37636636 G>A maps to NM_001085399.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:103629617 C>T maps to ENST00000428762 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:103293014 C>T maps to ENST00000428762 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr7:103294586 T>G maps to ENST00000428762 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:103293020 A>G maps to ENST00000428762 C580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:103113284 G>A maps to ENST00000428762 R3453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr7:103275918 A>G maps to ENST00000428762 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:103243937 C>A did not map to a codon.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr7:103155635 A>C maps to ENST00000428762 T2705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:103191602 G>A maps to ENST00000428762 T2071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:103338446 A>G maps to ENST00000428762 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:103230146 G>A maps to ENST00000428762 C1347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:103234872 G>A maps to ENST00000428762 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr7:103290822 G>A maps to ENST00000428762 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:103393638 G>A maps to ENST00000428762 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr7:103338414 C>T maps to ENST00000428762 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:73106158 G>A maps to NM_152222.1 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:73105599 G>A maps to NM_152222.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:73106269 G>T maps to NM_152222.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:73106533 T>C maps to NM_152222.1 *431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:73103472 G>A maps to NM_152222.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:30065685 C>T maps to NM_014012.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr20:30064400 C>T maps to NM_014012.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:30072049 C>T maps to NM_014012.4 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr1:204131140 G>A maps to NM_000537.3 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:204131188 C>T maps to NM_000537.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:204124194 G>A maps to NM_000537.3 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:204125410 G>A maps to NM_000537.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153207101 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153209856 T>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:153209077 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr23:153208372 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153208353 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:27850002 G>T maps to NM_001029874.1 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:150069775 C>T maps to NM_001099695.1 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr7:150066880 C>T maps to NM_001099695.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:150069805 C>T maps to NM_001099695.1 C549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:150068726 C>T maps to NM_001099695.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr7:150068854 G>A maps to NM_001099695.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:139241370 G>A maps to ENST00000367663 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr6:139251227 C>T maps to ENST00000367663 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:139235872 G>T maps to ENST00000367663 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:139266649 A>G maps to ENST00000367663 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:17156995 A>G did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:17080601 T>C did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:17024428 A>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:17092243 C>T did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr23:17073007 G>A did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:17153479 A>C did not map to a codon.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr23:17153510 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:17047708 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:17157019 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:8425884 C>T maps to NM_012102.3 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:8420773 C>T maps to NM_012102.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:8416190 G>A maps to NM_012102.3 H1485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:8419853 T>C maps to NM_012102.3 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:8418811 C>T maps to NM_012102.3 R1261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:8482842 G>A maps to NM_012102.3 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:8415660 T>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:15262150 G>A maps to NM_032918.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:15264337 T>C maps to NM_032918.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr12:15262279 A>G maps to NM_032918.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr12:15264289 G>A maps to NM_032918.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr4:57797538 G>T maps to NM_005612.4 E839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:43608349 C>T maps to NM_020975.4 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr10:43615632 C>G maps to NM_020975.4 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:43600616 C>T maps to NM_020975.4 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:43615132 C>T maps to NM_020975.4 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr10:43600607 C>T maps to NM_020975.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:43606911 A>G maps to NM_020975.4 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:7735135 C>T maps to NM_020415.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:7735186 C>T maps to NM_020415.3 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr2:85576704 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:100055711 A>G maps to NM_016316.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:111695099 A>G maps to NM_002912.3 F1486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr6:111685109 A>C maps to NM_002912.3 T2275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr6:111696719 A>T maps to NM_002912.3 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:111672876 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:111688942 G>A maps to NM_002912.3 Y2016Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:111697072 G>T maps to NM_002912.3 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:111709116 C>A did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr6:111652932 A>G maps to NM_002912.3 L2660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:111643875 G>A maps to NM_002912.3 G2749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:111701366 A>G maps to NM_002912.3 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:111695977 G>A maps to NM_002912.3 R1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:111695519 A>G maps to NM_002912.3 F1346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:111695846 A>G maps to NM_002912.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:111694064 G>A maps to NM_002912.3 D1831D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:1827533 C>T maps to NM_020695.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:1827734 C>T maps to NM_020695.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr19:1816465 G>A maps to NM_020695.3 I1140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:1828586 G>A maps to NM_020695.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr19:1820355 G>T maps to NM_020695.3 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:1826906 C>T maps to NM_020695.3 K627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:39290443 C>T maps to ENST00000381897 K1128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:39310256 G>A maps to ENST00000381897 H628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:39301995 T>C maps to ENST00000381897 G859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:39297316 G>T maps to ENST00000381897 T958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:39306530 G>A maps to ENST00000381897 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:73666757 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:73646516 C>T maps to NM_181471.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:34409329 T>C maps to NM_002915.3 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:34404129 T>G maps to NM_002915.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:118467595 C>T maps to NM_007370.4 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:33348713 T>C maps to NM_001017368.1 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:29837921 C>T maps to NM_021026.2 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:32587175 G>A maps to NM_001098527.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr22:32589216 A>G maps to NM_006605.3 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr22:32587232 G>A maps to NM_001098527.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr22:32586770 C>A maps to NM_001098527.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:32754282 T>C maps to NM_001098535.1 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:112671188 T>C maps to NM_001013734.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:16358729 G>A maps to NM_015150.1 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:16535298 A>G maps to NM_015150.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:16358499 G>A maps to NM_015150.1 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:16419243 A>G maps to NM_015150.1 H269H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D7-A6EY-01A-21D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr3:16475456 G>T maps to NM_015150.1 S78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr3:16399519 G>T maps to NM_015150.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:198540104 C>T maps to NM_144629.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:198511370 G>T maps to NM_144629.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:198436899 C>T maps to NM_144629.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:198498532 G>A maps to NM_144629.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:175956140 G>A maps to NM_022457.5 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:176118176 C>A maps to NM_022457.5 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:176012320 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr16:74670376 C>T maps to NM_018124.3 Q431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:14074438 G>A maps to NM_002918.4 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:14074061 G>A maps to NM_002918.4 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:14090270 G>A maps to NM_002918.4 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:6040185 G>A maps to NM_000635.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:5997112 G>A maps to NM_000635.3 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:6047471 C>T maps to NM_000635.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr19:6040128 G>A maps to NM_000635.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:6040095 G>A maps to NM_000635.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:6042052 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:3225155 G>A maps to NM_134428.1 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:3257055 G>T maps to NM_134428.1 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:3293098 G>A maps to NM_134428.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:107103143 G>T maps to ENST00000357881 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:107155090 C>T maps to ENST00000357881 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:106995083 G>A maps to ENST00000357881 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:151314728 A>T maps to NM_000449.3 L595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:151314769 T>C maps to NM_000449.3 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:117240335 G>A maps to NM_173560.3 W353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:117198977 T>C maps to NM_173560.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:56386814 G>A maps to NM_022841.5 D1037D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr15:56388647 C>T maps to NM_022841.5 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:56388134 G>A maps to NM_022841.5 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:56386688 G>A maps to NM_022841.5 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:56387072 T>C maps to NM_022841.5 T951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:37401882 C>A maps to NM_000538.3 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr3:101283801 A>G maps to NM_017819.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:100479325 T>C maps to NM_001134666.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:37763750 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:37768226 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:109695399 G>T did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:109697339 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:109697462 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:109696604 T>C did not map to a codon.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr23:109695525 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:109694907 C>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:109696505 A>G did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:109696913 T>G did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:109695154 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:109696170 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr23:109697185 C>T did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr23:109694939 A>G did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:109695008 G>T did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr23:109696086 T>A did not map to a codon.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr23:109696364 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:109694181 C>T did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:109695147 G>A did not map to a codon.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr23:71350835 G>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:71350735 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:71349877 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:71350380 T>C did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:71351349 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:71349752 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:71349919 C>T did not map to a codon.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr23:71349891 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:71349879 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr23:71349769 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:71350665 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:71351314 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:183885735 G>A maps to NM_015149.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr6:33263367 C>A maps to NM_004761.3 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr6:33260018 G>A maps to NM_004761.3 Q732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:33262518 G>A maps to NM_004761.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:93595501 C>T maps to NM_020211.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr15:93588401 G>A maps to NM_020211.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:98129123 C>T maps to NM_001012761.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:98115290 C>T maps to NM_001012761.2 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr5:98128976 C>A maps to NM_001012761.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr5:98128787 G>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:46943849 C>T did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:46949184 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:46951101 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:73069725 C>T maps to NM_001080479.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr5:73205301 C>T maps to NM_001080479.2 G1409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:73045774 C>T maps to NM_001080479.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:73048779 G>A maps to NM_001080479.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:73163797 A>T maps to NM_001080479.2 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:73205326 C>T maps to NM_001080479.2 R1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:73169026 A>C maps to NM_001080479.2 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:35750329 G>A maps to ENST00000456972 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:35751681 T>C maps to ENST00000456972 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr2:107041103 T>A maps to ENST00000304514 K1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:107074108 G>A maps to ENST00000304514 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr2:107041485 A>C maps to ENST00000304514 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr2:108477253 A>G maps to NM_182588.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr2:108488779 A>G maps to NM_182588.2 K1440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:108487645 A>G maps to NM_182588.2 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr2:108479239 C>T maps to NM_182588.2 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:113146042 T>C maps to NM_005054.2 V1493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:86012655 C>T maps to ENST00000358110 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr10:86008689 C>T maps to ENST00000358110 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:86017716 C>T maps to ENST00000358110 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:192547466 A>G maps to NM_002922.3 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:192545492 T>C maps to NM_002922.3 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:121275053 C>T maps to NM_001005339.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr10:121285597 A>G maps to NM_001005339.1 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr10:121259625 C>A maps to NM_001005339.1 *182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:321226 G>A maps to NM_183337.1 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:3318577 C>T maps to NM_198229.2 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:3424185 C>T maps to NM_198229.2 C974C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:3318442 A>G maps to NM_198229.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr4:3432141 G>T maps to NM_198229.2 E1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr4:3430428 G>T maps to NM_198229.2 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr4:3319264 G>A maps to NM_198229.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr4:3319252 C>T maps to NM_198229.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:3425304 G>A maps to NM_198229.2 T1057T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:3344687 G>T maps to NM_198229.2 G636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr4:3418744 C>T maps to NM_198229.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr4:3318307 C>T maps to NM_198229.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:176793199 C>A maps to ENST00000398128 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5716-01A-21D-1800-08 chr1:182569615 C>T maps to NM_002928.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:153347626 G>A maps to NM_012419.4 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:153347650 C>A maps to NM_012419.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr1:192153618 C>T maps to NM_130782.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr1:192150477 G>T maps to NM_130782.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:54791936 C>T maps to NM_170587.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:54791840 A>G maps to NM_170587.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr8:54792023 G>A maps to NM_170587.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:54791858 G>A maps to NM_170587.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr1:192335061 C>T maps to NM_001039152.3 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:192335170 C>T maps to NM_001039152.3 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:101018331 C>T maps to NM_015668.3 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:101065080 G>T maps to NM_015668.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr8:100999826 G>T maps to NM_015668.3 I1013I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr8:101092394 T>C maps to NM_015668.3 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:101083647 A>G maps to NM_015668.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:116359160 G>A maps to NM_144488.4 S1175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr9:116357900 C>T maps to NM_144488.4 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:116346499 G>A maps to NM_144488.4 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:116303691 G>A maps to NM_017790.3 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr9:116346511 G>A maps to NM_144488.4 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:116269752 C>A maps to NM_144488.4 C424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr9:116357984 G>A maps to NM_144488.4 K1117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:163043360 C>A maps to NM_001102445.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:163131753 G>A maps to NM_003617.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:72924982 A>G maps to NM_004296.4 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:72941374 C>T maps to NM_004296.4 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr14:72941365 C>T maps to NM_004296.4 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:72818834 C>T maps to NM_004296.4 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:72818894 C>T maps to NM_004296.4 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr14:72925030 A>G maps to NM_004296.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:240977012 C>A maps to ENST00000407727 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:240990445 C>A maps to ENST00000407727 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:240966227 C>T maps to ENST00000407727 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:240966236 A>G maps to ENST00000407727 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr5:63871703 C>T maps to NM_001029875.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr5:63871702 G>T maps to NM_001029875.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:182615869 C>T maps to NM_033345.2 *199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr17:63156396 C>T maps to NM_003835.3 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:63221142 C>T maps to NM_003835.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr17:63200382 C>T maps to NM_003835.3 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:33167819 C>T maps to NM_207391.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:33167774 C>G maps to NM_207391.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:33167384 C>T maps to NM_207391.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:49578747 G>A maps to NM_000324.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:227729645 G>A maps to NM_001167608.1 W79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:75511492 G>A maps to NM_001040456.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:29656436 C>T maps to NM_012265.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr22:29656463 A>G maps to NM_012265.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:29656788 G>A maps to NM_012265.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:111618 C>T maps to NM_022450.3 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr16:110495 G>A maps to NM_022450.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:74469918 A>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:74470844 G>T maps to NM_024599.5 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:74473081 G>A maps to NM_024599.5 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr17:74470538 G>A maps to NM_024599.5 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:726835 C>T maps to NM_003961.1 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:39358896 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:39381325 C>T maps to ENST00000372985 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:30616025 G>A maps to NM_138328.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:30615896 G>A maps to NM_138328.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr1:156351871 C>A maps to NM_020407.3 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:156351950 C>A maps to NM_020407.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr1:25712311 C>T maps to NM_020485.4 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:25715466 C>T maps to NM_020485.4 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr15:90023597 G>A maps to NM_016321.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:90021066 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:90023597 G>A maps to NM_016321.1 G188G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8680-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:25611079 C>T maps to ENST00000357542 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:25611169 G>A maps to ENST00000357542 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:25611169 G>A maps to ENST00000357542 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:151164246 G>A maps to NM_005614.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr7:151164205 C>A maps to NM_005614.3 *185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:49462854 G>A maps to NM_144593.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:129247929 C>A maps to NM_000539.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr2:20647765 G>A maps to NM_004040.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:62652725 C>A maps to NM_014836.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:62648942 C>T maps to NM_014836.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:62648729 G>T maps to NM_014836.4 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:22862132 C>T maps to NM_001160036.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:22864744 T>C maps to NM_001160036.1 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:22864861 C>T maps to NM_001160036.1 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr8:22864246 C>A maps to NM_001160036.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:22864480 G>A maps to NM_001160036.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:95072639 C>T maps to NM_014899.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:95099278 A>G maps to NM_014899.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr5:95072639 C>T maps to NM_014899.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:66838973 C>T maps to NM_014578.3 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:66833380 G>A maps to NM_014578.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:122218894 C>T maps to NM_019034.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:3849263 G>A maps to NM_001665.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:3849104 C>T maps to NM_001665.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:3849242 C>T maps to NM_001665.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:63671619 C>T maps to NM_020663.3 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr14:63735879 G>A maps to NM_020663.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:30536446 C>A maps to NM_001033568.1 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:721921 G>A maps to NM_138769.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:720499 C>T maps to NM_138769.1 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr16:720266 G>A maps to NM_138769.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:228879180 C>T maps to NM_021205.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:119243190 G>A did not map to a codon.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr23:119243202 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:119249596 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:119211109 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:119293199 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:119293303 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:119293251 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:119293197 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:119211085 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr23:119293305 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:144458724 G>T maps to ENST00000422773 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:144461521 G>A maps to ENST00000422773 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:144463996 C>T maps to ENST00000422773 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:144464011 A>G maps to ENST00000422773 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:144462874 C>T maps to ENST00000422773 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:33535189 G>A maps to NM_033103.4 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:33482842 C>T maps to NM_033103.4 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:53455529 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:53455586 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:53457856 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:53454958 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:53455347 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:53453323 C>T did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr22:45828194 C>T maps to NM_015653.3 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:45818284 C>T maps to NM_015653.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr12:107209072 G>T maps to ENST00000392837 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:12847419 G>A maps to NM_014859.4 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:12888088 G>A maps to NM_014859.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:38960544 C>T maps to ENST00000296782 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:38963141 G>A maps to ENST00000296782 R468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:39002698 G>A maps to ENST00000296782 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:38975689 G>A maps to ENST00000296782 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:38981988 G>A maps to ENST00000296782 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:38958789 G>A maps to ENST00000296782 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:152320290 G>A maps to NM_018151.4 R1419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr2:152300220 C>T maps to NM_018151.4 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr17:1551669 G>T maps to NM_031430.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:123970349 C>T maps to NM_178314.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:123915116 C>T maps to NM_145058.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:130898738 C>T maps to NM_015347.4 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr12:130898837 T>C maps to NM_015347.4 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:130929741 G>A maps to NM_015347.4 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:130935799 C>T maps to NM_015347.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:130926897 G>A maps to NM_015347.4 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:130923043 G>A maps to NM_015347.4 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:130921758 G>A maps to NM_015347.4 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:130929708 A>T maps to NM_015347.4 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr12:130892273 G>A maps to NM_015347.4 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:130898839 G>A maps to NM_015347.4 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr12:130912756 C>T maps to NM_015347.4 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr12:130927119 C>T maps to NM_015347.4 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr12:130926489 C>A maps to NM_015347.4 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr12:130898828 A>G maps to NM_015347.4 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:130926882 C>T maps to NM_015347.4 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:20458538 C>T maps to NM_015672.1 G921G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:42880350 C>A maps to NM_173642.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr12:8926379 A>C maps to NM_020734.2 *387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr6:72678731 A>C maps to NM_014989.4 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:73016980 C>T maps to NM_014989.4 R1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr6:72974728 G>A maps to NM_014989.4 Q1056Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:72892049 C>T maps to NM_014989.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:72892073 C>T maps to NM_014989.4 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr6:72984123 G>A maps to NM_014989.4 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr6:72678731 A>C maps to NM_014989.4 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:73000540 G>A maps to NM_014989.4 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr6:72596854 G>A maps to NM_014989.4 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr6:72892025 A>G maps to NM_014989.4 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:72806828 G>A maps to NM_014989.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:104897786 C>T maps to NM_001100117.2 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr8:104955137 A>G maps to NM_001100117.2 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr8:105260950 T>C maps to NM_001100117.2 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr8:104709364 A>G maps to NM_001100117.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr8:104940098 T>G maps to NM_001100117.2 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8364-01A-11D-2340-08 chr8:105257238 C>T maps to NM_001100117.2 R1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr8:104898305 T>G maps to NM_001100117.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:104897837 G>A maps to NM_001100117.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:105261817 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr8:104898095 T>A maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr8:104898168 T>C maps to NM_001100117.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr8:105026757 C>T maps to NM_001100117.2 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr8:104898095 T>C maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr8:104898095 T>C maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr8:104898338 C>T maps to NM_001100117.2 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr8:104898186 C>T maps to NM_001100117.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:105263282 C>T maps to NM_001100117.2 N1241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr8:105263870 T>G maps to NM_001100117.2 S1291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr8:104930677 G>A maps to NM_001100117.2 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr8:104898095 T>C maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr8:104898125 T>C maps to NM_001100117.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr8:104924393 C>A maps to NM_001100117.2 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:104898188 A>G maps to NM_001100117.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:104709389 C>T maps to NM_001100117.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:104948951 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr8:104922392 G>A maps to NM_001100117.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:41107429 G>A maps to NM_014747.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr20:43386770 C>T maps to NM_182970.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:66102300 C>T maps to NM_004292.2 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr11:66100172 C>T maps to NM_004292.2 K642K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:19981486 G>A maps to ENST00000255006 Q914Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:19981513 A>G maps to ENST00000255006 K923K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr20:19981540 C>T maps to ENST00000255006 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:19977341 C>T maps to ENST00000255006 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:93154422 C>T maps to NM_024832.3 D928D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr14:93118182 G>A maps to NM_024832.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:93043772 C>T maps to NM_024832.3 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:93142917 G>T maps to NM_024832.3 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:33179048 C>T maps to NM_002931.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:33179099 C>T maps to NM_002931.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:105182967 C>T maps to NM_021930.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:7411599 T>C maps to NM_031480.2 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:7393490 A>G maps to NM_031480.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:7405246 C>T maps to NM_031480.2 N363N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr5:96503523 G>A maps to NM_018343.2 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr18:21044005 G>A maps to NM_003831.3 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr18:21053569 A>G maps to NM_003831.3 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:21057189 C>T maps to NM_003831.3 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr18:21053584 C>T maps to NM_003831.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:21056995 T>C maps to NM_003831.3 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:3083440 G>A maps to NM_003804.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr6:3078165 C>T maps to NM_003804.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:90796354 T>C maps to NM_003821.5 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:90770377 C>T maps to NM_003821.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:90770395 C>T maps to NM_003821.5 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:90784970 A>G maps to NM_003821.5 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:90782082 A>C maps to NM_003821.5 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:24808694 C>T maps to NM_006871.3 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr21:43161711 G>A maps to ENST00000352483 H595H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:43162041 G>A maps to ENST00000352483 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:43169341 G>A maps to ENST00000352483 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr21:43187098 G>A maps to ENST00000352483 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:43160997 C>T maps to ENST00000352483 *833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:106146379 T>G did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr6:84563443 C>T maps to NM_001009994.1 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:84563820 C>T maps to NM_001009994.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:40503662 G>A maps to NM_002930.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:89758314 T>C maps to NM_000326.4 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:40705155 C>T maps to NM_012421.3 Y1594Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:40703530 A>C maps to NM_012421.3 R1053R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:40701664 G>T maps to NM_012421.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr1:40705332 G>A maps to NM_012421.3 G1653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:40702284 A>C maps to NM_012421.3 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:40704192 A>C maps to NM_012421.3 S1273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:73812654 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:73811802 A>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:73812035 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:73811612 G>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:73812786 A>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:73812035 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:73812323 A>C did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:73815738 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:5335448 C>T maps to NM_006911.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:67683870 G>A maps to NM_001013838.1 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr16:67690152 G>A maps to NM_001013838.1 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:67683768 G>A maps to NM_001013838.1 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:67685088 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:151766823 G>A maps to NM_017909.2 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr2:86998769 C>T maps to NM_022780.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:86993069 G>A maps to NM_022780.3 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:177571044 G>A maps to NM_022762.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:177571053 G>A maps to NM_022762.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr14:21270140 C>T maps to NM_198235.2 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr14:20978866 C>A maps to ENST00000430083 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:20978875 A>G maps to ENST00000430083 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:21052426 A>G maps to NM_145250.3 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:21052300 G>A maps to NM_145250.3 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr14:21058543 G>A maps to NM_001024822.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:21424362 C>T maps to NM_002934.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr14:21424359 C>T maps to NM_002934.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:21424362 C>T maps to NM_002934.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr14:21167712 G>A maps to NM_194431.1 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:21249932 T>C maps to NM_005615.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:21025060 G>A maps to NM_001110361.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:3604478 T>C maps to NM_002936.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:12918304 C>T maps to NM_006397.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:182550410 C>T maps to NM_021133.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:182550470 A>G maps to NM_021133.3 N598N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:182555836 G>A maps to NM_021133.3 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:182555271 G>A maps to NM_021133.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr1:182555203 T>G maps to NM_021133.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:31521240 C>T maps to NM_013235.4 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:31449475 A>G maps to NM_013235.4 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:31526885 G>A maps to NM_013235.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:151326554 C>T maps to NM_005168.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:151326680 G>A maps to NM_005168.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:151326680 G>A maps to NM_005168.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:120990438 C>T maps to ENST00000458409 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:121002880 C>T maps to ENST00000458409 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr12:120990360 C>T maps to ENST00000458409 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:86831535 A>G maps to NM_005667.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:86831013 C>T maps to NM_005667.3 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr15:59359011 T>C maps to ENST00000434298 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:59373219 G>A maps to ENST00000434298 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:59373168 T>C maps to ENST00000434298 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr15:59347955 G>A maps to ENST00000434298 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:59359225 C>T maps to ENST00000434298 Q544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:59373219 G>A maps to ENST00000434298 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:59387029 G>A maps to ENST00000434298 W981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr17:19318450 C>T maps to NM_007148.4 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:19316717 G>A maps to NM_007148.4 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr17:19314762 G>A maps to NM_007148.4 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:119005488 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:119005266 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:98829067 C>A maps to NM_178861.4 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:98828581 G>A maps to NM_178861.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:98829061 G>A maps to NM_178861.4 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:98828626 C>T maps to NM_178861.4 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr13:98828824 G>A maps to NM_178861.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:98828845 G>A maps to NM_178861.4 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:98828608 G>A maps to NM_178861.4 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:98828653 G>A maps to NM_178861.4 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr8:33416223 G>A maps to NM_024787.2 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:33406950 C>T maps to NM_024787.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:29645944 T>C maps to NM_017831.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr19:648885 G>A maps to ENST00000340092 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:106028293 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:105970508 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:105970348 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:105970425 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:105970198 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:106031182 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:106033491 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:149589942 T>C did not map to a codon.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr5:179393911 G>A maps to NM_018434.4 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:122338732 T>C maps to NM_139175.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr7:122338522 G>A maps to NM_139175.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:29693730 T>C maps to NM_001191324.1 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:125498441 G>A maps to NM_007218.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:125499066 C>T maps to NM_007218.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:125498141 A>G maps to NM_007218.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr8:125499248 C>T maps to NM_007218.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:141358223 T>C maps to NM_183399.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:141359743 G>A maps to NM_183399.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr5:141358325 C>T maps to NM_183399.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:7170254 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:7137147 C>T maps to NM_014746.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:158596041 C>T maps to NM_144726.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:158601052 G>A maps to NM_144726.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:158621767 A>T maps to NM_144726.2 Y111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:127608345 C>T maps to ENST00000368314 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:122342387 T>A maps to NM_198085.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:122342669 T>A maps to NM_198085.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:122342060 A>G maps to NM_198085.1 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:101924855 G>A maps to NM_173647.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:101924990 C>T maps to NM_173647.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:101910511 G>A maps to NM_173647.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr4:141888923 T>C maps to NM_020724.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:142053629 C>T maps to NM_020724.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:141888893 G>A maps to NM_020724.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr4:142053860 G>A maps to NM_020724.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr4:142053545 G>A maps to NM_020724.1 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:2018578 C>A maps to NM_174903.4 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr18:59483441 G>A maps to NM_173557.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr18:59483132 G>A maps to NM_173557.2 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr18:59483513 A>G maps to NM_173557.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:59483264 A>G maps to NM_173557.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:74155543 G>A maps to NM_052916.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr21:30365198 G>A maps to NM_015565.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr21:30339483 A>G maps to NM_015565.2 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr21:30302778 C>T maps to NM_015565.2 T1810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr21:30316134 T>G maps to NM_015565.2 L1404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr18:44013270 G>A maps to NM_152470.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:4846554 G>T maps to NM_015528.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4848157 G>A maps to NM_015528.1 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:196199487 G>A maps to NM_152617.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:196214415 C>A maps to NM_152617.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:196198764 G>A maps to NM_152617.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:196199223 G>T maps to NM_152617.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:196199009 G>T maps to NM_152617.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:74545756 T>C maps to NM_001098638.1 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:74547505 C>T maps to NM_001098638.1 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr13:25370392 T>C maps to ENST00000381927 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:25399908 C>T maps to ENST00000381927 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr13:25444737 T>G maps to ENST00000381927 T1485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:25353860 C>T maps to ENST00000381927 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:25376643 G>A maps to ENST00000381927 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:25425688 T>C maps to ENST00000381927 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:42716935 A>G maps to NM_030954.3 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:42742938 G>A maps to NM_030954.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr4:154633708 G>A maps to ENST00000274068 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:63510253 C>T maps to NM_001113561.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr5:63509835 C>A maps to NM_001113561.1 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:63509747 C>T maps to NM_001113561.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:63509836 A>G maps to NM_001113561.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr6:13977676 G>T maps to NM_001165033.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:13977655 A>T maps to NM_001165033.1 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:101300354 C>T maps to NM_183419.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:101300183 C>T maps to NM_183419.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr8:101300276 T>A maps to NM_183419.1 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:33402625 A>G maps to NM_153341.2 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:33402697 G>T maps to NM_153341.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:33402511 G>T maps to NM_153341.2 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:33407926 C>T maps to NM_153341.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr1:185068943 C>T maps to NM_007212.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:104312973 T>C maps to NM_019592.5 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:104309175 G>A maps to NM_019592.5 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr9:104317112 C>A maps to NM_019592.5 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:104302546 G>A maps to NM_019592.5 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:6272463 C>T maps to NM_207396.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:6278374 C>G maps to NM_207396.2 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:6266699 G>A maps to NM_207396.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:140115250 G>A maps to NM_031297.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:1066663 A>G maps to NM_001131034.3 *298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr17:78346773 G>C did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:78261819 G>A maps to NM_020914.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:78321527 C>T maps to NM_020914.4 L3180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:78346448 G>A maps to NM_020914.4 S4271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:78360231 T>C did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:78320621 G>A maps to NM_020914.4 Q2878Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr17:78350177 G>A maps to NM_020914.4 S4470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:78358855 G>T maps to NM_020914.4 L4829L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8361-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:78286810 G>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:78319490 C>T maps to NM_020914.4 H2501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:78360621 C>T maps to NM_020914.4 F5000F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:78318680 G>A maps to NM_020914.4 T2231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:78345685 A>G maps to NM_020914.4 V4195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:78356806 A>G maps to NM_020914.4 S4718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:78319325 C>A maps to NM_020914.4 T2446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:78280269 T>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:78363630 T>C maps to NM_020914.4 L5116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:78346439 C>T maps to NM_020914.4 N4268N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-A4GQ-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:78326794 T>C maps to NM_020914.4 S3502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr17:78321785 C>T maps to NM_020914.4 V3266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:78318475 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:117152803 T>C maps to NM_207343.2 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:117152788 C>A maps to NM_207343.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:117110518 T>C maps to NM_207343.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:5792587 C>T maps to NM_207111.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr7:5752386 G>A maps to NM_207111.2 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:5662562 G>A maps to NM_207111.2 F900F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-4442-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr7:5769125 G>A maps to NM_207111.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:5662685 G>A maps to NM_207111.2 F859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:5752371 C>T maps to NM_207111.2 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:5781308 C>T maps to NM_207111.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr6:125366469 C>G maps to NM_152553.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:125366442 G>A maps to NM_152553.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr6:125397988 C>T maps to NM_152553.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr13:79190392 C>T maps to NM_024546.3 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:79219068 A>G maps to NM_024546.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr13:79191058 G>A maps to NM_024546.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:79191257 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:45110699 C>T maps to ENST00000453887 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:45079870 G>A maps to ENST00000453887 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:45115604 C>T maps to ENST00000453887 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr1:44878226 T>A maps to ENST00000453887 L153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:44878011 C>A maps to ENST00000453887 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:44877960 C>T maps to ENST00000453887 N64N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-8602-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:44877942 G>A maps to ENST00000453887 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:3944541 G>T maps to NM_001134338.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:219529961 G>A maps to NM_022453.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:219529009 G>A maps to NM_022453.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:219528976 G>A maps to NM_022453.2 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:219529954 G>A maps to NM_022453.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:119206680 C>A maps to NM_032015.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:156469300 C>A maps to NM_001184997.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:121858579 C>A maps to NM_194271.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:121858091 C>T maps to NM_194271.1 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:36390589 T>C maps to NM_022781.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:36357921 G>A maps to NM_022781.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:30043317 C>T maps to NM_025236.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:30043020 G>A maps to NM_025236.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr6:30038979 G>A maps to NM_025236.3 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:30039130 G>A maps to NM_025236.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:2515434 C>T maps to NM_002938.4 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:30780691 C>T maps to NM_014771.2 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:30783164 C>T maps to NM_014771.2 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr16:30778078 G>A maps to NM_014771.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:30783173 G>C maps to NM_014771.2 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:30779278 A>G maps to NM_014771.2 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr16:30779422 G>C did not map to a codon.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr16:30777563 C>T maps to NM_014771.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:56601440 G>A maps to NM_194359.1 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:56435708 A>G maps to NM_017763.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:56439907 C>T maps to NM_017763.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr17:56438232 G>A maps to NM_017763.4 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr17:56438163 C>A maps to NM_017763.4 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:56436148 G>A maps to NM_017763.4 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:56440740 C>T maps to NM_017763.4 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr17:56435935 C>A maps to NM_017763.4 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:175958478 G>A maps to NM_014901.4 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:175959003 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:32146317 C>G maps to NM_006913.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr6:32146404 C>T maps to NM_006913.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:32147320 G>A maps to NM_006913.3 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:26792702 G>A maps to NM_005977.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:141457323 C>T maps to NM_014245.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr6:37344810 T>G did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr6:37342397 T>C maps to NM_003958.3 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:58035793 A>T maps to NM_016125.3 L235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:117204720 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:89614481 G>A maps to NM_003800.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:498026 G>A maps to NM_203389.1 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:502078 C>T maps to NM_203389.1 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:494952 G>A maps to NM_203389.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:494779 T>C did not map to a codon.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr10:90341417 C>T maps to NM_001031709.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:90122339 G>A maps to NM_001031709.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr10:90342920 G>A maps to NM_001031709.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:90342923 G>A maps to NM_001031709.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:90122462 C>T maps to NM_001031709.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:13742636 T>C maps to NM_003799.1 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr18:13742648 T>C maps to NM_003799.1 N379N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-7851-01A-11D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:686478 C>A maps to NM_018146.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:695113 C>A maps to NM_018146.2 G356G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-RD-A8N1-01A-12D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:241512588 C>T maps to NM_018226.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:241516114 C>T maps to NM_018226.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:241512609 G>A maps to NM_018226.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:241516003 G>A maps to NM_018226.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:241512588 C>T maps to NM_018226.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:156025074 A>C maps to NM_014017.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:78663930 C>T maps to NM_002941.3 A1434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:78685076 G>A maps to NM_002941.3 Y1073Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr3:78763663 G>A maps to NM_002941.3 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:78796029 G>A maps to NM_002941.3 Q174*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-5720-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:78717035 G>A maps to NM_002941.3 Q655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:78663795 A>G did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr3:78649330 T>G maps to NM_002941.3 R1625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:77147285 C>A maps to ENST00000332191 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:77607296 A>G maps to ENST00000332191 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:77526692 C>T maps to ENST00000332191 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:77684172 C>T maps to ENST00000332191 R1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr3:77666772 C>T maps to ENST00000332191 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr3:77542473 A>G maps to ENST00000332191 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr3:77526675 G>A maps to ENST00000332191 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr3:77147474 G>A maps to ENST00000332191 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr3:77607239 G>A maps to ENST00000332191 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr3:77572048 C>G maps to ENST00000332191 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:124747172 G>A maps to NM_022370.3 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:124742440 A>C maps to NM_022370.3 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:124744031 C>T maps to NM_022370.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr11:124739004 C>T maps to NM_022370.3 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:124738821 T>C maps to NM_022370.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:124765431 G>A maps to NM_019055.5 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr11:124766978 C>A maps to NM_019055.5 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:124765500 C>T maps to NM_019055.5 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:18564451 C>T maps to NM_005406.2 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr18:18564355 C>T maps to NM_005406.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:18622573 C>A maps to NM_005406.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:18629739 C>T did not map to a codon.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr18:18548821 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:18619430 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr18:18562782 C>A maps to NM_005406.2 G834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr18:18586551 C>A maps to NM_005406.2 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:18533606 C>T maps to NM_005406.2 T1331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:11351804 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:11359112 G>T maps to NM_004850.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:11351915 C>T maps to NM_004850.3 Q698Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:11355115 C>A maps to NM_004850.3 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:114997100 T>C maps to NM_001163790.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:4851559 C>A maps to NM_024589.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr16:4848161 C>T maps to NM_024589.1 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:34288779 C>T maps to NM_080748.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr3:123695731 C>T maps to NM_017578.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:125701222 C>T maps to NM_001012337.1 A169A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8363-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr5:10450087 T>C maps to NM_031916.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:10461309 G>A maps to NM_031916.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:10461378 G>A maps to NM_031916.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr5:10442329 G>A maps to NM_031916.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:64624766 C>T maps to NM_005012.2 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:64515459 C>A maps to NM_005012.2 P87P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-5726-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:94487068 C>T maps to NM_004560.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr9:94487065 C>G maps to NM_004560.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:94486804 G>A maps to NM_004560.2 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr9:94519611 G>A maps to NM_004560.2 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:94486426 G>A maps to NM_004560.2 N783N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:94495677 G>A maps to NM_004560.2 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr9:94487098 G>A maps to NM_004560.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:60907206 G>A maps to NM_002943.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:60803701 C>T maps to NM_134260.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:60806875 A>G maps to NM_134260.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr15:61521384 G>A maps to NM_134261.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:60792195 T>C maps to NM_134260.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr9:77300518 C>T maps to ENST00000396204 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:77112895 C>T maps to NM_006914.3 R2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr9:77282710 T>C maps to ENST00000396204 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:77277433 C>T maps to ENST00000396204 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:151787410 G>T maps to ENST00000392697 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:117650525 C>A maps to NM_002944.2 G1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr6:117642552 C>T maps to NM_002944.2 W1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr6:117641087 T>C maps to NM_002944.2 E1961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:117658373 C>A maps to NM_002944.2 E1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:117662565 T>C maps to NM_002944.2 L1633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:117710732 A>G maps to NM_002944.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr6:117724425 C>T maps to NM_002944.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:117709039 C>T maps to NM_002944.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:117706977 G>A maps to NM_002944.2 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:117622278 G>A maps to NM_002944.2 C2197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:117708087 C>A maps to NM_002944.2 G697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:55540062 T>C maps to NM_006269.1 D1207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:55542106 C>T maps to NM_006269.1 Q1889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:55533930 G>A maps to NM_006269.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:55534122 C>T maps to NM_006269.1 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:55540518 T>G maps to NM_006269.1 T1359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:55537788 C>T maps to NM_006269.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:55540959 G>A maps to NM_006269.1 L1506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr8:55534699 C>T maps to NM_006269.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:55542252 T>A maps to NM_006269.1 Y1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:55534684 C>T maps to NM_006269.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:55534131 C>T maps to NM_006269.1 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:55533672 C>T maps to NM_006269.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:55541305 G>T maps to NM_006269.1 E1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:55533897 G>C maps to NM_006269.1 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr8:55534053 C>T maps to NM_006269.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr8:55533558 C>A maps to NM_006269.1 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:10465955 C>T maps to NM_178857.5 Q1884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:10470815 C>T maps to NM_178857.5 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:10468220 C>T maps to NM_178857.5 E1129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:10469624 C>T maps to NM_178857.5 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr8:10480561 G>A maps to NM_178857.5 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:10468388 C>T maps to NM_178857.5 R1073R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:10470611 G>A maps to NM_178857.5 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:10466429 A>G maps to NM_178857.5 A1726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:10467746 C>T maps to NM_178857.5 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:10467650 C>T maps to NM_178857.5 A1319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:10467296 G>T maps to NM_178857.5 A1437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr8:10469918 G>T maps to NM_178857.5 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:10466732 G>A maps to NM_178857.5 G1625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr8:10469500 G>A maps to NM_178857.5 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:10466702 G>A maps to NM_178857.5 D1635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:10468838 G>A maps to NM_178857.5 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:10470599 C>T maps to NM_178857.5 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:10464632 G>A maps to NM_178857.5 S2325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:10470323 C>T maps to NM_178857.5 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:10480513 G>A maps to NM_178857.5 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr8:10473977 C>T maps to NM_178857.5 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr8:10466099 C>T maps to NM_178857.5 E1836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:10465474 C>A maps to NM_178857.5 E2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:10470515 G>A maps to NM_178857.5 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:10470641 G>A maps to NM_178857.5 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:10470815 C>T maps to NM_178857.5 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:46712974 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:46713333 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:46739136 G>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:33139021 G>A maps to NM_203288.1 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr17:1783865 C>T maps to NM_002945.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:1798334 T>C maps to NM_002945.3 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:96139887 C>T did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:96139826 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:96140045 G>A did not map to a codon.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr23:96139405 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:96139928 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:96140039 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:96139978 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:41815491 G>A maps to NM_015540.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:41813934 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:41822178 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:41814327 G>A maps to NM_015540.2 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:41813151 G>A maps to NM_015540.2 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:92811468 A>G maps to NM_024813.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:92767147 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:92789301 C>T maps to NM_024813.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:48073290 C>T maps to NM_024604.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr2:210884512 T>C maps to NM_199229.1 *229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:210880763 G>A maps to NM_199229.1 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:84961747 T>C did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr1:84961054 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:84961947 G>A maps to NM_025065.6 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:111320953 A>G maps to NM_032194.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:111320914 T>C maps to NM_032194.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr6:111336987 C>T maps to NM_032194.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr6:111329287 C>T maps to NM_032194.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:38129018 G>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:38169935 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:38158348 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr23:38176654 C>G did not map to a codon.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr23:38145179 C>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:38160590 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:38160590 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:38128997 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:21771651 T>C maps to NM_020366.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr14:21795818 C>T maps to NM_020366.3 N916N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:53675334 A>G maps to NM_015272.2 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:53720488 C>G did not map to a codon.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr16:53686794 G>A maps to NM_015272.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:113306353 A>G maps to NM_001143854.1 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:177322 G>A maps to NM_006987.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr2:89049501 G>T maps to NM_144563.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:153628914 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153626863 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:153627878 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153626867 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:153628829 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153628810 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr14:47120891 C>T maps to NM_080746.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr1:24018319 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:130210643 C>T maps to NM_000976.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:130210269 T>C did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:40499483 T>C did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:40500173 C>A maps to NM_001034996.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:23959967 C>T maps to NM_002948.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:47014894 C>T maps to NM_001035006.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:49120042 C>T maps to NM_000979.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr19:17972163 C>A maps to NM_000980.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:17973009 C>A maps to NM_000980.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:27830371 C>T maps to NM_000982.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:6246740 G>A maps to NM_000983.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:170586134 C>T maps to NM_001099645.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:101399980 A>G maps to NM_000986.3 *158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr3:101404712 C>G maps to NM_000986.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:8706387 T>C maps to NM_000990.4 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:55899502 G>A maps to NM_001136134.1 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:52027959 T>G maps to NM_000992.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:52027965 G>A maps to NM_000992.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:127620343 G>A maps to NM_007209.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:100646444 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:100646540 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:100646509 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:217364715 C>A maps to NM_000998.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:217366123 G>A maps to NM_000998.4 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:1996655 G>A maps to NM_005061.2 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:2003999 C>T maps to NM_005061.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:66792467 A>G maps to NM_000968.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:66793740 A>G maps to NM_000968.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:112843671 G>A maps to NM_001024662.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:136218178 C>T maps to NM_000972.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:136218199 A>G maps to NM_000972.2 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr8:146015799 C>T maps to NM_000973.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:146015748 C>A maps to NM_000973.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:146015266 G>A maps to NM_000973.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr12:120635142 G>C maps to NM_053275.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:128339382 C>T maps to NM_002950.3 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:128339334 C>T maps to NM_002950.3 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:128341189 G>A maps to NM_002950.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr20:35856961 C>T maps to NM_002951.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:58302680 A>G maps to NM_007042.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr10:92656135 G>A maps to ENST00000458617 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:92656099 C>T maps to ENST00000458617 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:15145360 G>A maps to NM_183005.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr10:15146038 T>G maps to NM_183005.3 P242P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F1-A448-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:15145414 C>T maps to NM_183005.3 S34S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:33613687 A>G maps to NM_018170.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:36668869 T>A maps to NM_021215.3 L62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:150443334 T>C maps to NM_015203.3 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr1:150429978 G>A maps to NM_015203.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:150445108 C>T maps to NM_015203.3 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:154334841 G>A maps to NM_019845.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:45056148 C>T maps to NM_203400.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:133138635 T>C maps to NM_001016.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr6:133138133 C>G maps to NM_001016.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr6:133138136 T>C maps to NM_001016.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr6:133138145 T>C maps to NM_001016.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:39923917 G>A maps to NM_001020.4 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr6:33244008 G>A maps to NM_022551.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:39925607 G>C maps to NM_194326.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:2012161 G>A maps to NM_002952.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:2012898 A>G maps to NM_002952.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr20:60962942 T>C maps to NM_001024.3 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:81573621 T>G maps to NM_001025.4 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr10:79795303 G>A maps to NM_001142285.1 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr23:71492542 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:71493690 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:71495453 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr24:2713760 C>T did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr24:22930848 C>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:22918665 C>A did not map to a codon.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr9:19378871 G>A maps to NM_001010.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:26883499 T>C maps to NM_001006665.1 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:26898395 G>T maps to NM_001006665.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:26898684 C>T maps to NM_001006665.1 N625N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:26878138 C>T maps to NM_001006665.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:166902366 C>T maps to ENST00000510118 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:166844006 C>T maps to ENST00000510118 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:166844006 C>T maps to ENST00000510118 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:166862226 G>A maps to ENST00000510118 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:166952164 G>T maps to ENST00000510118 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr6:166923826 G>T maps to ENST00000510118 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:166827347 C>T maps to ENST00000510118 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:20173604 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:20195148 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:20190976 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:20205969 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:20195137 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:20252923 C>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:64129374 G>A maps to NM_003942.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:91338513 G>A maps to NM_004755.2 H771H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr14:91341638 C>T maps to NM_004755.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:83352816 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:83359655 C>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:83403074 C>A did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:83359575 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:83359597 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:83362032 G>A did not map to a codon.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr23:83359568 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:83352807 C>A did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr23:83351319 C>T did not map to a codon.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr23:83357063 G>T did not map to a codon.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr23:83319319 G>A did not map to a codon.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr23:83411137 G>T did not map to a codon.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr23:83319381 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:83362681 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:83374986 G>A did not map to a codon.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr17:58024085 A>T maps to NM_003161.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:67201900 G>A maps to NM_003952.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr11:67201942 C>T maps to NM_003952.2 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:213341249 G>A maps to NM_012424.3 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:213445890 C>T maps to NM_012424.3 R1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:213445949 T>C maps to NM_012424.3 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:213403865 A>G maps to NM_012424.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:75376459 G>A maps to NM_031464.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:75376597 G>A maps to NM_031464.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:3627804 A>T maps to NM_001011.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:3628429 G>A maps to NM_001011.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:45244275 T>C maps to NM_001012.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:45243748 T>C maps to NM_001012.1 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:54710225 G>A maps to NM_001013.3 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr19:54710192 C>T maps to NM_001013.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:54711409 G>T maps to NM_001013.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:39452429 G>A maps to ENST00000443003 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr1:152129285 T>G maps to NM_001122965.1 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:152127240 G>A maps to NM_001122965.1 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:152127423 G>A maps to NM_001122965.1 H717H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:152128680 C>T maps to NM_001122965.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:78854243 C>T maps to NM_020761.2 N513N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:78923243 C>T maps to NM_020761.2 D1089D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:78938130 C>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:78867513 C>T maps to NM_020761.2 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:78599516 T>C maps to NM_020761.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr17:78896528 C>T maps to NM_020761.2 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:78727931 G>A maps to NM_020761.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:78899240 C>T maps to NM_020761.2 C960C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:78933960 C>T maps to NM_020761.2 D1187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:78933972 C>T maps to NM_020761.2 R1191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr17:78938108 G>A maps to NM_020761.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr17:78866670 T>G did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr16:836928 C>A did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr15:40866002 G>A maps to NM_152260.1 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:126073381 G>A maps to NM_032795.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:126081485 G>A maps to NM_032795.2 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr2:219458965 C>T maps to NM_005444.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr16:66956094 G>A maps to NM_004165.2 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:55757834 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:55748711 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:55757849 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:55777620 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:55748699 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:90097136 G>A maps to NM_021244.4 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:50140108 G>A maps to NM_006270.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr19:50140100 G>A maps to NM_006270.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:50143241 G>A maps to NM_006270.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:50138859 G>A maps to NM_006270.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr20:17606215 G>A maps to ENST00000377813 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:17607994 A>G maps to ENST00000377813 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:17617290 C>T maps to ENST00000377813 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr20:17641140 G>A maps to ENST00000377813 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:17617251 G>A maps to ENST00000377813 H769H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:17614256 G>A maps to ENST00000377813 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:7229285 C>T maps to NM_001003699.3 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:7247284 C>T maps to NM_001003699.3 S1534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:7226756 G>A maps to NM_001003699.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:7231268 T>C maps to NM_001003699.3 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:7182149 G>A maps to NM_001003699.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:7231874 C>T maps to NM_001003699.3 I1181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:7229264 C>T maps to NM_001003699.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:7230995 C>T maps to NM_001003699.3 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:7230881 C>T maps to NM_001003699.3 C850C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:7230608 C>T maps to NM_001003699.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr6:7229900 G>C maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:7229900 G>A maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:7230665 C>T maps to NM_001003699.3 R778R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:7246909 C>T maps to NM_001003699.3 D1409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:7229249 G>A maps to NM_001003699.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:7248771 C>T maps to NM_001003699.3 C1600C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:7247314 C>T maps to NM_001003699.3 S1544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:110757241 T>C maps to NM_006583.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:110756616 C>T maps to NM_006583.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:110754439 C>A maps to NM_006583.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr4:110756577 C>T maps to NM_006583.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:4150329 T>C maps to NM_001033.3 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr11:4150362 C>T maps to NM_001033.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:10263174 C>A maps to NM_001165931.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:15180275 A>G maps to NM_018427.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:15178533 G>A maps to NM_018427.3 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr21:45217943 C>T maps to NM_003683.5 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr21:45215075 C>A maps to NM_003683.5 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr10:99140564 C>G maps to NM_015179.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:99126539 C>T maps to NM_015179.3 E1058E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr10:99133604 G>A maps to NM_015179.3 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr10:99141531 C>A maps to NM_015179.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:99130742 G>A maps to NM_015179.3 H813H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:99132889 C>T maps to NM_015179.3 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr10:99116930 G>A maps to NM_015179.3 Q1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:45107916 C>T maps to NM_015056.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr21:45103226 C>A maps to NM_015056.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:42908939 G>A maps to NM_015703.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:42914118 A>C maps to NM_015703.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:6622701 A>G maps to NM_015324.2 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:6624663 T>C maps to NM_015324.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:6622580 G>A maps to NM_015324.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:6621763 T>C maps to NM_015324.2 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:51969428 A>G maps to NM_004704.3 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:67342428 G>T maps to NM_015169.3 G355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:67341434 C>T maps to NM_015169.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:18660169 A>C did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr23:18660254 G>A did not map to a codon.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr17:48562189 C>T maps to NM_018346.1 Q433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:48559583 C>T maps to NM_018346.1 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:7023619 G>A maps to NM_080657.4 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:114320290 A>G did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr7:77326149 C>T maps to NM_198467.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:77402578 C>T maps to NM_198467.2 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:77379030 C>T maps to NM_198467.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:77408241 T>C maps to NM_198467.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:15986908 A>G maps to NM_006511.1 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:15987412 G>A maps to NM_006511.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:77383227 G>A maps to NM_016578.3 R1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:77412130 C>A maps to NM_016578.3 E715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:77389134 T>C maps to NM_016578.3 G1043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:77388036 G>A maps to NM_016578.3 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:11933614 G>A maps to NM_015659.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:11941643 G>A maps to NM_015659.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr21:43905829 G>A maps to NM_080860.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:6836262 C>T maps to NM_173565.3 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr7:5984720 C>T maps to NM_173565.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:159399366 C>A maps to NM_031924.4 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr6:159401860 C>T maps to NM_031924.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:159420642 G>T maps to NM_031924.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:116949262 C>T maps to NM_001010892.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:116949322 C>T maps to NM_001010892.2 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:116938280 C>T maps to NM_001010892.2 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr19:46307638 G>A maps to NM_030785.3 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:46299144 G>A maps to NM_030785.3 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:46299144 G>A maps to NM_030785.3 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr19:46307602 G>A maps to NM_030785.3 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:46307884 G>A maps to NM_030785.3 Y426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:46313884 G>A maps to NM_030785.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:38082195 T>C maps to NM_001038633.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr8:108972949 C>A maps to NM_178565.4 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:127469862 A>G maps to ENST00000368317 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:127476518 T>C maps to ENST00000368317 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:127440346 C>T maps to ENST00000368317 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:947856 C>T maps to NM_001029871.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:57255239 C>T maps to NM_133368.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:57238590 C>T maps to NM_133368.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:157840088 T>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:122990115 A>G maps to NM_023012.5 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr12:122995656 T>C maps to NM_023012.5 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:123005955 G>A maps to NM_023012.5 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:16635392 T>G maps to NM_012425.3 *278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:100736175 A>G maps to NM_001130841.1 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:100733759 C>T maps to NM_001130841.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:100740490 A>G maps to NM_001130841.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:100756996 C>T maps to NM_001130841.1 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:23404005 G>A maps to NM_014433.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr22:23406129 G>A maps to NM_014433.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr22:23482459 A>G maps to NM_014433.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:23482436 G>A maps to NM_014433.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:62319288 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:62324279 C>A maps to ENST00000482936 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:62324526 G>A maps to ENST00000482936 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:62326157 C>T maps to ENST00000482936 H1058H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:62292793 G>A maps to ENST00000482936 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr20:62321131 G>A maps to ENST00000482936 Q685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr20:62326250 C>T maps to ENST00000482936 D1089D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:62293251 G>A maps to ENST00000482936 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:41772867 C>T maps to NM_015138.4 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:41762572 G>A maps to NM_015138.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:41772870 C>T maps to NM_015138.4 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:74657142 A>G maps to NM_001015055.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:74653512 G>A maps to NM_001015055.1 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:63959570 T>C maps to NM_145307.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:63959522 G>A maps to NM_145307.2 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr14:101348152 T>A maps to NM_001134888.2 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:101347456 G>A maps to NM_001134888.2 H1223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr14:101349301 G>A maps to NM_001134888.2 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr14:60069805 A>C maps to NM_021136.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:60074085 G>A maps to NM_021136.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:60063483 G>A maps to NM_021136.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr14:60072169 C>G maps to NM_021136.2 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr14:60194300 C>T maps to NM_021136.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:60213014 C>T maps to NM_021136.2 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr14:60194282 G>A maps to NM_021136.2 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr14:60194150 G>A maps to NM_021136.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:60194027 G>A maps to NM_021136.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:60097225 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:45997880 C>A maps to NM_005619.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr19:45997475 C>T maps to NM_005619.3 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:45998138 G>T maps to NM_005619.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:45989048 T>G did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr19:45997637 G>A maps to NM_005619.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:45998024 G>T maps to NM_005619.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:63472326 C>A maps to ENST00000377819 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:63488172 A>G maps to ENST00000377819 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:63487737 G>A maps to ENST00000377819 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr11:63487875 T>C maps to ENST00000377819 Y634Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr11:63520545 T>C maps to ENST00000377819 A961A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr2:55254235 C>T maps to NM_020532.4 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:55254421 T>C maps to NM_020532.4 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr6:107019879 A>G maps to NM_032730.4 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr6:107076782 A>T maps to NM_032730.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr6:107070694 C>A maps to NM_032730.4 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr6:107076788 G>T maps to NM_032730.4 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:20230372 G>A maps to ENST00000425986 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:20230156 G>A maps to ENST00000425986 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:20230609 G>A maps to ENST00000425986 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:1840944 C>T maps to NM_178568.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:1840971 G>A maps to NM_178568.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr11:57244116 C>T maps to NM_178570.1 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:57235091 G>A maps to NM_178570.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr11:57235418 G>A maps to NM_178570.1 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:57243697 C>T maps to NM_178570.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:186915362 C>T maps to NM_153708.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:187416492 G>T maps to NM_001004312.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:67695983 A>G maps to NM_173630.3 C1933C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:67813009 C>T maps to NM_173630.3 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:67860531 C>T maps to NM_173630.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr18:67817278 T>C maps to NM_173630.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:67869181 A>G maps to NM_173630.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:67817852 G>A maps to NM_173630.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:67788836 A>C maps to NM_173630.3 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:67817852 G>A maps to NM_173630.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:67755347 C>T maps to NM_173630.3 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:67715293 T>C maps to NM_173630.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:67781678 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:67742741 C>T maps to NM_173630.3 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:179012794 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:70138420 G>A maps to NM_001042417.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:70138357 C>T maps to NM_001042417.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:71660562 C>T maps to NM_001037442.2 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr4:71629278 T>G maps to NM_001037442.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:218940175 C>T maps to NM_198483.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr17:41143003 G>A maps to NM_173079.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:41143405 G>A maps to NM_173079.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:12121269 G>A maps to NM_032167.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:42390847 T>G maps to NM_001144825.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr7:87280191 T>G maps to NM_138290.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr7:87370835 G>T maps to NM_138290.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:87436694 C>T maps to NM_138290.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:87459245 G>A maps to NM_138290.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr21:36171640 G>A maps to NM_001754.4 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:36252917 G>A maps to NM_001754.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr21:36171664 C>T maps to NM_001754.4 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr21:36171736 G>C maps to NM_001754.4 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:93026962 A>G maps to NM_175634.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr8:93004117 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:93029538 C>T maps to NM_175634.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:93003865 C>T did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr8:92983011 C>T maps to NM_175634.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:92983011 C>T maps to NM_175634.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr8:92998513 G>A maps to NM_175634.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:92972631 A>G maps to NM_175634.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:93004020 A>G maps to NM_175634.2 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr6:45514960 C>T maps to ENST00000359524 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr6:45405708 C>T maps to ENST00000359524 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:45390580 G>T maps to ENST00000359524 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:45390459 G>A maps to ENST00000359524 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:45390603 C>T maps to ENST00000359524 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:25245749 G>A maps to NM_001031680.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr1:25229131 G>A maps to NM_001031680.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr1:155297949 T>C maps to NM_001105203.1 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:155300240 T>A maps to NM_001105203.1 L863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr1:155296537 C>T maps to NM_001105203.1 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:155294222 C>T maps to NM_001105205.1 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:35547294 C>T maps to NM_001135999.1 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:35547633 G>A maps to NM_001135999.1 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:35559221 G>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:35555606 G>A maps to NM_001135999.1 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:35547072 C>T maps to NM_001135999.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:35547550 A>C maps to NM_001135999.1 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr9:35560740 G>A maps to NM_001135999.1 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:49513256 G>A maps to NM_006666.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:49514565 C>T maps to NM_006666.1 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:49507565 A>T maps to NM_006666.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:83905672 C>T maps to NM_033411.3 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:83905456 A>G maps to NM_033411.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr21:30380586 C>T maps to NM_016940.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr4:184572390 G>A maps to ENST00000326397 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:159568162 A>G maps to ENST00000440678 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:159567985 C>T maps to ENST00000440678 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:159533351 C>T maps to ENST00000440678 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr13:32365958 C>T maps to NM_130806.3 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr5:33937954 G>A maps to NM_016568.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:33937042 G>A maps to NM_016568.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:33937523 C>T maps to NM_016568.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr5:33936974 C>T maps to NM_016568.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr5:33936964 C>T maps to NM_016568.3 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:33937424 C>T maps to NM_016568.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr5:33938065 C>T maps to NM_016568.3 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:33938197 C>T maps to NM_016568.3 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr5:33936955 G>A maps to NM_016568.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:155911940 G>A maps to NM_181885.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:137328339 G>A maps to NM_002957.4 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:137313625 C>T maps to NM_002957.4 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:33163387 G>A maps to ENST00000374685 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr6:33166233 G>C maps to ENST00000374685 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:33166100 G>A maps to ENST00000374685 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:38976508 G>A maps to NM_000540.2 T1738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:38976520 C>T maps to NM_000540.2 R1742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:38959975 C>T maps to NM_000540.2 G1196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:38976391 C>T maps to NM_000540.2 D1699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:38948732 G>A maps to NM_000540.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:39068583 C>T maps to NM_000540.2 Y4733Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:39051817 G>A maps to NM_000540.2 A4116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:39028589 G>A maps to NM_000540.2 G3893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:39019236 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:38980032 T>C maps to NM_000540.2 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:39034442 G>A maps to NM_000540.2 A3980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr19:38939332 C>T maps to NM_000540.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:38966080 C>T maps to NM_000540.2 N1428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:38968432 C>T maps to NM_000540.2 H1459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:38959604 G>T did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:38980002 G>T maps to NM_000540.2 E1912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr19:39066573 C>T maps to NM_000540.2 N4715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr19:38976355 C>T maps to NM_000540.2 H1687H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:38933086 C>A maps to NM_000540.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:38951152 C>T maps to NM_000540.2 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr19:38985209 C>T maps to NM_000540.2 L2165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr19:38966035 C>T maps to NM_000540.2 D1413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr19:39013755 G>A did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:39052021 C>T maps to NM_000540.2 G4184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr19:38949966 G>A maps to NM_000540.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:38951086 T>C maps to NM_000540.2 H811H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:38987105 C>T maps to NM_000540.2 R2241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr19:38939429 C>A maps to NM_000540.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:38985109 G>T maps to NM_000540.2 L2131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:38985046 C>T maps to NM_000540.2 F2110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr19:38954484 G>A maps to NM_000540.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr19:38924492 C>T maps to NM_000540.2 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:237777404 G>A maps to NM_001035.2 R1659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:237732549 C>T maps to NM_001035.2 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:237947035 C>T maps to NM_001035.2 N4008N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:237660038 T>C maps to NM_001035.2 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr1:237801712 G>A maps to NM_001035.2 K2283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:237617864 C>T maps to NM_001035.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr1:237675028 G>A maps to NM_001035.2 E920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:237777416 C>T maps to NM_001035.2 A1663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:237659952 G>T maps to NM_001035.2 G702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr1:237580423 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:237540728 G>A maps to NM_001035.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr1:237604731 T>C maps to NM_001035.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:237947275 C>T maps to NM_001035.2 H4088H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr1:237947446 C>A maps to NM_001035.2 I4145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:237791218 C>T maps to NM_001035.2 D2093D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:237872218 G>A maps to NM_001035.2 P3321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:237754061 C>T maps to NM_001035.2 C1310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:237961335 G>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:237756795 C>A maps to NM_001035.2 I1432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr1:237817654 G>T maps to NM_001035.2 E2636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:237550660 A>G maps to NM_001035.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr1:237947674 C>T maps to NM_001035.2 S4221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:237947293 C>T maps to NM_001035.2 I4094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:237923125 C>T maps to NM_001035.2 S3792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:237865296 T>C maps to NM_001035.2 S3129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:237947995 A>G maps to NM_001035.2 A4328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr1:237729907 C>T maps to NM_001035.2 R1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr1:237794732 T>A maps to NM_001035.2 I2149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:237802388 T>C maps to NM_001035.2 L2335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:237872338 A>G maps to NM_001035.2 T3361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr15:34080452 C>T maps to NM_001036.3 P3208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:34102717 G>A maps to NM_001036.3 R3355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:34072444 G>A maps to NM_001036.3 S3057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:34140607 G>A maps to NM_001036.3 L4538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr15:34111968 C>T maps to NM_001036.3 D3573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:33873840 C>T maps to NM_001036.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr15:34129189 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:34030748 G>A maps to NM_001036.3 T2538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:34150099 C>T maps to NM_001036.3 C4709C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr15:33916067 T>G maps to NM_001036.3 Y806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:34146650 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr15:33855183 T>G maps to NM_001036.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:34111968 C>T maps to NM_001036.3 D3573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:33954455 C>T maps to NM_001036.3 R1575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr15:33999124 G>A maps to NM_001036.3 V2163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:33855129 G>A maps to NM_001036.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:33988593 C>T maps to NM_001036.3 S2012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:34145781 C>T maps to NM_001036.3 Y4566Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:33938601 G>A maps to NM_001036.3 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:34032145 C>A maps to NM_001036.3 I2590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:34102804 A>G maps to NM_001036.3 P3384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:34123213 T>C maps to NM_001036.3 D3795D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr15:33993250 G>A maps to NM_001036.3 A2151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:33928728 C>T maps to NM_001036.3 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:33893741 C>T maps to NM_001036.3 N637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:34049794 C>T maps to NM_001036.3 A2901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:33873716 G>A maps to NM_001036.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:33893730 C>T maps to NM_001036.3 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr15:33855183 T>C maps to NM_001036.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:33941406 A>G maps to NM_001036.3 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:33999176 G>T maps to NM_001036.3 G2181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:34021136 C>T maps to NM_001036.3 R2371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:153598897 G>A maps to NM_001024210.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:153588310 G>A maps to NM_020672.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:153536278 G>A maps to ENST00000368707 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:153520238 A>G maps to NM_002960.1 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr1:153390569 T>A maps to NM_176823.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:153362987 G>T maps to NM_002964.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:153330872 A>G maps to NM_002965.3 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr21:48019326 G>T maps to NM_006272.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:33292200 G>A maps to NM_022753.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:33292404 G>A maps to NM_022753.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:101705310 C>T maps to NM_001400.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:101705023 C>T maps to NM_001400.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:10335347 G>A maps to NM_004230.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:10335473 G>A maps to NM_004230.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr9:91616714 C>T maps to NM_005226.2 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:91617002 C>T maps to NM_005226.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr9:91616510 C>T maps to NM_005226.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:91617032 G>A maps to NM_005226.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:3179783 C>T maps to NM_003775.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:10625084 G>A maps to NM_001166215.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr19:10624547 G>A maps to NM_001166215.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:18266952 G>A maps to NM_030754.4 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:64812121 C>T maps to ENST00000301885 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:45780147 C>T maps to NM_014016.3 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr3:45746627 C>T maps to NM_014016.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:23908270 C>T maps to NM_014363.4 W3248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:23942606 C>T maps to NM_014363.4 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr13:23908519 A>C maps to NM_014363.4 T3165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:23905258 A>G maps to NM_014363.4 S4252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr13:23905258 A>G maps to NM_014363.4 S4252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:23906233 C>T maps to NM_014363.4 A3927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:23906296 C>T maps to NM_014363.4 A3906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:23906839 A>G maps to NM_014363.4 G3725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:23913081 G>A maps to NM_014363.4 R1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr13:23910865 G>A maps to NM_014363.4 R2383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr13:23912947 A>G maps to NM_014363.4 S1689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr13:23942623 G>A maps to NM_014363.4 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr13:23905183 A>G maps to NM_014363.4 P4277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:23911666 G>A maps to NM_014363.4 P2116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr13:23914669 G>A maps to NM_014363.4 V1115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr13:23905615 A>G maps to NM_014363.4 G4133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:23906307 G>A maps to NM_014363.4 R3903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:23942606 C>T maps to NM_014363.4 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr13:23904754 G>A maps to NM_014363.4 C4420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:23909032 A>G maps to NM_014363.4 P2994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr13:23912385 G>A maps to NM_014363.4 R1877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:23908126 A>G maps to NM_014363.4 P3296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:5668283 C>T maps to ENST00000433404 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr19:5667091 C>T maps to ENST00000433404 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:5590401 G>A maps to NM_014649.2 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:5587936 G>A maps to NM_014649.2 R860R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:5587942 C>T maps to NM_014649.2 Q858Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:5587355 G>A maps to NM_014649.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:5590362 G>A maps to NM_014649.2 D817D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:5587292 A>G maps to NM_014649.2 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:5592762 G>A maps to NM_014649.2 I781I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:5587936 G>A maps to NM_014649.2 R860R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:234243631 T>G maps to NM_000541.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:134989195 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:134989147 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:134988581 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:134993907 G>C did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:134989589 G>T did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:134987487 G>A did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:134991105 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:134990643 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:134991089 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:134993841 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:134994096 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:134983780 A>G did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:134989522 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:134978400 G>A did not map to a codon.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr23:134986672 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr23:134983754 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:134995055 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:134983829 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:134989588 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:134986645 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:134993392 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr23:134993828 G>T did not map to a codon.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr16:51174296 G>A maps to ENST00000251020 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:51171373 G>A maps to ENST00000251020 G1208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:51174347 G>A maps to ENST00000251020 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:51175742 C>T maps to ENST00000251020 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:51171061 G>A maps to ENST00000251020 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:51174227 C>T maps to ENST00000251020 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:51173540 A>G maps to ENST00000251020 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr16:51174932 C>T maps to ENST00000251020 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:51173597 G>A maps to ENST00000251020 D845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:51185146 C>T maps to ENST00000251020 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr16:51175646 G>A maps to ENST00000251020 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:21993075 A>G maps to NM_005407.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr14:21992024 C>A maps to NM_005407.1 G613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:76753091 C>T maps to NM_171999.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:76754570 C>T maps to NM_171999.2 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr18:76754795 C>T maps to NM_171999.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr18:76753964 G>A maps to NM_171999.2 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr18:76754297 G>T maps to NM_171999.2 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:76752143 C>T maps to NM_171999.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr18:76757102 C>T maps to NM_171999.2 N1228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr18:76753439 G>A maps to NM_171999.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr18:76754621 C>T maps to NM_171999.2 N877N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:76753349 C>T maps to NM_171999.2 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:76754297 G>A maps to NM_171999.2 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:76752131 C>T maps to NM_171999.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:76753553 C>T maps to NM_171999.2 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr18:76757282 G>A maps to NM_171999.2 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:76752224 C>T maps to NM_171999.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:50407172 G>T maps to NM_020436.3 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:50400911 G>A maps to NM_020436.3 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr20:50406870 C>T maps to NM_020436.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr20:50406882 G>A maps to NM_020436.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr20:50407884 G>A maps to NM_020436.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:50407920 G>A maps to NM_020436.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:50418890 G>A maps to NM_020436.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr20:50408025 G>A maps to NM_020436.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr20:50406891 C>T maps to NM_020436.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr20:50405477 G>A maps to NM_020436.3 H888H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:50400935 G>A maps to NM_020436.3 N1010N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:119391936 G>A maps to NM_207506.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:130505665 C>T maps to ENST00000457563 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:55203854 C>T maps to NM_015589.4 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:55169044 G>A maps to NM_015589.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:39860436 C>T maps to NM_018028.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:39867346 C>T maps to NM_018028.2 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:169642897 A>G maps to NM_182610.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr10:76928352 C>T maps to ENST00000372690 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:76910645 C>T maps to ENST00000372690 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:92732008 C>T maps to NM_017654.3 W1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:92732374 T>C maps to NM_017654.3 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:92733451 T>C maps to NM_017654.3 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:92731908 G>A maps to NM_017654.3 Q1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr7:92760775 T>A maps to NM_152703.2 T1503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:92762802 G>A maps to NM_152703.2 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:92762824 G>A maps to NM_152703.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:92762802 G>A maps to NM_152703.2 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr7:92761612 G>T maps to NM_152703.2 S1224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr7:92764561 G>A maps to NM_152703.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:92761054 G>A maps to NM_152703.2 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:35521336 A>C maps to NM_015474.3 *627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr20:35555599 C>T maps to NM_015474.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr20:35526363 T>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:35539641 C>A maps to NM_015474.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr22:44379811 G>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:44368143 C>T maps to NM_015380.4 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr21:15882783 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:15893518 G>A maps to ENST00000285670 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr21:15872911 G>A maps to ENST00000285670 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr21:15858409 A>G maps to ENST00000285670 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr21:15889304 C>A maps to ENST00000285670 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:128707455 G>A maps to NM_001145928.1 D954D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:128707899 T>C maps to NM_001145928.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:128700068 G>A maps to NM_001145928.1 Q1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:128770680 G>A maps to NM_001145928.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:128712740 G>A maps to NM_001145928.1 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:128757639 C>T maps to NM_001145928.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:73664706 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:73699939 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:73698583 C>T maps to NM_013260.6 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:55742809 G>A maps to ENST00000443936 H871H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:55758267 G>A maps to ENST00000443936 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:55753610 G>A maps to ENST00000443936 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:50854559 T>C maps to ENST00000216061 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:50876601 G>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr22:50857309 T>A maps to ENST00000216061 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr10:71913592 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:133944076 A>C maps to NM_016103.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:133944177 C>A maps to NM_016103.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:133948426 A>G maps to NM_016103.3 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:136536720 C>T maps to NM_007101.3 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:136573486 G>A maps to NM_007101.3 Y464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:136536723 G>A maps to NM_007101.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr9:136573411 G>A maps to NM_007101.3 H489H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:136550365 G>A maps to NM_007101.3 N704N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:136596525 G>A maps to NM_007101.3 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:136577754 A>G maps to NM_007101.3 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:136594898 G>A maps to NM_007101.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr9:136550314 C>G maps to NM_007101.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:136573534 C>T maps to NM_007101.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:136529112 G>A maps to NM_007101.3 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:65746364 C>A maps to NM_005146.4 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:65732566 G>T maps to NM_005146.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr11:65743975 C>T maps to NM_005146.4 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr11:65744003 C>T maps to NM_005146.4 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr11:65732650 G>A maps to NM_005146.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:108954645 C>T maps to NM_014706.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:108924059 G>A maps to NM_014706.3 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:108926094 G>A maps to NM_014706.3 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:108918244 C>T maps to NM_014706.3 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:108917392 C>T maps to NM_014706.3 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:108931975 G>A maps to NM_014706.3 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr12:108920103 G>A maps to NM_014706.3 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:148808835 C>T maps to NM_015278.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:148854020 C>T maps to NM_015278.3 Y551Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:148711346 C>T maps to NM_015278.3 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:148848671 A>G maps to NM_015278.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:148840731 C>T maps to NM_015278.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:148865653 G>A maps to NM_015278.3 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:148865704 C>T maps to NM_015278.3 S1033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:148865428 C>T maps to NM_015278.3 H941H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:148852696 G>A maps to NM_015278.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:148761498 G>A maps to NM_015278.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:128924994 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:128926654 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:128925042 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:128914079 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:128927704 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:128926611 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:100587964 A>G maps to NM_194292.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:23801522 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:23803943 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:18456689 C>T maps to ENST00000332610 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:18391063 C>T maps to ENST00000332610 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:18391029 G>A maps to ENST00000332610 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr3:18435983 T>C maps to ENST00000332610 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:18458391 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:18462396 A>G maps to ENST00000332610 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr3:18457584 A>C maps to ENST00000332610 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:18390696 C>A maps to ENST00000332610 G787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:18393519 C>T maps to ENST00000332610 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:18435992 G>T maps to ENST00000332610 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:200298073 C>T maps to NM_001172509.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:200246469 G>A maps to NM_001172509.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:200298106 C>T maps to NM_001172509.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:200213630 G>A maps to NM_001172509.1 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr2:200298163 G>A maps to NM_001172509.1 H81H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:84363303 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:84363504 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:84363028 T>A did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:84363383 G>A did not map to a codon.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr23:84363372 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:84362914 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:84362934 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:84362427 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:84363313 G>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:84363666 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:51111570 G>A maps to NM_021818.2 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:51107478 T>G maps to NM_021818.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:66453458 G>A maps to NM_016038.2 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:50894790 G>A maps to ENST00000337034 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr22:50900899 C>T maps to ENST00000337034 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr22:50903025 G>A maps to ENST00000337034 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:50897732 C>T maps to ENST00000337034 S1269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:50900412 G>T maps to ENST00000337034 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:50886874 T>G did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr22:50900129 C>T maps to ENST00000337034 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:9861196 G>A maps to NM_030962.3 S1101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr16:28330502 C>T maps to NM_001024401.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:28331527 C>T maps to NM_001024401.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr19:56041243 G>A maps to NM_001101401.2 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:56047628 C>T maps to NM_001101401.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:123810083 G>A maps to NM_001167856.1 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:123794050 G>A maps to NM_001167856.1 H1174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:123782546 C>T maps to NM_001167856.1 T1339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr12:123810083 G>A maps to NM_001167856.1 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr12:123825558 C>T maps to NM_001167856.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:123794265 C>A maps to NM_001167856.1 G1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:1109759 G>A maps to NM_014963.2 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:1119038 C>A maps to NM_014963.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:1123581 C>T maps to NM_014963.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:1108859 G>A maps to NM_014963.2 I1178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:36018664 T>G maps to NM_001166034.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:36018973 G>A maps to NM_001166034.1 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr4:166254722 A>G maps to NM_006745.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:121178115 G>A maps to NM_001024956.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:121177764 G>A did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr19:50156861 C>T maps to NM_021228.2 D1072D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:50155637 G>A maps to NM_021228.2 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr19:50156699 A>C maps to NM_021228.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:50158030 C>G maps to NM_021228.2 G1174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:127764274 G>A maps to NM_173690.4 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:127781188 A>G maps to NM_173690.4 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:127828330 T>C maps to NM_173690.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:77717662 T>C maps to NM_004866.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:77717682 T>C maps to NM_004866.4 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:75146370 C>T maps to NM_005697.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr19:1918890 C>T maps to NM_079834.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:1918914 G>A maps to NM_079834.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr15:75309054 C>T maps to ENST00000361900 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr15:75310758 C>T maps to ENST00000361900 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr15:75308976 G>A maps to ENST00000361900 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr15:75308940 C>T maps to ENST00000361900 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr6:28539969 G>C maps to NM_052923.1 T1232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:28540668 G>A maps to NM_052923.1 C999C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:28541298 T>C maps to NM_052923.1 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:28540658 G>A maps to NM_052923.1 R1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr6:28542999 G>A maps to NM_052923.1 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:28543299 C>T maps to NM_052923.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:28540479 T>C maps to NM_052923.1 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:47466982 G>A maps to NM_012235.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:47465456 C>T maps to NM_012235.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:47467487 C>T maps to NM_012235.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:47468973 G>A maps to NM_012235.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:76643602 C>T maps to ENST00000324767 A1358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:76673781 T>C maps to ENST00000324767 Q1214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr15:76994110 T>C maps to ENST00000324767 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:77020933 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:27507228 C>T maps to NM_016240.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:27507231 C>T maps to NM_016240.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr8:27516484 C>T maps to NM_016240.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:27528558 C>T maps to NM_016240.2 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:27514296 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:27516064 G>A maps to NM_016240.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:27779235 G>A maps to NM_173833.5 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:27779529 C>T maps to NM_173833.5 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:27779547 C>T maps to NM_173833.5 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:27737173 G>A maps to NM_173833.5 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr8:27729525 G>A maps to NM_173833.5 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:27764716 G>A maps to NM_173833.5 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr12:125294826 G>A maps to NM_005505.4 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:125294751 G>T maps to NM_005505.4 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:125279751 G>A maps to NM_005505.4 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:77095432 A>G maps to NM_005506.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:1538420 G>A maps to NM_003693.2 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:1548907 G>A maps to NM_003693.2 H28H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:1548209 G>A maps to NM_003693.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:1538648 G>A maps to NM_003693.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr17:1538828 C>T maps to NM_003693.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr22:20780318 C>T maps to NM_153334.4 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr22:20785155 G>A maps to NM_153334.4 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr22:20780114 G>A maps to NM_153334.4 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:246921559 A>G maps to NM_016002.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:102107858 G>A maps to NM_005063.4 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:83602053 G>A maps to NM_001037582.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr4:83626456 G>A maps to NM_001037582.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr13:78133953 T>C maps to NM_144777.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:78177255 T>C maps to NM_144777.2 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr13:78130728 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:78191949 T>C maps to NM_144777.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr14:31191755 C>T maps to ENST00000311943 D617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr14:31119853 C>T maps to ENST00000311943 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:53773692 G>A maps to NM_152540.3 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:54231547 A>G maps to NM_152540.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:54231559 A>G maps to NM_152540.3 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:224463772 T>C maps to NM_003469.4 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:224462953 A>T maps to NM_003469.4 Y349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:224463301 G>T maps to NM_003469.4 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr2:224462647 C>T maps to NM_003469.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:224463091 G>T maps to NM_003469.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr2:224462278 C>T maps to NM_003469.4 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr15:51974744 A>G maps to NM_013243.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:32988791 G>A maps to NM_001144757.1 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:32936005 C>T maps to NM_001144757.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr15:32972070 C>T maps to NM_001144757.1 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:62186575 C>T maps to NM_003357.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr11:62064965 G>A maps to NM_206998.1 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:62064987 G>A maps to NM_206998.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr11:61977933 C>T maps to NM_002407.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:35085148 G>A maps to NM_001025591.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:25665220 C>T maps to NM_006998.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:25689705 T>C maps to NM_006998.3 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr6:25665244 C>T maps to NM_006998.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:159583996 G>T maps to NM_001197113.1 G345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr3:159614518 G>T maps to NM_001197113.1 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:12683794 C>T maps to NM_001112706.2 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr7:12680056 C>G maps to NM_001112706.2 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:129812261 G>A maps to NM_144643.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:129920858 G>A maps to NM_144643.2 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:129878252 T>C maps to NM_144643.2 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:41536330 C>T maps to NM_001031694.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:17768145 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:17771449 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:17771409 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:18260690 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:18264788 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:18274982 C>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:18278347 G>A did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:18352181 T>G did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:108066254 G>T maps to NM_198081.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:108067977 G>A maps to NM_198081.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:108067995 C>T maps to NM_198081.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr6:108068007 G>A maps to NM_198081.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:108070972 C>T maps to NM_198081.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:108041976 C>T maps to NM_198081.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:38802797 G>A maps to NM_006514.2 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:38753795 A>G maps to NM_006514.2 D1315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:38798266 G>C maps to NM_006514.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:38768330 G>T maps to NM_006514.2 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:38740024 T>C maps to NM_006514.2 S1562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:38793712 G>A maps to NM_006514.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:38793748 C>T maps to NM_006514.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr3:38739467 C>T maps to NM_006514.2 W1748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr3:38941491 G>A maps to ENST00000302328 R639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:38968334 T>A maps to ENST00000302328 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr3:38912934 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:38888508 A>G maps to ENST00000302328 D1684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:38889231 A>G maps to ENST00000302328 S1443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:38892064 C>A maps to ENST00000302328 E1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:38938680 A>C maps to ENST00000302328 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:38913773 G>A maps to ENST00000302328 T1135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr3:38913163 G>A maps to ENST00000302328 A1177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr3:38949574 A>C maps to ENST00000302328 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:166900483 G>A maps to NM_001165963.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:166848768 G>A maps to NM_001165963.1 N1672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:166911251 A>C maps to NM_001165963.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:166900451 G>A maps to NM_001165963.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr2:166852555 C>T maps to NM_001165963.1 S1516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:166908334 G>A maps to NM_001165963.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:166894546 G>A maps to NM_001165963.1 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr2:166848777 C>T maps to NM_001165963.1 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:166859077 G>A maps to NM_001165963.1 C1396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:166894492 A>G maps to NM_001165963.1 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:166892599 C>A maps to NM_001165963.1 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr2:166908379 G>T maps to NM_001165963.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:35523453 C>T maps to NM_199037.3 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:35523444 C>T maps to NM_199037.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:166226694 T>C maps to NM_001040142.1 A1245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr2:166245403 C>T maps to NM_001040142.1 N1696N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:166245808 A>T maps to NM_001040142.1 I1831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:166165864 T>C maps to NM_001040142.1 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:166246012 G>A maps to NM_001040142.1 T1899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:166223835 C>T maps to NM_001040142.1 F1210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:166229776 G>T maps to NM_001040142.1 E1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr2:166221687 G>A maps to NM_001040142.1 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr2:166179793 C>A maps to NM_001040142.1 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:166170515 C>A maps to NM_001040142.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:166152443 C>A maps to NM_001040142.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:166201249 T>C maps to NM_001040142.1 N916N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr2:165984254 G>A maps to NM_006922.3 F1093F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:165984284 G>A maps to NM_006922.3 Y1083Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:165997313 G>A maps to NM_006922.3 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:165947774 G>A maps to NM_006922.3 R1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:165996040 G>T maps to NM_006922.3 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:166021011 G>T maps to NM_006922.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:123508895 G>A maps to NM_018400.3 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:62020336 C>T maps to NM_000334.4 Q1379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:62045680 C>T maps to NM_000334.4 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr17:62018997 G>A maps to NM_000334.4 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr17:62025363 G>T maps to NM_000334.4 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:62036660 G>A maps to NM_000334.4 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:62020204 G>C maps to NM_000334.4 V1423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:62049997 G>A maps to NM_000334.4 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:62049080 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:62022371 G>T maps to NM_000334.4 R1257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr17:62049997 G>A maps to NM_000334.4 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:62028987 G>A maps to NM_000334.4 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:62018463 G>A maps to NM_000334.4 H1726H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr3:38591856 G>A maps to NM_001099404.1 A2002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:38591856 G>A maps to NM_001099404.1 A2002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:38592495 G>A maps to NM_001099404.1 D1789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:38640418 G>A maps to NM_001099404.1 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr3:38618179 G>C maps to NM_001099404.1 V1161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:38628974 G>A maps to NM_001099404.1 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr3:38640418 G>A maps to NM_001099404.1 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr3:38648285 G>A maps to NM_001099404.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:38601895 G>A maps to NM_001099404.1 G1329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:38639228 G>A maps to NM_001099404.1 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:38592795 G>A maps to NM_001099404.1 D1689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr3:38651270 G>A maps to NM_001099404.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr3:38651267 G>A maps to NM_001099404.1 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr3:38649646 G>A maps to NM_001099404.1 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:38592950 G>A maps to NM_001099404.1 R1638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:38597182 G>T maps to NM_001099404.1 G1502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:38616850 G>A maps to NM_001099404.1 I1201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:167298019 C>G maps to NM_002976.2 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:167262950 T>C maps to NM_002976.2 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:167304119 A>G did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr2:167284333 A>G maps to NM_002976.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:167288976 C>A maps to NM_002976.2 E815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:167289040 A>G maps to NM_002976.2 H793H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:52094953 C>T maps to NM_014191.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:52100213 G>A maps to NM_014191.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:52115619 G>A maps to NM_014191.2 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr12:52156330 A>T maps to NM_014191.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:52156378 C>T maps to NM_014191.2 D821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr12:52100393 G>A maps to NM_014191.2 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:52174461 C>T maps to NM_014191.2 A1283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr12:52200909 A>G maps to NM_014191.2 K1880K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr2:167133780 T>A maps to ENST00000303354 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:167133717 G>A maps to ENST00000303354 V884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr2:167060510 T>C maps to ENST00000303354 V1577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr12:6464508 C>A maps to NM_001159576.1 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:6457296 C>T maps to NM_001159576.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:23364328 C>T maps to ENST00000307331 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr16:23366786 C>T maps to ENST00000307331 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:23379278 C>T maps to ENST00000307331 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr16:23360099 C>T maps to ENST00000307331 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:23360159 C>T maps to ENST00000307331 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:1225649 G>T did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr16:23197804 C>T maps to NM_001039.3 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:23197804 C>T maps to NM_001039.3 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:23200703 T>C maps to NM_001039.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr16:23226786 C>G maps to NM_001039.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:23208717 A>C maps to NM_001039.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr16:23221165 C>T maps to NM_001039.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr16:23200993 T>A did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr16:23205500 G>A maps to NM_001039.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:50962177 G>A maps to NM_001169111.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr22:50962654 C>A maps to NM_001169111.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:53427302 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:53446174 C>T maps to NM_002979.4 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:55075764 C>T maps to NM_021626.2 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:55062740 C>T maps to NM_021626.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr17:55058575 G>T maps to NM_021626.2 L70L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-6452-01A-12D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:144891171 G>A maps to NM_182706.3 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:144893467 G>A maps to NM_182706.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:144895814 G>A maps to NM_182706.3 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:144874387 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:29994973 G>A maps to NM_001145514.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:29980469 A>G maps to NM_001145514.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:29983716 A>G maps to NM_001145514.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:45915934 G>A maps to NM_138355.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:145559732 C>T maps to NM_031309.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:145557212 G>A maps to NM_031309.4 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:145557014 C>T maps to NM_031309.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr20:644734 C>T maps to NM_033129.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr2:120236429 C>T maps to NM_002980.2 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:43604219 C>A maps to NM_173050.2 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr22:43610150 G>A maps to NM_173050.2 C666C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:43619154 G>A maps to NM_173050.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:43616480 G>A maps to NM_173050.2 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:43619154 G>A maps to NM_173050.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:43735242 T>C did not map to a codon.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr22:43600116 C>T maps to NM_173050.2 A951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:43623395 G>A maps to NM_173050.2 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:43735178 G>A maps to NM_173050.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:43610138 G>A maps to NM_173050.2 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:43687106 G>A maps to NM_173050.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:9077337 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:9100943 A>G maps to ENST00000457346 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:9111332 G>A maps to ENST00000457346 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr11:9090968 G>T maps to ENST00000457346 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr11:9096028 T>C maps to ENST00000457346 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:35201058 C>T maps to ENST00000394681 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr6:35209383 C>A maps to ENST00000394681 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:35210955 C>T maps to ENST00000394681 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:35196499 C>T maps to ENST00000394681 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:35196407 C>T maps to ENST00000394681 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr6:35210048 C>T maps to ENST00000394681 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:35205682 C>A maps to ENST00000394681 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:65294589 T>C did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:65298113 C>T maps to NM_020680.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:65305556 C>T maps to NM_020680.3 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr12:100685288 A>C maps to NM_017988.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:100732688 C>A maps to NM_017988.4 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:100732520 C>T maps to NM_017988.4 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:100708310 T>C maps to NM_017988.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:169823860 G>A maps to NM_181093.2 C573C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:169823857 C>T maps to NM_181093.2 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:169825072 G>A maps to NM_181093.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:20403768 C>A maps to NM_001006946.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:20402950 C>T maps to NM_001006946.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:97620627 C>T maps to NM_002998.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr8:97620627 C>T maps to NM_002998.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr20:43964514 G>A maps to NM_002999.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr20:43964514 G>A maps to NM_002999.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:59490614 G>A maps to NM_005625.3 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:1294130 C>T maps to NM_080489.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:1294127 G>A maps to NM_080489.4 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:50255863 C>T maps to NM_004713.3 K965K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr14:50298923 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:50269384 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:50298923 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:243433518 C>T maps to NM_006642.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:243542115 A>C maps to NM_006642.3 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:243433518 C>T maps to NM_006642.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr1:243579010 A>T maps to NM_006642.3 K542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr17:26982391 C>T maps to NM_006923.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:1154241 G>A maps to NM_016176.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr1:1153079 C>T maps to NM_016547.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:1152972 G>A maps to NM_016176.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr5:236616 G>A maps to NM_004168.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:230996 C>T maps to NM_004168.2 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:233709 G>A maps to NM_004168.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:256534 A>G maps to NM_004168.2 *665W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:235282 C>T maps to NM_004168.2 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:235261 C>T maps to NM_004168.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:17359569 T>G maps to NM_003000.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:111965594 G>A maps to NM_003002.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:4172019 G>A maps to NM_152744.3 W1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:4088995 G>A maps to NM_152744.3 P873P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8382-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:3681705 G>T maps to NM_152744.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr7:4002412 C>T maps to NM_152744.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:4002412 C>T maps to NM_152744.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:4185462 C>T maps to NM_152744.3 S1446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:4091418 C>T maps to NM_152744.3 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:4169721 A>G maps to NM_152744.3 K1374K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:4007007 A>T maps to NM_152744.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:4304865 A>G maps to NM_152744.3 A2164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr7:4116663 C>T maps to NM_152744.3 N1015N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:4304817 C>T maps to NM_152744.3 S2148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:4152941 C>T maps to NM_152744.3 N1152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:4304976 C>T maps to NM_152744.3 G2201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr7:4014045 G>A maps to NM_152744.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr7:4277372 C>T maps to NM_152744.3 L2029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr7:4285415 G>C maps to NM_152744.3 S2120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:4050652 C>T maps to NM_152744.3 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:3678716 A>G maps to NM_152744.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr7:3658796 C>T maps to NM_152744.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:71398133 G>A maps to NM_001144952.1 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr17:71391441 C>T maps to NM_001144952.1 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr17:71361523 A>G maps to NM_001144952.1 A1726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:71418541 C>A maps to NM_001144952.1 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:71346416 G>A maps to NM_001144952.1 S1999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:71382018 G>T maps to NM_001144952.1 P1512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:71389697 C>A did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr2:192701335 C>A maps to NM_004657.5 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:192711450 G>A maps to NM_004657.5 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:192700725 G>A maps to NM_004657.5 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:192700906 C>T maps to NM_004657.5 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:192711618 G>A maps to NM_004657.5 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:192701019 G>A maps to NM_004657.5 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:57224835 T>C maps to NM_138969.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:57317807 G>A maps to NM_148897.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr12:113837435 G>A maps to NM_006843.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:113830823 G>A maps to NM_006843.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr17:26692242 C>G maps to NM_001080837.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:85230952 G>A maps to NM_014300.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr3:10354287 G>A maps to ENST00000343726 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:75196654 G>A maps to NM_001039573.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr17:75209493 C>T maps to NM_001039573.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:75209490 C>T maps to NM_001039573.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr17:75196730 G>T maps to NM_001039573.2 G329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:75196726 C>T maps to NM_001039573.2 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr17:75209547 C>T maps to NM_001039573.2 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr17:75186882 A>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:75205425 C>T maps to NM_001039573.2 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr22:30812328 C>T maps to NM_012429.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr22:30857303 G>A maps to NM_174975.4 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr22:30891384 G>A maps to NM_174977.3 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:30887695 G>A maps to NM_174977.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:30891932 G>A maps to NM_174977.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr22:30890900 C>A maps to NM_174977.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:5058570 C>T maps to NM_014692.1 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr16:5064922 G>A maps to NM_014692.1 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr16:5064913 C>T maps to NM_014692.1 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:139358901 C>T maps to NM_014866.1 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:139361485 G>T maps to NM_014866.1 P1284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr9:139370904 G>T maps to NM_014866.1 S388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr9:139368956 A>C maps to NM_014866.1 L1037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr9:139342535 C>T maps to NM_014866.1 S2130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:139370018 C>T maps to NM_014866.1 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:139370930 T>C maps to NM_014866.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:139368830 C>T maps to NM_014866.1 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:139358970 A>G maps to NM_014866.1 H1449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:139341369 A>C maps to NM_014866.1 T2243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:139360441 G>A maps to NM_014866.1 A1425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:139369937 G>T maps to NM_014866.1 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:139342120 C>T maps to NM_014866.1 P2153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr9:139362891 A>G maps to NM_014866.1 Y1259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:139371656 C>T maps to NM_014866.1 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:177901699 C>A maps to NM_033127.2 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:122944100 A>G maps to NM_012430.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:145103955 C>T maps to NM_004892.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr1:145112422 A>C maps to NM_004892.4 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:145109529 T>C maps to NM_004892.4 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:42605069 G>T maps to NM_032970.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:42605165 G>A maps to NM_032970.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:39556130 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:39556143 A>G maps to NM_006364.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:39532545 A>G maps to NM_006364.2 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:39565193 T>C maps to NM_006364.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr20:18531752 C>T maps to NM_001172745.1 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr10:121691685 C>T maps to NM_007190.2 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr10:121658152 C>T maps to NM_007190.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:121658044 T>C maps to NM_007190.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr10:121652326 C>T maps to NM_007190.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:134011748 G>A maps to NM_021982.1 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:133997277 T>C did not map to a codon.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr5:134044578 G>T did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr5:134010342 C>T maps to NM_021982.1 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:110442691 C>T maps to NM_006323.2 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:110427545 A>G maps to NM_006323.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:110451568 G>T maps to NM_006323.2 A1067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr4:110460755 G>A maps to NM_006323.2 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:110384495 C>T maps to NM_006323.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr4:110446547 A>G maps to NM_006323.2 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:110384729 G>A maps to NM_006323.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr10:75520603 C>T maps to NM_198597.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:119644735 G>A maps to ENST00000379735 Y1012Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr4:119652577 G>A maps to ENST00000379735 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:83787986 G>A maps to ENST00000505472 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:83785681 G>A maps to ENST00000505472 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:83785627 G>A maps to ENST00000505472 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:83799933 C>T maps to ENST00000505472 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:83800029 G>T maps to ENST00000505472 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr10:102248650 C>T maps to NM_015490.3 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:102247504 C>A maps to NM_015490.3 V1136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:102265958 C>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:127786376 A>T maps to ENST00000464451 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr3:127779500 C>T maps to ENST00000464451 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr3:127785876 G>A maps to ENST00000464451 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr3:127785924 T>C maps to ENST00000464451 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:127778966 C>T maps to ENST00000464451 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr3:127786364 C>G maps to ENST00000464451 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:54823469 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:169710493 G>A maps to NM_003262.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:91964706 C>T maps to NM_024077.3 D585D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:49329873 A>G maps to NM_001193489.1 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr15:49284560 C>T maps to NM_001193489.1 G1062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:49303985 T>C maps to NM_001193489.1 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr15:49303925 A>G did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:49284488 C>T maps to NM_001193489.1 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:81952723 G>A maps to NM_005065.4 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:81993275 G>A maps to NM_005065.4 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:81993095 T>G maps to NM_005065.4 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:81945991 G>A maps to NM_005065.4 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:81952776 G>A maps to NM_005065.4 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:81953756 G>A maps to NM_005065.4 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:81993206 G>T maps to NM_005065.4 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:13846097 G>T maps to NM_025229.1 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:13839961 C>T maps to NM_025229.1 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:13912276 T>C maps to NM_025229.1 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:13847379 C>A maps to NM_025229.1 G458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:13894523 G>A maps to NM_025229.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:13847353 A>G maps to NM_025229.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:13867088 C>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:25806252 C>T maps to NM_015187.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr4:25849030 C>T maps to NM_015187.3 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:25769162 G>A maps to NM_015187.3 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:25834645 G>A maps to NM_015187.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:25806333 C>T maps to NM_015187.3 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:25849270 G>A maps to NM_015187.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:169697057 G>A maps to NM_000450.2 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:169696646 C>A maps to NM_000450.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:169699579 G>T maps to NM_000450.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:169701060 G>A maps to NM_000450.2 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:151337120 G>A maps to ENST00000435071 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:169676574 C>T maps to NM_000655.4 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:169677834 A>G maps to NM_000655.4 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr22:50649341 T>C did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:169562866 G>A maps to NM_003005.3 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:169559385 T>G maps to NM_003005.3 *831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:169581512 C>T maps to NM_003005.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:169586491 G>A maps to NM_003005.3 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:109017882 A>C maps to ENST00000228463 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr12:109017036 G>A maps to ENST00000228463 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:83591010 G>T maps to NM_006080.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:83739841 C>A maps to NM_006080.2 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:83590758 C>T maps to NM_006080.2 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:83689811 G>A maps to NM_006080.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:50313250 C>T maps to NM_004636.2 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:80418724 C>T maps to NM_006379.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr7:80418652 A>G maps to NM_006379.2 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:80374452 C>T maps to NM_006379.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr7:80418757 G>T maps to NM_006379.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:80374226 G>A maps to NM_006379.2 Q747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:84671485 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:84702391 T>C maps to NM_152754.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr7:84751063 G>T maps to NM_152754.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr7:84628756 T>C maps to NM_152754.2 *778W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:84649546 A>G did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr7:84629052 C>A maps to NM_152754.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:84666333 G>T maps to NM_152754.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:83032081 G>A maps to NM_012431.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:83029536 G>A maps to NM_012431.2 Y391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:83032028 G>A maps to NM_012431.2 N354N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:83037702 G>A maps to NM_012431.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:83119549 A>G maps to NM_012431.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:83119549 A>G maps to NM_012431.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr3:50211340 C>T maps to NM_004186.3 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:50219759 T>C maps to NM_004186.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:50211665 C>T maps to NM_004186.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:52469714 C>T maps to NM_020163.1 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:52469660 A>G maps to NM_020163.1 H769H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr1:156146217 C>T maps to NM_022367.3 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:156132885 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:156124509 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:156132857 C>T maps to NM_022367.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:97526806 C>T maps to NM_017789.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:92003857 C>T maps to NM_006378.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:92006232 C>A maps to NM_006378.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:91994491 C>T maps to NM_006378.3 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:92011708 G>A maps to NM_006378.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:92006307 G>A maps to NM_006378.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:92003640 G>A maps to NM_006378.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr9:91996135 C>T maps to NM_006378.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:92020308 C>T maps to NM_006378.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:74883727 T>C maps to NM_004263.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:74907035 C>T maps to NM_004263.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:74901668 G>A maps to NM_004263.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:74885008 C>T maps to NM_004263.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:74900804 C>T maps to NM_004263.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:102743182 C>T maps to NM_017893.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:102732746 G>A maps to NM_017893.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr10:102739928 G>A maps to NM_017893.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:102732746 G>A maps to NM_017893.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:102743284 C>T maps to NM_017893.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:102743486 C>T maps to NM_017893.2 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:9044646 G>A maps to NM_003966.2 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:9154619 G>A maps to NM_003966.2 C487C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:9054361 G>A maps to NM_003966.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:9136645 C>T maps to NM_003966.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr5:9108374 A>G maps to NM_003966.2 C650C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:9066626 G>T maps to NM_003966.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:9122805 C>T maps to NM_003966.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:9052129 C>T maps to NM_003966.2 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:9044505 G>A maps to NM_003966.2 Y1028Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:9108326 T>G maps to NM_003966.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr5:9054241 C>A maps to NM_003966.2 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr5:9238003 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr5:9043029 G>C maps to NM_003966.2 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr5:9044616 A>C maps to NM_003966.2 T991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:122632509 C>T maps to NM_001031702.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr3:122680089 C>T maps to NM_001031702.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr3:122629129 A>G maps to NM_001031702.2 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:122631807 G>A maps to NM_001031702.2 C869C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:122641180 G>T maps to NM_001031702.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:122632811 C>A maps to NM_001031702.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:115840538 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr5:115815858 G>A maps to ENST00000257414 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:4548327 C>T maps to NM_032108.3 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:4557219 G>A maps to NM_032108.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:4548309 G>A maps to NM_032108.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:4558376 C>T maps to NM_032108.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:4550160 C>T maps to NM_032108.3 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:4555999 G>A maps to NM_032108.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:4552636 G>A maps to NM_032108.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:4550833 C>T maps to NM_032108.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:151115070 G>C maps to NM_001178061.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:151112137 T>C maps to NM_001178061.1 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:151110552 C>T maps to NM_001178061.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:48052027 G>C maps to NM_153618.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr15:48062706 A>G maps to NM_153618.1 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:48063627 T>G maps to NM_153618.1 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:48063819 T>C maps to NM_153618.1 H1020H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:48056379 T>G maps to NM_153618.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr15:48056165 T>C maps to NM_153618.1 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:48052499 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:48052031 C>T maps to NM_153618.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr15:48052516 G>A maps to NM_153618.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr15:48056123 T>G maps to NM_153618.1 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr15:48056478 C>T maps to NM_153618.1 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr15:74708914 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:74703165 G>A maps to NM_003612.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr20:43837254 A>T maps to NM_003007.3 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr20:43836660 G>A maps to NM_003007.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr20:43837006 C>T maps to NM_003007.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr20:43850986 C>A maps to NM_003008.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr20:43851685 A>G maps to NM_003008.2 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:48477396 G>A maps to ENST00000004980 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:48441860 A>G maps to ENST00000004980 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:48441827 G>A maps to ENST00000004980 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:185318607 C>A maps to ENST00000427465 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:7468285 C>T maps to ENST00000321337 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:7466635 G>A maps to ENST00000321337 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr17:7468153 C>T maps to ENST00000321337 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:196626926 T>C maps to NM_152699.4 N584N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr3:196612954 T>C maps to NM_152699.4 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:196612798 G>A maps to NM_152699.4 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr6:76412459 T>C maps to NM_015571.2 C796C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:101083731 A>G maps to NM_020654.3 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:101083704 T>C maps to NM_020654.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr3:101062679 A>C maps to NM_020654.3 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:101060605 C>T maps to NM_020654.3 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:101136597 C>T maps to NM_020654.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:87333765 T>C maps to NM_004261.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr10:13370451 T>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:13364895 C>T maps to NM_012247.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:30455814 G>A maps to ENST00000478753 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr16:30456418 C>G maps to ENST00000478753 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:30455782 A>G maps to ENST00000478753 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:26131654 C>T maps to NM_020451.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr1:26131720 T>C maps to NM_020451.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:110310707 G>A maps to ENST00000356688 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:4834041 G>A maps to NM_144605.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr16:4835890 T>G did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:242265514 A>G maps to ENST00000391972 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr22:42383243 C>T maps to NM_145733.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:42377817 C>T maps to NM_145733.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr22:42390312 T>A maps to NM_145733.2 C295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:56598408 T>C maps to NM_004574.3 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:56604288 G>A maps to NM_004574.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:56598157 G>A maps to NM_004574.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:19707944 C>T maps to NM_002688.5 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:118797508 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:118763452 G>A did not map to a codon.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr23:118767451 T>C did not map to a codon.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr23:118767372 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:118763371 T>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:75398264 C>T maps to NM_001113491.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:67895977 A>G maps to NM_001018067.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:18028252 C>T maps to NM_012139.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:122768016 A>G maps to NM_020755.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr6:122779729 A>G maps to NM_020755.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:122768309 T>C maps to NM_020755.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:31901826 C>T maps to NM_178865.4 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:31896676 G>A maps to NM_178865.4 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:43142669 G>A maps to NM_006811.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:43141455 C>T maps to NM_006811.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:79498703 C>T did not map to a codon.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr5:79465283 A>G maps to NM_001174072.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:79446740 G>A maps to NM_001174072.1 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr14:94847293 G>A maps to NM_001127707.1 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:94849520 C>A maps to NM_001127707.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr14:94756414 A>G maps to NM_001100607.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:94754759 A>G maps to NM_001100607.1 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:94750337 C>G maps to NM_001100607.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:94754717 C>T maps to NM_001100607.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:94914994 C>T maps to NM_001080451.1 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:94964323 C>T maps to NM_173850.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr14:94964632 G>A maps to NM_173850.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:94964478 G>A maps to NM_173850.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:95081255 C>T maps to ENST00000393080 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr14:95088713 C>T maps to ENST00000393080 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr14:95081071 G>A maps to ENST00000393080 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:95030430 C>T maps to NM_006215.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:95033395 C>T maps to NM_006215.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:95033559 G>A maps to NM_006215.2 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:94780964 G>T maps to NM_001756.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:94772521 G>T maps to NM_001756.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:105279291 G>A did not map to a codon.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr23:105281008 A>C did not map to a codon.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr23:105279200 C>T did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr23:105281008 A>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:105280957 T>C did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:105278298 C>T did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:94936050 G>A maps to NM_175739.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr14:94933606 A>C maps to NM_175739.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:94929504 G>A maps to NM_175739.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr14:94936108 C>T maps to NM_175739.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr18:61223521 T>C maps to ENST00000382768 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr18:61231354 T>C did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:61260165 C>T maps to NM_012397.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:61260182 C>A maps to NM_012397.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr18:61260155 C>T maps to NM_012397.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:61264398 C>T maps to NM_012397.3 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:61562568 G>A maps to NM_001143818.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr18:61564332 T>A maps to NM_001143818.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr18:61326659 G>A maps to NM_006919.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:61323040 T>C maps to NM_006919.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:61323052 T>A maps to NM_006919.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:61323055 A>G maps to NM_006919.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr18:61323109 G>A maps to NM_006919.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:61326635 T>C maps to NM_006919.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:61322929 G>T maps to NM_006919.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:61154234 G>A maps to NM_002639.4 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:61156697 G>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:61170597 G>A maps to NM_002639.4 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:2948627 G>A maps to ENST00000316782 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:61471658 T>C maps to NM_001040147.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:61463516 C>T maps to NM_001040147.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:61649052 G>A maps to NM_198833.1 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr18:61649023 G>T maps to NM_198833.1 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:173883879 C>T maps to NM_000488.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:100775297 C>T maps to NM_000602.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:224863029 T>A maps to NM_001136530.1 K109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr17:1650310 A>C did not map to a codon.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr17:1657611 C>T maps to NM_000934.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:57373914 C>A maps to ENST00000403558 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:75280188 T>C maps to NM_001235.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:167510375 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr3:167508346 C>G maps to NM_005025.4 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:167189552 G>A maps to NM_006217.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr3:167159898 A>G maps to NM_006217.3 *406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr3:167189427 T>A maps to NM_006217.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:40928925 A>G maps to NM_013376.3 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:64863062 A>C maps to NM_014755.2 *315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:40947827 T>G maps to NM_203344.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:210415015 G>A maps to NM_019605.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:210415405 C>A maps to NM_019605.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr6:109311939 A>C maps to NM_014454.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:94922972 T>C maps to NM_144665.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr11:94923016 T>G maps to NM_144665.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179982317 G>A maps to NM_178123.4 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:179982317 G>A maps to NM_178123.4 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr2:179979929 T>C maps to NM_178123.4 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:42531131 C>T maps to NM_015559.2 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr18:42531917 T>C maps to NM_015559.2 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr18:42530072 C>A maps to NM_015559.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr18:42643633 C>T maps to NM_015559.2 R1588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:42530291 T>C maps to NM_015559.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr18:42532659 G>T maps to NM_015559.2 G1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:42531515 C>A maps to NM_015559.2 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr18:42532898 G>A maps to NM_015559.2 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:42531548 C>T maps to NM_015559.2 H748H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:42531686 C>T maps to NM_015559.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:42643098 C>T maps to NM_015559.2 C1409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:42533096 T>G maps to NM_015559.2 S1264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr18:42531905 C>T maps to NM_015559.2 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr18:42531539 C>T maps to NM_015559.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr18:42618510 A>C maps to NM_015559.2 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:42530474 C>T maps to NM_015559.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:30982822 C>G maps to NM_014712.1 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:30990955 G>A maps to NM_014712.1 S1283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:30990643 G>A maps to NM_014712.1 P1179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:30976310 G>A maps to NM_014712.1 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr16:30982810 C>A maps to NM_014712.1 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:30991057 C>A maps to NM_014712.1 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:30977127 G>A maps to NM_014712.1 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr16:30970467 C>T maps to NM_014712.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:30976103 C>A maps to NM_014712.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:30992461 C>T maps to NM_014712.1 D1591D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:47098829 T>C maps to NM_014159.6 S2148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:47142945 A>G did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:47098793 C>T maps to NM_014159.6 P2160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr3:47087997 C>A maps to NM_014159.6 G2359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr3:47127692 G>A maps to NM_014159.6 Q1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:99865306 C>T maps to NM_032233.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:99871570 G>T maps to NM_032233.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:99865306 C>T maps to NM_032233.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr14:99927669 G>A maps to NM_032233.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:99865450 G>A maps to NM_032233.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:37408416 A>G maps to NM_017438.3 *441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr21:37417936 C>T maps to NM_017438.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr21:37416161 G>A maps to NM_017438.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr21:37417921 G>A maps to NM_017438.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:9517750 C>T maps to ENST00000407969 V1454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:9482138 G>T did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr3:9515160 C>G maps to ENST00000407969 S1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:9483390 C>T maps to ENST00000407969 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:58549964 C>T maps to NM_001160305.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:58550380 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:140454489 G>T maps to NM_030648.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:140468096 C>T maps to NM_030648.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:123892234 G>A maps to NM_020382.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:123889558 C>T maps to NM_020382.3 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:123875277 T>C maps to NM_020382.3 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:123875316 C>T maps to NM_020382.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:150921646 C>T maps to NM_001145415.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:150921646 C>T maps to NM_001145415.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr1:150933456 C>T maps to NM_001145415.1 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:50050782 T>A maps to NM_031915.2 C171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:50055081 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr13:50062610 C>T maps to NM_031915.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:4355147 A>G maps to NM_006515.3 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:135202645 A>G maps to ENST00000372169 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:135203174 C>T maps to ENST00000372169 P1270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:135201785 C>T maps to ENST00000372169 V1733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:135187171 G>A maps to ENST00000372169 A1782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:135150683 C>T maps to ENST00000372169 T2353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:135221765 T>C maps to ENST00000372169 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:135152520 T>C maps to ENST00000372169 R2287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr9:135205648 G>A maps to ENST00000372169 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:135202829 G>A maps to ENST00000372169 D1385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr17:27284558 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:27308955 G>A maps to NM_178860.4 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:26688918 A>G maps to NM_021115.4 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr22:26706695 C>T maps to NM_021115.4 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:26688423 A>G maps to NM_021115.4 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:26747186 G>A maps to NM_021115.4 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr22:26688612 C>T maps to NM_021115.4 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr22:26707734 G>A maps to NM_021115.4 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr22:26688387 A>C maps to NM_021115.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr22:26688838 C>T maps to NM_021115.4 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:26701981 C>T maps to NM_021115.4 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:26747036 C>T maps to NM_021115.4 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:29884675 C>T maps to NM_201575.2 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:64535598 G>A maps to NM_201995.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:30730630 G>A maps to NM_005877.4 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:30734846 C>T maps to NM_005877.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:30734813 C>T maps to NM_005877.4 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:2247959 G>A maps to NM_007165.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:2246900 C>T maps to NM_007165.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:38449888 G>A maps to NM_006802.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:38444661 G>A maps to NM_006802.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:198273120 T>C maps to NM_012433.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:198257722 T>C maps to NM_012433.2 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:198265471 A>G maps to NM_012433.2 G895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:24291235 A>G maps to NM_016047.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:65824847 T>C did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:65827422 G>A maps to NM_006842.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:65825860 C>T maps to NM_006842.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:65822671 G>C maps to NM_006842.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:65828120 C>T maps to NM_006842.2 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:70590844 T>C maps to NM_012426.4 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:70597913 T>C maps to NM_012426.4 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:70575718 T>C maps to NM_012426.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:70599268 A>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:149898337 T>C maps to NM_005850.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr1:149898268 T>C maps to NM_005850.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:149898715 C>T maps to NM_005850.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:19391026 G>A maps to NM_172231.2 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:19390192 G>A maps to NM_172231.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:19388562 G>A maps to NM_172231.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:32000923 C>T maps to NM_001007467.1 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr22:32010835 C>T maps to NM_001007467.1 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:52962273 G>A maps to NM_016329.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:52950205 G>A maps to NM_016329.3 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr3:52941258 G>A maps to NM_016329.3 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:52962300 G>A maps to NM_016329.3 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:52966156 A>G maps to NM_016329.3 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:52945124 G>A maps to NM_016329.3 C600C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:7290521 C>T maps to NM_001018039.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:7409611 G>A maps to NM_001018039.1 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:7269821 G>A maps to NM_001018039.1 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:7214078 G>A maps to NM_001018039.1 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:7326037 A>G maps to NM_001018039.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:7213934 T>C maps to NM_001018039.1 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:7290595 G>T maps to NM_001018039.1 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:7239568 T>G maps to NM_001018039.1 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr10:7218090 G>A maps to NM_001018039.1 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr1:27189930 G>A maps to NM_006142.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:35658416 C>T maps to NM_005066.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:35652836 G>A maps to NM_005066.2 R611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr8:41161049 C>T maps to NM_003012.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:154709837 G>A maps to NM_003013.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:154702745 C>A maps to NM_003013.2 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:154709513 G>A maps to NM_003013.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr7:37951869 G>A maps to ENST00000223214 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr7:37955824 G>A maps to ENST00000223214 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:37947092 C>T maps to ENST00000223214 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr7:37947098 T>C maps to ENST00000223214 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:37955851 C>T maps to ENST00000223214 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:37947146 T>C maps to ENST00000223214 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr7:37955824 G>A maps to ENST00000223214 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr17:56084462 C>T maps to NM_006924.4 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:70700383 C>T maps to NM_004768.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:70694200 C>T maps to NM_004768.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:70700392 A>G maps to NM_004768.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:65473380 C>T maps to NM_001077199.1 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:65458073 G>A maps to NM_001077199.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:64036932 G>A maps to ENST00000513458 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:19112468 G>A maps to NM_001017392.3 R982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:19120787 C>T maps to NM_001017392.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:19115184 G>A maps to NM_001017392.3 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:19136832 G>A maps to NM_001017392.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:19135650 G>A maps to NM_001017392.3 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:19136067 A>G maps to NM_001017392.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:19136840 C>A maps to NM_001017392.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:19106050 G>A maps to NM_001017392.3 T1010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr21:33068879 A>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr21:33074094 G>A maps to NM_020706.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr21:33065756 G>A maps to NM_020706.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr21:33043942 C>T maps to NM_020706.2 E1071E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr21:33044065 C>T maps to NM_020706.2 R1030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:33057461 G>A maps to NM_020706.2 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr21:33044467 G>A maps to NM_020706.2 G896G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr21:33057744 A>G maps to NM_020706.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr21:33076195 G>C maps to NM_020706.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:33057482 C>T maps to NM_020706.2 V789V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:45543569 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:45573321 C>T maps to NM_007056.2 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:45570837 C>T maps to NM_007056.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:1720220 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:1712725 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:1712691 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1712481 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:1719899 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:1713016 A>G did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:1712645 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:1712435 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:1712693 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:1712813 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:1712982 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:1714398 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:1719943 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:99852512 G>A maps to NM_032870.2 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:99857154 T>C maps to NM_032870.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:99848924 G>A maps to NM_032870.2 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:46321968 C>T maps to NM_004719.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:46320291 A>G maps to NM_004719.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:46320407 C>A maps to NM_004719.2 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:46316820 C>T maps to NM_004719.2 S1341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:46322022 A>G maps to NM_004719.2 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:46316716 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:46325349 G>T maps to NM_004719.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:29475242 C>T maps to NM_005626.4 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:29475302 A>G maps to NM_005626.4 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:42089153 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:38975757 G>A maps to NM_001031684.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr12:132199457 G>A maps to NM_004592.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr12:120899956 A>C maps to NM_003769.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:166738050 G>A maps to NM_145169.1 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:81317087 G>A maps to NM_001098668.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr10:81317844 G>C maps to NM_001098668.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:81319122 G>A maps to NM_001098668.2 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr10:81317141 A>G maps to NM_001098668.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:81317024 T>G maps to NM_001098668.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:85890527 G>A maps to NM_198843.2 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:22020094 C>T maps to NM_003018.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr10:81706391 T>C maps to NM_003019.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:104491949 G>A maps to NM_178858.4 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:104486821 C>T maps to NM_178858.4 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr10:104492638 A>C maps to NM_178858.4 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:102795319 C>T maps to NM_030971.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr10:120925114 T>G maps to NM_213649.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:120921920 A>G maps to NM_213649.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:73198776 G>A maps to NM_144579.2 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:73198728 G>A maps to NM_144579.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr17:48252710 C>T maps to NM_000023.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:52895984 G>A maps to NM_000232.4 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:52895881 G>A maps to NM_000232.4 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:155771591 C>T maps to NM_000337.5 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr7:94229959 G>A maps to NM_001099401.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr7:94232733 C>T maps to NM_001099401.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr13:23894856 G>A maps to NM_000231.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr8:13965703 C>T maps to NM_139167.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:13965703 C>T maps to NM_139167.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr8:13948095 G>T maps to NM_139167.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr3:153840068 G>A maps to NM_015595.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr3:153840233 C>T maps to NM_015595.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7735-01A-11D-2053-08 chr3:153973255 C>T maps to NM_015595.3 N870N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr3:153840210 C>T maps to NM_015595.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr1:67147693 C>T maps to ENST00000237247 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr1:67148038 G>A maps to ENST00000237247 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:67147852 G>A maps to ENST00000237247 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:67101640 C>T maps to NM_032291.2 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr6:134494620 G>A maps to NM_001143676.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:42977374 G>A maps to NM_032237.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr20:42199270 G>A maps to NM_016276.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr20:42196349 G>A maps to NM_016276.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:8176713 C>T maps to NM_001080826.1 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:8185549 G>A maps to NM_001080826.1 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:8233917 C>T maps to NM_001080826.1 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:8234217 C>T maps to NM_001080826.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr8:8176269 C>T maps to NM_001080826.1 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:8185777 G>A maps to NM_001080826.1 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:8234931 G>T maps to NM_001080826.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:8234262 T>C maps to NM_001080826.1 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:8235192 G>A maps to NM_001080826.1 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:8176629 G>A maps to NM_001080826.1 C1085C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:8235347 C>A maps to NM_001080826.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:8185960 C>G maps to NM_001080826.1 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:8234139 G>A maps to NM_001080826.1 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:8176404 G>A maps to NM_001080826.1 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:8234244 C>T maps to NM_001080826.1 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:8235509 G>T maps to NM_001080826.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:77425508 G>A maps to NM_024776.2 C1305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr15:77473382 G>A maps to NM_024776.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:77426054 T>C maps to NM_024776.2 P1123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:77473379 G>A maps to NM_024776.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:67763156 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:67753311 T>C maps to NM_013257.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:67755775 T>C maps to NM_013257.3 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr17:26940279 C>T maps to NM_001174103.1 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:52103661 G>A maps to ENST00000361543 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:108824538 G>T maps to NM_152621.5 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:108816771 G>A maps to NM_152621.5 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:20219764 T>C maps to NM_001012410.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:20225108 T>C maps to NM_001012410.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:201437567 A>G maps to NM_152524.5 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:201435830 C>T maps to NM_152524.5 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr2:201440163 T>C maps to NM_152524.5 F1254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:201437240 T>C maps to NM_152524.5 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:72630884 T>C maps to NM_003901.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:72636412 G>T maps to NM_003901.3 G521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:25264716 C>T maps to NM_001039948.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:25294420 G>A maps to NM_001039948.2 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr22:25320201 C>T maps to NM_001039948.2 D1136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:25270529 G>A maps to NM_001039948.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr22:25264775 G>A maps to NM_001039948.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:25243745 G>A maps to NM_001039948.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr22:25294156 G>A maps to NM_001039948.2 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr22:25315859 G>A maps to NM_001039948.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:2279114 C>T maps to NM_014853.2 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:2280071 C>T maps to NM_014853.2 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:2275733 C>T maps to NM_014853.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:40801670 C>T maps to NM_015705.4 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:40805349 C>T maps to NM_015705.4 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:40802506 G>A maps to NM_015705.4 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:40803529 C>T maps to NM_015705.4 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:40802127 C>T maps to NM_015705.4 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:2767592 C>T maps to NM_003021.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr5:64967779 T>G maps to NM_019072.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:28883269 C>T maps to NM_001145795.1 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:28883541 C>T maps to NM_001145795.1 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:101952176 C>T maps to ENST00000306803 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:101944460 C>T maps to ENST00000306803 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:111886069 C>T maps to NM_005475.2 H564H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:123504038 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:162372592 C>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:156779192 G>A maps to NM_001161441.1 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:156779464 G>A maps to NM_001161441.1 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:6755213 C>T maps to NM_005490.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:6752654 C>T maps to NM_005490.2 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr9:130502090 T>C maps to NM_170600.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr9:130504084 A>G maps to NM_170600.2 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:130536741 G>A maps to NM_170600.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:130502624 C>T maps to NM_170600.2 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:130507378 C>T did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr9:130507126 G>A maps to NM_170600.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:130536606 C>T maps to NM_170600.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr8:19192367 A>C maps to NM_022071.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr8:19218775 G>A maps to NM_022071.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:21053505 G>A maps to ENST00000444387 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:21052442 G>A maps to ENST00000444387 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:21048380 G>A maps to ENST00000444387 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:21051062 C>T maps to ENST00000444387 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:21050921 C>T maps to ENST00000444387 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:85662597 T>C maps to NM_198482.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr15:78393575 C>A maps to NM_001101404.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:78390802 C>A maps to NM_001101404.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:78390310 C>T maps to NM_001101404.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:78384985 C>T maps to NM_001101404.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:80532614 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:80457738 A>G did not map to a codon.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr23:80552705 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:80406275 A>G maps to NM_031469.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:38039704 G>A maps to NM_018957.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:38051300 G>A maps to NM_018957.3 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:38046209 C>T maps to NM_018957.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:38040645 C>T maps to NM_018957.3 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:2828968 G>A maps to NM_001145856.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:2831296 C>A maps to NM_001145856.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:2824765 T>C did not map to a codon.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr4:2828986 C>T maps to NM_001145856.1 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:235943669 G>A maps to NM_014521.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:235951090 C>T maps to NM_014521.2 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:235950855 T>C maps to NM_014521.2 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr2:235951698 C>A maps to NM_014521.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8210-01A-11D-2340-08 chr2:235951625 C>A maps to NM_014521.2 S738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:235951623 C>A maps to NM_014521.2 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr2:235950501 G>A maps to NM_014521.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:235951517 G>A maps to NM_014521.2 W702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr3:15300336 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:15303784 C>T maps to NM_004844.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:249108713 G>A maps to NM_030645.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:249106188 G>A maps to NM_030645.1 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr1:249108782 C>T maps to NM_030645.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:249107333 G>T maps to NM_030645.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:249108742 G>A maps to NM_030645.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:152065097 G>A maps to NM_001009555.3 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:152069208 A>T maps to NM_001009555.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:4365542 C>T maps to NM_003025.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:4361737 G>A maps to NM_003025.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:4365590 C>A maps to NM_003025.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr19:4361602 C>T maps to NM_003025.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:4365575 C>A maps to NM_003025.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:4362733 C>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr19:4361686 G>A maps to NM_003025.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:17795623 C>T maps to NM_003026.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:17789412 T>G maps to NM_003026.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr9:17795578 C>T maps to NM_003026.2 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:17791293 C>T maps to NM_003026.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:84237296 A>G maps to ENST00000434347 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:84287032 T>G maps to ENST00000434347 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:84245408 C>T maps to ENST00000434347 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:84255836 C>T maps to ENST00000434347 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr1:87190088 G>C did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:131771010 G>A maps to ENST00000372554 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr23:19725083 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:19560085 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:19649996 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:19626151 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:19587235 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:19606846 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:19587261 C>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:19610205 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:19725093 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:19626053 A>C did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr23:19560205 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:19560112 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:19560253 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:19701964 T>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:171765729 G>A maps to NM_001017995.2 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:171821625 G>A maps to NM_001017995.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:171766815 C>T maps to NM_001017995.2 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:171765429 G>A maps to NM_001017995.2 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr5:171765918 C>T maps to NM_001017995.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:171766377 C>T maps to NM_001017995.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr5:171765750 G>A maps to NM_001017995.2 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:170041970 T>G maps to NM_020870.3 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:145442092 G>A maps to NM_152550.3 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr5:145439567 C>T maps to NM_152550.3 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:145439647 G>A maps to NM_152550.3 W592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:110015251 G>A maps to NM_001099289.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:109964323 C>T maps to NM_001099289.1 H256H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:8230087 C>T maps to NM_018986.3 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr4:8235215 C>T maps to NM_018986.3 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:8229514 G>A maps to NM_018986.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr4:8229025 C>T maps to NM_018986.3 D535D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr4:8229127 G>A maps to NM_018986.3 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr4:8233833 C>T maps to NM_018986.3 Q1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:8229487 G>A maps to NM_018986.3 E689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:148407407 G>A maps to NM_024577.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:148406226 C>T maps to NM_024577.3 W987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:148386494 G>C maps to NM_024577.3 Y1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:148386497 C>T maps to NM_024577.3 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:148388498 C>T maps to NM_024577.3 K1131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:148406584 G>A maps to NM_024577.3 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:148422395 G>A maps to NM_024577.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr5:148407353 G>A maps to NM_024577.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:51217084 G>A maps to ENST00000391814 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:51165361 G>A maps to ENST00000391814 R2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:51200865 G>A maps to ENST00000391814 Y639Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:51217126 A>T maps to ENST00000391814 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:51169600 A>G maps to ENST00000391814 S1880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:51220125 G>A maps to ENST00000391814 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:51170838 G>A maps to ENST00000391814 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:51170212 C>T maps to ENST00000391814 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:70332068 G>A maps to ENST00000338508 S1437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr11:70332305 G>C maps to ENST00000338508 A1358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:70319222 C>T maps to ENST00000338508 S1761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr11:70332290 G>A maps to ENST00000338508 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:70331990 T>C maps to ENST00000338508 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:70333184 G>A maps to ENST00000338508 S1065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:51117290 C>T maps to NM_001080420.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:51160715 G>A maps to NM_001080420.1 G1501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:51160523 G>A maps to NM_001080420.1 P1437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:51117056 G>A maps to NM_001080420.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr22:51115075 C>A maps to NM_001080420.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:51117810 C>T maps to NM_001080420.1 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:51117230 C>T maps to NM_001080420.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:51133314 G>A maps to NM_001080420.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:51143259 C>T maps to NM_001080420.1 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr22:51142342 C>T maps to NM_001080420.1 Y572Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr22:51159689 T>C maps to NM_001080420.1 F1159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145154001 G>A maps to NM_030974.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:38068426 G>A maps to NM_003028.2 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:154942609 G>A maps to NM_001130040.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:154942741 T>G maps to NM_001130040.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:422187 G>A maps to NM_012435.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr19:422148 G>A maps to NM_012435.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:422253 G>A maps to NM_012435.2 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:434720 C>T maps to NM_012435.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:91628424 G>A maps to NM_016848.5 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:91680486 A>G maps to NM_016848.5 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr9:91686167 C>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:91657076 C>T maps to NM_016848.5 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:49135609 G>A maps to NM_203349.3 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:49176492 C>T maps to NM_203349.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:49135636 G>T maps to NM_203349.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:46629543 G>A maps to NM_024745.4 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr16:46649917 C>T maps to NM_024745.4 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:4280239 T>C maps to NM_020209.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:154461770 G>T maps to NM_001010846.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:154461734 G>A maps to NM_001010846.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:96339060 C>T maps to ENST00000449279 K5K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GX-01A-12D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:155604759 G>A maps to NM_000193.2 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:155595710 C>T maps to NM_000193.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:155604792 C>T maps to NM_000193.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:155596157 C>T maps to NM_000193.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr13:26620776 G>A maps to NM_001007538.1 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:42403230 G>A maps to NM_001080505.1 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr4:42403248 G>A maps to NM_001080505.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:48510799 G>T maps to NM_016479.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:48510562 G>A maps to NM_016479.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:48510574 G>A maps to NM_016479.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:48520623 C>T maps to NM_016479.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:18233875 G>A maps to NM_004169.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:18232625 T>C maps to NM_004169.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:57625343 G>A did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr12:57628066 C>T maps to NM_005412.5 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr12:57626615 C>T maps to NM_005412.5 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:57626075 G>A did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr10:112769018 C>G maps to NM_007373.3 S433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:595435 C>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:595444 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:591663 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:601806 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:601734 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:601805 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:591691 C>T did not map to a codon.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr23:591690 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:595376 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:595436 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr23:591762 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:3518748 G>T maps to NM_013276.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:146269405 A>G did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:146243471 A>G maps to ENST00000367503 C1248C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:146247354 G>A maps to ENST00000367503 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:146266672 G>A maps to ENST00000367503 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:146267450 C>T maps to ENST00000367503 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:146276056 G>A maps to ENST00000367503 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr6:146244888 C>G maps to ENST00000367503 V1154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:146244836 G>A maps to ENST00000367503 R1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:146264430 G>A maps to ENST00000367503 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:146264881 G>A maps to ENST00000367503 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:72842080 C>T maps to NM_018130.2 W389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:132159957 C>T maps to NM_001172700.1 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:132158968 C>T maps to NM_001172700.1 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:132161100 A>G maps to NM_001172700.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:9912765 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:9914757 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:9900830 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:9864476 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:9862479 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:9864048 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:9905624 A>G did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:9900502 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:9863382 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:9862715 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:9900721 G>A did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:9905181 G>A did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:9864516 G>A did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:9863305 A>G did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:9864464 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:9863552 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:9864115 C>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:9859143 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:77661572 G>A maps to NM_020859.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr4:77677625 A>T maps to NM_020859.3 T1578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:77678004 C>T maps to NM_020859.3 R1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:77662484 C>T maps to NM_020859.3 S1053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr4:77675847 G>A maps to NM_020859.3 E1404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:50339873 C>T did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:50378090 G>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:50377324 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:50557008 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:50350730 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:50378664 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:50377846 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:50378058 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr23:50377349 G>A did not map to a codon.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr23:50376815 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr23:50350384 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:50350730 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:50377271 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:50350981 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:50377494 T>G did not map to a codon.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr23:50376643 T>G did not map to a codon.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr23:50377312 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:164709997 G>A maps to NM_001041.3 Y1650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:164764646 A>G maps to NM_001041.3 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:164755740 A>G maps to NM_001041.3 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:164758855 C>T maps to NM_001041.3 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr3:164700804 T>C maps to NM_001041.3 Q1744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:164700039 A>G maps to NM_001041.3 T1802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:164754249 T>C maps to NM_001041.3 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:164786977 A>G maps to NM_001041.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr3:164735641 A>C maps to NM_001041.3 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr3:164735641 A>C maps to NM_001041.3 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:164709250 G>A maps to NM_001041.3 G1666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr3:164764796 A>G maps to NM_001041.3 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:164777021 C>T maps to NM_001041.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:164755787 G>A maps to NM_001041.3 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr3:164735778 A>G maps to NM_001041.3 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr3:164735641 A>C maps to NM_001041.3 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:164781329 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr3:164764700 A>G maps to NM_001041.3 N605N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:124524548 A>G did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr11:124508509 A>C maps to NM_170601.3 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr11:124543598 G>C maps to NM_170601.3 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:124530685 C>T maps to NM_170601.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:48396330 A>G maps to NM_001006610.1 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:150460020 G>A maps to NM_005067.5 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:150460128 G>A maps to NM_005067.5 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr3:150480300 C>T maps to NM_005067.5 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:150480303 G>A maps to NM_005067.5 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr13:46358018 C>T maps to NM_198849.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:46357727 G>T maps to NM_198849.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:46357607 C>A maps to NM_198849.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:113320433 G>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:113286533 C>A maps to ENST00000393830 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:113321948 C>T maps to ENST00000393830 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:113329933 C>T maps to ENST00000393830 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:113320471 C>T maps to ENST00000393830 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:113329945 C>A maps to ENST00000393830 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:113295780 C>T maps to ENST00000393830 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:113321885 C>A maps to ENST00000393830 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:113345004 C>T maps to ENST00000393830 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:117066582 C>T maps to NM_001040455.1 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:117060708 C>T maps to NM_001040455.1 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr11:117053269 G>A maps to NM_001040455.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:117059505 C>T maps to NM_001040455.1 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:117066549 G>A maps to NM_001040455.1 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:406483 G>A maps to NM_021805.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:408789 G>T maps to NM_021805.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:3686655 C>T maps to NM_023068.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:3677371 A>G maps to NM_023068.3 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:3683916 A>G maps to NM_023068.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr20:3686511 G>A maps to NM_023068.3 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:3678697 C>T maps to NM_023068.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:3677392 A>G maps to NM_023068.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:3683940 C>T maps to NM_023068.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:3678775 G>T maps to NM_023068.3 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr20:3675128 G>A maps to NM_023068.3 R999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:51920663 C>T maps to NM_033130.4 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr19:51920006 G>A maps to NM_033130.4 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr19:51918540 C>T maps to NM_033130.4 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:51914439 C>T maps to NM_033130.4 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:51920399 C>T maps to NM_033130.4 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:50463679 T>C did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:51994930 G>A maps to NM_053003.2 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:52002706 G>A maps to NM_053003.2 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:52002869 C>T maps to NM_053003.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:52004969 T>C maps to NM_053003.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:52000163 G>A maps to NM_053003.2 D523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N2-01A-12D-A364-08 chr19:52149164 G>A maps to NM_001098612.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr18:43418863 G>A maps to NM_213602.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:52115549 C>T maps to ENST00000222107 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:52115534 G>A maps to ENST00000222107 D535D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:52023334 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:52033694 G>A maps to NM_001245.5 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:51647693 C>T maps to NM_014385.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:51958777 C>A maps to NM_014442.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:51955751 G>A maps to NM_014442.2 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:51960985 G>T maps to NM_014442.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:51955641 G>A maps to NM_014442.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr19:51960993 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:51961533 C>T maps to NM_014442.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:51957484 G>T maps to NM_014442.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr19:51958737 G>A maps to NM_014442.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:51958726 G>A maps to NM_014442.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:51629112 C>T maps to NM_014441.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr19:51629019 G>A maps to NM_014441.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:44840206 G>A maps to NM_173354.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:111582988 C>T maps to NM_015191.1 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:111558768 C>T maps to NM_015191.1 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:111594561 A>G maps to NM_015191.1 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:111594577 G>T maps to NM_015191.1 G836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:111591458 A>C maps to NM_015191.1 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:111594684 A>G maps to NM_015191.1 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr11:111572255 G>A maps to NM_015191.1 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr11:111571701 C>T maps to NM_015191.1 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:116744246 G>A maps to ENST00000445177 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr11:116734446 G>T maps to ENST00000445177 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr11:116719988 T>G maps to ENST00000445177 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:138282991 T>C maps to ENST00000509534 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:138287503 C>T maps to ENST00000509534 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:56355191 A>G maps to NM_006928.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:100841489 C>T maps to ENST00000262901 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:100838635 C>T maps to ENST00000262901 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:100838548 C>T maps to ENST00000262901 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:100896392 G>A maps to ENST00000262901 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:100896022 C>T maps to ENST00000262901 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:100838311 A>C maps to ENST00000262901 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:100896061 G>A maps to ENST00000262901 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:75664418 G>A maps to NM_001145357.1 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:75664483 C>A maps to NM_001145357.1 E1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr15:75703973 C>T maps to NM_001145357.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:75676744 G>A maps to NM_001145357.1 Q1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:75687178 G>A maps to NM_001145357.1 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:75676748 A>G maps to NM_001145357.1 C1017C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:16980623 G>A maps to NM_015260.1 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:16980659 G>A maps to NM_015260.1 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:16980512 G>A maps to NM_015260.1 E715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr19:16942379 C>T maps to NM_015260.1 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr19:16982064 C>T maps to NM_015260.1 Y848Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:16942352 G>A maps to NM_015260.1 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr11:65413831 G>A maps to NM_153253.29 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:65417118 T>C maps to NM_153253.29 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:65409995 G>A maps to NM_153253.29 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:65417934 G>A maps to NM_153253.29 Q989Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:65408616 C>T maps to NM_153253.29 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:72191398 C>T maps to NM_015556.1 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr14:72055764 G>A maps to NM_015556.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:72190561 C>T maps to NM_015556.1 P1490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:72117104 T>C maps to NM_015556.1 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:72128175 C>A maps to NM_015556.1 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:72117189 G>T maps to NM_015556.1 G653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:72128160 G>A maps to NM_015556.1 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:72056088 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:72191385 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:72191425 G>A maps to NM_015556.1 R1517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:232581354 C>T maps to NM_020808.3 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:232581414 A>G maps to NM_020808.3 T1071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:232579379 G>A maps to NM_020808.3 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:232650506 T>C maps to NM_020808.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:232581404 G>A maps to NM_020808.3 Q1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr1:232615459 C>T maps to NM_020808.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:232615459 C>T maps to NM_020808.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:232564164 G>A maps to NM_020808.3 R1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:232577108 G>A maps to NM_020808.3 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr1:232615429 G>A maps to NM_020808.3 Y676Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:38572894 C>T maps to NM_015073.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:38655201 C>T maps to NM_015073.1 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:38572873 C>T maps to NM_015073.1 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:38610321 T>C maps to NM_015073.1 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:38573488 G>A maps to NM_015073.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:38597246 C>A maps to NM_015073.1 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:38655372 C>T maps to NM_015073.1 G1345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:38684259 C>T maps to NM_015073.1 P1560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr19:38573566 C>T maps to NM_015073.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr19:38573203 G>A maps to NM_015073.1 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:38573386 C>T maps to NM_015073.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:38572720 C>T maps to NM_015073.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:1902287 C>T maps to ENST00000400068 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:1918078 G>A maps to ENST00000400068 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:1903214 G>A maps to ENST00000400068 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:1903085 C>A maps to ENST00000400068 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr20:1551634 G>T maps to NM_006065.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr20:1546811 G>A maps to NM_006065.3 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr20:1592288 C>A maps to NM_001135844.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:1559071 G>A maps to NM_006065.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:1459010 G>A maps to NM_001122962.1 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr20:1456814 C>T maps to NM_001122962.1 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr20:1456937 T>G maps to NM_001122962.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr10:69672624 T>G maps to NM_012238.4 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:69672418 C>T maps to NM_012238.4 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:69647247 C>A maps to NM_012238.4 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:69647187 C>T maps to NM_012238.4 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:39380358 G>A maps to NM_012237.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:120750796 T>C maps to NM_012240.2 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:13601127 C>T maps to NM_012241.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:4179213 G>A maps to NM_016539.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr19:4180846 C>T maps to NM_016539.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:79873484 A>G did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:105222981 C>T maps to NM_006427.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:61115820 G>A maps to NM_005982.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr14:61115475 C>T maps to NM_005982.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:45235979 T>C maps to NM_016932.4 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:45235952 G>A maps to NM_016932.4 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:45236174 G>A maps to NM_016932.4 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:45235937 G>A maps to NM_016932.4 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:45235934 G>A maps to NM_016932.4 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:45169749 G>A maps to NM_005413.3 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr2:45171769 G>A maps to NM_005413.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:45169608 C>T maps to NM_005413.3 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:45169338 C>T maps to NM_005413.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:45169644 G>A maps to NM_005413.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:45169311 C>T maps to NM_005413.3 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:45169422 C>T maps to NM_005413.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:45169647 C>T maps to NM_005413.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr14:61190153 T>C maps to NM_017420.4 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:61190675 C>A maps to NM_017420.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:46270343 C>T maps to NM_175875.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:60977804 C>T maps to ENST00000381716 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:60976476 C>T maps to ENST00000381716 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr14:60976190 C>T maps to ENST00000381716 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:60976275 C>T maps to ENST00000381716 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:60976625 G>A maps to ENST00000381716 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:47917529 T>C maps to NM_145060.3 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:57189646 T>C maps to NM_182620.3 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr13:21750537 G>A maps to NM_145061.5 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:46257473 C>A maps to NM_003726.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:2235476 C>T maps to NM_003036.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:2235476 C>T maps to NM_003036.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:2235329 C>T maps to NM_003036.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr1:2160477 C>T maps to NM_003036.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:170078370 C>T maps to NM_005414.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:170078514 C>T maps to NM_005414.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:31928059 C>A maps to NM_006929.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:31935512 A>C maps to NM_006929.4 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr6:31933768 A>G maps to NM_006929.4 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr6:31930556 C>T maps to NM_006929.4 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr6:31929355 C>T maps to NM_006929.4 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:54696083 C>T maps to NM_015360.4 D772D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr5:133502890 T>C maps to NM_170679.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:36182100 C>T maps to NM_005983.2 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:134072363 C>T maps to NM_006748.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:35269702 T>C maps to NM_032214.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:78318469 G>A maps to ENST00000389459 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:160580588 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:160604613 G>A maps to NM_003037.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:160607203 G>A maps to NM_003037.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:160460407 G>A maps to NM_001184714.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr1:160466139 G>A maps to NM_001184714.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:160722025 A>G maps to NM_021181.3 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:160721133 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:159799701 C>T maps to NM_020125.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:159923321 G>T maps to NM_033438.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:159922265 G>A maps to NM_033438.3 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:159923099 G>C maps to NM_033438.3 Y130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:70263857 G>A maps to NM_003049.3 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr13:103703659 C>T maps to NM_000452.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153717217 C>T did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:153716439 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153716403 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153716481 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:153715993 G>T did not map to a codon.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr23:153716808 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:153717160 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153716942 C>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:48490496 C>T maps to NM_152679.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:48486087 G>A maps to NM_152679.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:48490766 G>A maps to NM_152679.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:82605998 T>C maps to NM_001010893.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr4:87744984 G>A maps to NM_197965.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr4:87769920 G>A maps to NM_197965.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr2:219247695 C>A maps to NM_000578.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:219251368 C>T maps to NM_000578.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:219258850 C>T maps to NM_000578.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:51393179 G>A maps to NM_001174125.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:51394195 G>A maps to NM_001174125.1 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:48543968 T>G did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr15:48559801 G>A maps to NM_000338.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr15:48522587 A>C did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr15:48594955 C>T maps to NM_000338.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:48580324 A>G maps to NM_000338.2 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr15:48539657 G>T did not map to a codon.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr15:48536974 C>T maps to NM_000338.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:127520069 T>C maps to NM_001046.2 F1104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:127487002 A>T maps to NM_001046.2 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:127483311 A>G did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:56903668 G>A maps to NM_000339.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:67979672 C>T maps to NM_005072.4 E947E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:67980238 G>T maps to NM_005072.4 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:67991803 A>G maps to NM_005072.4 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:67984389 G>A maps to NM_005072.4 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:67982037 G>A maps to NM_005072.4 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:67978778 G>A maps to NM_005072.4 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr20:44680471 C>T maps to NM_001134771.1 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:44678260 G>A maps to NM_001134771.1 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:44683556 T>C maps to NM_001134771.1 H917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:44685203 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr20:44666017 C>A maps to NM_001134771.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr20:44681716 C>T maps to NM_001134771.1 H856H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr15:34528244 T>C maps to NM_133647.1 E1066E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:34531352 C>T maps to NM_133647.1 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:1081764 T>C maps to NM_006598.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:1075483 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:1081758 G>T maps to NM_006598.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:1081833 G>A maps to NM_006598.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:1076891 C>T maps to NM_006598.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:1078055 G>A maps to NM_006598.2 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:124826844 G>A maps to NM_001195483.1 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr3:124826631 G>T maps to NM_001195483.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:100459097 C>T maps to NM_020246.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:100453457 C>T maps to NM_020246.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr7:100457772 C>T maps to NM_020246.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr7:100454553 C>T maps to NM_020246.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr7:122765668 A>G maps to NM_022444.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:122757647 A>G maps to NM_022444.3 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr7:122765621 C>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:26821103 A>G maps to NM_001145975.1 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:26817362 A>T maps to NM_001145975.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:26820744 C>A maps to NM_001145975.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:45212283 G>A maps to NM_022829.5 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr20:45242253 G>T maps to NM_022829.5 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:135380131 G>A maps to NM_012450.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:135384170 G>T maps to NM_012450.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:135384206 G>A maps to NM_012450.2 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:135366415 T>C maps to NM_012450.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr7:135377114 G>A maps to NM_012450.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:6604365 G>A maps to NM_177550.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr17:6610070 G>T maps to NM_177550.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:6607254 G>A maps to NM_177550.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:43311061 A>G maps to NM_001146037.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:43253754 C>T maps to NM_007163.3 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr18:43262294 G>A maps to NM_007163.3 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr18:43262348 C>A maps to NM_007163.3 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:43224099 C>T maps to NM_007163.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr18:43253754 C>T maps to NM_007163.3 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:43262375 G>A maps to NM_007163.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr18:43216966 T>C maps to NM_007163.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr18:43204733 G>A maps to NM_007163.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr18:43205721 C>T maps to NM_007163.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr13:99338491 G>A maps to NM_005073.3 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:99354750 T>C maps to NM_005073.3 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:99337070 G>A maps to NM_005073.3 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:99376272 C>T maps to NM_005073.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr13:99376173 A>G maps to NM_005073.3 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:99378624 G>A maps to NM_005073.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:121658260 G>A maps to NM_021082.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:121648150 A>T maps to NM_021082.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:60711285 G>A maps to NM_016582.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr12:129293453 C>A maps to ENST00000376744 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:129293468 A>C maps to ENST00000376744 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:113460045 G>A maps to NM_003051.3 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:113464648 G>A maps to NM_003051.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:111540114 C>T maps to NM_018593.4 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:6945993 C>T maps to NM_153357.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:6945417 G>A maps to NM_153357.1 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:6945060 G>A maps to NM_153357.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:91196051 A>G maps to NM_213606.3 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:6943211 C>A maps to NM_201566.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:6941567 C>T maps to NM_201566.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:230911028 G>A maps to NM_152527.4 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:230911331 G>A maps to NM_152527.4 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr2:230902152 C>T maps to NM_152527.4 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:230911274 C>T maps to NM_152527.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:73749122 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:73744203 C>A did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:73745698 A>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:73641743 G>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:73749162 C>G did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:73740838 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:80196836 G>A maps to NM_001042423.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr17:80195527 C>T maps to NM_001042423.1 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:110921592 A>G maps to NM_004696.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr1:110925530 G>A maps to NM_004696.1 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:110925480 G>A maps to NM_004696.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:110919613 G>A maps to NM_004696.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:110924292 C>T maps to NM_004696.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:73089823 C>T maps to ENST00000450736 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:73096198 C>T maps to ENST00000450736 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:73096180 C>T maps to ENST00000450736 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:73094193 C>T maps to ENST00000450736 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:66267453 G>A maps to NM_004694.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:66265356 T>C maps to NM_004694.4 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:66270119 G>A maps to NM_004694.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:60168465 C>T maps to NM_004731.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:60169003 C>T maps to NM_004731.3 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr12:60098668 C>A maps to NM_004731.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:38476856 C>T maps to NM_013356.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr22:38476958 C>T maps to NM_013356.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:61412655 G>A maps to NM_194298.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr10:61432671 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:61413937 A>G maps to NM_194298.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr10:61424003 C>T maps to NM_194298.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:25813373 T>C maps to NM_005074.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:25819946 C>T maps to NM_005074.3 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr6:25820065 T>C maps to NM_005074.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr6:25813352 C>T maps to NM_005074.3 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:25851023 G>T maps to NM_001098486.1 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr6:25861881 G>A maps to NM_001098486.1 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr6:25855393 C>T maps to NM_001098486.1 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:25850130 G>A maps to NM_001098486.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:25769387 G>A maps to NM_005495.2 W89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr11:22364896 G>A maps to NM_020346.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr11:22380964 C>T maps to NM_020346.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr11:22360123 G>C maps to NM_020346.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr11:22399037 G>T maps to NM_020346.2 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:22360099 G>A maps to NM_020346.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr19:49939973 C>T maps to NM_020309.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:49934334 G>A maps to NM_020309.3 N442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:49933838 G>T maps to NM_020309.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:49933844 C>T maps to NM_020309.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:49934361 G>A maps to NM_020309.3 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:49936184 C>T maps to NM_020309.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:49934367 C>T maps to NM_020309.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:100790164 A>C maps to NM_139319.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:100806590 G>A maps to NM_139319.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr12:100811870 C>T maps to NM_139319.2 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:100813744 C>T maps to NM_139319.2 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr20:61593999 C>T maps to NM_022082.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:61593987 C>T maps to NM_022082.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr20:61588203 C>G maps to NM_022082.3 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr20:61598710 C>T maps to NM_022082.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr20:61598821 G>C maps to NM_022082.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr20:61594077 C>T maps to NM_022082.3 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr20:61595620 G>A maps to NM_022082.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr20:61588849 C>T maps to NM_022082.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr20:61594679 C>T maps to NM_022082.3 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:61588221 C>T maps to NM_022082.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr8:20008199 A>G maps to NM_001135691.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:20005153 G>A maps to NM_001135691.2 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:20005578 A>G maps to NM_001135691.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:20004786 C>T maps to NM_001135691.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:119001290 G>A maps to NM_003054.4 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:119001215 C>T maps to NM_003054.4 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr10:119014800 C>T maps to NM_003054.4 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:50819067 G>A maps to NM_003055.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:50820183 G>A maps to NM_003055.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:50819157 C>T maps to NM_003055.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:50819835 G>A maps to NM_003055.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:50819082 G>A maps to NM_003055.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr21:46951770 G>A maps to NM_194255.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr21:46951795 C>T maps to NM_194255.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:228563935 C>T maps to NM_025243.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:228563509 C>T maps to NM_025243.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:228564102 C>A maps to NM_025243.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:4561476 C>T maps to NM_004170.5 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:35339031 G>A maps to NM_004171.3 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:36686194 C>T maps to NM_004172.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr2:65217088 G>C maps to NM_003038.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:15065110 G>A maps to NM_005071.1 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:15072899 A>G maps to NM_005071.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:15063789 G>A maps to NM_005071.1 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr19:15072962 G>A maps to NM_005071.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr19:15063867 C>T maps to NM_005071.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr1:53558322 G>A maps to NM_006671.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:113414817 C>T maps to NM_005415.3 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:42323319 C>T maps to NM_006749.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:42294679 G>A maps to NM_006749.3 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:42295009 G>A maps to NM_006749.3 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:42275485 C>A did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:160543053 G>A maps to NM_003057.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:160543353 G>A maps to NM_003057.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:160553305 C>T maps to NM_003057.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:160560825 C>T maps to NM_003057.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr6:160543065 G>A maps to NM_003057.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:63066990 A>G maps to NM_001039752.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:63064834 C>T maps to NM_001039752.3 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:64337279 G>A maps to NM_018484.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:64337279 G>A maps to NM_018484.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:64367851 G>A maps to NM_144585.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr11:64360336 C>T maps to NM_144585.2 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:38316618 G>A maps to NM_004256.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:38318561 G>A maps to NM_004256.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:116609274 G>A maps to NM_018420.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:116534698 G>A maps to NM_018420.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:116534716 C>T maps to NM_018420.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:116609274 G>A maps to NM_018420.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:110763588 T>C maps to NM_033125.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:23818479 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr14:23817779 G>A maps to NM_020372.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:160670318 G>A maps to NM_003058.3 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:160679618 G>A maps to NM_003058.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:160679771 G>A maps to NM_003058.3 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:64981837 G>A maps to ENST00000438990 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:3287168 G>A maps to ENST00000436008 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:3324123 C>T maps to ENST00000436008 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:3273471 C>T maps to ENST00000436008 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr6:3298379 G>A maps to ENST00000436008 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr11:62933696 A>C maps to NM_199352.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:160863899 C>T maps to ENST00000392145 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:160831879 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:160829896 G>A maps to ENST00000392145 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:160864676 G>A maps to ENST00000392145 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:160864676 G>A maps to ENST00000392145 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:131658039 G>A maps to NM_003059.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:131647915 C>T maps to NM_003059.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr5:131671562 C>A maps to NM_003059.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:131719976 G>T maps to ENST00000435065 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:131728209 C>T maps to ENST00000435065 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:62744859 C>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:62744710 G>A maps to NM_004790.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:62751909 G>A maps to NM_004790.3 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr6:43267174 T>G maps to ENST00000372585 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:62766430 A>G maps to ENST00000430500 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:62760981 G>A maps to ENST00000430500 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr11:62760954 G>T maps to ENST00000430500 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr11:62782145 G>A maps to ENST00000430500 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:138718264 C>T maps to NM_152685.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:138715403 G>A maps to NM_152685.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:220033489 G>C maps to NM_001144890.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:220028196 G>A maps to NM_001144890.1 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:220034256 A>G maps to NM_001144890.1 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr2:220032916 C>T maps to NM_001144890.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:19516257 G>A maps to NM_020344.2 R627*. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:19576948 G>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr9:19786834 A>C maps to NM_020344.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:19619588 G>A maps to NM_020344.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr9:19786621 A>C maps to NM_020344.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr20:19677541 T>C maps to NM_020689.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:19665749 A>T maps to NM_020689.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr20:19662609 C>T maps to NM_020689.3 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr20:19634755 G>A maps to NM_020689.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr14:92915525 C>T maps to NM_153646.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr14:92790233 G>A maps to NM_153646.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:92790254 C>T maps to NM_153646.3 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:48413288 C>T maps to NM_205850.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr15:48434313 A>G maps to NM_205850.2 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr15:48428924 G>A maps to NM_205850.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:19163995 C>T maps to NM_005984.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:79686862 C>T maps to ENST00000331531 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:4842263 C>T maps to NM_003562.4 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:4841844 G>A maps to NM_003562.4 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:4841477 G>T maps to NM_003562.4 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:95814284 T>C maps to NM_001160210.1 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr7:95813718 G>A maps to NM_001160210.1 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:95750583 C>A maps to NM_001160210.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:95775885 C>A maps to NM_001160210.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:95751262 C>T maps to NM_001160210.1 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:129505598 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:129505598 T>C did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:129480610 T>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr13:41381559 C>A maps to NM_014252.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr13:41383754 C>G maps to NM_014252.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr13:41379283 C>T maps to NM_014252.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:70243269 A>G maps to NM_152707.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:18064144 G>A maps to NM_031481.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr22:18064126 C>T maps to NM_031481.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:73274290 G>A maps to NM_021734.4 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:140682858 C>A maps to NM_031947.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr3:48896997 C>A maps to NM_000387.4 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr3:48896992 T>A maps to NM_000387.4 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr14:37180669 A>C maps to NM_030631.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:792013 G>A maps to NM_001191061.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:792876 C>A maps to NM_001191061.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:6457518 C>T maps to NM_024103.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:108681755 G>A maps to NM_013386.3 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:108703902 A>G maps to NM_013386.3 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:130869722 A>G maps to ENST00000373069 *516W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr9:130860952 C>G maps to NM_052901.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:130868030 C>T maps to ENST00000373069 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:130863445 A>G maps to ENST00000373069 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:66428186 C>T maps to NM_173471.3 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:66419941 A>G maps to NM_173471.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:46630233 C>T maps to NM_004277.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr14:100765193 C>T maps to NM_001039355.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:100758769 C>T maps to NM_001039355.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:104414249 A>G maps to NM_030780.3 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:104413838 G>A maps to NM_030780.3 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:8194158 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:8195897 T>C maps to NM_201520.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr8:23429082 C>T maps to NM_016612.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:23425871 G>A maps to NM_016612.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:39432999 C>T maps to NM_017875.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr3:39433035 C>T maps to NM_017875.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:39433003 C>T maps to NM_017875.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:42398591 G>A maps to NM_001143780.1 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:42399084 G>A maps to NM_001143780.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:186068022 A>G maps to NM_001151.3 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr4:186067968 C>T maps to NM_001151.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:6429779 G>A maps to NM_173637.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:19218783 C>T maps to NM_178526.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:118586847 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:118540543 C>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:65144508 C>A maps to NM_182556.2 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:65147335 A>G did not map to a codon.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr11:65144355 C>T maps to NM_182556.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr5:110091221 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:110096993 C>T maps to NM_138773.1 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:118604462 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:118603923 C>T did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr23:118604440 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:118604436 G>A did not map to a codon.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr23:118604435 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:118604093 C>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:1505553 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1505570 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:1508485 G>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:1505588 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:1508410 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr23:1508410 C>T did not map to a codon.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr23:1508414 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:1506202 C>T did not map to a codon.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr4:983160 G>A maps to NM_213613.2 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:983844 C>T maps to NM_213613.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr12:58019452 T>G maps to NM_133489.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:78195442 G>A maps to NM_173626.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:78210883 C>A maps to NM_173626.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:78221998 C>T maps to NM_173626.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr17:78221950 C>T maps to NM_173626.3 C439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:149360037 C>T maps to NM_000112.3 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr5:149357286 A>C maps to NM_000112.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr7:107408209 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:107418724 A>C maps to NM_000111.2 L470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr7:107303836 C>T maps to NM_000441.1 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:107303782 G>A maps to NM_000441.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:107314666 C>T maps to NM_000441.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr7:107341589 G>A maps to NM_000441.1 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr7:107329563 C>T maps to NM_000441.1 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:107335116 C>T maps to NM_000441.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr7:107323651 G>T maps to NM_000441.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:103050936 G>A maps to ENST00000354356 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:103017302 T>A maps to ENST00000354356 K667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:48670410 G>A maps to NM_022911.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr3:48670959 C>T maps to NM_022911.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr8:92364078 C>A maps to NM_134266.1 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:92406185 G>A maps to NM_134266.1 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr8:92406059 A>G maps to NM_134266.1 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr6:35919038 G>A maps to NM_052961.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:35919041 G>A maps to NM_052961.3 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:205899106 G>A maps to NM_134325.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr1:205884253 G>A maps to NM_134325.2 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:205890726 G>A maps to NM_134325.2 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:205893530 G>A maps to NM_134325.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:17608215 C>T maps to NM_198580.1 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:17608191 G>A maps to NM_198580.1 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:17597506 C>T maps to NM_198580.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17597440 G>A maps to NM_198580.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17597524 G>A maps to NM_198580.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr9:131117770 C>T maps to NM_005094.3 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:131107805 C>A maps to NM_005094.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:131105563 C>T maps to NM_005094.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr9:131117713 C>A maps to NM_005094.3 Y500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:59021256 G>A maps to NM_012254.2 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:59011986 G>A maps to NM_012254.2 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:59012769 G>T maps to NM_012254.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:128365382 C>T maps to NM_001017372.1 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:128359404 T>C did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr5:128302291 A>G maps to NM_001017372.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:85478613 C>T maps to NM_004213.3 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:85478325 C>T maps to NM_004213.3 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:85438267 C>T maps to NM_004213.3 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:45564562 T>C maps to NM_004212.3 C573C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8210-01A-11D-2340-08 chr15:45564490 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:45561561 C>T maps to NM_004212.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:86924586 T>G maps to NM_022127.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:44197198 G>A maps to ENST00000313248 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:66131817 G>A maps to NM_001532.2 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:66136982 G>T maps to NM_001532.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:66136540 G>A maps to NM_001532.2 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr11:66134944 G>C maps to NM_001532.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr11:66133937 C>T maps to NM_001532.2 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:66136991 C>T maps to NM_001532.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr10:73111462 C>T maps to NM_018344.5 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:73082558 C>A maps to NM_018344.5 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr10:73082525 A>C maps to NM_018344.5 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:73115850 C>T maps to NM_018344.5 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:73111354 G>A maps to NM_018344.5 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:5334525 C>T maps to NM_153247.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:5331432 C>T maps to NM_153247.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:5338626 A>G maps to NM_153247.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:5336804 C>T maps to NM_153247.2 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr7:5327608 G>A maps to NM_153247.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:5330863 C>T maps to NM_153247.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:5331405 C>T maps to NM_153247.2 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:43396802 C>T maps to NM_006516.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:43393383 G>A maps to NM_006516.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:43393338 G>A maps to NM_006516.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:43396473 C>T maps to NM_006516.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:43393458 G>T maps to NM_006516.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:43394614 C>T maps to NM_006516.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:45353774 C>T maps to NM_030777.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr20:45354454 C>A maps to NM_030777.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr6:134350401 G>A maps to NM_145176.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:134323145 C>T maps to NM_145176.2 E563E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:40158331 T>A maps to NM_052885.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr12:40223996 G>A maps to NM_052885.3 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:40223948 A>G maps to NM_052885.3 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr12:40265615 G>T maps to NM_052885.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:7981303 C>T maps to NM_153449.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:7970450 G>A maps to NM_153449.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:7967112 G>A maps to NM_153449.2 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr12:7982593 G>C maps to NM_153449.2 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:170727810 A>G maps to NM_000340.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:170716930 G>A maps to NM_000340.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:170715714 G>A maps to NM_000340.1 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr12:8074089 G>A maps to NM_006931.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr12:8083957 G>A maps to NM_006931.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr12:8077068 A>G maps to NM_006931.2 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:7186562 G>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:62373772 C>T maps to NM_020062.3 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:9097692 C>T maps to NM_003039.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:9107747 C>T maps to NM_003039.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:9097964 C>T maps to NM_003039.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:9079301 G>A maps to NM_207420.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr1:9063463 G>A maps to NM_207420.2 N478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:9067417 G>T maps to NM_207420.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:9078423 G>A maps to NM_207420.2 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr9:130165961 G>A maps to NM_014580.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:130167202 A>G maps to NM_014580.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:9836621 C>T maps to NM_020041.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:10022956 G>A maps to NM_020041.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:9922007 C>G did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr4:10023014 G>A maps to NM_020041.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:211751693 G>A maps to NM_021194.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr1:220091651 C>T maps to NM_018713.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:220091798 G>A maps to NM_018713.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:220101752 C>T maps to NM_018713.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:26370879 A>G maps to NM_001004434.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:26365782 G>A maps to NM_001004434.1 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:27480770 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:68411811 C>T maps to NM_022902.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:32417984 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:32399178 C>T maps to NM_001193513.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr2:32399182 C>T maps to NM_001193513.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:101431475 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:101361883 C>T maps to NM_133496.4 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:118170035 G>A maps to NM_173851.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:118159294 G>A maps to NM_173851.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:118165288 G>A maps to NM_173851.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:42065101 A>T maps to NM_006345.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:37356231 C>T maps to NM_080552.2 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:37357011 C>T maps to NM_080552.2 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr20:37356213 G>A maps to NM_080552.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:37356972 C>T maps to NM_080552.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr20:37353477 G>A maps to NM_080552.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr20:37356774 C>T maps to NM_080552.2 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr20:37356420 G>A maps to NM_080552.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:37356948 C>T maps to NM_080552.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr20:37357017 G>A maps to NM_080552.2 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:37353747 C>T maps to NM_080552.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr20:37353699 C>T maps to NM_080552.2 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:176823996 T>C maps to NM_003052.4 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:176814839 C>T maps to NM_003052.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr5:176815003 G>A maps to NM_003052.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:176813054 G>A maps to NM_003052.4 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:176815129 C>T maps to NM_003052.4 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:176821194 G>A maps to NM_003052.4 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:25665887 C>T maps to NM_006424.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:25672388 A>G maps to NM_006424.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:25677872 T>A maps to NM_006424.2 Y525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:25665875 G>A maps to NM_006424.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:25678187 C>A maps to NM_006424.2 C630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:140127156 T>C did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:140127501 A>G maps to NM_080877.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:140127763 C>T maps to NM_080877.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr9:140128708 G>C maps to NM_080877.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:88187197 C>A maps to NM_006416.4 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:88210913 C>T maps to NM_006416.4 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:48761970 C>A did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr23:48762574 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:48762401 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:100480963 A>G maps to ENST00000370153 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:139947623 C>T maps to NM_080670.2 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:112292734 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:112299707 C>T maps to NM_017945.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:112300134 C>T maps to NM_017945.2 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr17:47784417 C>T maps to ENST00000415270 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:47785120 A>C maps to ENST00000415270 Y62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr17:47783607 G>A maps to ENST00000415270 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr17:47782506 G>A maps to ENST00000415270 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:47785132 G>T maps to ENST00000415270 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:8428258 G>A maps to NM_001142540.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:8430201 G>A maps to NM_001142540.1 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:8428192 C>T maps to NM_001142540.1 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr7:133984323 G>A maps to NM_032826.4 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:45832636 C>T maps to NM_018389.4 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:45832396 C>T maps to NM_018389.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:45832609 C>T maps to NM_018389.4 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:45827873 C>T maps to NM_018389.4 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr6:137245221 C>T maps to NM_001008783.1 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:137245684 C>T maps to NM_001008783.1 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:137243811 G>A maps to NM_001008783.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr19:16682352 C>T maps to NM_024881.4 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:69140372 G>A maps to NM_018656.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:118475667 C>A maps to NM_001029858.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr6:118635387 A>G maps to NM_001029858.3 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr6:118556703 A>C maps to NM_001029858.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr6:118556700 C>T maps to NM_001029858.3 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:118228993 C>T maps to NM_001029858.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:234367373 G>A maps to NM_173508.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr1:234367424 G>A maps to NM_173508.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr1:234458880 C>G maps to NM_173508.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:234041292 G>A maps to NM_173508.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:234367305 C>T maps to NM_173508.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr14:58063438 T>G maps to NM_001080455.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:58038710 G>A maps to NM_001080455.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:58056070 T>C maps to NM_001080455.1 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:58063405 T>C maps to NM_001080455.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:114512831 A>G maps to NM_025181.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr2:114500331 C>G maps to NM_025181.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:150844682 A>G maps to NM_078483.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr5:150858881 T>C maps to NM_078483.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:150718650 G>A maps to NM_181776.2 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:150682786 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:150660641 G>A maps to NM_001145017.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:150660653 C>T maps to NM_001145017.1 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:92914013 C>T maps to NM_152313.2 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:43955630 G>A maps to NM_018964.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr21:43962554 C>T maps to NM_018964.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr21:43963563 G>A maps to NM_018964.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:124955001 C>T maps to NM_198277.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:124954764 C>T maps to NM_198277.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr7:140037082 C>T did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:140082275 G>A maps to NM_207113.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:140035243 G>A maps to NM_207113.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:118895937 A>G maps to NM_001164278.1 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr11:118895781 G>A maps to NM_001164278.1 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:46598113 A>G maps to NM_030674.3 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:79234092 G>A maps to NM_001037984.1 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:79246343 G>A maps to NM_001037984.1 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr17:79219697 G>A maps to NM_001037984.1 D1006D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:165768193 A>G maps to ENST00000409662 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:165755180 C>T maps to ENST00000409662 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:165754991 C>T maps to ENST00000409662 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:46764392 G>T maps to NM_018976.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:46758169 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:46758282 G>A maps to NM_018976.4 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:46761056 A>G maps to NM_018976.4 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr12:47172328 A>G maps to NM_018018.4 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr12:47173393 C>T maps to NM_018018.4 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr12:47172532 G>T maps to NM_018018.4 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:48325405 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:48319067 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:48320458 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:48319468 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr14:61519065 G>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr16:58706103 G>A maps to NM_018231.1 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:58713973 G>A maps to NM_018231.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr16:84075603 G>A maps to NM_001080442.1 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:84067035 G>A maps to NM_001080442.1 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:84050848 G>A maps to NM_001080442.1 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:54941646 G>T maps to NM_173514.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:54960629 A>G maps to NM_173514.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:153935109 C>A maps to NM_014437.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:196573390 A>G maps to NM_001127257.1 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:196545251 G>T maps to NM_001127257.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:196571394 C>T maps to NM_001127257.1 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr2:196581721 C>T maps to NM_001127257.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr2:196581415 T>C maps to NM_001127257.1 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:70943933 A>G maps to NM_001159770.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr17:70943978 C>T maps to NM_001159770.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:71084849 G>A maps to NM_001159770.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:70645063 G>A maps to NM_001159770.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr17:70732814 C>T maps to NM_001159770.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:71084795 C>T maps to NM_001159770.1 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:18292280 T>C maps to NM_001145195.1 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:18242333 G>A maps to NM_001145195.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:18276519 G>A maps to NM_001145195.1 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:18250726 C>A maps to NM_001145195.1 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr10:18242354 C>G maps to NM_001145195.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr10:18250550 T>C maps to NM_001145195.1 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:47431803 C>T maps to NM_001128225.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:47431803 C>T maps to NM_001128225.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr11:47431842 C>T maps to NM_001128225.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:22262400 C>T maps to NM_001135153.1 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:22273424 G>A maps to NM_001135153.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:22265944 C>A maps to NM_001135153.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:2737213 G>A maps to NM_144564.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:2733009 G>A maps to NM_144564.4 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:145638279 G>A maps to NM_130849.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145641442 G>A maps to NM_130849.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:145638295 G>A maps to NM_130849.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:145641415 C>T maps to NM_130849.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:145640737 G>A maps to NM_130849.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:145640187 G>A maps to NM_130849.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr12:56630232 G>A maps to NM_001135195.1 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:56630229 G>A maps to NM_001135195.1 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr12:56630724 C>T maps to NM_001135195.1 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:56628732 C>T maps to NM_001135195.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:56629007 G>A maps to NM_001135195.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:33706547 C>T maps to NM_012319.3 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:33694126 G>A maps to NM_012319.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:33689576 G>A maps to NM_012319.3 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:33694075 G>A maps to NM_012319.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:103228643 C>T maps to NM_001135146.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:103189152 C>T maps to NM_001135146.1 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:103228706 T>A maps to NM_001135146.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr14:69925108 C>T maps to NM_018375.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:44528254 C>T maps to NM_000341.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:44539838 G>T maps to NM_000341.3 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr2:44547600 C>T maps to NM_000341.3 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:44547360 G>A maps to NM_000341.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:190445147 G>A maps to NM_014585.5 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6803-01A-11D-1882-08 chr2:190426750 G>T maps to NM_014585.5 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:190430307 G>A maps to NM_014585.5 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:205766094 G>A maps to NM_173854.4 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:105199106 G>A maps to NM_032148.3 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:105321864 C>T maps to NM_032148.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:125741770 C>G maps to NM_001008485.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr3:125725936 G>C maps to NM_017836.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:125775343 G>A maps to NM_001008487.1 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:57263538 G>A maps to NM_003627.5 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:57263583 G>A maps to NM_003627.5 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:1518294 C>T maps to ENST00000382147 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:1486542 G>A maps to ENST00000382147 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:57184136 G>A maps to ENST00000428603 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr11:57182109 G>C maps to ENST00000428603 Y359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:108126851 T>C maps to NM_080546.3 N368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:108097857 T>A maps to NM_080546.3 L95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:108126836 C>T maps to NM_080546.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:108118606 T>C maps to NM_080546.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:10747091 C>T maps to NM_020428.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr1:95303424 T>G maps to NM_001114106.1 L223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr1:95330394 C>A maps to NM_001114106.1 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr6:31832428 G>A maps to NM_025257.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:75716927 G>T maps to NM_152697.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:75679470 C>A maps to NM_152697.4 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:75740674 G>A maps to NM_152697.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:75862265 A>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:8384691 C>T maps to ENST00000377479 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:8399673 G>A maps to ENST00000377479 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr1:8390935 C>T maps to ENST00000377479 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:8390764 C>T maps to ENST00000377479 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:8384691 C>T maps to ENST00000377479 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:8404000 G>A maps to ENST00000377479 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr1:8399613 C>T maps to ENST00000377479 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr1:8390542 G>A maps to ENST00000377479 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:8384497 C>T maps to ENST00000377479 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:33944917 G>A maps to NM_016180.3 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr5:33951725 G>A maps to NM_016180.3 Y363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr5:33951680 G>A maps to NM_016180.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:205628385 G>A maps to NM_033102.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:142222397 C>T maps to NM_001080431.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:142222469 C>T maps to NM_001080431.1 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr8:142228979 G>A maps to NM_001080431.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:142228904 G>A maps to NM_001080431.1 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr8:142227210 G>A maps to NM_001080431.1 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr8:142228730 G>A maps to NM_001080431.1 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:142228523 G>T maps to NM_001080431.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:142228559 G>A maps to NM_001080431.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:142222439 C>T maps to NM_001080431.1 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:142225980 G>A maps to NM_001080431.1 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:142228484 C>T maps to NM_001080431.1 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:142221612 G>T maps to NM_001080431.1 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:142222397 C>T maps to NM_001080431.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:142228928 G>A maps to NM_001080431.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:142231718 G>A maps to NM_001080431.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:115642092 C>A maps to NM_033051.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:115652550 G>A maps to NM_033051.3 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr9:115652544 C>T maps to NM_033051.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr13:29284951 C>T maps to NM_001135919.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr17:19458974 G>A maps to ENST00000395585 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:19618074 C>A maps to NM_152908.3 G85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:19618512 C>T maps to NM_152908.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:42334897 G>A maps to NM_000342.3 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr17:42340028 G>A maps to NM_000342.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:42328568 G>A maps to NM_000342.3 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr2:162738865 G>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:162805660 C>T maps to NM_001178015.1 R757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr2:162821607 G>A maps to NM_001178015.1 T1028T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:162696413 C>T maps to NM_001178015.1 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr2:162762259 C>T maps to NM_001178015.1 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:3215451 G>A maps to NM_001174090.1 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:3209804 G>A maps to NM_001174090.1 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr20:3218213 G>A maps to NM_001174090.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:3211444 G>A maps to NM_001174090.1 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr20:3210180 T>C maps to NM_001174090.1 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:3209500 G>A maps to NM_001174090.1 N768N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr2:27892202 T>C maps to NM_018158.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:150759082 C>T maps to NM_003040.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:150771576 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:220494916 G>A maps to NM_201574.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:220500177 C>T maps to NM_201574.2 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr2:220504269 C>A maps to NM_201574.2 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:220495066 C>T maps to NM_201574.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:220504356 G>A maps to NM_201574.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:220501407 C>T maps to NM_201574.2 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr2:220500551 C>T maps to NM_201574.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:72429507 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:72222755 C>T maps to NM_001098484.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:72429586 C>T maps to NM_001098484.2 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr4:72313450 G>T did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr4:72425946 A>T maps to NM_001098484.2 G1025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr4:72338535 G>A maps to NM_001098484.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:74452026 T>C maps to NM_021196.3 K1078K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:74482996 G>A maps to NM_021196.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:74489327 G>A maps to NM_021196.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:74513012 C>T maps to NM_021196.3 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:74474175 G>A maps to NM_021196.3 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:74459681 C>A maps to NM_021196.3 T896T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:27460078 G>C maps to ENST00000454389 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:27427493 C>T maps to ENST00000454389 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:27465553 C>A maps to ENST00000454389 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:27436203 G>T maps to ENST00000454389 C974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:27436566 C>A maps to ENST00000454389 G915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:51865098 C>T maps to NM_001039960.1 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:51856143 G>A maps to NM_001039960.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:139750732 G>A maps to ENST00000507527 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:139739838 A>C maps to ENST00000507527 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:32462977 C>T maps to NM_000343.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:18923662 C>T maps to NM_152351.3 H586H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr17:18862515 G>A maps to NM_152351.3 A84A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-8372-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:18862464 C>T maps to NM_152351.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:18922780 C>T maps to NM_152351.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:24922694 G>A maps to NM_052944.2 W623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr16:24881233 T>C maps to NM_052944.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:26714069 G>A maps to NM_178498.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:26725160 A>C maps to NM_178498.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:26700346 A>G maps to NM_178498.3 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:26708083 T>C maps to NM_178498.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr11:26725133 G>T maps to NM_178498.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:26743063 C>A maps to NM_178498.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr16:31500610 C>A maps to ENST00000431354 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:31499964 G>A maps to ENST00000431354 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:31497186 T>G maps to ENST00000431354 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr16:31500027 C>T maps to ENST00000431354 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr22:32625329 T>C maps to NM_014227.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:32620256 T>C maps to NM_014227.2 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:32628913 C>T maps to NM_014227.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:32650197 C>T maps to NM_014227.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:32628913 C>T maps to NM_014227.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr22:32644747 A>G maps to NM_014227.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr22:32650149 A>G maps to NM_014227.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr22:32644771 C>T maps to NM_014227.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:17983486 T>C did not map to a codon.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr19:18001722 G>A maps to NM_000453.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17983358 G>A maps to NM_000453.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:27423327 G>A maps to NM_021095.2 C628C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:27430332 C>T maps to NM_021095.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:27424661 G>A maps to NM_021095.2 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr2:27427687 G>A maps to NM_021095.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:27429797 G>A maps to NM_021095.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:27430422 G>A maps to NM_021095.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr2:27424275 G>T maps to NM_021095.2 Y530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:27430356 A>G maps to NM_021095.2 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:101588917 G>A maps to NM_145913.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:101603515 G>A maps to NM_145913.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:101581229 G>A maps to NM_145913.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:101603422 G>A maps to NM_145913.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:48703365 C>T maps to NM_001135181.1 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:48708211 C>T maps to NM_001135181.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:48701404 G>A maps to NM_001135181.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:48697256 G>A maps to NM_001135181.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:11059527 G>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:11060284 C>T maps to NM_003042.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr3:11060365 G>A maps to NM_003042.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr3:11058950 C>T maps to NM_003042.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr3:10960115 C>A maps to NM_014229.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:335649 G>A maps to NM_016615.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:332298 G>A maps to NM_016615.3 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:115582756 G>A did not map to a codon.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr23:115586616 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:115572198 T>G did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:115574827 A>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:115582793 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:115585599 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:115582605 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:85266866 G>A maps to NM_182767.4 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:85264416 G>A maps to NM_182767.4 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:85277606 G>A maps to NM_018057.5 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr12:85285643 G>A maps to NM_182767.4 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr19:49793508 G>A maps to NM_014037.2 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr19:49814454 T>C maps to NM_014037.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:49812143 G>T maps to NM_014037.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:110737373 G>A maps to NM_001010898.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:110737211 C>T maps to NM_001010898.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr1:110716596 C>A maps to NM_001010898.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr1:110737325 C>T maps to NM_001010898.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:1235725 C>A maps to NM_182632.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr5:1239617 C>T maps to NM_182632.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:1235778 T>C did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr5:1243677 G>A maps to NM_182632.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr5:1212544 C>T maps to NM_001003841.2 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:55730215 C>T maps to NM_001043.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:55731865 C>T maps to NM_001043.3 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr16:55690821 C>T maps to NM_001043.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:1409198 G>A maps to NM_001044.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr5:1409886 C>T maps to NM_001044.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:1432616 G>A maps to NM_001044.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:1441510 C>A maps to NM_001044.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:1416274 G>A maps to NM_001044.4 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:1432616 G>A maps to NM_001044.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr5:1406320 G>A maps to NM_001044.4 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:1432799 C>T maps to NM_001044.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:28545191 G>A maps to ENST00000394821 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:28545145 C>A maps to ENST00000394821 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr17:28538389 C>T maps to ENST00000394821 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr17:28539848 C>T maps to ENST00000394821 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:28545341 G>T maps to ENST00000394821 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:28537664 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:28548904 G>A maps to ENST00000394821 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:20673935 T>C maps to NM_004211.3 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr11:20657904 C>G maps to NM_004211.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr11:20652344 G>A maps to NM_004211.3 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:20629139 C>T maps to NM_004211.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:14485231 T>C maps to NM_001134367.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr3:14489114 T>C maps to NM_001134367.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr3:14508103 C>T maps to NM_001134367.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:149576671 C>T maps to NM_014228.3 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:149584483 G>A maps to NM_014228.3 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:149576689 C>T maps to NM_014228.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:152958730 C>T did not map to a codon.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr23:152960202 C>T did not map to a codon.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr23:152960075 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:44468043 G>A maps to NM_201649.2 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:44466468 G>A maps to NM_201649.2 C575C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:44482787 C>T maps to NM_201649.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:44466865 G>A maps to NM_201649.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:44467244 G>A maps to NM_201649.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:30104718 C>T maps to NM_003045.4 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr13:30109977 G>A maps to NM_003045.4 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr13:30096481 G>A maps to NM_003045.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr13:30110028 G>A maps to NM_003045.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr13:30107024 G>A maps to NM_003045.4 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:33700229 A>G maps to NM_019849.2 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:33706709 G>A maps to NM_019849.2 Y107Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:139101902 G>A maps to ENST00000280612 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:139162992 G>A maps to ENST00000280612 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr4:139153454 T>C maps to ENST00000280612 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:170219126 G>T maps to NM_020949.2 C104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:170244704 C>T maps to NM_020949.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:170218994 C>T maps to NM_020949.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:170201191 C>T maps to NM_020949.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:170219000 G>A maps to NM_020949.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr8:17412505 G>T maps to NM_003046.5 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:17401120 C>T maps to NM_001164771.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:17401102 C>T maps to NM_001164771.1 C125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:17400835 G>A maps to NM_001164771.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:17407890 T>C maps to NM_001164771.1 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:17409423 G>A maps to NM_001164771.1 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:17417857 C>T maps to NM_001164771.1 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:70149775 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:70148104 A>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:70149576 C>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:70149827 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:70147374 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:70148312 T>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:70147354 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:70149523 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:70147195 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr22:21385708 G>A maps to NM_004173.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:68330528 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:68330567 C>T maps to NM_003983.4 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:68338045 G>A maps to NM_032178.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr16:68344763 A>C maps to NM_032178.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:68335177 T>C maps to NM_032178.2 *310W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr14:23634554 C>T maps to NM_012244.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:33355553 G>A maps to NM_014270.4 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:33355637 A>G maps to NM_014270.4 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:33353424 C>T maps to NM_014270.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:33353055 C>T maps to NM_014270.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:33353079 C>T maps to NM_014270.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr19:33350776 G>A maps to NM_014270.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:40657162 G>A maps to NM_021097.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:40656481 A>G maps to NM_021097.2 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:40657278 C>A maps to NM_021097.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:40656426 C>A maps to NM_021097.2 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr2:40366565 G>A maps to NM_021097.2 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr2:40656258 T>G maps to NM_021097.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:40366802 G>A maps to NM_021097.2 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:40655875 A>G maps to NM_021097.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr2:40366763 G>A maps to NM_021097.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr2:40342431 G>A maps to NM_021097.2 F961F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:40656003 T>A maps to NM_021097.2 K473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:40657011 G>A maps to NM_021097.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr19:47969321 G>A maps to NM_015063.2 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:47951331 G>A maps to NM_015063.2 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:47951489 T>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:47969507 C>T maps to NM_015063.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:70633945 G>T maps to NM_183002.1 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:70517818 C>T maps to NM_183002.1 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr14:70512798 C>T maps to NM_183002.1 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:27480471 A>G did not map to a codon.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr1:27428928 C>T maps to NM_003047.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:27426920 G>A maps to NM_003047.3 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:111921156 T>C maps to NM_183061.1 Q754Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:111898416 T>C maps to NM_183061.1 E960E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr1:173526565 C>T maps to NM_178527.3 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:173506087 G>A maps to NM_178527.3 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:173494046 A>G maps to NM_178527.3 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr1:173506169 A>G maps to NM_178527.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:173503802 A>G maps to NM_178527.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr1:173552663 G>A maps to NM_178527.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:173545801 A>G maps to NM_178527.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr2:103318932 C>G maps to NM_003048.3 S606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:103281692 G>A maps to NM_003048.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:103322333 C>A maps to NM_003048.3 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:103274236 G>A maps to NM_003048.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:492079 C>T maps to NM_004174.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:488454 C>T maps to NM_004174.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:481729 C>T maps to NM_004174.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:482224 G>A maps to NM_004174.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:477514 G>A maps to NM_004174.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr5:475095 C>T maps to NM_004174.2 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:476159 C>T maps to NM_004174.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:485313 C>T maps to NM_004174.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:476454 C>T maps to NM_004174.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:72764647 G>A maps to NM_004252.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:103090418 G>A maps to NM_001011552.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:103095358 G>C maps to NM_001011552.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:103149074 G>A maps to NM_001011552.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:103119968 C>T maps to NM_001011552.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:67286607 G>A maps to NM_004594.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:67290883 G>C maps to NM_004594.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr16:67292310 C>T maps to NM_004594.2 Y529Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr23:135084304 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:135067950 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:135080302 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:135080678 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:135126866 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:135067849 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:135095106 C>T did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:46508174 A>C did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:46508231 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:46541837 T>C did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:46618278 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:46521971 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:46513102 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:46466413 T>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:48503377 C>T maps to ENST00000417961 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:48472052 C>T maps to ENST00000417961 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr20:48494551 T>A maps to ENST00000417961 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:143185919 A>G maps to NM_173653.3 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:143185876 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:143292990 G>A maps to NM_173653.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:21325708 C>T maps to NM_006446.4 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr12:21377656 A>G maps to NM_006446.4 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr12:21331642 T>G maps to NM_006446.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr12:20876090 T>A maps to NM_017435.4 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:20886039 T>C did not map to a codon.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr12:20903615 C>A maps to NM_017435.4 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:133664052 C>T maps to NM_005630.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:133661492 C>T maps to NM_005630.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr3:133661594 G>A maps to NM_005630.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:133673822 C>T maps to NM_005630.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:133698393 G>A maps to NM_005630.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:133673819 G>T maps to NM_005630.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:74913972 G>A maps to NM_007256.4 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:92669300 G>A maps to NM_013272.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:92459656 C>T maps to NM_013272.3 H205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:92669420 C>T maps to NM_013272.3 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr15:92459374 C>T maps to NM_013272.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr20:61287964 C>T maps to NM_016354.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:101592919 A>G maps to NM_180991.4 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:101631747 C>T maps to NM_180991.4 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:101606334 G>A maps to NM_180991.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:101627088 G>A maps to NM_180991.4 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr5:101631705 A>C maps to NM_180991.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr5:101631702 G>C maps to NM_180991.4 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:101583011 A>G maps to NM_180991.4 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr5:101597685 C>T maps to NM_180991.4 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr5:101585437 C>T maps to NM_180991.4 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr5:101631697 C>T maps to NM_180991.4 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr5:101583041 C>T maps to NM_180991.4 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:70744650 C>T maps to NM_030958.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:70744650 C>T maps to NM_030958.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:70744008 C>T maps to NM_030958.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr8:70744272 G>A maps to NM_030958.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr5:101834416 G>A maps to NM_173488.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:101735413 T>A maps to NM_173488.3 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:101816043 G>A maps to NM_173488.3 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr5:101813378 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr5:101815968 A>C maps to NM_173488.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:33679650 A>G maps to NM_152270.3 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:33689812 G>A maps to NM_152270.3 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:33747356 C>T maps to NM_018042.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:33738392 A>G maps to NM_018042.3 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:33749720 T>C maps to NM_018042.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr17:33749726 C>G maps to NM_018042.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr17:33738911 G>A maps to NM_018042.3 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr17:33806363 G>A maps to ENST00000361112 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr17:33802292 T>G maps to ENST00000361112 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:33767970 A>G maps to NM_144682.5 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:33767862 G>A maps to NM_144682.5 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr17:33592741 C>T maps to NM_144975.3 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:33586500 C>T maps to NM_144975.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:41483495 G>A maps to NM_144990.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr1:41483645 G>A maps to NM_144990.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:41486095 C>T maps to NM_144990.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:41486227 C>T maps to NM_144990.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr10:98806445 G>A maps to NM_003061.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr10:98823347 G>A maps to NM_003061.2 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:98766416 A>G maps to NM_003061.2 T1134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:98766410 G>A maps to NM_003061.2 C1136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:98807475 A>G maps to NM_003061.2 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:98764577 G>T maps to NM_003061.2 V1194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr10:98778862 A>G maps to NM_003061.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:98807529 G>A maps to NM_003061.2 C517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:20597355 C>T maps to ENST00000273739 C1086C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:20620583 C>T maps to ENST00000273739 D1527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:20521007 C>T maps to ENST00000273739 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:20597433 G>A maps to ENST00000273739 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr4:20619220 G>A maps to ENST00000273739 G1445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr4:20618692 C>T maps to ENST00000273739 C1349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:20487858 G>A maps to ENST00000273739 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr4:20535275 G>A maps to ENST00000273739 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr4:20533666 T>C maps to ENST00000273739 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr4:20597370 C>T maps to ENST00000273739 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr4:20487825 T>C maps to ENST00000273739 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr4:20525484 C>T maps to ENST00000273739 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:168671758 G>A maps to NM_003062.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:168244400 G>A maps to NM_003062.2 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:168096821 G>A maps to NM_003062.2 C1434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:168187940 C>T maps to NM_003062.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:168112862 G>T maps to NM_003062.2 C1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr5:168175344 G>A maps to NM_003062.2 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr5:168201355 G>A maps to NM_003062.2 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:168244440 G>T maps to NM_003062.2 C219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:84453980 G>A maps to NM_052910.1 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:84454846 G>A maps to NM_052910.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr13:84454001 C>T maps to NM_052910.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:84455033 A>G maps to NM_052910.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:84454826 C>T maps to NM_052910.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr13:84455201 C>G maps to NM_052910.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr13:84453959 C>T maps to NM_052910.1 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr13:84454670 C>A maps to NM_052910.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr13:84453563 C>T maps to NM_052910.1 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr13:84454970 T>C maps to NM_052910.1 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr13:84455456 A>G maps to NM_052910.1 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr13:84454724 G>A maps to NM_052910.1 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr13:84454739 T>C maps to NM_052910.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr13:84453671 G>A maps to NM_052910.1 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr13:84453794 G>T maps to NM_052910.1 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:84453788 C>T maps to NM_052910.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:84454064 G>T maps to NM_052910.1 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:144904762 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:144905423 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:144905692 T>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:144904850 G>A did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:144906220 G>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:144904103 T>G did not map to a codon.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr23:144905745 G>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:144905441 A>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:144906158 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:144906226 C>T did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:144903991 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:144905392 C>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:144904205 C>T did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:144905445 G>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:144903976 A>G did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:144904232 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:144906228 A>G did not map to a codon.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr23:144905374 C>G did not map to a codon.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr23:144904388 T>C did not map to a codon.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr23:144904987 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:144904310 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:144905986 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr23:144905048 A>T did not map to a codon.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr23:144906416 A>C did not map to a codon.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr23:144905266 A>T did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:144906325 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr23:144905138 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:164906122 C>T maps to NM_014926.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:164906365 G>A maps to NM_014926.2 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr3:164905855 T>C maps to NM_014926.2 Q921Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr3:164907652 A>C maps to NM_014926.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:164906062 T>C maps to NM_014926.2 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:164906923 G>A maps to NM_014926.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:164906580 G>A maps to NM_014926.2 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:142717005 A>T did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr23:142718110 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:142718540 A>T did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:142716879 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:142718308 C>T did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:142718453 C>T did not map to a codon.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr23:142717774 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:142718125 C>T did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:142718164 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:88327789 C>T maps to NM_015567.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:88328764 T>C maps to NM_015567.1 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr13:88329874 C>T maps to NM_015567.1 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr13:88327909 C>T maps to NM_015567.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr13:88328683 G>A maps to NM_015567.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr13:88329454 C>A maps to NM_015567.1 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr13:88328926 C>T maps to NM_015567.1 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:88328995 C>T maps to NM_015567.1 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:88329436 C>T maps to NM_015567.1 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr13:88330471 G>A maps to NM_015567.1 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:88329913 C>T maps to NM_015567.1 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr13:88327807 G>A maps to NM_015567.1 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr13:88327711 G>A maps to NM_015567.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr13:88330081 G>C maps to NM_015567.1 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:88329082 G>A maps to NM_015567.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr13:88329121 C>T maps to NM_015567.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr13:88330442 G>T maps to NM_015567.1 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr13:88328905 C>T maps to NM_015567.1 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:88329580 C>T maps to NM_015567.1 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr13:88329508 G>A maps to NM_015567.1 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr13:88328995 C>T maps to NM_015567.1 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:88330267 G>A maps to NM_015567.1 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:88328902 C>A maps to NM_015567.1 Y420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:88329622 G>A maps to NM_015567.1 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:88330042 G>A maps to NM_015567.1 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr13:88328752 G>A maps to NM_015567.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr13:88328416 G>C maps to NM_015567.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr13:88328836 C>A maps to NM_015567.1 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr13:88329637 G>T maps to NM_015567.1 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr13:88327783 C>T maps to NM_015567.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:88328680 T>C maps to NM_015567.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr13:86368163 A>C maps to NM_032229.2 L827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr10:105750528 T>C maps to NM_014720.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:105761203 T>C maps to NM_014720.2 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:105761302 T>C maps to NM_014720.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:105758875 G>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr10:105778620 T>C maps to NM_014720.2 D1029D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:57913111 A>G maps to ENST00000428312 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:57743470 C>T maps to ENST00000428312 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:57913084 C>T maps to ENST00000428312 Y819Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:57817174 C>T maps to ENST00000428312 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:57847675 C>T maps to ENST00000428312 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr20:57610085 T>C maps to NM_016045.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:107578562 A>G maps to NM_003063.2 *32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:59186116 A>G maps to NM_024755.2 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:59181693 T>C maps to NM_024755.2 Q713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr15:59191665 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:159835379 G>A maps to NM_006425.4 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:143823791 G>T maps to NM_020427.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:146474972 C>T maps to NM_001003688.1 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:146468015 C>T maps to NM_001003688.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:146436031 C>T maps to NM_001003688.1 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr18:45368210 G>C maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:45374881 G>A maps to NM_001003652.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr18:45368210 G>C maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr18:45374870 C>T maps to NM_001003652.2 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr18:45423025 A>G maps to NM_001003652.2 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr18:45395638 G>C maps to NM_001003652.2 Y165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr15:67457388 C>T maps to NM_005902.3 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:48603090 C>T maps to NM_005359.5 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr18:48575208 C>T maps to NM_005359.5 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:135496656 G>A maps to NM_001001419.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:67073422 T>A maps to NM_005585.4 Y347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:46448236 G>A maps to NM_005904.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr13:37453529 C>T maps to NM_001127217.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr13:37453415 T>C maps to NM_001127217.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr13:37439851 C>T maps to NM_001127217.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr13:37439800 G>A maps to NM_001127217.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr13:37439796 G>A maps to NM_001127217.2 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:37427645 G>A maps to NM_001127217.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:71442156 T>C maps to NM_001044305.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr6:71562282 G>A maps to NM_001044305.1 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:40887721 C>T maps to NM_022733.2 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:40872412 C>T maps to NM_022733.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:40881882 C>T maps to NM_022733.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:40879886 G>A maps to NM_022733.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr1:40887655 G>A maps to NM_022733.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:40880950 T>C maps to NM_022733.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:40872513 C>T maps to NM_022733.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:128645815 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:128599864 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:128621095 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:128599548 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:128599863 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:128615122 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr23:128622972 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:128599894 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:128615069 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:128614735 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr23:128650353 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:128626045 G>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr23:128638728 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:2039853 G>A maps to NM_003070.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr9:2123849 A>G maps to NM_003070.3 E1298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:2161876 C>T maps to NM_003070.3 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr9:2039787 G>A maps to NM_003070.3 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:2039811 G>A maps to NM_003070.3 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr9:2084120 G>A maps to NM_003070.3 Q817Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:2123849 A>G maps to NM_003070.3 E1298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:2123795 G>A maps to NM_003070.3 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:2182187 G>A maps to NM_003070.3 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr9:2039766 G>A maps to NM_003070.3 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:2039817 A>G maps to NM_003070.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:2088614 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:2039685 G>A maps to NM_003070.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr9:2033023 C>T maps to NM_003070.3 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr19:11138520 C>T maps to NM_001128849.1 R1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:11096046 G>C maps to NM_001128849.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:11107210 G>A maps to NM_001128849.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:11138594 G>A maps to NM_001128849.1 A1117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:11144498 G>A maps to NM_001128849.1 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:11145660 C>T maps to NM_001128849.1 D1341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:11132480 G>A maps to NM_001128849.1 T899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:11134300 C>T maps to NM_001128849.1 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:11145783 A>G maps to NM_001128849.1 S1382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:11129650 G>A maps to NM_001128849.1 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:11118654 A>C maps to NM_001128849.1 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:144468577 G>A maps to NM_003601.2 E898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:144449037 C>T maps to NM_003601.2 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:95191963 G>T maps to NM_001128429.1 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:217285158 C>T maps to NM_014140.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:217279807 A>G maps to NM_014140.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:217285118 C>T maps to NM_014140.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:217285158 C>T maps to NM_014140.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr2:217285090 C>A maps to NM_014140.3 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr22:24135749 C>T maps to NM_003073.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr22:24145517 C>T maps to NM_003073.3 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr22:24135749 C>T maps to NM_003073.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:24145517 C>T maps to NM_003073.3 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:47712177 C>T maps to NM_003074.3 W623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:47651781 G>A maps to NM_003074.3 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:47629764 T>C maps to NM_003074.3 P1084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr3:47651741 G>A maps to NM_003074.3 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:47651721 T>C maps to NM_003074.3 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:56563354 G>A maps to NM_003075.3 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr12:56559401 G>T maps to NM_003075.3 R947R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:56575375 G>A maps to NM_003075.3 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:56565505 G>A maps to NM_003075.3 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:56572297 C>T maps to NM_003075.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:56563584 G>A maps to NM_003075.3 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:56581045 C>T maps to NM_003075.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr12:56572210 G>A maps to NM_003075.3 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr12:56578894 C>T maps to NM_003075.3 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr12:50480098 C>G maps to NM_003076.4 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr17:61911082 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:150937305 C>T maps to NM_003078.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:150937241 G>A maps to NM_003078.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:38793824 C>A did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:53438753 T>C did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:53436051 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:53440053 A>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:53436411 C>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:53440337 A>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:53432884 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:53426555 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:53410092 G>A did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr23:53436107 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr22:45755789 C>T maps to NM_148674.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr22:45767385 G>A maps to NM_148674.3 R760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:45750989 T>C maps to NM_148674.3 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:45809406 C>T maps to NM_148674.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr22:45755828 C>A maps to NM_148674.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:45779372 G>A maps to NM_148674.3 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr9:106874034 T>C maps to NM_001042550.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:112349458 G>T maps to NM_005445.3 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:112361627 C>T maps to NM_005445.3 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr10:112328745 C>G maps to NM_005445.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr10:112350787 G>A maps to NM_005445.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:160138559 C>T maps to NM_005496.3 D630D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:160146610 A>G maps to NM_005496.3 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:160141301 A>G maps to NM_005496.3 K703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:160141238 C>T maps to NM_005496.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:160142780 C>T maps to NM_005496.3 L818L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-MX-A5UJ-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:72897462 C>T maps to NM_015110.3 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:72897375 A>G maps to NM_015110.3 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:72962061 G>A maps to NM_015110.3 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:72901114 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:72893537 C>T maps to NM_015110.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:72965071 C>T maps to NM_015110.3 R978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:72913006 C>T maps to NM_015110.3 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:17877641 G>A maps to ENST00000381272 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:17899379 A>G maps to ENST00000381272 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:17884435 A>G maps to ENST00000381272 Y736Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:2724948 C>T maps to NM_015295.2 R886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:2775769 G>A maps to NM_015295.2 A1738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:2771568 C>T maps to NM_015295.2 R1669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:2688391 T>C maps to NM_015295.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:2752538 C>T maps to NM_015295.2 C1445C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr18:2732471 T>G maps to NM_015295.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152856942 C>T maps to NM_030663.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:18167651 C>T maps to NM_148886.1 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:39909859 C>T maps to NM_019008.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:39910324 G>A maps to NM_019008.4 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:39907380 C>A maps to NM_019008.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr22:39908396 T>C maps to NM_019008.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr22:39910084 C>T maps to NM_019008.4 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:39907949 C>T maps to NM_019008.4 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:18225951 C>T maps to NM_144775.2 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:91925132 T>C maps to ENST00000417249 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:55825626 A>C maps to NM_001122964.1 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:55806899 T>C maps to NM_001122964.1 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:18856806 G>A maps to ENST00000389467 L2055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:18847477 A>G maps to ENST00000389467 L2612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:18847463 G>A maps to ENST00000389467 C2616C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:18880519 C>T maps to ENST00000389467 W913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:18859269 A>G maps to ENST00000389467 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:18863427 A>G maps to ENST00000389467 G1671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:18844442 G>A maps to ENST00000389467 R2871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:18861334 A>G maps to ENST00000389467 H1799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:18858832 G>A maps to ENST00000389467 R1980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr16:18853075 G>A maps to ENST00000389467 F2169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:156237903 A>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:156230292 G>A maps to NM_015327.2 H744H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:156244427 C>T maps to NM_015327.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr1:156222290 G>A maps to NM_015327.2 I889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr1:156220711 G>A maps to NM_015327.2 G968G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:2202207 C>T maps to NM_017575.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:2203278 C>T maps to NM_017575.4 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:2200608 C>T maps to NM_017575.4 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr17:2202840 C>A maps to NM_017575.4 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:2202633 C>T maps to NM_017575.4 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:2201201 C>T maps to NM_017575.4 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:2203722 A>G maps to NM_017575.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr17:2090056 G>A maps to NM_017575.4 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:2186146 G>A maps to NM_017575.4 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:183486864 C>T maps to ENST00000367537 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:183511261 C>T maps to ENST00000367537 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:128850230 G>A maps to NM_005631.4 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:128845469 G>A maps to NM_005631.4 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:128845084 C>T maps to NM_005631.4 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:128845573 C>T maps to NM_005631.4 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:70477654 C>A maps to NM_001034852.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr14:70478204 C>T maps to NM_001034852.1 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr14:70490003 C>T maps to NM_001034852.1 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:168947784 C>T maps to NM_022138.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:168947818 T>C maps to NM_022138.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:169064766 T>C maps to NM_022138.2 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:168949812 T>C maps to NM_022138.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr6:169051409 G>A maps to NM_022138.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:168999603 A>G maps to NM_022138.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr6:168927116 C>T maps to NM_022138.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:4163472 G>A maps to ENST00000443211 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:6413035 C>T maps to NM_000543.4 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr11:6411929 C>G maps to NM_000543.4 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:6412940 C>T maps to NM_000543.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:68405943 C>T maps to NM_018667.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:68395143 G>A maps to NM_018667.3 R645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:68404953 C>T maps to NM_018667.3 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:68405382 G>A maps to NM_018667.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:68405289 G>A maps to NM_018667.3 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:130931133 G>A maps to NM_017951.4 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr2:130931166 G>A maps to NM_017951.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:130930890 A>G maps to NM_017951.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:123122519 A>G maps to NM_006714.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:28285219 C>T maps to NM_014474.2 H413H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:21985315 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:22012434 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:21995316 G>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:21995194 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:21985369 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:21990052 T>C did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:31496922 C>T maps to ENST00000454496 R971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:31491332 G>A maps to ENST00000454496 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:31487682 G>A maps to ENST00000454496 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr11:57310171 G>A maps to ENST00000457912 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:57310768 C>T maps to ENST00000457912 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:57313371 C>T maps to ENST00000457912 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:4497135 G>A maps to NM_001114974.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:4496329 G>A maps to NM_001114974.1 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:54576053 A>G maps to NM_014311.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:98649828 G>A maps to NM_020429.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:98655119 A>T maps to NM_020429.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:98655152 C>T maps to NM_020429.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:98636090 G>A maps to NM_020429.2 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:98655079 G>A maps to NM_020429.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr7:98638149 C>T maps to NM_020429.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:62574629 C>T maps to NM_022739.3 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:62587238 C>T maps to NM_022739.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:62594567 A>G maps to NM_022739.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:62551005 A>G maps to NM_022739.3 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:88409943 C>T maps to NM_198274.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:88409943 C>A maps to NM_198274.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:88384011 G>C did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr2:88402651 G>T maps to NM_198274.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr1:214507651 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:246027161 C>T maps to NM_001167740.1 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:245912888 G>A maps to NM_001167740.1 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:1686414 A>G maps to NM_052928.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:1690196 G>A maps to NM_052928.2 C597C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:1684733 C>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr17:1703658 T>A maps to NM_052928.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:1686366 G>A maps to NM_052928.2 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr17:1690238 G>A maps to NM_052928.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:73449012 T>C maps to NM_006062.2 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:73449938 C>T maps to NM_006062.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:49832563 G>A maps to NM_003068.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:49833818 C>T maps to NM_003068.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:49831371 T>C maps to NM_003068.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:88744867 G>A maps to NM_178310.3 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:88747889 T>C maps to NM_178310.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:88747835 G>T maps to NM_178310.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr16:88748081 C>T maps to NM_178310.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:88747937 G>T maps to NM_178310.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:88747850 T>C maps to NM_178310.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr15:42823657 G>A maps to NM_003825.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:10277683 C>T maps to NM_130811.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr1:227954658 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:227935497 C>T maps to NM_053052.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:84302946 T>G maps to NM_014841.2 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:84417538 G>A maps to NM_014841.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:84265952 G>A maps to NM_014841.2 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr6:84269909 G>A maps to NM_014841.2 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:15423074 G>A maps to NM_001039697.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:15459747 G>T maps to NM_001039697.1 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:139272333 G>A maps to NM_003086.2 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:139287156 G>A maps to NM_003086.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:139288729 C>T maps to NM_003086.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr9:139273163 C>A maps to NM_003086.2 E1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:139273209 G>A maps to NM_003086.2 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:139277745 C>T maps to NM_003086.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr9:139275293 G>A maps to NM_003086.2 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:139282004 G>A maps to NM_003086.2 Y419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr5:121739510 G>A maps to ENST00000379533 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:121767673 T>A maps to ENST00000379533 L445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:121786635 A>C maps to ENST00000379533 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr5:121786899 T>C maps to ENST00000379533 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr5:121739485 A>C did not map to a codon.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr5:121787256 A>G maps to ENST00000379533 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:176048238 C>A maps to NM_003085.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:176056535 G>A maps to NM_003085.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr5:176056613 G>A maps to NM_003085.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:127729626 C>T maps to NM_014390.2 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:127361417 C>T maps to NM_014390.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:127729668 C>T maps to NM_014390.2 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:127447554 G>A maps to NM_014390.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:127725810 C>A maps to NM_014390.2 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:127338981 C>A maps to NM_014390.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr7:127725832 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:127361421 C>T maps to NM_014390.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:242021173 C>T maps to NM_001080437.1 C1333C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:241969711 C>T maps to NM_001080437.1 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:242002304 C>T maps to NM_001080437.1 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:38006326 C>T maps to NM_024700.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:38006092 A>G maps to NM_024700.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:38003354 G>A maps to NM_024700.2 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:1281355 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:1285977 G>A maps to ENST00000381876 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:1285980 C>T maps to ENST00000381876 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:1277014 C>T maps to ENST00000381876 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:43381976 A>G maps to NM_017719.4 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:43344904 G>A maps to NM_017719.4 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:43389109 G>A maps to NM_017719.4 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:96956090 G>A maps to NM_014014.3 I905I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr2:96967312 G>A maps to NM_014014.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr2:96949032 G>A maps to NM_014014.3 S1607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:96944057 G>A maps to NM_014014.3 R1843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:96945251 G>A maps to NM_014014.3 H1690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr2:96944339 C>T maps to NM_014014.3 A1811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:96943573 G>A maps to NM_014014.3 Q1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:96943303 A>G maps to NM_014014.3 S1968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:96948968 G>A maps to NM_014014.3 R1629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:96940785 A>G maps to NM_014014.3 D2125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr2:96952127 G>A maps to NM_014014.3 P1308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:70131384 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:70123577 C>T maps to NM_006857.1 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr12:123950368 C>T maps to NM_180699.2 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:7595260 T>C maps to NM_152551.3 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr19:41263267 C>T maps to NM_004596.4 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr19:41269578 C>T maps to NM_004596.4 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:101833228 C>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:101835368 C>T maps to NM_003090.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr15:101833363 G>A maps to NM_003090.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:2446419 G>A maps to ENST00000339610 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:16721538 T>C maps to NM_198220.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:16712391 T>C maps to NM_198220.2 N15N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr18:19203787 G>A maps to NM_006938.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:19203853 A>G maps to NM_006938.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:19203787 G>A maps to NM_006938.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr22:24953725 T>C maps to NM_004175.3 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr15:25222130 T>G maps to NM_022805.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:32005721 A>G maps to NM_003098.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:32026767 C>T maps to NM_003098.2 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr8:121823875 T>G maps to NM_021021.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:121644749 C>T maps to NM_021021.3 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:121823711 C>T maps to NM_021021.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:121554211 A>G maps to NM_021021.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:121823612 G>A maps to NM_021021.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr8:121644791 G>A maps to NM_021021.3 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:69334793 G>A maps to NM_006750.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:51314810 G>A maps to NM_018967.2 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr8:51621477 T>C maps to NM_018967.2 H408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr8:51571220 A>T maps to NM_018967.2 K346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr8:51664598 T>G maps to NM_018967.2 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:51449299 C>T maps to NM_018967.2 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:51465607 A>G did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr2:1094064 C>T maps to NM_018968.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:1251208 T>C maps to NM_018968.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:1243520 G>A maps to NM_018968.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:1263212 G>A maps to NM_018968.3 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:1271264 C>T maps to NM_018968.3 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:1161256 C>T maps to NM_018968.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:1204898 C>T maps to NM_018968.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr3:63645449 G>A maps to NM_001080537.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr3:63649695 C>T maps to NM_001080537.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:78198881 G>A maps to NM_012245.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:78198842 G>T maps to NM_012245.2 Y292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:78203417 T>C maps to NM_012245.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:64419452 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:64423956 T>C maps to NM_003099.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:46189965 C>T maps to NM_152244.1 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:17836500 G>A maps to ENST00000417048 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:17890482 T>C maps to ENST00000417048 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:17890473 A>G maps to ENST00000417048 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:86267736 T>C maps to NM_153816.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:86281933 C>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:86283981 T>C maps to NM_153816.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:64802340 C>T maps to NM_013306.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:64806047 C>T maps to NM_013306.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:82752104 A>C maps to NM_152836.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:82751882 C>A maps to NM_152836.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr2:27598552 C>T maps to NM_014748.2 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:27598768 C>T maps to NM_014748.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:27596741 C>A maps to NM_014748.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:27594137 C>A maps to NM_014748.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:53814453 C>A maps to NM_052870.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:53814786 G>A maps to NM_052870.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr5:53815332 C>T maps to NM_052870.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:53814891 G>A maps to NM_052870.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:53815131 C>T maps to NM_052870.2 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:53815284 C>T maps to NM_052870.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:130784706 C>T maps to NM_014758.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:50707742 G>A maps to NM_182854.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:50707934 G>A maps to NM_182854.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr16:50707964 G>A maps to NM_182854.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:44469498 G>A maps to NM_033421.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:44469309 G>A maps to NM_033421.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:64446652 T>C maps to NM_024798.2 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:122281824 C>T maps to ENST00000395451 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:122272427 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:186272693 G>A maps to NM_031953.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:151634670 G>C maps to ENST00000458013 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:151638413 C>T maps to ENST00000458013 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:151611549 G>A maps to ENST00000458013 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr16:12662458 C>T maps to NM_001080530.2 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr16:12293529 A>G maps to NM_001080530.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:12662398 G>A maps to NM_001080530.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:12371841 G>A maps to NM_001080530.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr9:115579986 T>C maps to NM_001012994.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:101601119 G>A maps to NM_152628.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:101648122 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:101608890 C>T maps to NM_152628.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr15:75941856 C>T maps to NM_153271.1 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:125216989 C>T maps to NM_003794.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:125216989 C>T maps to NM_003794.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:17937585 C>T maps to NM_152227.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:17930822 T>C maps to NM_152227.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr20:17928169 G>A maps to NM_152227.1 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr14:35037120 G>A maps to NM_152233.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr14:35036957 T>C maps to NM_152233.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr1:99164433 G>A maps to NM_015976.4 E337E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-4370-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:2297143 C>T maps to NM_013321.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:2311526 G>A maps to NM_013321.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:2296637 C>T maps to NM_013321.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:158359771 G>A maps to NM_016224.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:158349642 C>T maps to NM_016224.3 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:158349699 G>A maps to NM_016224.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:158330998 C>T maps to NM_016224.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:158296186 G>A maps to NM_016224.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:53516882 C>T maps to NM_003578.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:53517579 C>T maps to NM_003578.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr12:53499019 T>C maps to NM_003578.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr12:53512990 C>T maps to NM_003578.3 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:107908369 C>T maps to NM_018013.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:107908292 G>T maps to NM_018013.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:107854723 C>A maps to NM_018013.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr6:107956312 G>A maps to NM_018013.3 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:107955682 C>T maps to NM_018013.3 H545H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr6:107827632 T>C did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr14:55510976 C>T maps to NM_199421.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:46986748 C>T maps to NM_144949.2 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr2:46985770 C>T maps to NM_144949.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:46985743 C>T maps to NM_144949.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:67993121 T>C maps to NM_004232.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:67992101 C>T maps to NM_004232.3 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:24801295 G>A maps to NM_003102.2 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:138585511 A>G maps to NM_001101677.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr9:138588458 T>C maps to NM_001101677.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr9:138588518 C>T maps to NM_001101677.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:36776104 C>T maps to ENST00000511166 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr13:36776104 C>T maps to ENST00000511166 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:597773 C>T maps to NM_005632.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:603449 C>T maps to NM_005632.2 S1065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr16:597503 C>T maps to NM_005632.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:599088 C>T maps to NM_005632.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:34923141 G>A maps to NM_138927.1 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr21:34922886 G>A maps to NM_138927.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr21:34922823 G>C maps to NM_138927.1 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:34922610 G>A maps to NM_138927.1 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:34923450 G>A maps to NM_138927.1 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr21:34925014 T>C maps to NM_138927.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr21:34918578 G>A maps to NM_138927.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr21:34924324 T>C maps to NM_138927.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr21:34921956 G>A maps to NM_138927.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr21:34924269 T>G maps to NM_138927.1 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:97101122 T>C maps to NM_001034954.1 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr10:97141492 G>A maps to NM_001034954.1 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:97117445 G>A maps to NM_001034954.1 D690D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:186545448 G>A maps to ENST00000355634 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:186533059 T>C maps to ENST00000355634 Q1086Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:186544614 G>A maps to ENST00000355634 H752H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:186545526 T>C maps to ENST00000355634 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:186544767 G>A maps to ENST00000355634 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:108489835 C>T maps to NM_001013031.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:108923732 G>A maps to NM_001013031.1 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr10:108380194 G>A maps to NM_001013031.1 N929N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr10:108923822 C>A maps to NM_001013031.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:108389107 G>A maps to NM_001013031.1 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:108469078 G>A maps to NM_001013031.1 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr10:108924011 C>T maps to NM_001013031.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:108923945 C>T maps to NM_001013031.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr10:108923843 C>T maps to NM_001013031.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr10:108432661 G>C maps to NM_001013031.1 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr10:108923912 C>T maps to NM_001013031.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr10:108459100 T>C maps to NM_001013031.1 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:7705056 C>T maps to NM_020777.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:7706005 C>A maps to NM_020777.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:7726879 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:7728580 C>T maps to NM_020777.2 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:7666179 C>T maps to NM_020777.2 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:7728547 G>A maps to NM_020777.2 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:7194810 G>A maps to NM_020777.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:7714522 A>G maps to NM_020777.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:7533274 G>A maps to NM_020777.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr10:106976776 C>T maps to NM_014978.1 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:106899199 G>T maps to NM_014978.1 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr10:106865236 T>C maps to NM_014978.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr10:106959783 C>T maps to NM_014978.1 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr10:107005352 C>T maps to NM_014978.1 T974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr10:106849593 G>T maps to NM_014978.1 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:106924109 C>A maps to NM_014978.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:45353326 C>T maps to NM_003104.5 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:121448107 C>T maps to NM_003105.5 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:121475016 T>C maps to NM_003105.5 D1545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:121429395 G>T maps to NM_003105.5 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr11:121420785 G>A maps to NM_003105.5 R723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:121454236 G>A maps to NM_003105.5 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:121454269 C>T maps to NM_003105.5 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr11:121425951 G>A maps to NM_003105.5 E832E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:121421292 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:109910091 G>T maps to NM_002959.4 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:109883433 T>C maps to NM_002959.4 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:109897120 A>G maps to NM_002959.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:39262442 G>A maps to NM_005633.3 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr2:39213363 C>T maps to NM_005633.3 R1201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:39222339 C>T maps to NM_005633.3 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:39249714 G>A maps to NM_005633.3 Y618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:39213083 G>A maps to NM_005633.3 R1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:50585160 A>T maps to NM_006939.2 P1300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr14:50666573 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:50616748 T>C maps to NM_006939.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:41835989 G>A maps to NM_025237.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:41832757 G>A maps to NM_025237.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:41835926 G>A maps to NM_025237.2 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr7:16502238 G>T maps to ENST00000396652 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr13:112722289 G>A maps to NM_005986.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr13:112722295 C>T maps to NM_005986.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:5833107 G>A maps to NM_003108.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:5833131 C>T maps to NM_003108.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:5833530 C>T maps to NM_003108.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr2:5833491 G>A maps to NM_003108.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:5833866 G>A maps to NM_003108.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:204092325 C>T maps to ENST00000367206 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr3:137484051 G>T maps to NM_004189.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:137483757 C>T maps to NM_004189.2 A44A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D7-6818-01A-11D-1882-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:55372485 C>T maps to NM_022454.3 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:55372548 C>T maps to NM_022454.3 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr8:55371954 C>T maps to NM_022454.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:55370865 C>T maps to NM_022454.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr8:55371954 C>T maps to NM_022454.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr8:55370847 G>A maps to NM_022454.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:62680253 C>T maps to NM_018419.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:62679698 G>A maps to NM_018419.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr20:62680315 C>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:62679563 C>T maps to NM_018419.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:181430414 G>A maps to NM_003106.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:181430541 C>T maps to NM_003106.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:139586577 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:139586638 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:139586595 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:139586755 A>G did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr23:139586542 C>T did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:139586728 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:139586637 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:139586053 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:139586356 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:157053374 T>C maps to NM_178424.1 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr5:157073788 G>A maps to NM_178424.1 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:157078489 C>T maps to NM_178424.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:157073824 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:23728679 A>C maps to NM_006940.4 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:23999034 G>A maps to NM_006940.4 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:24048768 C>T maps to NM_006940.4 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr12:23908617 T>C maps to NM_006940.4 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:23893941 C>T maps to NM_006940.4 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr11:15994600 G>A maps to NM_001145819.1 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:16119152 A>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:16071412 C>T maps to NM_001145819.1 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:16208343 G>A maps to NM_001145819.1 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:15994576 C>T maps to NM_001145819.1 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:10583475 G>A maps to ENST00000354846 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:10583280 C>T maps to ENST00000354846 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr8:10583556 C>T maps to ENST00000354846 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr8:10583691 C>T maps to ENST00000354846 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr16:1035325 C>T maps to NM_014587.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:70120257 C>T maps to NM_000346.3 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:53777398 T>C maps to NM_138473.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:53776717 T>C maps to NM_138473.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr12:53776034 C>T maps to NM_138473.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:53775575 C>T maps to NM_138473.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:53776183 C>T maps to NM_138473.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:231372705 A>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:231328833 A>G maps to NM_001080391.1 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:231368992 C>T maps to NM_001080391.1 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:231379967 C>A maps to NM_003113.3 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:231033860 G>A maps to NM_080424.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:231037654 G>A maps to NM_080424.2 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:231042313 G>A maps to NM_080424.2 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:231042331 G>A maps to NM_080424.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:231036426 C>T maps to NM_080424.2 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:231041382 A>G maps to NM_001185015.1 *556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr2:231077539 C>T maps to NM_080424.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:231134618 A>G maps to NM_007237.4 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:231150515 C>T maps to NM_007237.4 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:231120197 T>C maps to NM_007237.4 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr2:231115696 G>A maps to NM_007237.4 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:231155280 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:231110597 C>T maps to NM_007237.4 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:231103097 T>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:231264897 C>T maps to NM_138402.4 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:46002399 C>T maps to NM_003110.5 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:46002809 G>A maps to NM_003110.5 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr2:174820641 C>A maps to NM_003111.4 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:21469088 G>A maps to NM_003112.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:21550661 G>A maps to NM_003112.3 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:171573001 G>A maps to NM_001003845.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:171572827 C>T maps to NM_001003845.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:171573013 G>A maps to NM_001003845.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:171573682 C>T maps to NM_001003845.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:171573715 C>T maps to NM_001003845.2 C333C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:171572953 G>A maps to NM_001003845.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:171572882 C>T maps to NM_001003845.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:45924730 G>A maps to NM_199262.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr17:45924988 C>T maps to NM_199262.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:45925465 C>T maps to NM_199262.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:53723084 C>T maps to NM_001173467.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:53722415 G>A maps to NM_001173467.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr7:20824640 C>T maps to NM_182700.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:20825339 C>T maps to NM_182700.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:20824268 C>T maps to NM_182700.4 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:20825186 C>T maps to NM_182700.4 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr7:20824583 G>A maps to NM_182700.4 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:20824805 C>T maps to NM_182700.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:31324542 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:31322544 C>T maps to NM_173847.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:31322544 C>T maps to NM_173847.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:49110327 C>A maps to NM_133498.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:101243517 C>T did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr8:101195649 C>T maps to NM_003114.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:101196204 T>C maps to NM_003114.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr8:101252665 A>C maps to NM_003114.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:101206482 C>A maps to NM_003114.3 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr2:215013943 C>T maps to NM_024532.3 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:214354766 C>T maps to NM_024532.3 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:215274981 C>T maps to NM_024532.3 H613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:214354793 C>G maps to NM_024532.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:214160815 T>C maps to NM_024532.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:214149344 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:214215284 T>C maps to NM_024532.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr1:118550747 G>A maps to NM_206996.2 I1502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:118514667 C>A maps to NM_206996.2 V2048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:118583458 G>A maps to NM_206996.2 H1020H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr1:118584643 G>A maps to NM_206996.2 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:118527386 T>G maps to NM_206996.2 T1896T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr1:118566056 C>T maps to NM_206996.2 R1313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr1:118538990 A>C did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr1:118624179 C>T maps to NM_206996.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:118693872 C>T maps to NM_206996.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:118617200 G>A maps to NM_206996.2 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:118634279 A>G maps to NM_206996.2 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:34206048 G>A maps to NM_003116.1 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:26906802 G>T maps to NM_006461.3 T950T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:22676750 G>A did not map to a codon.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr10:22657512 A>C maps to ENST00000376603 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:22634742 C>T maps to ENST00000376603 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:35808274 G>A maps to NM_172312.1 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:49098615 G>A maps to ENST00000376407 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:49075878 G>A maps to ENST00000376407 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:49043749 T>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:49057238 G>A maps to ENST00000376407 R1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:49048212 T>C maps to ENST00000376407 Q1236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:123594151 T>C maps to NM_001174046.1 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr7:123599596 C>T maps to NM_001174046.1 N368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:140335783 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:140336518 C>T did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:140335817 C>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:140336550 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:140785778 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:140785770 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:140785701 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr23:140785823 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:140785810 C>T did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:144337214 T>G did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:144337293 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:144329134 G>T did not map to a codon.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr23:144337214 T>G did not map to a codon.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr23:144337198 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:144329174 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:142795422 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:142795584 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:142795350 T>C did not map to a codon.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr23:142795338 T>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:142605182 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:142596774 C>T did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr23:142596855 G>T did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr23:142121815 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:151043780 G>A maps to NM_003118.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:151045950 G>A maps to NM_003118.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:151052747 C>T maps to NM_003118.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr5:151051232 G>T maps to NM_003118.2 C77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr5:151047129 G>A maps to NM_003118.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr4:88414916 G>A maps to NM_004684.4 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr2:32289151 C>G maps to NM_014946.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr2:32362006 A>G maps to NM_014946.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:32289086 C>T maps to NM_014946.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr1:84991559 A>G maps to ENST00000263717 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:24860365 C>T maps to ENST00000424834 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:24858405 T>C maps to ENST00000424834 N803N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:24865019 C>T maps to ENST00000424834 H1063H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr13:24876889 G>A maps to ENST00000424834 R1308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:172607479 A>C maps to NM_031955.5 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:172631533 G>A maps to NM_031955.5 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:172834945 G>A maps to NM_031955.5 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr3:172674584 A>G maps to NM_031955.5 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:172834945 G>A maps to NM_031955.5 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:218036153 A>G maps to NM_138796.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:218036113 A>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:217975156 C>T maps to NM_138796.2 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:218036192 A>G maps to NM_138796.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:217947759 C>T maps to NM_138796.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr1:217824480 A>G maps to NM_138796.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:52945918 C>T maps to NM_145263.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:52943100 G>A maps to NM_145263.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr4:52944992 T>C maps to NM_145263.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:133714469 T>A maps to NM_174927.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:48523039 G>A maps to NM_006038.3 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:48522569 G>A maps to NM_006038.3 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:48522560 G>A maps to NM_006038.3 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:48628887 C>T maps to NM_022827.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:48632977 G>A maps to NM_022827.2 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:16736337 C>T maps to NM_198546.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:16748033 G>A maps to NM_198546.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:89764299 G>A maps to NM_152339.3 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:89764415 G>A maps to NM_152339.3 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:89764596 G>A maps to NM_152339.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:177105978 A>C maps to NM_144644.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:177113868 G>A maps to NM_144644.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr4:123868602 A>G maps to NM_145207.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:123949495 A>G maps to NM_145207.2 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:123855261 T>C maps to NM_145207.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr4:123850211 T>G maps to NM_145207.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:45694911 C>T maps to NM_024063.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:45706831 G>T maps to NM_024063.2 G500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:48917263 C>T maps to NM_019073.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:48771535 T>C maps to NM_019073.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:97328283 T>C maps to NM_173499.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:97326896 T>C maps to NM_173499.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr5:95011142 C>T maps to NM_031952.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:94994503 A>C maps to NM_031952.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:95011301 A>G maps to NM_031952.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr8:145095739 C>T maps to NM_198572.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:145101718 C>T maps to NM_198572.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr8:145096244 C>G maps to NM_198572.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:145095790 T>C maps to NM_198572.2 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:145095490 C>A maps to NM_198572.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr8:145095526 G>A maps to NM_198572.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:145095766 C>A maps to NM_198572.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:49893962 C>T maps to NM_023071.3 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:49883336 A>G maps to NM_023071.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:201342741 G>A maps to ENST00000409151 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:201284106 C>T maps to ENST00000409151 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:169732593 G>A maps to NM_020675.3 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:169746005 A>C maps to NM_020675.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:74688036 T>C maps to NM_014752.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr6:34508911 C>T maps to NM_012391.1 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:34512184 G>C maps to NM_012391.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:34512082 C>T maps to NM_012391.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:29039041 C>T maps to NM_182756.3 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:64939751 C>T maps to NM_001008778.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr11:64940348 C>T maps to NM_001008778.1 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr7:99909533 C>T maps to NM_001004351.4 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:35806993 T>C maps to NM_024867.3 S1732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr5:35814619 A>C maps to NM_024867.3 R1812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:35649521 A>G maps to NM_024867.3 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:35659270 C>T maps to NM_024867.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:35628562 T>C maps to NM_024867.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr5:35667220 A>G maps to NM_024867.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr5:35654722 A>G maps to NM_024867.3 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:35667344 C>T maps to NM_024867.3 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:35641742 A>G maps to NM_024867.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr5:35771826 C>G maps to NM_024867.3 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:220353848 C>T maps to NM_005876.4 G2741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:220312962 C>T maps to NM_005876.4 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:220336947 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:220354352 G>A maps to NM_005876.4 E2871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:220349087 G>A maps to NM_005876.4 P2301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:220354262 A>G maps to NM_005876.4 P2841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:220355248 C>T maps to NM_005876.4 L3014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:220331920 C>T maps to NM_005876.4 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:220329301 G>A maps to NM_005876.4 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:220299719 G>A maps to NM_005876.4 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr2:220312959 G>A maps to NM_005876.4 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:220349009 C>T maps to NM_005876.4 H2275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:220313049 G>A maps to NM_005876.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:220348727 C>T maps to NM_005876.4 P2181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:220343907 C>T maps to NM_005876.4 T1690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:220329223 C>T maps to NM_005876.4 C925C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:220353256 C>A maps to NM_005876.4 I2632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:220346103 C>T maps to NM_005876.4 F1816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr2:220353343 C>T maps to NM_005876.4 N2661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:220348544 C>T maps to NM_005876.4 L2120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:220333584 C>T maps to NM_005876.4 C1102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:7324281 C>T maps to NM_199339.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:16258452 C>T maps to NM_015001.2 S1906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:16256109 G>A maps to NM_015001.2 E1125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr1:16260873 C>A maps to NM_015001.2 A2713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:16199577 T>C maps to NM_015001.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:16256979 A>G maps to NM_015001.2 L1415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:16261326 G>A maps to NM_015001.2 S2864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:16263674 T>C maps to NM_015001.2 G3348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:16262481 C>T maps to NM_015001.2 P3249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:16248845 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:16259758 C>T maps to NM_015001.2 R2342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:16262481 C>T maps to NM_015001.2 P3249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:16265253 C>T maps to NM_015001.2 G3582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:16254748 C>T maps to NM_015001.2 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:16257669 A>G maps to NM_015001.2 V1645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:16262529 T>C maps to NM_015001.2 G3265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:16259136 A>G maps to NM_015001.2 S2134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:16257561 A>G maps to NM_015001.2 K1609K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:16199370 T>C maps to NM_015001.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:16261497 G>A maps to NM_015001.2 T2921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:16263926 C>A maps to NM_015001.2 P3432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:16260225 G>A maps to NM_015001.2 K2497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr1:16255131 G>T maps to NM_015001.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:16262613 G>A maps to NM_015001.2 V3293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr13:46287418 C>T maps to NM_152719.1 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr13:46287450 C>T maps to NM_152719.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:46287327 C>T maps to NM_152719.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr13:46287489 C>T maps to NM_152719.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr13:46287534 C>T maps to NM_152719.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr13:46287708 C>T maps to NM_152719.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr13:46288455 C>T maps to NM_152719.1 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:46287831 G>A maps to NM_152719.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:44877947 A>G maps to NM_025137.3 L1669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr15:44913992 G>A maps to NM_025137.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:44944094 C>T maps to NM_025137.3 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:44913996 T>C maps to NM_025137.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr15:44888502 C>T maps to NM_025137.3 R1404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:44951448 T>C maps to NM_025137.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:36878522 C>T maps to NM_001142294.1 E660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr13:36888424 G>T maps to NM_001142294.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:36905565 C>A maps to NM_001142294.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:65257734 G>T maps to NM_016630.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:89590438 C>T maps to NM_003119.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:89592861 A>G maps to NM_003119.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:89598457 C>T maps to NM_003119.2 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr17:74382949 G>A maps to NM_182965.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:49132183 C>T maps to NM_020126.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:49132081 C>T maps to NM_020126.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:49132885 C>T maps to NM_020126.3 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:228884213 A>G maps to NM_001142644.1 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:228883826 G>A maps to NM_001142644.1 C581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:228884735 T>C maps to NM_001142644.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:228846498 G>T maps to NM_001142644.1 C1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:228886658 G>A maps to NM_001142644.1 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:228882350 G>A maps to NM_001142644.1 D1073D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr2:228881276 A>G maps to NM_001142644.1 I1431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:228882971 G>A maps to NM_001142644.1 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr2:228883843 T>A maps to NM_001142644.1 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:47377074 C>A maps to NM_001080547.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:47399892 C>T maps to NM_001080547.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:101880329 C>T maps to ENST00000299272 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:101876580 G>A maps to ENST00000299272 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr9:91083395 C>T maps to NM_006717.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:57162585 C>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:57021143 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:62570000 T>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:62570005 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:62570233 G>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:33240247 C>A maps to NM_014471.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:147499621 C>T maps to NM_001127698.1 C788C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr5:147491380 T>C maps to NM_001127698.1 C581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:147480950 A>G maps to NM_001127698.1 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr5:147505094 C>T maps to NM_001127698.1 C916C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr18:12463379 C>T maps to NM_001128626.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr18:12506562 G>A maps to NM_001128626.1 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:12479830 G>T maps to NM_001128626.1 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr18:12463376 C>T maps to NM_001128626.1 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr18:12449699 G>A maps to NM_001128626.1 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:89936520 C>T maps to NM_032451.1 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:89916878 C>T maps to NM_032451.1 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:89927100 C>T maps to NM_032451.1 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:89936598 C>T maps to NM_032451.1 D688D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:28993368 C>A maps to NM_032038.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:28993317 C>T maps to NM_032038.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:4352607 G>A maps to NM_182538.4 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:32280648 G>A maps to NM_144569.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:32262280 C>T maps to NM_144569.4 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:32256814 G>A maps to NM_144569.4 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:136602744 C>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:136834172 G>A maps to NM_004598.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:136448204 C>T maps to NM_004598.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:73848011 G>A maps to NM_014767.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:73826723 G>T maps to NM_014767.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:73823933 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:167675863 G>T maps to NM_016950.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr4:167921513 C>T maps to NM_016950.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr4:167833842 G>A maps to NM_016950.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:14276112 G>A maps to NM_006108.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr11:13984525 G>A maps to NM_006108.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:14284394 C>T maps to NM_006108.2 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:1165658 C>T maps to NM_012445.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:1165269 G>A maps to NM_012445.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:1165158 C>T maps to NM_012445.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:47700148 T>C maps to NM_003563.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr17:47679345 G>A maps to NM_003563.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:139308135 T>C maps to NM_001001664.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:139316734 A>G maps to NM_001001664.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:88903759 C>T maps to NM_001040058.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:88902838 C>T maps to NM_001040058.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:2353032 G>A maps to NM_152988.2 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:2353173 G>A maps to NM_152988.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:2345251 G>A maps to NM_152988.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:121229360 C>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:73115581 C>A maps to NM_003124.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr2:73118534 C>T maps to NM_003124.4 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:38643474 T>G maps to NM_152594.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:38632011 G>A maps to NM_152594.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr15:38591730 C>T maps to NM_152594.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr15:38643534 C>T maps to NM_152594.2 C335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:65571869 G>A maps to NM_181784.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:65541009 C>A maps to NM_181784.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:65571936 G>A maps to NM_181784.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:65659115 G>T maps to NM_181784.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:65540703 G>A maps to NM_181784.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:65571869 G>A maps to NM_181784.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:65559174 C>T maps to NM_181784.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:65540907 G>A maps to NM_181784.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:65541234 G>A maps to NM_181784.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:152957780 C>T maps to NM_005987.3 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:153004878 C>T maps to NM_003125.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:153004967 C>T maps to NM_003125.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:153029004 C>T maps to NM_005988.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:153066038 G>A maps to NM_001024209.2 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:153085020 G>A maps to NM_001014450.1 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:152975732 G>A maps to NM_005416.2 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:124323693 T>C maps to NM_199327.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr13:80911384 C>T maps to NM_005842.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:155003997 C>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:155003588 G>A did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:155004391 T>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:155004071 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:155004341 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:155003540 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:155004290 A>T did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:155003812 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:155003624 C>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:141694196 G>A maps to NM_030964.3 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:141694394 G>A maps to NM_030964.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:141694676 G>A maps to NM_030964.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:55658771 T>C maps to NM_032681.3 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:55656477 G>C did not map to a codon.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr11:55653660 G>C maps to NM_032681.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:9427507 C>T maps to NM_025106.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:9416345 C>T maps to NM_025106.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:9427588 G>A maps to NM_025106.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:6981673 C>T maps to NM_032641.3 W131*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-A4CR-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:158622283 C>T maps to NM_003126.2 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr1:158646086 T>G did not map to a codon.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr1:158651376 G>A maps to NM_003126.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:158596640 C>A maps to NM_003126.2 E1941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:158641956 G>A maps to NM_003126.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:158644338 C>T maps to NM_003126.2 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr1:158654935 A>G maps to NM_003126.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr1:158613203 G>T maps to NM_003126.2 I1450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr1:158621189 T>C maps to NM_003126.2 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr1:158653163 C>T maps to NM_003126.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr1:158604449 T>C maps to NM_003126.2 E1816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr1:158589971 A>G maps to NM_003126.2 S2135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr1:158617462 T>C maps to NM_003126.2 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr1:158623115 G>A maps to NM_003126.2 R1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:158647572 G>T maps to NM_003126.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:158632693 T>C maps to NM_003126.2 E754E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:158653169 T>C maps to NM_003126.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr1:158618324 T>G maps to NM_003126.2 R1230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:158639573 A>G maps to NM_003126.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr1:158650414 C>T maps to NM_003126.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:158592946 T>C maps to NM_003126.2 Q1982Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr1:158604388 C>A maps to NM_003126.2 E1837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:158637646 C>T did not map to a codon.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr1:158623115 G>A maps to NM_003126.2 R1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:131395516 C>T maps to NM_001130438.2 C2446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr9:131329151 C>T maps to NM_001130438.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:131395597 G>A maps to NM_001130438.2 S2473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:131369951 C>T maps to NM_001130438.2 T1372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr9:131381149 G>C maps to NM_001130438.2 R1867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr9:131329030 T>C maps to NM_001130438.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:131346760 G>A maps to NM_001130438.2 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:131339689 A>G maps to NM_001130438.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:131375679 C>T maps to NM_001130438.2 S1688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:131353799 G>A maps to NM_001130438.2 P1017P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr9:131353778 C>T maps to NM_001130438.2 N1010N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:131392620 G>A maps to NM_001130438.2 S2243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:131353805 G>A maps to NM_001130438.2 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr14:65253381 G>A maps to ENST00000389723 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:65239522 G>A maps to ENST00000389723 N1780N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:65262177 C>T maps to ENST00000389723 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:65260265 C>T maps to ENST00000389723 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:65241932 G>A maps to ENST00000389723 N1588N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr14:65259824 C>T maps to ENST00000389723 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:65260556 G>A maps to ENST00000389723 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr14:65268105 G>A maps to ENST00000389723 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr14:65262291 G>A maps to ENST00000389723 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr14:65237840 G>A maps to ENST00000389723 Q1858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:65240060 C>T maps to ENST00000389723 K1689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:65252320 G>A maps to ENST00000389723 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:54856268 C>T maps to NM_003128.2 Y666Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:54858255 C>T maps to NM_003128.2 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:54895585 C>T maps to NM_003128.2 R2325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:54839398 G>A maps to NM_003128.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:54858498 G>A maps to NM_003128.2 E1105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:54855379 C>T maps to NM_003128.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:54895522 C>T maps to NM_003128.2 S2304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:54874380 C>T maps to NM_003128.2 A1660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr2:54856334 C>T maps to NM_003128.2 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:54872403 C>T maps to NM_003128.2 I1436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:54880819 G>A maps to NM_003128.2 K1884K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:54893177 C>T maps to NM_003128.2 C2262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:66456222 C>T maps to NM_006946.2 T2044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:66475076 G>A maps to NM_006946.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66453563 G>A maps to NM_006946.2 S2317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66476408 C>T maps to NM_006946.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:66472907 C>T maps to NM_006946.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:66458925 G>A maps to NM_006946.2 A1798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:66468626 G>A maps to NM_006946.2 I981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:66483312 C>T maps to NM_006946.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:66460057 G>A maps to NM_006946.2 R1713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:41012168 G>C maps to NM_020971.2 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:40993658 C>T maps to NM_020971.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:41026036 G>A maps to NM_020971.2 A1211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:41071343 G>T maps to NM_020971.2 V1977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:41040081 C>T maps to NM_020971.2 S1397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:41078035 G>A maps to NM_020971.2 L2477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:41062145 G>A maps to NM_020971.2 E1747E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr19:41063306 C>T maps to NM_020971.2 Q1890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr19:41062936 G>A maps to NM_020971.2 Q1766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:42148706 G>A maps to ENST00000320955 A2966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:42147510 G>A maps to ENST00000320955 R3112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr15:42150832 G>A maps to ENST00000320955 D2731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr15:42180151 G>T maps to ENST00000320955 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:42171951 C>T maps to ENST00000320955 Q974Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr15:42185100 G>A maps to ENST00000320955 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr15:42143985 G>A maps to ENST00000320955 G3549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:42151168 C>T maps to ENST00000320955 A2666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:94809514 C>T maps to NM_006415.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:94809484 A>G maps to NM_006415.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:94843196 G>A maps to NM_006415.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:13098371 G>A maps to NM_018327.2 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:13074180 G>A maps to NM_018327.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:13098151 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:18636592 G>A maps to NM_194285.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:18637192 G>A maps to NM_194285.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:18636446 G>T maps to NM_194285.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr11:18637506 G>C maps to NM_194285.2 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr11:18636836 A>T maps to NM_194285.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:18633955 G>A maps to NM_194285.2 Y597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:126023789 G>T maps to NM_003129.3 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:126021226 A>G maps to NM_003129.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:126021271 C>T maps to NM_003129.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr5:179263586 G>A maps to NM_003900.4 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:142773862 G>A maps to NM_001080415.1 S951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:142741773 G>A maps to NM_001080415.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:142741773 G>A maps to NM_001080415.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:139930497 T>C did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:139931629 A>T maps to NM_001035235.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:45778339 A>C maps to NM_018079.4 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:45800477 G>A maps to NM_018079.4 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:45826799 C>A maps to NM_018079.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:36031230 C>A maps to ENST00000373558 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr16:30723018 C>T maps to NM_006662.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr16:30723590 G>A maps to NM_006662.2 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:30750684 A>G maps to NM_006662.2 P3108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr16:30727523 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:30734368 A>G maps to NM_006662.2 P1326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:30745250 A>T maps to NM_006662.2 L2177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr16:30732219 C>G maps to NM_006662.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:30727670 G>A maps to NM_006662.2 Q896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:30735943 T>G maps to NM_006662.2 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr16:30715407 C>G maps to NM_006662.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:30750429 C>T maps to NM_006662.2 P3023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:30744599 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:30723462 G>A maps to NM_006662.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr16:30750657 C>T maps to NM_006662.2 S3099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr16:30727757 C>T maps to NM_006662.2 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:30723027 G>A maps to NM_006662.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:30745869 C>T maps to NM_006662.2 S2221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:36717697 C>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr17:36707420 G>A maps to NM_025248.2 R978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:76029798 G>A maps to NM_080744.1 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:76019657 G>A maps to NM_080744.1 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr7:76027009 G>A maps to NM_080744.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:6663022 G>A maps to NM_001047.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr5:6652020 G>A maps to NM_001047.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr2:31754395 G>A maps to NM_000348.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr2:31805765 C>T maps to NM_000348.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:56236242 A>G maps to NM_024592.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:56225591 G>T maps to NM_024592.3 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:17723593 C>T maps to NM_001005291.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:17722983 C>T maps to NM_001005291.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr17:17726907 C>G maps to NM_001005291.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:17720699 C>T maps to NM_001005291.2 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:17723584 G>A maps to NM_001005291.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr22:42276823 C>T maps to NM_004599.2 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr22:42264621 G>A maps to NM_004599.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr22:42271598 G>T maps to NM_004599.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr22:42290836 G>A maps to NM_004599.2 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:42276928 C>T maps to NM_004599.2 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:43141604 G>A maps to NM_003131.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:43143530 C>T maps to NM_003131.2 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr5:121311042 A>G maps to NM_152546.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr5:121356467 C>T maps to NM_152546.2 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:121309938 C>T maps to NM_152546.2 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:64488719 A>T maps to NM_020762.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr12:64458980 C>G maps to NM_020762.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:64519880 C>T maps to NM_020762.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr12:64521658 G>A maps to NM_020762.2 E853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:64456869 G>A maps to NM_020762.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:64491075 C>T maps to NM_020762.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr12:64456869 G>A maps to NM_020762.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:9027592 C>T maps to NM_014850.2 T970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr3:9027388 G>A maps to NM_014850.2 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:9057340 G>A maps to NM_014850.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr3:9057395 G>A maps to NM_014850.2 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr3:9100111 C>T maps to NM_014850.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:9027583 G>A maps to NM_014850.2 H973H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:9036100 C>T maps to NM_014850.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:87840205 T>C maps to NM_003130.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:4247797 A>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:62178750 C>T maps to NM_080823.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr20:62172299 C>T maps to NM_080823.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr5:112197084 T>A maps to NM_003135.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:74068512 A>G maps to NM_014230.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:74042210 G>A maps to NM_014230.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:74042187 C>T maps to NM_014230.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr4:57354155 G>T maps to NM_006947.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IZ-01A-32D-A25D-08 chr4:57356811 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:225977010 C>T maps to NM_003133.5 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:35854498 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:104783606 G>A maps to ENST00000336613 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:104783674 G>A maps to ENST00000336613 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:153050421 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:153047268 T>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:153050912 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:153048549 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:153050930 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153046775 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153049821 C>T did not map to a codon.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr23:153047059 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:126135201 G>A maps to NM_003139.3 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:126137068 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:126136743 G>A maps to NM_003139.3 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:133534432 G>T did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:38019422 G>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:38008989 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:38024076 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:99919890 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:99924334 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:99920637 C>A did not map to a codon.
Sequencing variant TCGA-CD-8526-01A-11D-2340-08 chr23:99919930 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:99920260 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:99920542 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:99920364 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:2226992 A>G maps to NM_021947.1 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:24993348 C>T maps to NM_005839.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:24996799 G>A maps to NM_005839.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:24979062 G>A maps to NM_005839.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:2809395 C>T maps to NM_016333.3 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:2812490 A>G maps to NM_016333.3 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:2814126 C>T maps to NM_016333.3 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:2813633 C>G maps to NM_016333.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:2817371 T>C maps to NM_016333.3 A2281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr16:2815031 A>G maps to NM_016333.3 S1501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:2819192 C>G maps to NM_016333.3 S2643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr16:2816492 G>A maps to NM_016333.3 P1988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:2811590 G>A maps to NM_016333.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:2812422 C>T maps to NM_016333.3 R632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr7:75889226 G>A maps to ENST00000388802 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:75896576 C>T maps to ENST00000388802 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:75896680 G>A maps to ENST00000388802 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:75896629 C>T maps to ENST00000388802 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:119592099 C>T maps to NM_194286.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr12:119588836 G>A maps to NM_194286.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:119588944 C>A maps to NM_194286.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:119563239 G>A maps to NM_194286.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:119594347 C>T maps to NM_194286.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:100478929 C>T maps to NM_015908.5 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr24:2655594 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr24:2655178 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:2655459 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:60737940 C>T maps to NM_198935.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:141443376 C>T maps to NM_003143.1 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:80762803 A>G maps to ENST00000380182 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:80770363 T>C maps to ENST00000380182 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr5:80738510 A>C maps to ENST00000380182 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:81046803 C>A maps to ENST00000380182 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:54867611 A>G maps to NM_145716.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:54694478 C>T maps to NM_145716.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:54870572 C>T maps to NM_145716.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:182786931 G>A maps to NM_001130445.1 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:182784160 C>A maps to NM_001130445.1 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:182786911 C>T maps to NM_001130445.1 R1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr2:182780323 G>T maps to NM_001130445.1 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:109192888 G>A maps to NM_018984.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:109182491 G>A maps to NM_018984.3 Q808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr12:109182914 G>A maps to NM_018984.3 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:28003847 G>A maps to NM_033389.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:27963594 T>C maps to NM_033389.2 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:27958632 G>A maps to NM_033389.2 S1166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:27957927 G>A maps to NM_033389.2 H1401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:27958581 G>A maps to NM_033389.2 S1183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:27957939 G>A maps to NM_033389.2 H1397H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:28030049 A>G maps to NM_033389.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:67077277 C>T maps to NM_017857.3 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:26348817 C>A maps to NM_005086.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:149485989 C>T maps to NM_198455.2 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:149522373 C>T maps to NM_198455.2 R4674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr7:149489037 G>A maps to NM_198455.2 L1794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:149500829 C>T maps to NM_198455.2 C2717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr7:149475867 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:149477453 C>T maps to NM_198455.2 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:149497408 G>A maps to NM_198455.2 V2390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:149475867 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:149498834 A>G maps to NM_198455.2 L2430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr7:149489757 C>T maps to NM_198455.2 N1939N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr7:149490472 C>G maps to NM_198455.2 G1984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr7:149480253 C>T maps to NM_198455.2 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:149489157 T>G maps to NM_198455.2 P1802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:149500638 C>T maps to NM_198455.2 G2681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:149495202 G>A maps to NM_198455.2 T2318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr7:149481148 C>T maps to NM_198455.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:149515105 C>T maps to NM_198455.2 T3835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:155989859 G>A maps to ENST00000368312 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:156272761 C>T maps to ENST00000467789 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:153063225 A>G did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:153063826 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:153063256 C>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:57099954 G>A maps to NM_003146.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:65339168 G>A maps to NM_006396.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr11:65338860 G>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr14:38678776 C>A maps to NM_001049.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:38679661 C>T maps to NM_001049.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:38679607 A>T maps to NM_001049.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:38679517 G>A maps to NM_001049.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:71166189 C>T maps to NM_001050.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:37603821 T>C maps to NM_001051.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:37603059 G>A maps to NM_001051.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:37603074 C>T maps to NM_001051.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr22:37603677 G>A maps to NM_001051.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr22:37603002 G>A maps to NM_001051.2 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:37602723 C>T maps to NM_001051.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:37602726 G>A maps to NM_001051.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr20:23016704 C>T maps to NM_001052.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:23016533 C>T maps to NM_001052.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:1129608 G>A maps to NM_001053.3 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:1129860 C>T maps to NM_001053.3 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:1129866 G>A maps to NM_001053.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:1129227 C>T maps to NM_001053.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr16:1129557 G>A maps to NM_001053.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr23:48116744 G>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:48123235 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:85128058 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:85136859 C>A maps to NM_001166417.1 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:48209551 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:48244823 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:48053564 C>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:48054731 C>T did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:48054787 C>T did not map to a codon.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr23:48054779 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr23:48053652 C>G did not map to a codon.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr23:48053629 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:52682510 G>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:52677444 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:52674498 G>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:52677308 A>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:52681368 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:52677332 A>G did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:52677311 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:41222544 C>T maps to NM_003932.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr11:130066231 A>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:130060403 G>A maps to NM_021978.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr8:53092688 A>G maps to NM_014682.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:134472081 G>A maps to NM_173344.2 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:134474126 G>T maps to NM_173344.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr8:134477157 C>T maps to NM_173344.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr16:70422403 G>A maps to NM_006927.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:44202013 G>A maps to NM_174963.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:44303914 C>T maps to NM_174963.2 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:86067344 C>T maps to NM_003896.3 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:86073607 G>A maps to NM_003896.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:86075231 G>A maps to NM_003896.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:86073607 G>A maps to NM_003896.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:98510728 G>A maps to ENST00000493584 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr3:98489734 G>A maps to ENST00000493584 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr11:8720765 C>A maps to NM_005418.3 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:8739285 A>G did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr11:8732692 C>T maps to NM_005418.3 W753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:8739391 G>A maps to NM_005418.3 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:8752500 G>A maps to NM_005418.3 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:8752323 C>T maps to NM_005418.3 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:8751552 C>T maps to NM_005418.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr11:8752512 C>T maps to NM_005418.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:186761060 G>A maps to NM_003032.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr3:186761056 C>G maps to NM_003032.2 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr2:107459866 G>A maps to NM_001142351.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:107459974 G>C maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr2:107450507 C>T maps to NM_001142351.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:107459934 G>A maps to NM_001142351.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:107459881 G>A maps to NM_001142351.1 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:107459500 G>A maps to NM_001142351.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr2:107460328 G>A maps to NM_001142351.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:74623162 G>A maps to NM_018414.3 H386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:74621503 G>A maps to NM_018414.3 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:74623282 G>A maps to NM_018414.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr17:74569350 G>A maps to NM_006456.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:74562347 A>G maps to NM_006456.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr9:130653085 G>A maps to NM_013443.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:130653118 C>T maps to NM_013443.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:130648925 C>T maps to NM_013443.3 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:130653010 C>T maps to NM_013443.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr7:116759769 C>T maps to ENST00000323984 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:116849977 T>C maps to ENST00000323984 C464C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:22408251 G>A maps to NM_003034.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:22487106 C>T maps to NM_003034.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:22408308 C>T maps to NM_003034.3 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:22487141 G>A maps to NM_003034.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:22354737 C>G maps to NM_003034.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:92973322 T>A maps to NM_006011.3 L48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:93007590 C>T maps to NM_006011.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr15:92977596 G>A maps to NM_006011.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr18:55020154 G>A maps to NM_015879.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:100238557 C>T maps to NM_005668.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:100238557 C>T maps to NM_005668.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr5:100192066 T>A maps to NM_005668.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr5:100147762 T>A maps to NM_005668.4 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr5:100222284 A>G maps to NM_005668.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:44260100 G>A maps to NM_013305.4 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr18:44336459 C>T maps to NM_013305.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr18:44260169 C>T maps to NM_013305.4 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:44260370 G>A maps to NM_013305.4 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr18:44336399 G>A maps to NM_013305.4 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr18:44260283 G>A maps to NM_013305.4 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr18:44260337 G>A maps to NM_013305.4 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr18:44272145 C>T maps to NM_013305.4 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr18:44266171 G>A maps to NM_013305.4 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr18:44260211 C>T maps to NM_013305.4 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:44260148 C>T maps to NM_013305.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:17432534 C>T maps to NM_001004470.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr10:17369098 A>T maps to NM_001004470.1 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr3:52556203 C>T maps to NM_015136.2 R2141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:52537420 G>A maps to NM_015136.2 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:52556631 G>A maps to NM_015136.2 S2224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:52551964 C>T maps to NM_015136.2 C1569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:52551615 C>T maps to NM_015136.2 C1538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:52554480 C>T maps to NM_015136.2 G1855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:52552860 C>T maps to NM_015136.2 H1670H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:103981260 C>T maps to NM_017564.9 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:104155079 G>A maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:104078852 C>T maps to NM_017564.9 N996N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:104152954 C>T maps to NM_017564.9 S2384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:104121067 C>T maps to NM_017564.9 V1625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:104049337 C>T maps to NM_017564.9 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr12:104157270 C>A maps to NM_017564.9 S2497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:104049337 C>T maps to NM_017564.9 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:104144469 C>T maps to NM_017564.9 D2184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:104049046 C>T maps to NM_017564.9 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr12:104099462 C>A maps to NM_017564.9 T1318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:104134517 C>T maps to NM_017564.9 F1955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:104140393 G>A maps to NM_017564.9 T2052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:104142933 G>A maps to NM_017564.9 P2146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:36485022 G>A maps to NM_003149.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:36422209 G>A maps to NM_003149.1 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr3:36534689 C>T maps to NM_003149.1 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr3:36422158 C>T maps to NM_003149.1 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UG-01A-21D-A31L-08 chr3:36485103 C>T maps to NM_003149.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr3:36527668 C>T maps to NM_003149.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:57638743 G>A maps to NM_145064.1 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:57637987 G>A maps to NM_145064.1 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:57643004 C>T maps to NM_145064.1 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:136240171 G>A maps to NM_005862.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr3:136117671 C>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:123185029 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:123229278 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:123196830 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:123217381 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:123205130 G>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:123196990 C>G did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:123164874 C>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:123185061 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:123171426 A>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:123202433 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:123217305 C>A did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:123220422 C>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:123220559 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:123171416 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-BR-4184-01A-01D-1126-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-8366-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr7:99808703 G>A maps to NM_012447.2 P1103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:99779802 G>A maps to NM_012447.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:99796139 C>T maps to NM_012447.2 V429V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8484-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr7:99808775 A>G maps to NM_012447.2 E1127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:99796124 G>A maps to NM_012447.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:99779802 G>A maps to NM_012447.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:99809480 A>G maps to NM_012447.2 E1193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:72470007 C>A maps to ENST00000308103 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr2:152992029 A>C maps to NM_005843.4 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:74089387 C>T did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr2:74077570 C>T maps to NM_213622.1 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:74086400 G>A maps to NM_213622.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:74089387 C>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr4:68447129 C>T maps to NM_012108.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr4:68441206 A>C maps to NM_012108.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:68472068 T>C maps to NM_012108.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr19:4325404 C>A maps to ENST00000314714 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:38005719 G>A maps to NM_000349.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:72466073 C>T maps to NM_006645.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:33686931 C>T maps to NM_178007.2 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr13:33686967 G>A maps to NM_178007.2 N786N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:33701652 C>T maps to NM_178007.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr13:33741703 G>A maps to NM_178007.2 Y67Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:33704264 A>G maps to NM_178007.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:33704014 G>A maps to NM_178007.2 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr13:33703175 C>T maps to NM_178007.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr13:33701559 G>A maps to NM_178007.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr17:37814752 C>A maps to NM_006804.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:38247158 C>T maps to NM_032016.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:81611719 C>T maps to NM_181900.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr15:81611764 G>A maps to NM_181900.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr18:51880422 C>T did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:67941415 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:67941914 G>A did not map to a codon.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr23:67943489 G>A did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr23:67941950 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:67941512 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:67935146 C>T did not map to a codon.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr23:67940948 C>A did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:67937257 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:67940851 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:67940211 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:67941390 T>A did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:67936224 G>C did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr2:191851577 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:191841683 G>A maps to NM_007315.3 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr17:40474480 G>A maps to NM_139276.2 Y640Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:40467786 C>T maps to NM_139276.2 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr17:40476995 C>T maps to NM_139276.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:191897687 G>A maps to NM_003151.2 C680C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:191898231 C>A maps to NM_003151.2 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr2:191934455 G>A maps to NM_003151.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr2:191922751 G>A maps to NM_003151.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:40441494 C>T maps to NM_003152.3 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:40458335 C>T maps to NM_003152.3 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:40447789 C>T maps to NM_003152.3 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:40359648 G>A maps to NM_012448.3 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:40369448 G>A maps to NM_012448.3 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:40369448 G>A maps to NM_012448.3 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr12:57501477 G>A maps to NM_003153.4 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:57499294 C>T maps to NM_003153.4 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:57493154 G>A maps to NM_003153.4 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:57501037 T>A maps to NM_003153.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:47741115 C>A maps to NM_017453.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:47734394 G>T maps to NM_017453.2 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:47734556 G>A maps to NM_017453.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:74526052 T>A maps to NM_001164380.1 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:74601000 T>C maps to NM_001164380.1 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr4:77230708 T>C maps to NM_003943.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr4:77230639 C>T maps to NM_003943.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:77230675 C>T maps to NM_003943.3 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:23709799 G>A maps to NM_003155.2 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:23709859 G>A maps to NM_003155.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:172755133 C>T maps to NM_003714.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:172744948 G>T maps to NM_003714.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:89793831 C>T maps to ENST00000433102 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr7:89856640 T>C maps to NM_152999.3 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:89854551 C>T maps to NM_152999.3 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr7:89856418 T>C maps to NM_152999.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:120005644 C>T maps to NM_182915.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:120020820 C>T maps to NM_182915.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:120012378 G>A maps to NM_182915.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:120005391 G>A maps to NM_182915.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr2:120005613 C>T maps to NM_182915.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:120003323 G>A maps to NM_182915.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:120005697 C>T maps to NM_182915.2 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr2:120005307 G>A maps to NM_182915.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr7:87913436 G>A maps to NM_024636.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:47716885 T>C maps to NM_001048166.1 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:47717401 A>G maps to NM_001048166.1 C1091C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:47717512 T>C maps to NM_001048166.1 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:47746068 T>C maps to NM_001048166.1 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:47717263 T>C maps to NM_001048166.1 E1137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr1:47746464 G>A maps to NM_001048166.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:4103493 G>A maps to NM_003156.3 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:4112532 G>A maps to NM_003156.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:4112931 T>A maps to NM_003156.3 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:4080586 C>T maps to NM_003156.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:27024458 C>T maps to ENST00000382009 R789R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:27024296 G>A maps to ENST00000382009 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:27019549 G>A maps to ENST00000382009 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:26997035 T>C maps to ENST00000382009 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:63965053 C>T maps to ENST00000358794 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr5:171523474 G>A maps to NM_005990.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:171523525 C>T maps to NM_005990.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:171517366 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr19:1207202 G>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:220471012 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:220476440 G>A maps to NM_052902.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:43664347 T>A maps to NM_004760.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:197002221 G>A maps to NM_004226.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:197002359 G>T maps to NM_004226.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:197004483 T>C maps to NM_004226.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:31939919 C>T maps to NM_032454.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr13:99109503 G>A maps to NM_003576.3 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:99539029 A>G maps to ENST00000354930 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:99468225 C>T maps to ENST00000354930 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:99761545 G>A maps to ENST00000354930 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:23809299 C>T maps to NM_031414.3 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:23749936 C>G maps to NM_031414.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:23826128 C>A maps to NM_031414.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr7:23749936 C>T maps to NM_031414.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:23827645 G>A maps to NM_031414.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr7:23749943 G>T maps to NM_031414.3 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:146750299 C>A maps to NM_001112724.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:146750334 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr4:5468446 C>T maps to NM_018401.1 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:5458559 G>A maps to NM_018401.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr4:5170043 C>T maps to NM_018401.1 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr4:5500794 T>G maps to NM_018401.1 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr10:134021590 C>A maps to NM_173575.2 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:134039073 G>A maps to NM_173575.2 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:8478888 A>G maps to NM_030906.2 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:2097714 A>G maps to NM_080836.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr20:2097951 T>C maps to NM_080836.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:2097723 G>A maps to NM_080836.3 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:219563570 G>T maps to NM_015690.3 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:219561248 G>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:36475325 A>G maps to NM_007271.2 H241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:169103918 C>T maps to NM_013233.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:168931517 G>A maps to NM_013233.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:36807451 G>A maps to ENST00000373130 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:36809854 G>A maps to ENST00000373130 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:36823905 G>A maps to ENST00000373130 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:80567156 C>T maps to NM_007029.3 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:27094410 G>A maps to NM_030795.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:124111493 G>T maps to NM_004099.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:124116897 T>C maps to NM_004099.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:74277087 G>T maps to NM_004809.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:39544432 A>G maps to NM_145286.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:48809430 G>A maps to NM_172311.2 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:48808803 C>T maps to NM_172311.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:48808755 T>C maps to NM_172311.2 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:48808507 A>C maps to NM_172311.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:81743797 G>A maps to NM_033104.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:81744922 T>C maps to NM_033104.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:81743535 G>A maps to NM_033104.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:81744679 G>T maps to NM_033104.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:81837458 A>G maps to NM_033104.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:81744276 G>A maps to NM_033104.2 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:70644169 G>A maps to NM_001130161.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr10:70645582 C>A maps to NM_001130161.2 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:70644584 C>T maps to NM_001130161.2 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:70645237 A>G maps to NM_001130161.2 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr10:70644496 C>G maps to NM_001130161.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:184931901 C>T maps to NM_020225.1 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:184931727 C>A maps to NM_020225.1 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:74487705 C>T maps to ENST00000449139 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:74490098 C>T maps to ENST00000449139 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:74483817 G>A maps to ENST00000449139 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:134925393 C>T maps to NM_182489.1 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:134928081 C>A maps to NM_182489.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr17:61780973 G>A maps to NM_001003787.2 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:61781921 G>A maps to NM_001003787.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:61788154 G>A maps to NM_001003787.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:61804043 C>T maps to NM_001003787.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr2:202340423 G>A maps to NM_018571.5 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:202323571 T>C maps to NM_018571.5 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:125898430 G>A maps to NM_018387.4 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:43896936 C>A maps to NM_153700.2 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr15:43900401 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:37129803 C>T maps to NM_003162.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:37143269 G>A maps to NM_003162.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:37126677 A>G maps to NM_003162.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:31424868 C>T maps to NM_001083893.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:31416423 C>T maps to NM_001083893.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:47228902 C>T maps to NM_001039877.1 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr19:47230795 G>A maps to NM_001039877.1 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:7177677 T>C did not map to a codon.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr23:7177443 C>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:7252075 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:7267952 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:7268248 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:7268042 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:7252076 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:7268106 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:31621491 T>C maps to NM_178862.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr3:31661246 C>T maps to NM_178862.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr16:731246 C>T maps to NM_005861.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:731216 G>A maps to NM_005861.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:731435 A>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:144507853 C>T maps to NM_003764.3 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:144507946 C>T maps to NM_003764.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr6:144508429 C>T maps to NM_003764.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:144508015 C>T maps to NM_003764.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:57246272 C>T maps to NM_001001433.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:93734062 G>T maps to NM_001001850.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:73118586 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:131297516 G>A maps to NM_194356.1 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr11:59564790 G>A maps to NM_004177.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr16:31049877 G>A maps to NM_004604.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:180959170 C>T maps to NM_005819.4 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:132792739 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:132796763 T>C maps to NM_003569.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:9408352 A>G did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:130442512 C>T maps to NM_003165.3 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:130416037 C>T maps to NM_003165.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:130416037 C>T maps to NM_003165.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:53108539 T>A maps to NM_178509.5 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:53158485 G>A maps to NM_178509.5 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:53078194 A>G maps to NM_178509.5 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:147680278 G>T maps to NM_001127715.1 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:147703986 C>T maps to NM_001127715.1 G1089G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:147612299 T>C maps to NM_001127715.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:147588296 T>C maps to NM_001127715.1 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:120957877 A>G maps to NM_014980.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr3:120976117 T>G maps to NM_014980.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr3:121097668 A>G maps to NM_014980.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:10782234 G>A maps to NM_018423.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:75633121 C>T maps to NM_016086.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:75630222 G>A maps to NM_016086.2 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:48570975 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:84658721 G>A maps to NM_003849.3 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:84676771 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:84660506 C>T maps to NM_003849.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:84668520 A>G maps to NM_003849.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:67559309 C>T maps to NM_003848.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr3:151598579 T>A maps to NM_033050.4 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:151598715 C>T maps to NM_033050.4 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:118828953 C>T maps to NM_022491.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:118828947 A>C maps to NM_022491.2 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr12:118841253 C>T maps to NM_022491.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:104356985 C>T maps to NM_016169.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr10:104264031 C>T maps to NM_016169.3 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:104389821 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:53239777 C>T maps to NM_001130912.1 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:53250417 G>A maps to NM_001130912.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:70501232 C>T maps to NM_001128206.1 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:70517124 C>T maps to NM_001128206.1 C445C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:70536318 A>G maps to NM_001128206.1 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:70533370 C>T maps to NM_001128206.1 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr8:70517160 G>A maps to NM_001128206.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:70533325 A>C maps to NM_001128206.1 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:70498607 C>T maps to NM_001128206.1 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr20:46290515 C>T did not map to a codon.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr20:46331298 G>A maps to NM_001161841.1 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:46295173 G>A maps to NM_001161841.1 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:46301065 G>A maps to NM_001161841.1 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr20:46319006 G>A maps to NM_001161841.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:46295089 G>A maps to NM_001161841.1 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:28618377 G>A maps to NM_177529.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:28619924 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr16:28620029 G>A maps to NM_177529.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:28617171 G>A maps to NM_177529.1 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:28606996 C>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:70620450 G>A maps to NM_014465.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:108868905 A>G maps to NM_001008743.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:108875196 C>T maps to NM_001008743.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:108872146 C>T maps to NM_001008743.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:108994804 C>T maps to NM_006588.2 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr2:108999962 G>A maps to NM_006588.2 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr4:70723266 C>T maps to NM_005420.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:48385410 C>T maps to NM_003167.3 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:48386831 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:49100123 G>A maps to NM_177973.1 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:44258196 G>A maps to NM_014351.3 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:37402357 T>G maps to NM_001032377.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:37410582 G>A maps to NM_001032377.1 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:56132071 G>A did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr7:56132001 C>T maps to ENST00000395437 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:56141898 A>G maps to ENST00000395437 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:149721598 A>G maps to NM_001002255.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:39148606 C>T maps to ENST00000405018 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr22:39148609 G>A maps to ENST00000405018 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr22:39146906 G>A maps to ENST00000405018 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:39135930 C>T maps to ENST00000405018 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:39146930 C>T maps to ENST00000405018 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:39148567 G>A maps to ENST00000405018 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr12:56397745 G>A maps to NM_001032387.1 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:21833072 T>C maps to NM_007192.3 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:21827735 C>T maps to NM_007192.3 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr14:21829372 C>T did not map to a codon.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr14:21840167 G>A maps to NM_007192.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr14:21826586 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:21829014 G>A maps to NM_007192.3 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:45333005 A>G maps to NM_003599.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr6:44921155 T>C did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:56424576 C>T maps to NM_003168.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:39949668 C>T maps to NM_003169.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:39961096 C>T maps to NM_003169.3 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:39961139 C>T maps to NM_003169.3 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:39964162 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr19:39963887 G>A maps to NM_003169.3 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr19:39957334 G>A maps to NM_003169.3 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:27013674 C>T maps to NM_003170.3 D856D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:27011677 C>T maps to NM_003170.3 D768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:27016470 A>G maps to NM_003170.3 E1078E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:27024690 C>A maps to NM_003170.3 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:27009835 C>T maps to NM_003170.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:27014188 C>A maps to NM_003170.3 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:70968475 G>T maps to NM_003171.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:70951475 T>C maps to NM_003171.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:70968514 C>T maps to NM_003171.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:136234222 G>A maps to NM_033161.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:136198851 G>A maps to NM_006753.4 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:136198881 C>T maps to NM_006753.4 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:24581754 G>A maps to NM_019601.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:24580866 T>C maps to NM_019601.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:24583690 C>T maps to NM_019601.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr22:24582116 G>A maps to NM_019601.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr22:24579169 C>T maps to NM_019601.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr22:24581667 G>A maps to NM_019601.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr22:24580149 C>T maps to NM_019601.3 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:95838254 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:95841806 C>T maps to NM_145006.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr1:223465897 G>A maps to NM_017982.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:33194479 C>T maps to NM_015551.1 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr3:33194482 G>A maps to NM_015551.1 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:33194680 A>C maps to NM_015551.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr23:48558961 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:48558746 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48559088 T>A did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:48564697 G>T did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:48558720 C>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:48559087 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:48559109 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:48559122 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:67926306 G>A maps to NM_017635.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:67926057 C>T maps to NM_017635.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:67926240 A>G maps to NM_017635.3 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:67942633 C>A maps to NM_017635.3 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:149884987 G>A maps to NM_014849.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:149882376 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:149882202 G>A maps to NM_014849.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:149880799 G>T maps to NM_014849.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr1:149882467 G>A maps to NM_014849.3 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:91769546 C>T maps to NM_014848.4 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91769873 C>T maps to NM_014848.4 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:91835607 C>A maps to NM_014848.4 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:91811772 C>T maps to NM_014848.4 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:91801723 C>A maps to NM_014848.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr5:75621290 C>A maps to NM_014979.1 I701I. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr5:75427934 A>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:113168501 C>T maps to ENST00000374463 P3129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:113243564 G>A maps to ENST00000374463 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr9:113261432 C>T maps to ENST00000374463 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:113217885 G>A maps to ENST00000374463 C1257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:113141744 T>C maps to ENST00000374463 V3433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:113170529 G>T maps to ENST00000374463 I2453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:113221385 A>G maps to ENST00000374463 C1110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr9:113220819 C>T maps to ENST00000374463 A1169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:113228187 G>A maps to ENST00000374463 T1093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr9:113234517 G>A maps to ENST00000374463 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr9:113276306 G>A maps to ENST00000374463 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr9:113171165 G>A maps to ENST00000374463 V2241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:113208196 G>A maps to ENST00000374463 D1461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:113312288 C>T maps to ENST00000374463 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:113312183 G>A maps to ENST00000374463 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:113192680 T>C maps to ENST00000374463 S1804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr9:113173396 C>T maps to ENST00000374463 T2201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:113168516 G>T maps to ENST00000374463 S3124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:29811361 G>A maps to NM_021738.2 S1122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr10:29813445 G>A maps to NM_021738.2 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:29770533 G>A maps to NM_021738.2 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr10:29821495 C>T maps to NM_021738.2 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:29813567 C>A maps to NM_021738.2 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr10:29839532 G>A maps to NM_021738.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:29821471 G>A maps to NM_021738.2 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr10:29769634 A>T maps to NM_021738.2 Y1736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:29754536 G>A maps to NM_021738.2 S2040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:29775127 A>G maps to NM_021738.2 Y1555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:29747512 C>T maps to NM_021738.2 T2136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:29813556 G>A maps to NM_021738.2 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:29759314 G>A maps to NM_021738.2 S1911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:29821714 G>A maps to NM_021738.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:138333864 G>A maps to NM_001139456.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:138333798 G>A maps to NM_001139456.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:16778385 G>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:16773178 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:16775392 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:110587851 A>G maps to NM_001099744.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:110587155 G>A maps to NM_001099744.1 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr8:110588229 G>T maps to NM_001099744.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:110587965 T>C maps to NM_001099744.1 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:115537371 A>G maps to NM_003176.2 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:115418727 T>G maps to NM_003176.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:115428198 T>C maps to NM_003176.2 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:58456997 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:58482428 G>A maps to NM_014258.2 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr20:58467644 C>T maps to NM_014258.2 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:58467110 A>G maps to NM_014258.2 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:58476793 C>A maps to NM_014258.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr20:58440687 A>C maps to NM_014258.2 T1466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr20:58495500 C>T maps to NM_014258.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:58486831 G>T maps to NM_014258.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:10924768 G>A maps to NM_001040274.2 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:10924822 G>A maps to NM_001040274.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr6:10894338 C>T maps to NM_001040274.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:10928674 C>T maps to NM_001040274.2 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr6:10903118 T>C maps to NM_001040274.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:15224404 G>A maps to NM_033025.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:15222473 C>A maps to NM_033025.4 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:15224479 C>T maps to NM_033025.4 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:85666190 C>T maps to NM_032184.1 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:85648625 G>A maps to NM_032184.1 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:85666013 G>T maps to NM_032184.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr1:85648218 G>C maps to NM_032184.1 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:93650879 C>T maps to NM_003177.5 Y602Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:93607754 C>T maps to NM_003177.5 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:93636993 C>T maps to NM_003177.5 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:46355622 T>G maps to NM_004819.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr19:46347309 G>T maps to NM_004819.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:46355586 G>C maps to NM_004819.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:47478770 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:47478893 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:47478908 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:47464743 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47464760 A>C did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr23:47435944 T>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:47434137 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:47434573 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:33327400 G>A maps to NM_003490.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:32924964 C>A maps to NM_003490.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:32929823 G>A maps to NM_003490.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:33149690 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:86329092 C>A maps to NM_006372.4 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr6:86329065 G>A maps to NM_006372.4 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr6:152651514 T>G maps to NM_182961.2 R4769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:152631933 G>A maps to NM_182961.2 S5595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr6:152631074 G>A maps to NM_182961.2 P5699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:152557372 T>C maps to NM_182961.2 R6755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:152718064 A>G maps to NM_182961.2 T2467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:152847247 A>G maps to NM_182961.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:152740726 G>A maps to NM_182961.2 Q1800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:152558017 G>A maps to NM_182961.2 S6711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:152599229 G>A maps to NM_182961.2 N6189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr6:152651704 G>A maps to NM_182961.2 A4705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr6:152590340 T>C maps to NM_182961.2 Q6218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr6:152658020 A>G maps to NM_182961.2 S4161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:152476160 G>A maps to NM_182961.2 R7999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:152583313 A>G maps to NM_182961.2 P6275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:152542667 C>T maps to NM_182961.2 Q7183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr6:152651700 C>A maps to NM_182961.2 E4707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr6:152725383 T>C maps to NM_182961.2 E2263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr6:152631869 G>A maps to NM_182961.2 R5617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:152590319 C>T maps to NM_182961.2 Q6225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:152658026 C>T maps to NM_182961.2 R4159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:152725424 T>G maps to NM_182961.2 R2250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr6:152652592 G>A maps to NM_182961.2 D4409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr6:152542604 G>T maps to NM_182961.2 P7204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr6:152647756 A>C maps to NM_182961.2 T4989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:152823875 G>A maps to NM_182961.2 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr6:152469369 A>G maps to NM_182961.2 A8262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr6:152671374 G>A maps to NM_182961.2 G3943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:152734581 A>G maps to NM_182961.2 I2045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:152832705 C>T maps to NM_033071.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:152454425 C>A maps to NM_182961.2 V8662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr6:152652265 G>A maps to NM_182961.2 R4518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:152643021 C>T did not map to a codon.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr6:152711422 G>A maps to NM_182961.2 H2723H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:152737699 C>A maps to NM_182961.2 E1958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr6:152708290 G>A maps to NM_182961.2 Y2801Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr6:152804312 G>A maps to NM_182961.2 Y419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr6:152737733 A>C maps to NM_182961.2 T1946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr6:152782806 A>G maps to NM_182961.2 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr6:152651713 G>A maps to NM_182961.2 T4702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:152772295 A>G maps to NM_182961.2 I1024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:152683403 C>T maps to NM_182961.2 Q3400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:152443750 G>A maps to NM_182961.2 R8738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr6:152563499 G>A maps to NM_182961.2 Q6590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:152605133 C>T maps to NM_182961.2 S6062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr6:152557949 A>C did not map to a codon.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr6:152847283 A>G maps to NM_182961.2 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:152540257 C>T maps to NM_182961.2 E7308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:152621777 G>A maps to NM_182961.2 Q5894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:152623081 G>A maps to NM_182961.2 V5821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr6:152711428 G>A maps to NM_182961.2 S2721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr6:152560817 A>G maps to NM_182961.2 S6639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr6:152652349 G>A maps to NM_182961.2 S4490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr6:152614776 G>A maps to NM_182961.2 L5986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:152615187 G>A maps to NM_182961.2 S5919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:152665290 G>T maps to NM_182961.2 A4050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:152804218 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr6:152716742 C>T maps to NM_182961.2 T2540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr6:152782821 C>T maps to NM_182961.2 K768K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr14:64375919 C>T maps to NM_182914.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:64519033 C>T maps to NM_182914.2 G2801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:64542722 C>T maps to NM_182914.2 R3643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:64634308 T>C maps to NM_182914.2 D5619D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:64630226 G>A maps to NM_182914.2 P5469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr14:64483264 A>G maps to NM_182914.2 L1601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr14:64628975 A>C maps to NM_182914.2 P5427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:64469919 T>G maps to NM_182914.2 T1423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:64491107 T>A maps to NM_182914.2 L1924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:64675597 G>A maps to NM_182914.2 Q6108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:64542722 C>T maps to NM_182914.2 R3643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr14:64596519 G>C maps to NM_182914.2 V4680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr14:64518713 G>T maps to NM_182914.2 G2695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr14:64493364 C>T maps to NM_182914.2 S2107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:64522714 C>T maps to NM_182914.2 T3266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr14:64518334 A>G maps to NM_182914.2 E2568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr14:64675618 A>G maps to NM_182914.2 R6115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:64522808 C>T maps to NM_182914.2 R3298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr14:64520290 T>G maps to NM_182914.2 S3220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:64587646 T>C maps to NM_182914.2 H4342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:64692111 C>A maps to NM_182914.2 L6864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:33403338 C>T maps to NM_006772.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:33411214 C>T maps to NM_006772.2 H962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:33411217 T>C maps to NM_006772.2 H963H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:33411172 C>T maps to NM_006772.2 G948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:33409507 C>T maps to NM_006772.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8365-01A-21D-2340-08 chr6:33410695 A>C maps to NM_006772.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr6:33410695 A>C maps to NM_006772.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:33393627 G>A maps to NM_006772.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:33411373 T>G maps to NM_006772.2 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr6:33410695 A>C maps to NM_006772.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:33406231 C>A maps to NM_006772.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:39777831 G>A maps to NM_004711.4 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr22:39772141 C>T maps to NM_004711.4 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr19:48878948 C>T maps to NM_012451.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:48879532 C>T maps to NM_012451.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr21:34045775 G>A maps to NM_003895.3 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:158517269 C>T maps to NM_003898.3 G1455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:158483058 G>A maps to NM_003898.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:158484820 A>C did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:158487476 G>A maps to NM_003898.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:158516708 G>A maps to NM_003898.3 P1268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:158516906 G>A maps to NM_003898.3 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:158505105 C>T maps to NM_003898.3 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:99671249 G>A maps to ENST00000336292 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:99670475 C>T maps to ENST00000336292 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:150027978 C>A maps to NM_001166209.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:150029321 C>T maps to NM_001166209.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:150029195 C>A maps to NM_001166209.1 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr4:119951943 G>T maps to NM_133477.2 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:75406538 T>A maps to NM_001114133.1 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:75410663 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr10:75408253 G>A maps to NM_001114133.1 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr3:63542314 C>T maps to NM_001130003.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:35902365 C>T maps to NM_007247.4 T970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:35914084 T>C maps to NM_007247.4 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:35914111 G>A maps to NM_007247.4 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:35913721 A>C maps to NM_007247.4 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:35880673 T>A maps to NM_007247.4 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:35902350 A>G maps to NM_007247.4 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr17:35899296 C>T maps to NM_007247.4 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:35902431 C>T maps to NM_007247.4 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:49049792 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:49050713 G>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:43995542 C>T maps to NM_033542.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr12:79611373 C>T maps to NM_005639.2 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:79611355 G>A maps to NM_005639.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:33538208 A>G maps to NM_198992.3 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:33532784 G>A maps to NM_198992.3 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr12:33579287 C>T maps to NM_198992.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr12:33529821 C>T maps to NM_198992.3 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr12:33532787 C>T maps to NM_198992.3 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:33532871 T>C maps to NM_198992.3 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr12:33559903 A>C maps to NM_198992.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:155838036 C>T maps to NM_152280.4 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:155850289 G>T did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr11:66807436 C>G maps to NM_001177880.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr11:66807454 C>A maps to NM_001177880.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:45273977 T>G maps to NM_020826.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:45267973 C>T maps to NM_020826.2 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr11:45273974 C>A maps to NM_020826.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:210334371 G>A maps to NM_001146261.1 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:46969271 C>T maps to NM_031912.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:46962095 G>A maps to NM_031912.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:62551035 G>A maps to NM_031914.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:62551093 C>T maps to NM_031914.2 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:19195129 C>T maps to NM_016524.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr16:19278367 C>T maps to NM_016524.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:19194967 C>T maps to NM_016524.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:202568474 C>T maps to NM_177402.4 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:202572237 G>A maps to NM_177402.4 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr19:51132646 G>A maps to NM_001160329.1 H395H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:51128720 C>T maps to NM_001160329.1 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr18:40850587 G>A maps to NM_020783.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr18:40851686 G>C maps to NM_020783.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr18:40854219 C>T maps to NM_020783.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:55686653 G>A maps to NM_003180.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:55686554 C>T maps to NM_003180.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:114641765 C>T maps to ENST00000369545 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr1:114682264 G>A maps to ENST00000369545 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr1:114640393 G>A maps to ENST00000369545 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr11:61300594 A>G maps to NM_004200.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:61290642 G>A maps to NM_004200.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:61323635 G>A maps to NM_004200.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:7324615 G>A maps to NM_175733.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:7439227 A>T maps to NM_175733.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:7334763 C>T maps to NM_175733.3 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr11:7334763 C>T maps to NM_175733.3 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr11:7324552 G>C maps to NM_175733.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:27679866 C>T maps to NM_001193308.1 Y479Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:27680309 A>G maps to NM_001193308.1 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:85411567 C>T maps to ENST00000359152 E1627E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:85445390 C>A maps to NM_001162953.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:99942124 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:99942072 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:99943431 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:99942203 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:99934399 C>T did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:99943431 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:99956504 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:99936232 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:99931116 G>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:37984760 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:37984741 G>A did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:37893210 C>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:37961643 A>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:37935886 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:37984695 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:37955457 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:37948784 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:64897647 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:64895928 A>G maps to NM_172230.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:166580220 C>T maps to NM_003181.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:166571817 C>T maps to NM_003181.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr6:166580184 G>A maps to NM_003181.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:166579294 G>A maps to NM_003181.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:166580163 C>T maps to NM_003181.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:166580268 G>A maps to NM_003181.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:132938519 C>T maps to NM_001033080.1 W275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:132910624 C>T maps to NM_003967.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:132910579 A>G maps to NM_003967.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr22:39826040 G>T maps to NM_006116.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr22:39817855 C>T maps to NM_006116.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:39826199 C>T maps to NM_006116.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:39826094 C>A maps to NM_006116.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:30872569 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:30877627 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:30870904 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:30849564 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:30849601 A>G did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:30870903 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:30872537 G>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:30870980 G>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr23:30870900 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:30873125 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:30849626 G>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr7:97362034 C>T maps to NM_003182.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:97363045 G>A maps to NM_003182.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr10:123843295 T>A maps to NM_206862.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:123845447 C>T maps to NM_206862.2 Q1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:123845455 G>A maps to NM_206862.2 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:124009083 C>T maps to NM_206862.2 R2896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:123971211 G>A maps to NM_206862.2 T2424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr10:123970398 G>A maps to NM_206862.2 T2153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:124013540 C>T maps to NM_206862.2 D2939D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:123847468 T>C maps to NM_206862.2 T1818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr10:123843196 C>T maps to NM_206862.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:123842650 G>A maps to NM_206862.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:123845554 C>A maps to NM_206862.2 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:1730103 C>T maps to NM_006342.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:1739043 C>T maps to NM_006342.1 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:61685280 C>T maps to NM_016360.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:61684817 T>G maps to NM_016360.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:75347719 C>T maps to NM_001058.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:75278553 G>A maps to NM_001058.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:75347802 G>A maps to NM_001058.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:71174708 C>T maps to NM_001057.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:71175905 G>A maps to NM_001057.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr10:71168821 G>T maps to NM_001057.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:104640559 C>T maps to NM_001059.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:104640757 G>A maps to NM_001059.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr4:104640439 G>A maps to NM_001059.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr4:104577406 C>A maps to NM_001059.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr4:104640664 G>A maps to NM_001059.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr1:59042471 G>A maps to NM_002353.2 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:59042210 C>T maps to NM_002353.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr1:59042366 G>A maps to NM_002353.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr1:166833123 G>A maps to NM_053053.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:166827445 C>T maps to NM_053053.3 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:166831571 C>T maps to NM_053053.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:7056450 G>A maps to NM_152293.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:70618473 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:70598857 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:70603862 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:70602919 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:70683798 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:70598811 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:70618465 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:70612473 A>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:70597030 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:70601750 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:70608625 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:70627983 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:70598121 A>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:70604864 T>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:70608208 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:70674046 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:70613282 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:70586332 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:70618459 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:70627997 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:70586173 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:6632167 C>T maps to NM_006284.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:34850722 C>T maps to NM_005643.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:28948572 T>C maps to NM_005644.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr17:34173907 A>T did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr17:34171904 C>T maps to NM_139215.1 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:34171770 C>T maps to NM_139215.1 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr17:34171857 C>T maps to NM_139215.1 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:222757580 A>G maps to NM_005681.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr2:10015997 G>A maps to NM_005680.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:10059230 A>T maps to NM_005680.2 K445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr16:84218552 G>A maps to NM_005679.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:84218534 G>A maps to NM_005679.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:84217342 C>T maps to NM_005679.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr16:84217036 G>A maps to NM_005679.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:84215811 C>T maps to NM_005679.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:84215473 G>T maps to NM_005679.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:93471427 T>A maps to NM_024116.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:93469379 T>A maps to NM_024116.3 K262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr9:32630717 G>A maps to NM_153809.2 Y1620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:32630783 A>G maps to NM_153809.2 S1598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr9:32634836 G>A maps to NM_153809.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:32630585 C>T maps to NM_153809.2 Q1664Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:32631545 G>A maps to NM_153809.2 F1344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr9:32633110 G>A maps to NM_153809.2 R823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr9:32631118 G>A maps to NM_153809.2 Q1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:32633057 C>T maps to NM_153809.2 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:32633762 C>A maps to NM_153809.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:120754888 C>T maps to NM_003184.3 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:120795638 A>G maps to NM_003184.3 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:120818520 A>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:120844732 C>T maps to NM_003184.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr10:8006408 T>C maps to NM_031923.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:8056702 C>T maps to NM_031923.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:8005988 T>C maps to NM_031923.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:7866404 G>A maps to NM_031923.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr10:8006453 G>A maps to NM_031923.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr10:8007449 A>G maps to NM_031923.2 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:60585188 C>T maps to NM_003185.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr20:60584157 G>A maps to NM_003185.3 Q612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr20:60587990 C>T did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:60589623 G>A maps to NM_003185.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr18:23866045 G>A maps to ENST00000418698 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr10:105146934 C>G maps to NM_006951.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:105138237 T>C maps to NM_006951.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:229737983 G>A maps to NM_014409.3 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:229737983 G>A maps to NM_014409.3 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:229738208 G>A maps to NM_014409.3 N235N. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:229738169 G>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:229730769 C>G maps to NM_014409.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:99709349 C>T did not map to a codon.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr7:99711236 A>G did not map to a codon.
Multiple mappings detected for codon TCGA-CG-5721-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:99709440 G>A maps to ENST00000472509 N327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr7:99710532 T>C maps to ENST00000472509 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:99706052 C>T maps to ENST00000472509 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:62554756 T>C maps to NM_006473.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:62545463 C>T maps to NM_006473.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MV-01A-11D-A364-08 chr11:62554692 G>C maps to NM_006473.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:140699523 T>G maps to NM_005642.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:100532687 T>C did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:100536733 T>A did not map to a codon.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr23:100533035 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:100536707 C>T did not map to a codon.
Alternatively spliced codon TCGA-BR-8590-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr6:42044975 A>T maps to NM_138572.2 K307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:42034051 G>A maps to NM_138572.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:77393266 C>T did not map to a codon.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr23:77393256 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:77387181 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:77393319 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr6:159456920 G>A maps to NM_054114.3 R712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:159457404 G>A maps to NM_054114.3 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:117073839 G>A maps to NM_003186.3 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:117073797 C>T maps to NM_003186.3 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:159889526 G>A maps to ENST00000368096 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:47691500 G>A maps to ENST00000371883 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr1:47685496 C>T maps to ENST00000371883 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:759007 G>T maps to NM_006755.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:764846 G>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:159922469 C>T maps to NM_033394.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:160027036 C>T maps to NM_033394.2 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:160086949 C>T maps to NM_033394.2 S1671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:160050844 C>T maps to NM_033394.2 C940C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:160019917 C>T maps to NM_033394.2 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:160080768 C>T maps to NM_033394.2 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:160025863 T>C maps to NM_033394.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:61498805 C>T maps to ENST00000389520 D1831D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:61498205 C>T maps to ENST00000389520 A1631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr17:61497863 G>A maps to ENST00000389520 P1517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:61498412 A>T maps to ENST00000389520 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:61498448 C>T maps to ENST00000389520 S1712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:27869580 T>C maps to NM_020791.2 I849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:27869899 C>T maps to NM_020791.2 R956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr17:27844527 C>T maps to NM_020791.2 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:27802737 T>C maps to NM_020791.2 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:27825385 T>C maps to NM_020791.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:27861209 G>A maps to NM_020791.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:29989426 T>C maps to NM_016151.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:30002181 C>T maps to NM_004783.2 N841N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:29997695 G>A maps to NM_016151.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:29994825 C>T maps to NM_016151.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr16:29998919 G>A maps to NM_016151.2 R1109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr16:29998847 G>A maps to NM_016151.2 W1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:29999114 G>A maps to NM_016151.2 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:30002181 C>T maps to NM_004783.2 N841N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:118599654 G>A maps to NM_016281.3 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:118598097 T>C maps to NM_016281.3 K735K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:118636897 G>A maps to NM_016281.3 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr12:118598019 C>T maps to NM_016281.3 Q761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:118590073 T>C maps to NM_016281.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr12:118619208 C>A maps to NM_016281.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr12:118590079 C>T maps to NM_016281.3 Q829Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr6:32821353 G>C maps to NM_000593.5 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:32815288 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:32818228 C>T maps to NM_000593.5 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:32820912 G>A maps to NM_000593.5 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr6:32805902 T>C maps to ENST00000452392 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:33281219 C>G maps to NM_172208.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:33281126 C>T maps to NM_172208.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:33281603 G>A maps to NM_172208.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr6:33272849 G>A maps to NM_172208.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:33272170 G>C maps to NM_172208.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr12:6562380 C>T maps to NM_018009.4 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:6561437 C>T maps to NM_018009.4 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:6562829 G>A maps to NM_018009.4 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:16165118 G>A maps to NM_153365.2 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr1:234586216 T>C maps to NM_005646.3 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:234541715 C>A maps to NM_005646.3 E1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:234553889 A>G maps to NM_005646.3 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:234601427 C>T maps to NM_005646.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:234565960 C>T maps to NM_005646.3 E827E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:234565022 C>T maps to NM_005646.3 A973A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:234566029 A>G maps to NM_005646.3 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:53899913 C>T maps to NM_134323.1 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr12:53899823 C>T maps to NM_134323.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:11082566 C>T maps to NM_007375.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:11076928 T>C maps to NM_007375.3 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:33455787 A>G maps to ENST00000455217 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:33467668 T>G maps to ENST00000455217 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:33457406 C>T maps to ENST00000455217 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr5:33455056 G>A maps to ENST00000455217 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:150460422 C>T maps to NM_025150.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:150477183 C>T maps to NM_025150.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:102224298 G>A maps to NM_152334.2 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:102197158 T>C maps to NM_152334.2 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr15:102211871 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:6634951 G>T maps to NM_138697.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:19166728 G>T maps to NM_152232.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:19166143 C>T maps to NM_152232.2 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr1:19166575 G>A maps to NM_152232.2 Y679Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:19180946 G>A maps to NM_152232.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr1:19180733 G>T maps to NM_152232.2 C410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:1269810 C>T maps to NM_152228.1 D842D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr1:1268155 C>T maps to NM_152228.1 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:1267837 C>T maps to NM_152228.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr5:9629276 T>A maps to NM_019599.2 K290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:10978046 T>G maps to NM_023921.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:10978268 A>G maps to NM_023921.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:11061807 G>A maps to NM_023920.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:122635649 G>T maps to NM_016945.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:122635117 G>A maps to NM_016945.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:122635649 G>T maps to NM_016945.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:11174709 C>T maps to NM_176888.1 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:11150027 C>T maps to NM_176889.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:11149589 C>T maps to NM_176889.2 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:141464525 C>T maps to NM_016943.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr12:11286387 A>C maps to NM_001097643.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr12:11183703 A>G maps to NM_176885.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:141478687 C>T maps to NM_016944.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:141478797 C>A maps to NM_016944.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr7:141478665 C>T maps to NM_016944.1 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:11338669 G>A maps to NM_181429.1 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:11139174 G>A maps to NM_176890.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:143141231 T>C maps to NM_177437.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr7:143141468 G>A maps to NM_177437.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr12:10954758 G>A maps to NM_023919.2 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr12:10954758 G>A maps to NM_023919.2 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:13561608 C>A maps to NM_017714.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:13514761 C>T maps to NM_017714.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:71605529 A>G maps to NM_000353.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr16:71606200 C>A maps to NM_000353.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:71609921 A>G maps to NM_000353.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:71602118 G>A maps to NM_000353.2 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:125506108 G>A maps to NM_032026.3 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:10311864 G>A maps to NM_014760.3 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr7:27832692 T>C maps to ENST00000409980 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:27824918 C>T maps to ENST00000409980 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:27868390 G>A maps to ENST00000409980 Q795Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:153640244 G>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:38023250 C>T maps to NM_015173.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:38016290 C>T maps to NM_015173.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:38016278 G>A maps to NM_015173.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:38138781 T>C maps to NM_015173.2 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:38022258 C>T maps to NM_015173.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:38016512 C>T maps to NM_015173.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr22:30689912 C>A maps to ENST00000403477 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr22:30691727 G>A maps to ENST00000403477 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr9:131570100 C>A maps to NM_018201.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:131559483 G>T maps to NM_018201.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:131559378 C>G maps to NM_018201.3 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74B-01A-12D-A33T-08 chr9:131565731 G>A maps to NM_018201.3 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:131565554 G>A maps to NM_018201.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:6925151 C>T maps to NM_001113361.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:6925427 C>A maps to NM_001113361.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:6925448 G>A maps to NM_001113361.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:72307609 T>C maps to NM_022771.4 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:72265949 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr12:72288102 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:77926508 G>A maps to NM_019020.2 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr17:77924238 G>A maps to NM_019020.2 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr19:50390982 G>A maps to NM_024682.2 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:26685313 G>A maps to NM_018317.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:26750038 C>T maps to NM_018317.2 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:100983198 C>T maps to NM_018421.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:100961815 C>T maps to NM_018421.3 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100963772 G>A maps to NM_018421.3 Y815Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:419298 C>T maps to ENST00000246077 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr20:420909 C>T maps to ENST00000246077 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:47507444 C>T maps to NM_014346.2 C457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:47188434 T>C maps to NM_014346.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:47189607 G>A maps to NM_014346.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:47370252 C>T maps to NM_014346.2 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:37237384 T>C maps to NM_017772.2 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:37298879 C>T maps to NM_017772.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:2546754 G>A maps to ENST00000434757 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:2546589 C>T maps to ENST00000434757 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:2547018 C>T maps to ENST00000434757 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:2546161 G>T maps to ENST00000434757 G5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:48399810 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48418074 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:48417709 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:48417658 C>T did not map to a codon.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr23:48403294 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:48418770 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:48417658 C>T did not map to a codon.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr23:48418149 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr23:48419179 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:48399741 C>T did not map to a codon.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr17:28887642 C>T maps to NM_015594.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:78316782 G>A maps to NM_144572.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr15:78316587 G>A maps to NM_144572.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:34500227 C>T maps to NM_001001417.5 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:75861152 A>G maps to ENST00000431480 H1225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:75901920 A>G maps to ENST00000431480 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:76055810 T>C maps to ENST00000431480 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:75900463 C>T maps to ENST00000431480 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr13:76055891 G>A maps to ENST00000431480 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr13:75866264 G>T maps to ENST00000431480 T1154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr13:75936260 G>A maps to ENST00000431480 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:76055435 G>A maps to ENST00000431480 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr3:17279754 A>G maps to NM_001134381.1 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr3:17208257 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:17202724 G>A maps to NM_001134381.1 C728C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:17550028 G>A maps to NM_001134381.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:13306707 A>G maps to NM_016495.4 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:13321204 C>A maps to NM_016495.4 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:101627910 G>A did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr2:101654161 G>C maps to NM_001102426.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:101644788 C>T maps to NM_001102426.1 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:106070450 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:106070527 C>T did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr23:106110047 T>C did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:106066490 C>T did not map to a codon.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr23:106069406 T>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:106083919 A>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:106083330 A>G did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:106110053 A>G did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr23:106069424 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:106046089 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:141598176 G>A maps to NM_015130.2 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr4:141543720 G>A maps to NM_015130.2 N1143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr4:141590134 C>T maps to NM_015130.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:141590793 C>T maps to NM_015130.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:141583178 C>T maps to NM_015130.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr4:141607596 G>A maps to NM_015130.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:141592016 G>A maps to NM_015130.2 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:179302056 G>A maps to NM_198868.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:179302017 G>A maps to NM_198868.2 C690C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:179301924 G>A maps to NM_198868.2 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:179320378 G>A maps to NM_198868.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:36612465 C>T maps to NM_001281.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:42712854 G>A maps to NM_003192.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:80772781 C>T maps to NM_005993.4 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:80714083 G>A maps to NM_005993.4 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:80763855 C>T maps to NM_005993.4 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:80858556 G>A maps to NM_005993.4 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr17:80726294 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:80885160 C>T maps to NM_005993.4 D857D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:80765496 C>T maps to NM_005993.4 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr17:80865645 G>A maps to NM_005993.4 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:120930726 C>T maps to NM_152715.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr11:120924330 G>A maps to NM_152715.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:120957639 A>G maps to NM_152715.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr4:107170075 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:107154786 G>A maps to NM_001163436.1 Y490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:64878158 C>T maps to NM_013254.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:64878158 C>T maps to NM_013254.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:64883862 A>G maps to NM_013254.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr17:45776812 C>T maps to NM_014726.2 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:9656276 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:9660158 A>G did not map to a codon.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr23:9665415 T>G did not map to a codon.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:9622285 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:9679716 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:9679786 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:9679768 T>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:9656196 T>G did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:9677344 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:9661210 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:9656060 G>A did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:9656114 T>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr3:176756100 C>T maps to NM_024665.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:176769373 T>G maps to NM_024665.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:176768321 A>G maps to NM_024665.4 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr24:6954380 C>A did not map to a codon.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr24:6955426 T>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:72988314 G>A maps to NM_012453.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:72985187 A>G maps to NM_012453.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr7:72984995 C>T maps to NM_012453.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:72992828 C>T maps to NM_012453.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:72985265 C>T maps to NM_012453.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:72988760 C>T maps to NM_012453.2 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:2026276 C>T maps to NM_006453.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr6:170871099 G>A maps to NM_003194.4 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr6:170871033 G>A maps to NM_003194.4 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:170871006 A>G maps to NM_003194.4 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:170871033 G>A maps to NM_003194.4 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:55903505 G>A maps to NM_199047.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr14:55881107 T>A maps to NM_199047.2 K373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr14:55907215 C>T maps to NM_199047.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:55895631 G>A maps to NM_199047.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:162279996 C>T maps to NM_006593.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:162280611 G>A maps to NM_006593.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:162280647 G>A maps to NM_006593.2 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:162280584 C>T maps to NM_006593.2 Y632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:162273268 G>A maps to NM_006593.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:162274318 C>T maps to NM_006593.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:162280035 G>A maps to NM_006593.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:162273010 C>T maps to NM_006593.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:124496846 C>T maps to NM_032811.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:45142091 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:19752590 C>T maps to NM_080647.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr22:19766890 C>T maps to NM_080646.1 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:19748692 G>A maps to NM_080647.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr22:19751828 C>T maps to NM_080647.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:19752521 C>T maps to NM_080647.1 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr11:67402651 C>T maps to NM_005995.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr11:67399228 C>T maps to NM_005995.4 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:67399795 C>T maps to NM_005995.4 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:119441699 A>C maps to ENST00000369429 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr1:119428074 A>G maps to ENST00000369429 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr1:119427516 G>A maps to ENST00000369429 N549N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:119469234 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:85446855 A>G maps to NM_001080508.1 Y457Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:85446534 C>T maps to NM_001080508.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:85472389 C>T maps to NM_001080508.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:85446534 C>T maps to NM_001080508.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:85446534 C>A maps to NM_001080508.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:85472392 C>T maps to NM_001080508.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr6:85472320 G>A maps to NM_001080508.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:85473683 G>A maps to NM_001080508.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:59482854 G>A maps to NM_005994.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:59479293 C>T maps to NM_005994.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr17:59485554 C>T maps to NM_005994.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:59477551 G>A maps to NM_005994.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr7:35284587 G>T maps to NM_001077653.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr7:35293165 C>A maps to NM_001077653.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr7:35293168 G>A maps to NM_001077653.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:45822602 C>T maps to NM_013351.1 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:45822677 T>G maps to NM_013351.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:45822578 G>A maps to NM_013351.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:45822164 T>C maps to NM_013351.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:79277873 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:79279655 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:79278707 G>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:79282368 T>A did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:79279617 A>G did not map to a codon.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr23:79279564 G>T did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr23:79286561 C>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:79282758 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr23:79283521 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr23:79278611 G>A did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:115120666 C>T maps to NM_016569.3 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:115114184 T>C maps to NM_016569.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:115117307 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:59560870 C>T maps to ENST00000393853 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:59560378 C>T maps to ENST00000393853 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr17:59557597 C>T maps to ENST00000393853 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:59560759 G>A maps to ENST00000393853 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr12:114841664 C>T maps to NM_000192.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:114793516 G>T maps to NM_000192.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:114832668 C>T maps to NM_000192.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr12:114841688 G>A maps to NM_000192.3 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:114793420 A>G maps to NM_000192.3 H491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr12:114823290 T>G maps to NM_000192.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr12:114793453 G>A maps to NM_000192.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:114793462 C>T maps to NM_000192.3 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:30100494 G>A maps to NM_004608.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:30097644 C>T maps to NM_004608.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:30097590 G>A maps to NM_004608.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:3600359 C>T maps to NM_201636.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:3600362 G>A maps to NM_201636.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:3600326 G>A maps to NM_201636.2 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:3600079 G>A maps to NM_201636.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:3600212 G>A maps to NM_201636.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:3600353 G>A maps to NM_201636.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:3600461 C>T maps to NM_201636.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:3595832 G>A maps to NM_201636.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:3600068 G>A maps to NM_201636.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:3600152 C>T maps to NM_201636.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:139719829 G>A maps to NM_001166253.1 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:139719835 G>A maps to NM_001166253.1 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:139706976 T>G maps to NM_001166253.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr14:92258734 A>G maps to NM_001128596.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr17:37822310 A>C maps to NM_003673.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:54899527 T>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:54891665 A>G maps to NM_006756.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr1:23724339 C>T maps to NM_003196.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:102885265 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:102885194 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:101382345 A>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:101381918 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:101382091 G>T did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr23:101382430 T>A did not map to a codon.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr23:102864219 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:102864511 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:102864034 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:102864314 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:102864294 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:102842090 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr23:102529209 G>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:102529303 T>G did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:102529129 T>G did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:102529175 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:102529120 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:102529190 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:101395935 T>G did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:101396154 G>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:101396122 C>T did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:101395817 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:101396253 T>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:101396011 C>T did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr23:101396190 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:102586398 G>A did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:102586596 A>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:13681447 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr8:74858990 C>T maps to NM_005648.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:2822059 C>T maps to NM_207013.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:24083514 T>C maps to NM_003198.2 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:24080851 G>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:24077883 C>A maps to NM_003198.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:24083457 G>A maps to NM_003198.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:24083478 T>C maps to NM_003198.2 H733H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:24080895 C>T maps to NM_003198.2 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr18:44560579 C>T maps to NM_016427.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr18:44560000 G>A maps to NM_016427.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:44561191 A>G maps to NM_016427.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr18:44561455 C>T maps to NM_016427.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr18:44560350 T>A maps to NM_016427.2 K429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:44561338 G>A maps to NM_016427.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr18:44560468 G>A maps to NM_016427.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr18:44559961 A>G maps to NM_016427.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr18:44543288 C>T maps to NM_001100817.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:145878171 C>A maps to NM_006706.3 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr5:145838679 A>G maps to NM_006706.3 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:145838610 A>C maps to NM_006706.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:145838613 A>G maps to NM_006706.3 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:145838628 T>G maps to NM_006706.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:145838634 T>G maps to NM_006706.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:145838640 C>T maps to NM_006706.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:145838592 G>A maps to NM_006706.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:145838595 G>A maps to NM_006706.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:132944907 C>T maps to NM_174937.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr10:133107427 A>T maps to NM_174937.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:132915124 C>T maps to NM_174937.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr10:132891574 C>T maps to NM_174937.3 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:57565311 A>G maps to NM_207036.1 E610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:31130319 C>T maps to NM_007109.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:31127380 G>A maps to NM_007109.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:42610102 C>T maps to NM_005650.1 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:42610372 C>T maps to NM_005650.1 Q313Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:42609856 G>T maps to NM_005650.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr22:42611136 G>A maps to NM_005650.1 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr22:42609754 T>C maps to NM_005650.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr22:42609402 T>G maps to NM_005650.1 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr22:42611292 G>A maps to NM_005650.1 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:42608371 C>T maps to NM_005650.1 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr22:42611136 G>A maps to NM_005650.1 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:42610357 C>T maps to NM_005650.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:134210811 C>T maps to NM_003206.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:134210720 G>A maps to NM_003206.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr2:27373193 G>A maps to NM_175769.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:27373193 G>A maps to NM_175769.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:89977609 C>T maps to NM_014972.2 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:1615427 G>A maps to NM_003200.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:52924544 C>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr18:52899753 A>C maps to ENST00000398339 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:52899780 G>A maps to ENST00000398339 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:133473799 A>G maps to ENST00000395029 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr5:133478791 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:133473835 G>A maps to ENST00000395029 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:85361485 G>A maps to NM_031283.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:85533373 C>T maps to NM_031283.2 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr2:85536583 A>G maps to NM_031283.2 *589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:114925316 A>G maps to NM_030756.4 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:114911585 C>A maps to NM_030756.4 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:114920411 C>T maps to NM_001146274.1 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:114925565 C>T maps to NM_030756.4 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:114925397 G>A maps to NM_030756.4 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:114925706 G>A maps to NM_030756.4 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:114900992 G>A maps to NM_030756.4 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr20:61488982 C>T maps to NM_006602.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:152082229 T>G maps to NM_007113.2 R1155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:152081441 G>A maps to NM_007113.2 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:152082433 G>A maps to NM_007113.2 Q1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:152083745 G>A maps to NM_007113.2 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:152083993 G>A maps to NM_007113.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr1:152084186 C>T maps to NM_007113.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr1:152080901 G>A maps to NM_007113.2 F1597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:152086499 G>A maps to NM_007113.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:152081441 G>A maps to NM_007113.2 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:152081492 G>A maps to NM_007113.2 R1400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:152081258 C>T maps to NM_007113.2 L1478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr1:152059397 G>A maps to NM_001008536.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:152057613 G>T maps to NM_001008536.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr1:152059359 T>C maps to NM_001008536.1 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr1:152059359 T>C maps to NM_001008536.1 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr12:110345341 C>T maps to NM_032300.4 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:67816416 C>T maps to NM_006019.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:67815009 C>T maps to NM_006019.3 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:96157233 C>T maps to NM_004918.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:59629105 G>A maps to NM_001062.3 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr22:31022487 C>T maps to NM_000355.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:149776322 G>A maps to ENST00000451292 E1457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:149755411 C>T maps to ENST00000451292 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:149751642 G>A maps to ENST00000451292 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:149755682 C>T maps to ENST00000451292 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr5:149767628 C>T maps to ENST00000451292 P1045P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr6:160201119 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr21:33951126 A>T maps to NM_144659.5 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr6:167585757 C>T maps to NM_001145121.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:167587431 C>T maps to NM_001145121.1 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:33087458 C>T maps to NM_001145541.1 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:33087383 A>G maps to NM_001145541.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:33083247 C>T maps to NM_001145541.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr11:33087509 G>A maps to NM_001145541.1 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:106715424 C>T maps to NM_152772.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr12:106729907 G>A maps to NM_152772.1 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:44248037 G>A maps to NM_182539.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:44250297 T>C did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:44253919 G>A maps to NM_182539.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:196018209 A>G maps to NM_152773.3 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:45271716 C>T maps to NM_001013632.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:111072571 G>A maps to NM_001082538.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr12:124156630 G>T maps to NM_024809.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr12:124171417 G>T maps to NM_024809.3 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:124171429 C>T maps to NM_024809.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:124192157 G>T maps to NM_024809.3 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:97447372 A>T maps to ENST00000371217 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr10:97444351 A>T maps to ENST00000371217 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr10:97440351 A>C maps to ENST00000371217 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:97423994 C>T maps to ENST00000371217 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:104376688 G>A maps to NM_003211.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr12:104380724 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr4:156832686 A>T maps to NM_005651.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr4:156838588 T>C maps to NM_005651.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:156825179 A>T maps to NM_005651.2 K16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:90450953 T>C maps to NM_018319.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:90429694 C>T maps to NM_018319.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:24653308 G>A maps to NM_016614.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:24651210 A>G maps to NM_016614.2 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr10:115959053 T>G maps to NM_198795.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr10:115970505 C>A maps to NM_198795.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:115962035 G>A maps to NM_198795.1 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:154493837 A>C maps to NM_001098475.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:154516453 G>A maps to NM_001098475.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr1:154479755 G>C maps to NM_001098475.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:154516465 G>A maps to NM_001098475.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr13:61103093 C>T maps to NM_001146070.1 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr13:61103081 C>T maps to NM_001146070.1 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:61102744 A>T maps to NM_001146070.1 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:179620045 C>T maps to ENST00000444136 C615C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:179600005 A>G maps to ENST00000444136 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:179632553 G>A maps to ENST00000444136 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:179564916 G>A maps to ENST00000444136 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr1:179631421 G>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:46659716 A>G maps to NM_001010870.2 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:46656521 C>T maps to NM_001010870.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:46657578 C>T maps to NM_001010870.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:46656497 C>T maps to NM_001010870.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:46661522 C>T maps to NM_001010870.2 G1886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:46657304 T>G maps to NM_001010870.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr6:46657610 C>T maps to NM_001010870.2 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr6:46658066 T>G maps to NM_001010870.2 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr6:46656737 G>A maps to NM_001010870.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr6:46660185 C>A maps to NM_001010870.2 R1441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:46656548 G>A maps to NM_001010870.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:46658574 C>T maps to NM_001010870.2 Q904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:46660830 G>T maps to NM_001010870.2 E1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:46661432 A>G maps to NM_001010870.2 L1856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr6:46657943 G>A maps to NM_001010870.2 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:46657610 C>T maps to NM_001010870.2 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:100204027 G>A maps to NM_014290.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:100245399 C>T maps to NM_014290.2 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:100249528 C>T maps to NM_014290.2 H997H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:100227189 T>C maps to NM_014290.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:100245264 T>C maps to NM_014290.2 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr1:151748569 A>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:151748696 T>C maps to NM_001083965.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:49863215 C>T maps to NM_003598.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:49863200 C>T maps to NM_003598.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:49850572 G>A maps to NM_003598.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:49845793 C>T maps to NM_003598.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:35443480 G>A maps to ENST00000357281 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:35443480 G>A maps to ENST00000357281 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr6:35443211 C>T maps to ENST00000357281 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr12:3104141 C>T maps to NM_003213.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:3149556 G>A maps to NM_003213.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:48230565 C>T maps to NM_003215.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:48169969 G>A maps to NM_003215.2 R166*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CG-5721-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:48173384 C>A maps to NM_003215.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:97850997 C>T maps to ENST00000379795 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:97866137 C>T maps to ENST00000379795 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:97860430 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:97850994 C>T maps to ENST00000379795 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:97862156 G>A maps to ENST00000379795 Y601Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:97861205 G>A maps to ENST00000379795 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr7:97860370 C>T maps to ENST00000379795 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:97852433 G>T maps to ENST00000379795 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr14:102880990 C>T maps to NM_014844.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:102918743 G>A maps to NM_014844.3 W1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:102918788 C>T maps to NM_014844.3 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:102901154 C>T maps to NM_014844.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr14:102918809 G>A maps to NM_014844.3 T1162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr14:102931610 T>A maps to NM_014844.3 I1258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:102964446 G>A maps to NM_014844.3 A1363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr14:102910039 C>T maps to NM_014844.3 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr4:65188508 G>A maps to NM_001010874.4 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr4:65188412 C>T maps to NM_001010874.4 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr4:65175597 G>T maps to NM_001010874.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr4:65275045 G>A maps to NM_001010874.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr4:65240923 A>T maps to NM_001010874.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:65275039 C>T maps to NM_001010874.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:120996336 C>T maps to NM_005422.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:121038773 G>A maps to NM_005422.2 T1866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:120996432 C>T maps to NM_005422.2 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:121038921 C>T maps to NM_005422.2 L1916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:121060507 C>T maps to NM_005422.2 Q2096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr11:120996138 C>T maps to NM_005422.2 Y444Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:121037452 C>A maps to NM_005422.2 I1850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr11:121028581 G>A maps to NM_005422.2 T1446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:121023728 C>T maps to NM_005422.2 N1415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:121023677 C>T maps to NM_005422.2 C1398C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr11:121037374 T>G maps to NM_005422.2 G1824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:121016688 C>T maps to NM_005422.2 F1323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:121000441 C>T maps to NM_005422.2 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:121000756 C>T maps to NM_005422.2 C926C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:121016727 C>T maps to NM_005422.2 G1336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:120983878 C>T maps to NM_005422.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr11:120998578 C>T maps to NM_005422.2 C631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr11:121023710 C>T maps to NM_005422.2 D1409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:120996399 C>T maps to NM_005422.2 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr11:121016670 A>G maps to NM_005422.2 K1317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr11:120989024 T>A maps to NM_005422.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:114059302 C>T maps to NM_058222.1 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:114045826 A>G did not map to a codon.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr9:27158094 C>T maps to NM_000459.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:27204915 G>A maps to NM_000459.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr9:27185586 G>A maps to NM_000459.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr9:27203085 T>C maps to NM_000459.3 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:6718525 T>C maps to NM_053285.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr17:6704226 A>T maps to NM_053285.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:15212063 G>A maps to NM_031898.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:15217492 C>T maps to NM_031898.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:95537770 C>T maps to NM_144705.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:95539787 C>T maps to NM_144705.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:95537500 C>T maps to NM_144705.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:10729709 C>T maps to NM_144674.1 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:10721646 G>A maps to NM_144674.1 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr16:10721580 C>T maps to NM_144674.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr16:1556267 C>T maps to NM_016111.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr16:1552704 A>T maps to NM_016111.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:1551759 C>T maps to NM_016111.3 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr16:1552758 C>T maps to NM_016111.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:53446254 G>A maps to NM_170754.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:53451887 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:53457554 G>A maps to NM_170754.2 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:53453431 C>T maps to NM_170754.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:53448185 G>A maps to NM_170754.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:53451886 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:20853142 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:20846984 G>A maps to NM_007110.4 Y1760Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:20850793 C>T maps to NM_007110.4 T1376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr14:20851685 C>T maps to NM_007110.4 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr14:20854231 A>G did not map to a codon.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr14:20849162 G>A maps to NM_007110.4 T1563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr14:20876370 G>A maps to NM_007110.4 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:20871977 C>T maps to NM_007110.4 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:20841474 G>T maps to NM_007110.4 A2256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr14:20851709 A>G maps to NM_007110.4 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:20850792 G>A maps to NM_007110.4 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:58011824 G>A maps to NM_199046.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:58019818 T>C maps to NM_199046.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr8:73942615 A>G maps to NM_017489.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr8:73951417 G>A maps to NM_017489.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr16:69400707 A>G did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:75681990 C>T maps to NM_018975.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:1264610 C>T maps to NM_198253.2 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:1294622 C>T maps to NM_198253.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:1272353 G>A maps to NM_198253.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:1294532 G>A maps to NM_198253.2 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4301-01A-01D-1158-08 chr5:1272311 G>A maps to NM_198253.2 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:1268636 G>A maps to NM_198253.2 D860D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:1282620 C>T maps to NM_198253.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:1268636 G>A maps to NM_198253.2 D860D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:1253878 C>T maps to NM_198253.2 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:1294214 C>T maps to NM_198253.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:1294685 G>A maps to NM_198253.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:35609378 C>T maps to NM_006285.2 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:35609367 C>T maps to NM_006285.2 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:35609489 G>A maps to NM_006285.2 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr9:35609003 A>G maps to NM_006285.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:35605978 A>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:45813597 G>A maps to NM_007170.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:45851581 A>G did not map to a codon.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr1:45810643 G>T maps to NM_007170.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:70446169 C>T maps to NM_030625.2 Q1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:70426986 C>T maps to NM_030625.2 T1549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:70450634 A>G maps to NM_030625.2 S1825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:70451498 C>A maps to NM_030625.2 T2113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:70405605 A>G maps to NM_030625.2 P1040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr10:70446267 C>T maps to NM_030625.2 V1736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr10:70333411 A>G maps to NM_030625.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:70406187 A>T maps to NM_030625.2 T1234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:70333732 C>A maps to NM_030625.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:106155656 G>A maps to ENST00000513237 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:106157192 G>T maps to ENST00000513237 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr4:106158509 T>C maps to NM_017628.3 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:106158464 A>G maps to ENST00000513237 T1143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:74317032 C>T maps to ENST00000409262 C873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:74327751 C>T maps to ENST00000409262 Y1186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:74307622 A>G did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr2:74300716 T>C maps to ENST00000409262 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:74273835 G>A maps to ENST00000409262 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:74273649 C>A maps to ENST00000409262 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:74328867 C>T maps to ENST00000409262 I1558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:74327751 C>T maps to ENST00000409262 Y1186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr2:74328639 G>C maps to ENST00000409262 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:74327910 C>T maps to ENST00000409262 Y1239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:103111627 T>C maps to NM_017746.3 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr9:103092224 G>A maps to NM_017746.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:103111561 A>G maps to NM_017746.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:103070933 C>T maps to NM_017746.3 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:43920323 G>A maps to NM_031451.4 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:70127624 A>G did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:69772061 G>A did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:69849511 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr23:70080717 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:104464984 C>T did not map to a codon.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr23:104464112 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:107224609 G>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:107225021 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr23:107225139 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr23:107224568 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:107224598 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:107225280 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:107224323 G>A did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr17:56651573 T>C maps to ENST00000240361 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr17:56676671 A>G maps to ENST00000240361 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:56657024 C>A did not map to a codon.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr17:56665027 C>G did not map to a codon.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr8:30699690 A>T maps to NM_031271.3 P2281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:30695218 G>A maps to NM_031271.3 Q2478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:30704619 T>C maps to NM_031271.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr8:30701488 A>C maps to NM_031271.3 L1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:30703660 G>T maps to NM_031271.3 S958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr8:30701928 C>T maps to NM_031271.3 P1535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:30699726 C>T maps to NM_031271.3 K2269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:30701384 G>A maps to NM_031271.3 R1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:30705315 T>C maps to NM_031271.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr8:30694921 C>A maps to NM_031271.3 E2577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:30702407 G>A maps to NM_031271.3 Q1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:30704078 C>A maps to NM_031271.3 G819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr8:30695502 A>C maps to NM_031271.3 L2383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:30701327 C>A maps to NM_031271.3 G1736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:80320037 G>A maps to NM_207459.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:62290152 C>T maps to NM_018469.3 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:71218968 G>A maps to NM_144582.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr3:51733460 C>T maps to NM_015926.4 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:51733579 G>T maps to NM_015926.4 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr3:133494370 G>A maps to NM_001063.3 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:133476767 C>T maps to NM_001063.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:133475799 C>T maps to NM_001063.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:133475164 G>A maps to NM_001063.3 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:133495909 C>T maps to NM_001063.3 N630N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr10:60154713 C>T maps to NM_003201.1 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr6:10398871 G>A maps to ENST00000379613 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr6:50803903 G>A maps to ENST00000263046 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr6:50810963 C>T maps to ENST00000263046 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:50810888 G>A maps to ENST00000263046 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:50810817 G>T maps to ENST00000263046 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:50807908 C>T maps to ENST00000263046 C336C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:50807914 G>A maps to ENST00000263046 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:50810909 G>A maps to ENST00000263046 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:55206379 G>A maps to NM_003222.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr20:55211735 A>G maps to NM_003222.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr20:55208569 C>T maps to NM_003222.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr20:55212939 G>A maps to NM_003222.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr20:55211786 G>A maps to NM_003222.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:50681776 T>C maps to NM_172238.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:50696581 G>A maps to NM_172238.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr6:50712856 T>C maps to NM_172238.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:50683049 C>T maps to NM_172238.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:50681808 T>A did not map to a codon.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr6:50696967 T>C maps to NM_172238.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:4312635 G>A maps to NM_003223.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:4312554 G>A maps to NM_003223.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:4308192 G>A maps to NM_003223.2 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr16:4312623 G>A maps to NM_003223.2 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:155581522 G>A maps to NM_016020.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:155581416 G>A maps to NM_016020.3 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:51492669 T>C maps to NM_005653.4 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:51502901 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:51511512 G>A maps to NM_005653.4 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:121997198 G>A maps to NM_014553.2 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr2:122007203 T>A maps to NM_014553.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr2:122004465 C>T maps to NM_014553.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:121997153 G>A maps to NM_014553.2 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:121997186 G>A maps to NM_014553.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:114287549 C>T maps to NM_007111.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr13:114265369 C>T maps to NM_007111.4 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr13:114286056 C>T maps to NM_007111.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:141682679 G>T maps to NM_001178139.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr3:141682771 G>A maps to NM_001178139.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr23:132351693 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:132351558 G>A did not map to a codon.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr23:132351940 A>G did not map to a codon.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr23:132351882 G>A did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:132351470 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:48891238 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:48887805 C>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:48891040 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:48887693 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:48891049 G>A did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:41657474 G>T maps to ENST00000343317 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:115590980 A>G maps to NM_012252.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr3:100463761 T>C maps to NM_001007565.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:26895228 G>A maps to NM_012143.2 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:26902875 C>T maps to NM_012143.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:188348878 C>T maps to NM_006287.4 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr7:93519521 G>A maps to NM_006528.2 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:93518425 G>A maps to NM_006528.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:93519533 G>A maps to NM_006528.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:54611542 G>A maps to NM_013342.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:54618064 C>A maps to NM_013342.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:100218518 C>T maps to NM_003227.3 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:100218518 C>T maps to NM_003227.3 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:100228629 G>A maps to NM_003227.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr7:100218617 G>A maps to NM_003227.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:195798335 G>A maps to NM_001128148.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:195787074 C>T maps to NM_001128148.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:195789784 A>G maps to NM_001128148.1 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:195800859 A>G maps to NM_001128148.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:133898949 C>T maps to NM_003235.4 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:133881991 C>T maps to NM_003235.4 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr8:133900553 G>A maps to NM_003235.4 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr8:133898732 G>A maps to NM_003235.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr8:133895188 C>T maps to NM_003235.4 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr8:133895149 G>A maps to NM_003235.4 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:133906121 G>A maps to NM_003235.4 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:134144190 G>T did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:133894711 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:133879301 C>T maps to NM_003235.4 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:133883659 C>A maps to NM_003235.4 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr8:133885382 G>A maps to NM_003235.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:133898732 G>A maps to NM_003235.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:133920512 C>T maps to NM_003235.4 Y1310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:95230366 T>C maps to NM_014305.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:95243104 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:70677990 T>C maps to NM_003236.2 *161W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31487397 C>A maps to NM_001042454.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:31487821 C>T maps to NM_001042454.2 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:218607500 C>T maps to NM_001135599.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:218520237 G>A maps to NM_001135599.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr1:218520216 T>G maps to NM_001135599.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:218614598 C>T maps to NM_001135599.2 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:76437517 C>T maps to NM_003239.2 W199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:76427264 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:76427331 G>T maps to NM_003239.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:76437954 G>T maps to NM_003239.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:135382976 C>T maps to NM_000358.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr9:101891356 C>A maps to NM_004612.2 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr9:101904869 A>T maps to NM_004612.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr9:101891276 C>T maps to NM_004612.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:30648431 T>C maps to NM_001024847.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:30729961 C>T maps to NM_001024847.2 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr3:30713930 T>G did not map to a codon.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr3:30686362 C>T maps to NM_001024847.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:92178027 G>A maps to NM_003243.4 N646N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:92161319 C>A maps to NM_003243.4 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:92174325 G>A maps to NM_003243.4 D727D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr1:92182210 C>A maps to NM_003243.4 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr1:92200484 G>T maps to NM_003243.4 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:105886049 C>T maps to NM_004257.4 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr2:105924383 G>A maps to NM_004257.4 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:105915106 C>T maps to NM_004257.4 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr2:105889360 C>T maps to NM_004257.4 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr2:105885781 G>A maps to NM_004257.4 Q785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr2:105900789 T>C maps to NM_004257.4 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr2:105900791 C>A maps to NM_004257.4 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr18:3452123 C>A maps to NM_170695.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:89177517 A>C did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr23:89177430 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:89177107 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:89177209 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr23:89177517 A>G did not map to a codon.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr23:89177653 G>A did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr23:89177143 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:89177503 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:89177298 A>C did not map to a codon.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr23:89177508 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr23:89177252 T>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr24:3447295 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr24:3447604 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr24:3447739 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr24:3447603 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr14:24731000 G>A maps to NM_000359.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:24729875 C>T maps to NM_000359.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:24729875 C>T maps to NM_000359.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:24730997 G>A maps to NM_000359.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:24718707 C>T maps to NM_000359.2 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:36779457 C>T maps to NM_004613.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:36770551 C>A maps to NM_004613.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:36767988 A>G maps to NM_004613.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:36779432 C>A maps to NM_004613.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:36759565 A>C maps to NM_004613.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:36758716 C>T maps to NM_004613.2 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:36767985 C>T maps to NM_004613.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:2312867 C>T maps to NM_003245.3 N518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:2308988 G>A maps to NM_003245.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr20:2312664 C>T maps to NM_003245.3 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr20:2308982 C>T maps to NM_003245.3 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr20:2297996 G>A maps to NM_003245.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr20:2315906 C>A maps to NM_003245.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:2321151 G>A maps to NM_003245.3 K669K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr3:44951843 G>A maps to NM_003241.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:44929184 G>A maps to NM_003241.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:44952775 C>T maps to NM_003241.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr15:43531358 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:43531013 C>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:43548789 G>T maps to NM_201631.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:43525819 C>T maps to NM_201631.3 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:43527730 G>A maps to NM_201631.3 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:43531379 T>C maps to NM_201631.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:2384383 G>A maps to NM_198994.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:2397896 G>A maps to NM_198994.2 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:2378637 C>T maps to NM_198994.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr20:2397899 G>A maps to NM_198994.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr20:2413183 C>T maps to NM_198994.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr20:2384320 C>T maps to NM_198994.2 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr15:43585662 G>T maps to NM_052955.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:43585152 C>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr15:43577064 C>T maps to NM_052955.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:43584952 A>C maps to NM_052955.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr15:43577112 G>C maps to NM_052955.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:43568757 C>T maps to NM_052955.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr15:43569079 G>A maps to NM_052955.2 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr15:43569088 G>A maps to NM_052955.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:85554668 A>G maps to ENST00000409015 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:56698410 A>G maps to NM_024831.6 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:56698903 C>T maps to NM_024831.6 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr8:56717539 C>T maps to NM_024831.6 D696D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:2186586 C>T maps to NM_199292.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:2186544 C>A maps to NM_199292.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr11:2192944 C>T maps to NM_199292.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr20:57568777 C>T maps to NM_198976.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A8CX-01A-11D-A364-08 chr20:57568759 C>T maps to NM_198976.1 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr20:57568759 C>T maps to NM_198976.1 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:43779351 A>C maps to ENST00000330266 L935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr2:43802125 A>G maps to ENST00000330266 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr2:43732808 T>C maps to ENST00000330266 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr8:42693376 G>A maps to NM_018105.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:42693173 G>A maps to NM_018105.2 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:67877119 C>A maps to NM_020457.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr16:67876786 G>A maps to NM_020457.2 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr16:67876795 A>G maps to NM_020457.2 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:72068120 A>G maps to NM_031435.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr12:72070861 A>T maps to NM_031435.3 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr2:242573184 C>T maps to NM_015963.5 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:242572944 G>A maps to NM_015963.5 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr7:108205297 T>C maps to NM_001130475.1 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:76452234 C>T maps to NM_144721.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:83838783 G>A maps to NM_024672.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr4:83822020 C>A maps to NM_024672.4 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:23028797 G>A maps to NM_000361.2 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:23028479 G>A maps to NM_000361.2 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:23028479 G>A maps to NM_000361.2 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr20:23028938 C>T maps to NM_000361.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:23029061 G>A maps to NM_000361.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:23028479 G>A maps to NM_000361.2 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:39885658 C>T maps to NM_003246.2 D1019D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:39874865 C>T maps to NM_003246.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr15:39877764 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:39882121 C>T maps to NM_003246.2 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:39874865 C>T maps to NM_003246.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr15:39874700 G>A maps to NM_003246.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:169648976 G>A maps to NM_003247.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr6:169637337 C>T maps to NM_003247.2 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:169641949 G>A maps to NM_003247.2 C266C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr6:169622297 C>T maps to NM_003247.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:169632788 G>A maps to NM_003247.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:169625315 A>G maps to NM_003247.2 D899D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:169625354 G>A maps to NM_003247.2 D886D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6817-01A-11D-1882-08 chr6:169632104 G>A maps to NM_003247.2 C707C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr6:169626378 G>A maps to NM_003247.2 R812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:169648547 G>A maps to NM_003247.2 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:169629756 C>T maps to NM_003247.2 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:169641958 G>T maps to NM_003247.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr1:155170257 G>A maps to NM_007112.3 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:155167337 G>A maps to NM_007112.3 Y805Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:155175988 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:155175054 C>T maps to NM_007112.3 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:155172138 G>A maps to NM_007112.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:79357546 G>A maps to NM_003248.4 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:79372824 A>G maps to NM_003248.4 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:79366473 C>T maps to NM_003248.4 C487C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr5:79331428 C>T maps to NM_003248.4 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:79355571 G>A maps to NM_003248.4 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr19:375954 G>A maps to NM_016585.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:151861727 G>A maps to NM_053055.3 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:151849480 C>T maps to NM_053055.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:151825966 C>T maps to NM_182578.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:128134765 G>A maps to NM_001164685.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:128150815 C>A maps to NM_001164685.1 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:157158483 C>A maps to NM_017872.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr10:25314059 G>A maps to NM_024838.4 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:25312242 C>T maps to NM_024838.4 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:88474158 T>C maps to NM_018271.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:214853 A>C maps to NM_005131.2 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr18:260236 C>T maps to NM_005131.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:122755145 C>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:122805586 G>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:122830675 G>A did not map to a codon.
Sequencing variant TCGA-BR-6456-01A-11D-1800-08 chr23:122744806 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:122765539 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:122755186 A>G did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:122830586 T>G did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:122820397 C>G did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:122829948 G>C did not map to a codon.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr23:122829932 C>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:122766891 C>A did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:122759790 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:122769998 A>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:122799588 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:122801083 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:122767862 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:122755100 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:122799611 T>C did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:79846239 A>G maps to NM_005782.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:79846260 G>A maps to NM_005782.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr22:29907261 C>T maps to NM_003678.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:29925228 C>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:3077500 G>A maps to NM_024339.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:63825342 G>A maps to NM_025075.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:2813273 A>C maps to NM_003249.3 *690C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:2807509 G>A maps to NM_003249.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr19:2807485 G>A maps to NM_003249.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:2807515 C>T maps to NM_003249.3 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:38244712 G>T maps to NM_003250.5 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:38243030 C>T maps to NM_003250.5 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:38249571 G>A maps to NM_003250.5 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:38233861 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:38249547 C>T maps to NM_003250.5 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:36748266 C>T maps to NM_005119.3 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:36769579 C>T maps to NM_005119.3 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:36752134 G>T maps to NM_005119.3 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:36754727 G>T maps to NM_005119.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:24193952 G>A maps to NM_001128177.1 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:24169074 G>T maps to NM_001128177.1 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:24185081 G>A maps to NM_001128177.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr3:24185036 C>T maps to NM_001128177.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:77775269 C>T maps to NM_003251.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:52952904 T>C maps to NM_018676.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:52960304 C>T maps to NM_018676.3 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr13:52972168 A>G maps to NM_018676.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:52952736 G>T maps to NM_018676.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr15:72020960 C>T maps to NM_024817.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:72040764 G>T maps to NM_024817.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:71535236 G>A maps to NM_024817.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:72057441 C>T maps to NM_024817.2 D891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:72023518 C>T maps to NM_024817.2 N531N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr15:72057435 G>T maps to NM_024817.2 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:11464342 G>A maps to ENST00000423059 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:11441595 C>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr7:11675887 G>A maps to ENST00000423059 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:11676577 G>A maps to ENST00000423059 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:11676524 C>T maps to ENST00000423059 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:11514154 T>C maps to ENST00000423059 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:11521444 G>A maps to ENST00000423059 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:11521424 C>T maps to ENST00000423059 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:11415489 T>C maps to ENST00000423059 K1635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:11676322 A>G maps to ENST00000423059 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr7:11676524 C>T maps to ENST00000423059 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr7:11630117 G>A maps to ENST00000423059 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:11676472 G>A maps to ENST00000423059 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:11445993 G>A maps to ENST00000423059 D1390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:11676160 G>A maps to ENST00000423059 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr2:138169182 A>G maps to ENST00000272643 K900K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr2:138373776 T>G maps to ENST00000272643 T1155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:137872831 A>T maps to ENST00000272643 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr2:137990640 A>G maps to ENST00000272643 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:137990634 T>C maps to ENST00000272643 C694C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:138400059 C>T maps to ENST00000272643 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:137814206 C>T maps to ENST00000272643 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr2:138033525 A>G maps to ENST00000272643 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:138320843 A>G maps to ENST00000272643 V1067V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:137928467 G>T maps to ENST00000272643 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr2:137814005 T>C maps to ENST00000272643 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr2:137928506 C>T maps to ENST00000272643 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:138000025 G>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:137852592 C>T maps to ENST00000272643 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr2:138169312 A>C maps to ENST00000272643 R944R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr2:137872774 G>A maps to ENST00000272643 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr2:39983100 C>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:39964117 G>A maps to NM_025264.4 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:9426222 C>T maps to NM_015453.2 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:119290950 G>A maps to NM_006288.3 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:70454865 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:27400905 G>A maps to NM_004740.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:121336660 C>T maps to NM_001033925.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr21:32493036 G>A maps to NM_003253.2 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:32638370 A>G maps to NM_003253.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr21:32639180 C>T maps to NM_003253.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr21:32595733 C>T maps to NM_003253.2 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr21:32492733 A>G maps to NM_003253.2 V1576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8367-01A-11D-2340-08 chr21:32638955 G>A maps to NM_003253.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr21:32624208 C>T maps to NM_003253.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5799-01A-11D-1600-08 chr21:32493036 G>A maps to NM_003253.2 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr21:32508290 C>T maps to NM_003253.2 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr21:32513433 A>G did not map to a codon.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr21:32617947 G>A maps to NM_003253.2 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:32502564 C>T maps to NM_003253.2 T1337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:32624199 C>T maps to NM_003253.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr21:32624208 C>T maps to NM_003253.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr6:155485682 G>A maps to ENST00000456144 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:155574158 G>A maps to ENST00000456144 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:155458396 T>C maps to ENST00000456144 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:155561731 G>A maps to ENST00000456144 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:155465746 G>A maps to ENST00000456144 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:155561782 T>C maps to ENST00000456144 D1096D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:155469425 C>T maps to ENST00000456144 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:4817759 G>A maps to NM_182919.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:4817393 C>T maps to NM_182919.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:4816901 C>T maps to NM_182919.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:4818092 C>T maps to NM_182919.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:4816265 C>T maps to NM_182919.2 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:4817189 G>T maps to NM_182919.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:4818197 C>T maps to NM_182919.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:4817840 G>A maps to NM_182919.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:4818122 G>A maps to NM_182919.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:43772882 C>T maps to NM_005424.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr1:43778102 C>T maps to NM_005424.2 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:43770627 C>T maps to NM_005424.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:43774660 G>T maps to NM_005424.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:43777468 G>A maps to NM_005424.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:43778273 T>C did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr1:43778819 C>T maps to NM_005424.2 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:43778240 G>A maps to NM_005424.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr5:134785359 C>T maps to NM_001099221.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr11:65123434 G>A maps to NM_145719.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr4:153691553 G>A maps to NM_145720.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:153691841 A>C maps to NM_145720.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:153691220 A>G maps to NM_145720.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr8:144681749 G>A maps to NM_032862.4 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:149375677 A>G maps to NM_030953.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:3349372 G>A maps to NM_033208.3 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:114014390 G>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:156381462 G>A maps to NM_138379.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:56817438 C>T maps to NM_003920.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:56811706 A>G maps to NM_003920.3 D1180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:56822331 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr12:56817450 T>C maps to NM_003920.3 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:56817447 C>T maps to NM_003920.3 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:201926415 C>T maps to NM_006335.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:201938667 C>T maps to NM_006335.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:48754134 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:48751228 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:902816 T>G maps to NM_013337.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:900432 T>C maps to NM_013337.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:7998750 G>A maps to NM_006351.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:7999072 G>T maps to NM_006351.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:39971318 G>C maps to NM_001001563.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:39971204 G>A maps to NM_001001563.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:100601605 C>T did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr14:58875880 G>A maps to NM_012460.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr23:47444706 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:54219399 C>T maps to NM_014464.3 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:32049151 G>A maps to NM_022164.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:32050769 C>T maps to NM_022164.2 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:156396199 C>T maps to NM_015508.4 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:156395503 C>T maps to NM_015508.4 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:66643868 A>G maps to NM_017858.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:168169138 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:168169163 G>A maps to NM_152902.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:126162736 C>T maps to NM_148910.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:126160800 G>A maps to NM_148910.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr6:43473499 C>T maps to NM_001146016.1 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:43472923 T>C maps to NM_001146016.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr15:30010322 C>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:30029533 T>C maps to NM_003257.3 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:30024732 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:30011318 G>A maps to NM_003257.3 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:30001144 G>A maps to NM_003257.3 R1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:30053364 C>T maps to NM_003257.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr15:30010841 A>G maps to NM_003257.3 H1168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:71836210 C>T maps to NM_004817.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:3736171 C>T maps to NM_014428.1 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:3734421 C>T maps to NM_014428.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr19:3746571 C>A maps to NM_014428.1 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:3733890 C>T maps to NM_014428.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:3746580 G>A maps to NM_014428.1 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:66547631 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:53275201 C>T maps to ENST00000423516 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:53263293 A>G did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:153537724 G>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:153524228 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:153533695 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:153539310 G>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:153549179 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:153541073 A>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:153556270 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:153549109 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:153551556 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:153557990 A>G did not map to a codon.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr23:153524216 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:153539339 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:153539212 A>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:164393887 G>A maps to NM_032136.4 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:164394214 G>T maps to NM_032136.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:164394016 T>C maps to NM_032136.4 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr4:164393458 G>T maps to NM_032136.4 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:164394289 G>A maps to NM_032136.4 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr4:164394543 G>A maps to NM_032136.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr4:164394748 C>T maps to NM_032136.4 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:84225139 C>T maps to NM_005077.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:84205814 G>A maps to NM_005077.3 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:84226806 G>A maps to NM_005077.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr9:84226722 G>A maps to NM_005077.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:3009701 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:3009626 G>A maps to NM_003260.4 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:70346946 C>T maps to NM_005078.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:70344722 G>A maps to NM_005078.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:82242306 C>T maps to ENST00000376537 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:2991982 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:2993497 G>A maps to NM_001143986.1 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:2987968 C>T maps to NM_001143986.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr19:2987153 G>A maps to NM_001143986.1 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:171853206 C>A maps to ENST00000360843 E715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr2:171854266 T>C maps to ENST00000360843 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:171867900 G>A maps to ENST00000360843 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:60558533 G>A maps to ENST00000326270 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:60689889 A>G maps to ENST00000326270 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:167022026 A>G maps to ENST00000507499 *1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:166999180 T>G maps to ENST00000507499 L837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr4:166915614 C>A maps to ENST00000507499 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:166910563 T>C maps to ENST00000507499 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr4:166981210 C>T maps to ENST00000507499 N649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:166915566 A>G maps to ENST00000507499 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:166795139 C>T maps to ENST00000507499 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:166795223 C>T maps to ENST00000507499 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:166986980 A>G maps to ENST00000507499 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr4:166960519 A>C maps to ENST00000507499 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:98138802 G>A maps to NM_012465.3 C747C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:98192585 G>A maps to NM_012465.3 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr10:98192669 G>A maps to NM_012465.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:98170229 C>T maps to NM_012465.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr10:98127886 G>A maps to NM_012465.3 Y1002Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:35713238 G>A maps to NM_006289.3 I1102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:35706051 G>A maps to NM_006289.3 A1806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:35711591 C>T maps to NM_006289.3 P1293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:35725613 G>A maps to NM_006289.3 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr9:35700199 A>T maps to NM_006289.3 L2216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:63009876 C>T maps to NM_015059.2 Q956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:63019351 C>T maps to NM_015059.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:62994287 C>T maps to NM_015059.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:63031734 C>T maps to NM_015059.2 G1292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr15:63089447 G>A maps to NM_015059.2 L2027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr15:63111821 T>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:63029189 C>T maps to NM_015059.2 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:63047786 C>T maps to NM_015059.2 C1511C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:63004188 C>T maps to NM_015059.2 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:63044601 T>A maps to NM_015059.2 C1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:63000708 C>T maps to NM_015059.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr15:63040576 C>G maps to NM_015059.2 L1351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr15:63008618 C>A maps to NM_015059.2 A908A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:62945496 G>A maps to NM_015059.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:62978907 C>T maps to NM_015059.2 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:63089582 C>T maps to NM_015059.2 S2072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:63069084 C>T maps to NM_015059.2 D1830D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:63031560 G>A maps to NM_015059.2 T1234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:63017303 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:62990051 C>T maps to NM_015059.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:63069042 C>T maps to NM_015059.2 N1816N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:38798649 G>A maps to NM_003263.3 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:38799486 G>T maps to NM_003263.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:38799939 T>C maps to NM_003263.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:38776167 C>T maps to NM_030956.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:38774897 G>A maps to NM_030956.3 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:38775960 G>A maps to NM_030956.3 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr4:38774897 G>A maps to NM_030956.3 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr4:154624400 T>C maps to NM_003264.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:154624622 C>T maps to NM_003264.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:154625729 T>C maps to NM_003264.3 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:154625774 C>A maps to NM_003264.3 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr4:154625489 G>A maps to NM_003264.3 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:154625490 C>T maps to NM_003264.3 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:187004018 G>A maps to NM_003265.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:186997811 C>T maps to NM_003265.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:187000109 A>G maps to NM_003265.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:186998141 G>A maps to NM_003265.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:120474909 T>C maps to NM_138554.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr9:120476847 C>G maps to NM_138554.3 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr9:120475242 C>T maps to NM_138554.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr9:120476157 T>G maps to NM_138554.3 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:223286172 G>T maps to NM_003268.5 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:223285359 G>A maps to NM_003268.5 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:223285098 C>T maps to NM_003268.5 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr4:38829330 G>A maps to NM_006068.3 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr4:38830758 C>T maps to NM_006068.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr4:38830419 C>T maps to NM_006068.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:12905874 C>T did not map to a codon.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr23:12906521 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:12903717 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:12904490 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:12906072 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:12905083 C>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:12905417 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:12904061 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr23:12906378 G>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:12939515 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:12939202 A>G did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:12940243 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:12937959 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:12939420 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:12938573 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:12937485 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:12937550 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:12940035 T>G did not map to a codon.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr23:12939189 G>T did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:12937480 G>A did not map to a codon.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr23:12940243 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:12937804 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:12938122 T>G did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr3:52255256 G>A maps to ENST00000494383 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr10:102896609 G>A maps to NM_005521.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:102893953 G>A maps to NM_005521.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:74742967 G>A maps to NM_016170.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:170736524 G>A maps to NM_021025.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:170736690 C>T maps to NM_021025.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr5:170736746 C>A maps to NM_021025.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:170736617 G>A maps to NM_021025.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:38851173 G>A maps to NM_031940.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr8:38853730 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:38851131 G>A maps to NM_031940.3 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:38851176 G>A maps to NM_031940.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr8:38853952 C>T maps to NM_078473.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:102182720 A>G maps to NM_078474.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:149051031 G>A maps to NM_138786.3 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:196050828 G>A maps to NM_138461.2 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:196054329 G>A maps to NM_138461.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:228228628 C>T maps to NM_024795.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:228228610 A>G maps to NM_024795.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr3:149192780 C>T maps to NM_004617.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:149192828 C>T maps to NM_004617.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:4685808 G>A maps to NM_003963.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:4685823 G>A maps to NM_003963.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:4686187 C>T maps to NM_003963.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:4686289 C>T maps to NM_003963.2 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr15:83790729 T>G maps to NM_023003.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr15:83790678 T>G maps to NM_023003.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:19381885 G>A maps to NM_001001524.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:19375643 G>A maps to NM_001001524.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:105361019 T>C maps to NM_030788.2 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:105361782 G>T maps to NM_030788.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr8:105368423 T>C maps to NM_030788.2 *471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:105360959 G>A maps to NM_030788.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr14:24664213 T>C maps to NM_006405.5 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:24664129 G>A maps to NM_006405.5 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr14:24662100 G>A maps to NM_006405.5 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr13:100196199 C>T maps to NM_004800.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:98303916 T>G maps to NM_020123.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:98287918 C>T maps to NM_020123.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr10:98287045 C>T maps to NM_020123.3 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr20:30729459 C>T maps to NM_014742.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:30720865 C>T maps to NM_014742.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr20:30742949 A>G maps to NM_014742.3 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr20:30730867 C>T maps to NM_014742.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:66546104 C>T maps to ENST00000286424 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:75406887 C>T maps to NM_138691.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:75369790 C>T maps to NM_138691.2 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:75420335 C>A maps to NM_138691.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:2593877 G>A maps to NM_080751.2 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr20:2582791 G>T maps to NM_080751.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:2616614 C>T maps to NM_080751.2 R784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:2582902 C>T maps to NM_080751.2 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr15:81636295 A>G maps to ENST00000454937 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr15:81650757 G>A maps to ENST00000454937 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr15:81625266 G>T maps to ENST00000454937 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:81631012 G>A maps to ENST00000454937 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:81625551 C>T maps to ENST00000454937 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:54664874 G>A maps to NM_001145303.1 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:54664209 T>C maps to NM_001145303.1 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr16:19451389 T>C maps to NM_001105248.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr16:19451956 A>T maps to NM_001105248.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr16:19468201 C>T maps to NM_024780.4 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr16:19483450 G>A maps to NM_001105248.1 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr17:76113968 G>T maps to NM_007267.6 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:76117720 C>T maps to NM_007267.6 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr17:76121029 G>C maps to NM_007267.6 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:76117687 G>A maps to NM_007267.6 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr16:19056298 C>T maps to NM_024847.3 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:19063045 G>A maps to NM_024847.3 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:76134467 C>A maps to NM_152468.4 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:76137108 G>A maps to NM_152468.4 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr17:76134464 G>T maps to NM_152468.4 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr17:76129506 C>G maps to NM_152468.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:129389915 G>A maps to NM_001017395.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:129370587 C>T maps to NM_001017395.3 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:205241212 C>T maps to NM_014858.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:205238586 C>T maps to NM_014858.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:205211129 C>T maps to NM_014858.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr1:205238337 C>T maps to NM_014858.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:205238751 C>T maps to NM_014858.3 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:205238925 C>T maps to NM_014858.3 H532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:205210850 C>T maps to NM_014858.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:205238715 C>T maps to NM_014858.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr1:205238130 C>T maps to NM_014858.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr12:94976110 C>T maps to NM_020698.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr12:94972169 C>T maps to NM_020698.2 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:94975588 G>A maps to NM_020698.2 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:165712523 C>T maps to NM_019026.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:40717164 C>T maps to NM_001008740.3 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr13:114174949 C>T maps to NM_017905.4 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr13:114188556 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:114152697 T>C maps to NM_017905.4 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:20020974 G>A maps to NM_181719.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr1:20097940 G>A maps to NM_181719.4 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:20009856 G>A maps to NM_181719.4 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:20009613 G>A maps to NM_181719.4 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:140024250 C>T maps to ENST00000252100 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:140023146 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr5:140021627 C>G maps to ENST00000252100 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:68941411 C>T maps to NM_024562.1 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:69117395 C>T maps to NM_024562.1 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:68877537 C>A maps to NM_024562.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr19:10943723 G>A maps to NM_006858.2 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr14:75614414 G>A maps to NM_006827.5 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:79603624 C>T maps to NM_007364.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:79606184 C>T maps to NM_007364.2 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:79614412 C>T maps to NM_007364.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:69377540 G>A maps to NM_144676.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr14:77808278 A>T maps to NM_213601.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:193059202 G>A maps to NM_016192.2 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr2:193059094 G>A maps to NM_016192.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:42090430 G>A maps to NM_032376.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr17:7339810 T>C maps to NM_178518.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr17:7340374 C>T maps to NM_178518.2 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:7339930 T>C maps to NM_178518.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr17:72832360 C>T maps to NM_017728.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:79287759 G>A maps to NM_178520.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:12263968 C>T maps to NM_018374.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:12254540 C>A maps to NM_018374.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:48361045 T>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:8077914 A>G maps to NM_032354.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr3:133098806 G>A maps to NM_001136469.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:60688365 C>T maps to NM_024092.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:60689420 C>T maps to NM_024092.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:60689456 C>T maps to NM_024092.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:21101783 C>T maps to NM_003876.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:21101951 C>T maps to NM_003876.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:10018665 C>T maps to NM_018447.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr3:50396053 C>G maps to NM_007024.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr12:112374525 G>T maps to NM_001193531.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:44782427 G>T maps to NM_032256.1 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:44782313 C>T maps to NM_032256.1 C468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:44782313 C>A maps to NM_032256.1 C468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr12:108985736 A>G maps to NM_181724.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:122181539 G>A maps to NM_001080825.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr14:105995482 G>A maps to NM_025268.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:43738911 C>T maps to NM_144626.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:43738891 C>T maps to NM_144626.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:43738509 C>T maps to NM_144626.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:85367434 T>C maps to NM_032273.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:85365182 C>T maps to NM_032273.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:85345228 T>C maps to NM_018480.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr11:85345128 G>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:4248029 T>C maps to ENST00000382753 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:98453802 G>A maps to NM_001134450.1 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:98460916 G>A maps to NM_001134450.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:98409164 C>T maps to NM_015348.1 A1276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:60704375 C>A maps to NM_017870.3 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:60696228 C>T maps to NM_017870.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:60703651 G>A maps to NM_017870.3 W783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:60703478 C>T maps to NM_017870.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:60699529 C>T maps to NM_017870.3 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:126004053 G>A maps to NM_052907.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr12:126137112 C>T maps to NM_052907.2 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:125834259 T>C maps to NM_052907.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr12:126138172 C>T maps to NM_052907.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr12:126138781 G>A maps to NM_052907.2 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr12:126138478 C>T maps to NM_052907.2 R820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr12:126135432 G>A maps to NM_052907.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr12:126139126 C>T maps to NM_052907.2 D1036D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:126135276 A>G maps to NM_052907.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:130184914 G>A maps to NM_133448.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:129566528 G>A maps to NM_133448.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr12:129566417 T>C maps to NM_133448.2 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr12:130185231 G>T maps to NM_133448.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr12:129694076 T>C maps to NM_133448.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:129559043 C>A maps to NM_133448.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:130184740 G>A maps to NM_133448.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:130184751 G>A maps to NM_133448.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr12:129558600 G>C maps to NM_133448.2 S1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr12:129566426 T>G maps to NM_133448.2 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:129559010 C>A maps to NM_133448.2 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr12:129559435 C>A maps to NM_133448.2 G762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:130184677 G>A maps to NM_133448.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr12:129694196 G>A maps to NM_133448.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr12:129559291 T>G maps to NM_133448.2 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:32962033 C>T maps to NM_207313.1 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:32953467 C>T maps to NM_207313.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr17:32955599 T>C maps to NM_207313.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:32953297 C>T maps to NM_207313.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:32959853 C>T maps to NM_207313.1 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:67232301 C>T maps to NM_025124.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:67234858 G>A maps to NM_025124.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:87029198 T>C maps to NM_022918.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:87025589 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr11:87006866 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:87029213 T>C maps to NM_022918.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:48863430 T>C maps to NM_018273.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:48845825 C>T maps to NM_018273.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:48845963 C>T maps to NM_018273.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:48846618 G>T maps to NM_018273.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr4:159140504 C>T maps to NM_018342.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:42827838 T>C maps to ENST00000406159 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:42819215 C>T maps to ENST00000406159 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:5778542 C>T maps to NM_152784.3 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:5745967 G>T maps to NM_152784.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:36038231 C>T maps to NM_032635.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:36036858 G>A maps to NM_032635.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr19:36037608 G>T maps to NM_032635.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:36038037 G>A maps to NM_032635.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:36232024 C>T maps to NM_024660.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:36230719 G>A maps to NM_024660.2 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr6:10751369 C>T maps to NM_030969.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:85829044 G>A maps to NM_001031738.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:55828274 G>A maps to NM_001085488.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr4:83406786 G>A maps to NM_001080506.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:66061809 G>A maps to NM_153266.3 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:66061944 C>T maps to NM_153266.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr11:66061971 G>A maps to NM_153266.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:153573843 G>A maps to NM_152680.2 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr4:38990474 C>T maps to NM_024943.1 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:87536643 T>C maps to NM_153354.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr2:135309654 G>A maps to NM_030923.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:135215679 C>T maps to NM_030923.4 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:109247078 G>T did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:112407371 G>A maps to NM_022484.4 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:112423776 C>T maps to NM_022484.4 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr7:112424363 A>G maps to NM_022484.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr7:112412890 C>T maps to NM_022484.4 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:216960850 C>T maps to NM_138390.3 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:216964783 C>A maps to NM_138390.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:216960775 G>A maps to NM_138390.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr2:216964985 G>A maps to NM_138390.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr2:216964916 C>T maps to NM_138390.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr5:72419283 C>T maps to NM_173490.6 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:138860444 T>C maps to NM_198282.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:72469396 G>A maps to NM_153217.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:72469087 C>T maps to NM_153217.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:949615 C>T maps to NM_032326.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr4:941649 C>T maps to NM_032326.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:941595 C>T maps to NM_032326.2 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr4:952214 C>T maps to NM_032326.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr4:951692 G>A maps to NM_032326.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr7:150493585 G>A maps to NM_014020.3 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:120439193 G>A maps to NM_030577.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:120438596 G>A maps to NM_030577.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:120438935 C>T maps to NM_030577.2 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:120439106 C>T maps to NM_030577.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr2:120439334 G>A maps to NM_030577.2 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:120439016 C>T maps to NM_030577.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:39944309 T>C maps to NM_152390.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:39944177 T>G maps to NM_152390.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr11:62557410 C>T maps to NM_199337.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:675582 G>A maps to NM_152834.2 H35H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:669840 C>T maps to NM_152834.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:104230499 G>A maps to NM_024789.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:104230586 G>A maps to NM_024789.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr10:104233734 G>A maps to NM_024789.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:159028322 C>T maps to NM_020823.1 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:159029368 G>A maps to NM_020823.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr6:159044608 C>T maps to NM_020823.1 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:103431204 A>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:202976929 T>C maps to NM_001079809.1 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:202985124 C>T maps to NM_001079809.1 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:202992113 C>T maps to NM_001079809.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:202977771 A>G maps to NM_001079809.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:202992134 G>A maps to NM_001079809.1 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:202985096 G>A maps to NM_001079809.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr7:1589975 G>A maps to NM_001097620.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:1587534 C>T maps to NM_001097620.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:38620837 G>A maps to NM_012264.4 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr22:38620888 C>T maps to NM_012264.4 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr16:8889879 G>A maps to NM_015421.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:153247848 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:153247940 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:48741642 G>A maps to NM_199129.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr20:48744536 G>A maps to NM_199203.2 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:55889218 C>T maps to NM_139172.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr4:166000875 C>T maps to NM_001100389.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr4:166000863 C>T maps to NM_001100389.1 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr4:166021836 A>G maps to NM_001100389.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:57466636 G>A maps to NM_001130963.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr12:57454642 G>A maps to NM_001130963.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr7:15425181 G>A maps to NM_001004320.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr7:15584445 G>C maps to NM_001004320.1 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr2:220414534 G>T maps to NM_001005209.1 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:220412243 G>A maps to NM_001005209.1 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr17:26686414 C>T maps to ENST00000457710 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:74312963 C>T maps to NM_013390.2 P1178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr9:74319524 G>A maps to NM_013390.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:95660775 C>T maps to NM_001134658.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:130762847 C>T maps to NM_052913.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:29447581 G>T maps to NM_001003682.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr18:5890541 C>T maps to NM_001080209.1 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr18:5890352 C>T maps to NM_001080209.1 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr18:5890415 C>T maps to NM_001080209.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr18:5891516 G>A maps to NM_001080209.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr18:5891792 C>T maps to NM_001080209.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr18:5891852 C>T maps to NM_001080209.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr18:5890439 C>A maps to NM_001080209.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:5890415 C>A maps to NM_001080209.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:5891843 G>T maps to NM_001080209.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:9656942 C>T maps to NM_001130924.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:9656055 C>T maps to NM_001130924.2 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:72691175 C>T maps to NM_001080462.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:72691046 G>A maps to NM_001080462.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:1604918 C>T maps to NM_024600.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:190158095 G>A maps to NM_207316.1 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr16:67262460 C>T maps to NM_014187.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:67262460 C>T maps to NM_014187.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:129815399 G>A maps to NM_032842.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr7:129825118 C>T maps to NM_032842.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:138487645 C>T maps to ENST00000422794 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:27263302 C>T maps to NM_017727.4 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:27259613 C>T maps to NM_017727.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr9:32784495 G>A maps to NM_212558.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:67940343 G>A maps to NM_182526.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr16:75574029 C>T maps to NM_001077416.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:75579360 C>T maps to NM_001077416.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:118403004 C>T maps to NM_032780.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:63188895 A>G maps to NM_178505.6 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:63191021 C>T maps to NM_178505.6 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:63170262 T>C maps to NM_178505.6 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr10:63188733 C>T maps to NM_178505.6 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr23:15657775 G>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr14:61747019 G>T maps to NM_001017970.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:61747055 G>A maps to NM_001017970.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:41956147 C>T maps to NM_018126.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:41941380 A>G maps to NM_018126.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100334081 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100349661 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100349841 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:100349692 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr23:100349860 T>C did not map to a codon.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:120194859 C>T maps to NM_183240.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:120195017 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:120194652 G>A maps to NM_183240.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:16790892 G>T maps to NM_024074.1 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:108536264 A>G maps to NM_018112.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:119165904 G>A maps to NM_018266.1 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:32566072 C>T maps to NM_018056.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:32568261 C>T maps to NM_018056.2 H489H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:32557329 C>T maps to NM_018056.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr1:32557494 C>T maps to NM_018056.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:12783955 C>A maps to ENST00000431022 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr3:12790208 G>A maps to ENST00000431022 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr3:12778266 G>A maps to ENST00000431022 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr3:185214765 C>T maps to NM_080652.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr11:9305015 A>G maps to NM_015012.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:44905705 C>T maps to NM_144638.1 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:14176276 C>T maps to NM_024334.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:14183165 G>A maps to NM_024334.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr3:14176342 T>A maps to NM_024334.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:194344284 C>T maps to NM_001166305.1 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr3:100275724 G>C maps to ENST00000403410 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr11:129725627 C>T maps to NM_138788.3 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:129724712 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:129725621 C>T maps to NM_138788.3 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr23:34657452 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:34657418 G>A did not map to a codon.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr23:34648572 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:34648576 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:34675057 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:54266462 A>G maps to NM_018087.4 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr1:54298163 T>C maps to NM_018087.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr12:64196137 C>T maps to NM_014254.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr12:64202852 T>G maps to NM_014254.1 L438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:15541717 T>C maps to NM_018022.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:1849797 G>A maps to NM_178545.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:45120722 G>A maps to NM_024587.2 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:45120566 G>A maps to NM_024587.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr8:92030644 C>G maps to NM_018710.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr14:20928394 G>T maps to NM_001100814.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr1:95639440 C>T maps to NM_152487.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:95657378 A>G maps to NM_152487.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:95657234 C>T maps to NM_152487.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:25818034 C>T maps to NM_018202.4 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:25775372 G>A maps to NM_018202.4 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:25812244 A>G maps to NM_018202.4 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:25818070 C>A maps to NM_018202.4 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:25783149 G>T maps to NM_018202.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:54509117 G>A maps to ENST00000371338 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:54506484 C>T maps to ENST00000371338 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:54509066 G>A maps to ENST00000371338 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:18729232 C>T maps to NM_012109.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr19:18729277 G>A maps to NM_012109.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:77423306 G>T maps to NM_032936.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:55457571 G>C maps to NM_182532.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:226058795 C>T maps to NM_014698.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:226037669 A>G maps to NM_014698.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:226041488 G>A maps to NM_014698.2 C546C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:226044663 G>A maps to NM_014698.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:226048597 C>T maps to NM_014698.2 W395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:226044615 C>T maps to NM_014698.2 W493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:226062013 G>A maps to NM_014698.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:44115222 C>T maps to NM_018426.1 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr14:77708713 C>T maps to NM_020431.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr14:77722963 G>A maps to NM_020431.2 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:77712358 G>T maps to NM_020431.2 G509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:77715751 G>A maps to NM_020431.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr14:77710780 C>T maps to NM_020431.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr8:91643832 C>A maps to NM_001008495.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:91657389 C>T maps to NM_001008495.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:91637964 G>T maps to NM_001008495.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr8:125334365 C>A maps to NM_194291.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:125326275 G>A maps to NM_194291.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:56663663 T>C maps to ENST00000434581 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:74888566 C>T maps to NM_017866.5 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr8:133764098 G>A maps to ENST00000395406 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr8:133759332 G>A maps to ENST00000395406 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr10:45427457 C>T maps to NM_001123376.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:109796625 C>T maps to NM_153015.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:109796742 A>T maps to NM_153015.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:156256096 G>A maps to NM_032323.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:156256063 C>T maps to NM_032323.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:156256114 G>A maps to NM_032323.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:205052682 A>G maps to NM_203376.1 *256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:16071010 G>A maps to NM_001013641.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:16073509 C>T maps to NM_001013641.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:18723138 G>A maps to NM_153347.1 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:55738704 G>A maps to NM_173804.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:42529647 G>A maps to ENST00000389834 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:42512334 T>C did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:112832490 T>C maps to NM_032824.2 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:112865399 C>A maps to NM_032824.2 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:112847267 T>G maps to NM_032824.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:48658931 C>T maps to NM_001008269.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:426712 C>T maps to NM_021259.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr16:426760 G>A maps to NM_021259.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr16:427479 G>A maps to NM_021259.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:35846468 C>T maps to ENST00000360192 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:35852918 C>T maps to NM_001042590.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr9:136379889 A>G maps to NM_001080483.2 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:136389957 C>T maps to NM_001080483.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:136385356 G>A maps to NM_001080483.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr14:74874599 G>C maps to NM_001105579.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr14:74874689 G>A maps to NM_001105579.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr20:24523879 G>A maps to NM_024893.1 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr20:24524023 C>T maps to NM_024893.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr20:24524023 C>T maps to NM_024893.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr20:24524044 C>T maps to NM_024893.1 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr19:41889657 A>G maps to NM_001098821.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:41884321 A>G maps to NM_001098821.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:31260323 G>A did not map to a codon.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr17:38990821 T>C maps to NM_001195386.1 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:69097099 A>G maps to NM_007114.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr3:69072369 G>A maps to NM_007114.2 Y1080Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:4292679 G>A maps to NM_144615.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:4292733 C>T maps to NM_144615.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:154754276 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:154741378 G>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:154736702 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:154754196 C>T did not map to a codon.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr23:154736648 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:154741368 C>T did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:154743753 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr23:154743876 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:100328203 C>T maps to NM_003275.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:52069168 C>T maps to NM_014548.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr15:52075000 T>C maps to NM_014548.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:52161499 A>T maps to NM_014547.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr12:98921764 C>T maps to NM_003276.2 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:98928111 A>T maps to NM_003276.2 K693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr12:98927558 A>G maps to NM_003276.2 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr12:98926790 T>C maps to NM_003276.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:98927396 C>T maps to NM_003276.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:33134736 A>G maps to NM_001039770.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr3:33134421 G>A maps to NM_001039770.2 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr4:68784829 G>A maps to NM_182606.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:68788632 G>A maps to NM_182606.3 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr4:69094500 A>G maps to NM_182502.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr4:68693132 A>G maps to NM_004262.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:68688174 C>T maps to NM_004262.2 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:68930555 C>A maps to NM_207407.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:68930610 T>C maps to NM_207407.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:51237697 C>T maps to NM_182559.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:117787927 G>A maps to ENST00000413475 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr11:117789463 G>T maps to ENST00000413475 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr21:19647633 C>T maps to NM_002772.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr21:19725235 A>C maps to NM_002772.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:19775801 G>A maps to NM_002772.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr21:19642428 C>A maps to NM_002772.2 G973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr21:19666642 G>A maps to NM_002772.2 C810C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr21:19737467 C>T maps to NM_002772.2 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:19653413 G>A maps to NM_002772.2 R871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:19666594 G>A maps to NM_002772.2 C826C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr21:19725235 A>G maps to NM_002772.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr21:19687478 T>G maps to NM_002772.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:19744528 G>A maps to NM_002772.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr21:19666653 G>A maps to NM_002772.2 R807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr21:19704476 T>C maps to NM_002772.2 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr21:19666926 G>A maps to NM_002772.2 N768N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr21:42866319 C>T maps to NM_001135099.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:42852404 A>G maps to NM_001135099.1 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr21:43795902 G>A maps to ENST00000380399 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr21:43803161 A>G maps to ENST00000380399 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:117985943 C>T maps to NM_019894.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:117982546 C>T maps to NM_019894.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:37462910 G>A maps to ENST00000381792 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:37462146 G>A maps to ENST00000381792 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:37482377 G>A maps to ENST00000381792 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:37499364 A>G maps to ENST00000381792 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:37482392 G>A maps to ENST00000381792 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr22:37462910 G>A maps to ENST00000381792 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:37491982 G>A maps to ENST00000381792 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr3:111799888 C>T maps to ENST00000443106 N818N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:111766640 G>A maps to ENST00000443106 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:111795815 C>T maps to ENST00000443106 H671H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:2405447 G>A maps to NM_182973.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:2422183 T>C maps to NM_182973.1 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr19:2403176 C>T maps to NM_182973.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:2399112 C>T maps to NM_182973.1 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:12994448 G>A did not map to a codon.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr12:29670472 A>G maps to NM_001193451.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:83526059 C>T maps to NM_152588.1 N801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:83250836 G>A maps to NM_152588.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:83379734 C>T maps to NM_152588.1 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr12:83250836 G>A maps to NM_152588.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:101287384 G>A maps to NM_032813.2 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr13:101266645 C>T maps to NM_032813.2 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr13:101278037 C>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:101287178 G>A maps to NM_032813.2 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:101288799 G>A maps to NM_032813.2 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr7:150779626 A>G maps to NM_031434.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:150779569 G>T maps to NM_031434.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:42267868 C>T maps to NM_001076674.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr14:51713860 C>T maps to NM_030755.4 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr14:51713848 G>A maps to NM_030755.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:57505490 C>A maps to NM_015959.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:66346762 T>C maps to NM_019022.3 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:66377366 C>T maps to NM_019022.3 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:7980389 C>T maps to NM_021156.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr9:117849382 G>A maps to NM_002160.2 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:117838693 T>C maps to NM_002160.2 Q945Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr9:117853060 C>T maps to NM_002160.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:117846647 C>T maps to NM_002160.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:117849316 G>A maps to NM_002160.2 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:117852870 C>A maps to NM_002160.2 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:117840405 G>A maps to NM_002160.2 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr9:117845083 A>G maps to NM_002160.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:117852841 T>C maps to NM_002160.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr9:117848974 G>T maps to NM_002160.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:117849199 G>A maps to NM_002160.2 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:117849112 G>A maps to NM_002160.2 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr9:117825394 C>T maps to NM_002160.2 T1278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:117849040 G>A maps to NM_002160.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:117844968 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:117849132 G>A maps to NM_002160.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:26669335 C>T maps to NM_021137.4 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr17:26667425 A>G maps to NM_021137.4 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:26666693 C>T maps to NM_021137.4 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr17:26667473 G>A maps to NM_021137.4 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr14:103600063 G>T maps to NM_006291.2 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr6:138196896 C>T maps to NM_006290.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:138196150 G>A maps to NM_006290.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:138201244 G>A maps to NM_006290.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:138200309 G>A maps to NM_006290.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:138201286 C>T maps to NM_006290.2 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:152220547 C>T maps to NM_007115.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:4651946 G>A maps to NM_152362.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:51350347 G>A maps to NM_207381.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr15:51350608 C>T maps to NM_207381.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:23058107 C>A maps to NM_003844.3 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr8:23057398 C>T maps to NM_003844.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:22900648 A>G did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:22972206 G>A maps to ENST00000356864 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:22969280 C>T maps to ENST00000356864 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:22995436 G>A maps to NM_003840.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:60036436 C>T maps to NM_003839.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr18:60021738 C>T maps to NM_003839.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr8:119945335 G>A maps to NM_002546.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr8:119938850 G>A maps to NM_002546.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr8:119941042 T>A maps to NM_002546.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:119938901 C>T maps to NM_002546.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:119936807 G>A maps to NM_002546.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr8:119945314 G>A maps to NM_002546.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:119945473 G>A maps to NM_002546.3 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr22:42321375 G>A maps to NM_052945.3 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:2493159 C>T maps to NM_003820.2 H200H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HU-8244-01A-11D-2340-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr13:24190109 C>T maps to NM_018647.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr13:24233282 C>T maps to NM_018647.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:6439830 A>G maps to NM_001065.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr12:6440067 C>T maps to NM_001065.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:12251951 C>T maps to NM_001066.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:12262064 C>T maps to NM_001066.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:12262148 G>A maps to NM_001066.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:6521664 G>T maps to ENST00000355862 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:6522201 G>A maps to ENST00000355862 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr20:62329756 G>A maps to NM_003823.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:12202467 T>C maps to NM_001243.3 H556H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:12202500 G>A maps to NM_001243.3 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:7993306 C>T maps to NM_001561.5 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr13:43175103 C>T maps to NM_003701.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr13:43180927 C>T maps to NM_003701.3 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr13:43180636 C>T maps to NM_003701.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:6669902 G>A maps to NM_003807.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr19:6665137 G>A maps to NM_003807.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr1:173010834 C>T maps to NM_005092.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:173176215 G>A maps to NM_003326.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:173155858 G>A maps to NM_003326.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:6535070 G>A maps to NM_003811.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr3:170805247 A>G maps to NM_015028.2 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:170784472 C>A maps to NM_015028.2 G1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:170857332 G>A maps to NM_015028.2 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:170801979 G>A maps to NM_015028.2 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr3:170857276 A>G maps to NM_015028.2 H467H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:170843726 G>A maps to NM_015028.2 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr5:150422225 C>A maps to NM_006058.3 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr5:150436491 G>A maps to NM_006058.3 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr5:150436497 A>G maps to NM_006058.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:150411907 G>A maps to NM_006058.3 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:2746453 C>T maps to NM_024309.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:2744178 G>A maps to NM_024309.3 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:122078293 G>A maps to ENST00000509841 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:7287071 G>A maps to NM_003985.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr17:7291746 A>G maps to NM_003985.3 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:195594642 G>A maps to NM_001010938.1 Y905Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:9634227 C>T maps to NM_003747.2 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:9413538 A>G maps to NM_003747.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:9562211 C>T maps to NM_003747.2 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:9609198 A>G maps to NM_003747.2 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:9623890 A>G maps to NM_003747.2 T1232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:9609294 C>T maps to NM_003747.2 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:9609123 C>T maps to NM_003747.2 D946D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:9437750 G>A maps to NM_003747.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:57076124 C>A maps to NM_033396.2 E1354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:57076650 A>G maps to NM_033396.2 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:57069611 A>G maps to NM_033396.2 P1590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr11:57080877 G>A maps to NM_033396.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:93609347 A>G maps to NM_025235.3 E897E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:93602098 A>G maps to NM_025235.3 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:93579760 T>C maps to NM_025235.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr10:93582082 T>G maps to NM_025235.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:93596679 T>C maps to NM_025235.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:99854132 G>A did not map to a codon.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr23:99854067 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:175046766 G>A maps to NM_022093.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4187-01A-01D-1126-08 chr1:175046730 C>T maps to NM_022093.1 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr1:175049335 G>A maps to NM_022093.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:175048796 C>T maps to NM_022093.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:175046770 T>C maps to NM_022093.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr1:175067561 C>T maps to NM_022093.1 Y650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr1:175048580 G>A maps to NM_022093.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:175086195 C>T maps to NM_022093.1 D747D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:175048556 C>T maps to NM_022093.1 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:175097761 C>T maps to NM_022093.1 C1070C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:175092539 T>C maps to NM_022093.1 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr1:175066622 G>A maps to NM_022093.1 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:175046697 C>T maps to NM_022093.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr1:175066550 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:52485812 G>A maps to NM_003280.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:52486161 A>G maps to NM_003280.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:201380607 C>T maps to ENST00000367312 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr1:201380577 G>A maps to ENST00000367312 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr19:55665448 G>A maps to ENST00000344887 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:55665462 G>T maps to ENST00000344887 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:55663273 C>T maps to ENST00000344887 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:74954889 T>G maps to NM_001112808.2 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr1:75009633 C>T maps to NM_001112808.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:201332435 A>G maps to ENST00000421663 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:11362891 A>G maps to NM_005425.4 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr5:72144270 G>A maps to NM_002270.3 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:72201191 T>C maps to NM_002270.3 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:72201158 C>T maps to NM_002270.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:72173152 A>G maps to NM_002270.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:12829854 G>A maps to NM_001136196.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:12830078 T>C maps to NM_001136196.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:12813688 C>T maps to NM_001136196.1 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:128610201 C>T maps to ENST00000471166 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:128619045 T>A maps to ENST00000471166 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:128645195 T>C maps to ENST00000471166 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:128630032 G>A maps to ENST00000471166 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr1:175324674 A>G maps to NM_003285.2 Y1071Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:175306813 T>C maps to NM_003285.2 G1128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr1:175325572 G>A maps to NM_003285.2 D1000D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:175334353 A>G maps to NM_003285.2 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:175325524 G>A maps to NM_003285.2 H1016H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:175372720 G>A maps to NM_003285.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr1:175293535 G>T maps to NM_003285.2 R1305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:175372558 G>A maps to NM_003285.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:175331847 G>A maps to NM_003285.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr1:175355351 G>T maps to NM_003285.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:175306747 C>A maps to NM_003285.2 G1150G. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr1:175324650 G>C does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr1:175355234 G>A maps to NM_003285.2 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr1:175365678 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr1:175332855 G>A maps to NM_003285.2 R899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:5396805 G>A maps to NM_001080495.2 P1645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:5352148 G>A maps to NM_001080495.2 F2791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:5410795 C>T maps to NM_001080495.2 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:5415826 C>T maps to NM_001080495.2 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr7:5410957 C>T maps to NM_001080495.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:5391705 G>A maps to NM_001080495.2 D1738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr7:5410912 G>A maps to NM_001080495.2 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:5347922 C>T maps to NM_001080495.2 S2907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:5352184 G>A maps to NM_001080495.2 A2779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:5347889 C>T maps to NM_001080495.2 S2918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:5348942 G>A maps to NM_001080495.2 G2815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr7:5348864 G>T maps to NM_001080495.2 I2841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr7:5410471 G>A maps to NM_001080495.2 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:24831652 G>A maps to NM_014494.2 W1758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:24788434 G>A maps to NM_014494.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr16:24802782 A>T maps to NM_014494.2 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:24834863 C>T maps to NM_014494.2 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:24815624 T>C maps to NM_014494.2 N1274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr22:40657920 C>T maps to ENST00000454349 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr22:40675997 G>A did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr22:40660881 C>T maps to ENST00000454349 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:76046099 C>T maps to NM_001142640.1 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:76083022 G>A maps to NM_001142640.1 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:76047110 G>T maps to NM_001142640.1 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:218669295 G>A maps to NM_022648.4 G1698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:218712548 C>T maps to NM_022648.4 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr2:218747128 G>A maps to NM_022648.4 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:218757702 C>T maps to NM_022648.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:218762538 T>C maps to NM_022648.4 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr2:218712773 C>T maps to NM_022648.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr2:218712302 A>C maps to NM_022648.4 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:218712866 C>T maps to NM_022648.4 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:218673323 A>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:218682830 G>A maps to NM_022648.4 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:218700767 G>A maps to NM_022648.4 I933I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:218713076 G>T maps to NM_022648.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:218683202 C>T maps to NM_022648.4 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:218674598 G>A maps to NM_022648.4 I1636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr2:218683457 C>T maps to NM_022648.4 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:218713673 T>C maps to NM_022648.4 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr2:218712302 A>C maps to NM_022648.4 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:47385796 C>T maps to NM_022748.11 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:47343040 G>A maps to NM_022748.11 F988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:47408172 C>T maps to NM_022748.11 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:47408193 G>A maps to NM_022748.11 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr7:47333331 G>A maps to NM_022748.11 F1257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:47440451 C>T maps to NM_022748.11 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:47341844 G>A maps to NM_022748.11 I1161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr7:47463778 G>A maps to NM_022748.11 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:47408880 G>T maps to NM_022748.11 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:47474966 C>T maps to NM_022748.11 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:47385877 C>T maps to NM_022748.11 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:47344500 C>T maps to NM_022748.11 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:47408745 C>T maps to NM_022748.11 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:38645086 G>A maps to NM_032865.5 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr17:38645215 T>A maps to NM_032865.5 K149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:32063526 G>A maps to ENST00000375244 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:32065870 T>C maps to ENST00000375244 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:32064255 G>A maps to ENST00000375244 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:32035684 C>A maps to ENST00000375244 G2099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr6:32020587 G>T maps to ENST00000375244 R2992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr6:32036743 G>A maps to ENST00000375244 D1919D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:32036821 C>T maps to ENST00000375244 T1893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:32023711 C>A maps to ENST00000375244 E2795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr6:32052313 G>A maps to ENST00000375244 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:32036212 G>A maps to ENST00000375244 F2058F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr6:32017047 C>T maps to ENST00000375244 T3252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr6:32049828 C>T maps to ENST00000375244 T1240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:32063939 G>A maps to ENST00000375244 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:32065795 G>A maps to ENST00000375244 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:32015706 C>A maps to ENST00000375244 T3376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:32037369 G>A maps to ENST00000375244 H1849H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8249-01A-11D-2340-08 chr6:32017143 G>A maps to ENST00000375244 T3220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:32065915 T>G maps to ENST00000375244 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr6:32029204 G>A maps to ENST00000375244 R2487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:32017098 G>A maps to ENST00000375244 Y3235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:32063931 G>A maps to ENST00000375244 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:32063460 G>A maps to ENST00000375244 C723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr17:48940664 C>T maps to NM_005749.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:41833201 G>A maps to NM_016272.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:45809250 T>C maps to NM_025077.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:45808126 G>A maps to NM_025077.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr11:1311590 G>A maps to ENST00000382211 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:35743187 C>T maps to ENST00000451197 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:35730402 G>A maps to ENST00000451197 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:17766052 C>T maps to NM_001082968.1 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr17:17797055 G>A maps to NM_001082968.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:17788063 G>A maps to NM_001082968.1 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:17764787 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:17764837 G>A maps to NM_001082968.1 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr1:235292024 C>G maps to NM_014765.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:235277208 G>A maps to NM_014765.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr20:43572150 C>T maps to NM_006809.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:45406320 G>A maps to NM_006114.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:45406423 T>C maps to NM_006114.2 *362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:161196287 C>T maps to NM_032174.4 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:100096644 C>T maps to NM_014820.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:39744079 G>A did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:39726978 T>C did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr20:39728845 C>T maps to NM_003286.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr8:144400004 C>T maps to NM_052963.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:144403475 G>A maps to NM_052963.1 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:144406744 G>A maps to NM_052963.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr8:144399935 G>A maps to NM_052963.1 N429N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr17:38562634 C>T did not map to a codon.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr17:38546402 G>C maps to ENST00000357601 T1464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:38556277 C>T maps to ENST00000357601 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:25665876 A>G maps to ENST00000264331 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:25641011 G>A maps to ENST00000264331 R1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:25674014 A>C maps to ENST00000264331 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:18205933 G>A maps to NM_004618.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:18205933 G>A maps to NM_004618.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:18181367 G>A maps to NM_004618.3 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:18211671 G>A maps to NM_004618.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:133375668 G>A maps to NM_007027.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:133320110 G>A maps to NM_007027.3 R1518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:133356833 G>A maps to NM_007027.3 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:133358932 A>G maps to NM_007027.3 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:133377883 G>A maps to NM_007027.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:133375668 G>A maps to NM_007027.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:32550786 C>T maps to NM_005802.4 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:32542035 T>C maps to NM_005802.4 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:32543960 G>A maps to NM_005802.4 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:32541438 C>T maps to NM_005802.4 S1028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:132584973 G>A maps to ENST00000437532 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr1:179873151 C>G maps to ENST00000398836 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr9:132571732 C>A maps to NM_014506.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr9:132569558 C>A maps to NM_014506.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:130496637 G>A maps to NM_001085347.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr9:130496679 C>A maps to NM_001085347.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:179063239 C>T maps to NM_022371.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:59728226 C>T maps to NM_014729.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:59728046 A>C maps to NM_014729.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr8:59750663 G>A maps to NM_014729.2 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr8:59750732 G>A maps to NM_014729.2 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:59764295 T>C maps to NM_014729.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:59727934 G>A maps to NM_014729.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:52484317 G>A maps to ENST00000407228 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr16:52473871 A>G maps to ENST00000407228 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr16:52473730 G>A maps to ENST00000407228 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:52479907 G>A maps to ENST00000407228 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr14:21960501 A>C maps to NM_014828.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:21955821 C>T maps to NM_014828.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr14:21955782 C>T maps to NM_014828.2 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:21957486 T>C maps to NM_014828.2 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr14:21957498 T>C maps to NM_014828.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:21957414 T>C maps to NM_014828.2 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr17:7578430 G>A maps to NM_001126112.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr17:7577155 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr17:7579310 C>T did not map to a codon.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr17:7579310 C>T did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr17:7579405 G>C maps to NM_001126112.1 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr17:7579311 C>G maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr17:7577496 A>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr17:7578452 G>C maps to NM_001126112.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr17:7578178 C>A maps to NM_001126112.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr17:7578374 G>A maps to NM_001126112.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr15:43784281 G>T maps to NM_001141980.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:43724631 A>G maps to NM_001141980.1 S1145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr15:43701940 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:43714074 G>A maps to NM_001141980.1 R1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:223971920 C>A maps to NM_001031685.2 G1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:223976851 T>C maps to NM_001031685.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:223984002 C>T maps to NM_001031685.2 E746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:44958447 C>T maps to NM_006034.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:27898872 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:44003969 A>C maps to NM_014477.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr3:189612027 C>T maps to NM_003722.4 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:189349367 T>C did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr3:189584564 G>A maps to NM_003722.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:189526242 C>T maps to NM_003722.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:189526314 G>A maps to NM_003722.4 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:189597918 C>T maps to NM_001114979.1 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr1:3638706 G>A maps to NM_005427.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr1:3638767 G>T maps to NM_005427.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr1:3638721 C>T maps to NM_005427.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:3646620 C>T maps to NM_005427.2 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:3644759 C>T maps to NM_005427.2 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr6:83074848 G>A maps to NM_006670.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:68822753 C>A maps to NM_139075.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr8:80954872 T>C maps to NM_001025252.1 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr6:125550287 C>T maps to NM_003287.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr20:62500697 G>A maps to NM_199360.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr20:62520578 T>C maps to NM_199360.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr11:18062240 G>C maps to ENST00000341556 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr12:72332846 G>A maps to ENST00000389376 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:72335392 C>T maps to ENST00000389376 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr12:72416244 G>T maps to ENST00000389376 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:6979534 T>C maps to NM_001159287.1 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr7:144463011 G>A maps to NM_022445.3 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:63353933 G>T maps to ENST00000357980 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:63336324 G>T maps to ENST00000357980 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:35689706 G>A maps to ENST00000329305 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:35685135 G>A maps to NM_213674.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:35685729 C>T maps to ENST00000329305 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:154145589 A>G maps to NM_001043351.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:18148085 A>G maps to NM_000367.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:1480976 G>A maps to NM_000547.5 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:1418198 C>T maps to NM_000547.5 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:1437320 A>G maps to NM_000547.5 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:1418191 C>G maps to NM_000547.5 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:1491614 A>G maps to NM_000547.5 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:1544464 G>A maps to NM_000547.5 P906P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr2:1499797 C>T maps to NM_000547.5 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr2:1544473 C>T maps to NM_000547.5 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:1437208 G>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr2:1481015 G>A maps to NM_000547.5 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:1418178 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:1491734 G>A maps to NM_000547.5 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:6638382 C>T maps to ENST00000453338 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IZ-01A-32D-A25D-08 chr11:6637937 C>G maps to ENST00000453338 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:6638583 C>T maps to ENST00000453338 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr11:6638270 G>A maps to ENST00000453338 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr13:103282503 A>G maps to ENST00000376052 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr13:103295690 G>T maps to ENST00000376052 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:103286305 C>T maps to ENST00000376052 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:103257198 C>T maps to ENST00000376052 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:103292683 C>T maps to ENST00000376052 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr5:665396 C>A maps to NM_007030.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:666084 C>A maps to NM_007030.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr5:677911 G>C maps to NM_007030.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr16:67424888 G>A maps to NM_016140.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:186305775 C>T maps to NM_003292.2 V1519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:186304583 A>G maps to NM_003292.2 I1599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:186302449 A>C maps to NM_003292.2 P1753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:186300650 A>G maps to NM_003292.2 D1889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:186325511 C>T maps to NM_003292.2 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr1:186310499 G>A maps to NM_003292.2 Q1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:186301401 T>C maps to NM_003292.2 S1843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr1:186340107 G>A maps to NM_003292.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:186302467 G>A maps to NM_003292.2 S1747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:127292483 C>T maps to NM_001136053.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:127295856 C>T maps to NM_001136053.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:188925187 G>T maps to NM_198485.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:3544201 A>G maps to NM_182752.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:3545082 C>T maps to NM_182752.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:73957864 T>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:73961663 G>A maps to ENST00000409716 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:140093981 G>A maps to NM_001128228.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:140087029 C>T maps to NM_001128228.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr9:140094140 C>A maps to NM_001128228.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr16:1306980 G>A maps to NM_012217.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:1306673 G>A maps to NM_012217.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:1306688 G>A did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr16:1306317 C>T maps to NM_012217.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr16:1308364 G>C maps to NM_012217.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr16:1272742 C>G maps to NM_012467.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:1273478 G>A maps to NM_012467.3 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:1272024 A>G maps to NM_012467.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:26937371 G>A maps to NM_003595.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr22:26932451 C>T maps to NM_003595.3 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:26937533 C>T maps to NM_003595.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:26937080 C>T maps to NM_003595.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr13:45914127 C>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:10942994 G>A maps to NM_199261.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr21:10942729 T>G maps to NM_199261.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:10951414 A>C maps to NM_199261.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr21:10951270 T>C maps to NM_199261.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr21:10934994 T>C maps to NM_199261.2 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr21:10951263 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:10916385 A>G maps to NM_199261.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr21:10941946 T>C maps to NM_199261.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr21:10969091 C>T maps to NM_199261.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr21:10934966 G>A maps to NM_199261.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr21:10941928 A>C maps to NM_199261.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr21:10906910 G>A maps to NM_199261.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr13:19999106 C>G maps to NM_199254.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr13:20048103 A>G maps to NM_199254.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr20:30345299 T>G maps to ENST00000340513 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:30370193 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:30359470 T>C maps to ENST00000340513 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:30381658 C>T maps to ENST00000340513 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr20:30370127 T>C maps to ENST00000340513 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr7:23547124 C>T maps to NM_013293.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:23545391 G>A maps to NM_013293.3 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:50635770 C>A maps to NM_025204.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:50633391 C>T maps to NM_025204.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:50636356 C>T maps to NM_025204.2 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr16:67189148 G>A maps to NM_003789.3 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:123671570 C>T maps to NM_001190945.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr9:123675800 G>A maps to NM_001190945.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:123686063 G>A maps to NM_001190945.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr9:139820132 A>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:139814795 C>T maps to ENST00000359662 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:139814906 C>A maps to ENST00000359662 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:103372096 T>C maps to NM_145725.2 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr14:103371926 C>T maps to NM_145725.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr14:103338277 G>A maps to NM_145725.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:239306239 C>T maps to NM_015650.3 D610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:239237440 G>T maps to NM_015650.3 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:111912542 C>T maps to ENST00000340026 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:111896927 C>T maps to ENST00000340026 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:111884185 G>A maps to ENST00000340026 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:209955412 C>T maps to NM_025228.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:209936185 A>C maps to NM_025228.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:27076099 T>C maps to NM_004295.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:211546013 C>T maps to ENST00000427925 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:211526724 C>T maps to ENST00000427925 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr11:36511801 G>A maps to NM_145803.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr11:36511399 A>G maps to NM_145803.1 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:2222337 C>T maps to NM_032271.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr16:2226123 C>T maps to NM_032271.2 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:2215905 C>T maps to NM_032271.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:2226330 G>A maps to NM_032271.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr12:112587665 A>T maps to NM_006700.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:49879889 C>A maps to NM_005879.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:49866634 T>C maps to NM_005879.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:49869389 G>A maps to NM_005879.2 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:42240733 T>C maps to NM_001042646.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:42264628 C>T maps to NM_001042646.1 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:42244236 G>A maps to NM_001042646.1 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:42166996 C>T maps to NM_001042646.1 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:42244032 G>A maps to NM_001042646.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:42251454 A>C maps to NM_001042646.1 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr3:42240697 G>A maps to NM_001042646.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:42244182 C>T maps to NM_001042646.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:202257732 C>A maps to NM_015049.2 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:71495949 G>A maps to NM_014294.5 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr8:71510487 C>A maps to NM_014294.5 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:118005712 C>T maps to NM_152402.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr4:118006000 G>C maps to NM_152402.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:118005619 G>A maps to NM_152402.2 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:118005712 C>T maps to NM_152402.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr3:36898083 G>A maps to NM_014831.2 D999D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:36893683 G>A maps to NM_014831.2 R1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:36874328 C>A maps to NM_014831.2 E2205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr3:36896946 C>T maps to NM_014831.2 S1378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:36887886 G>A maps to NM_014831.2 N1637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:36872547 G>A maps to NM_014831.2 H2798H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:36873741 T>C maps to NM_014831.2 P2400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr3:36887886 G>A maps to NM_014831.2 N1637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:36897722 C>A maps to NM_014831.2 G1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:36899406 G>A maps to NM_014831.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr3:36872532 C>T maps to NM_014831.2 P2803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr16:3714316 C>T maps to NM_016292.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:3740885 G>A maps to NM_016292.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr16:3739121 A>G maps to NM_016292.2 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:3713497 C>T maps to NM_016292.2 K545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:3714424 C>T maps to NM_016292.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:7834328 C>T maps to NM_001166621.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:7834357 G>A maps to NM_001166621.1 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:7834013 C>T maps to NM_001166621.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr21:45511890 C>T maps to NM_003274.4 T986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr21:45499967 G>A maps to NM_003274.4 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr21:45507598 G>A maps to NM_003274.4 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:45511869 T>C maps to NM_003274.4 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr1:36603532 C>T maps to NM_014408.3 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:7747585 G>A maps to NM_001042461.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:141461466 G>A maps to NM_031466.5 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:141461250 G>A maps to NM_031466.5 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:141461073 A>T maps to NM_031466.5 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:141297704 A>G did not map to a codon.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr6:123786069 C>T maps to NM_006073.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:118529108 C>A maps to ENST00000264029 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:41126728 C>T maps to NM_018965.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr6:41162571 C>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:41162311 G>A maps to ENST00000373108 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:42227308 G>A maps to NM_033502.2 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr6:42231246 C>T maps to NM_033502.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:42227275 C>T maps to NM_033502.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:42196139 G>A maps to NM_033502.2 T1182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:152710779 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:152710794 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:129695920 T>C maps to NM_007117.3 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:129695848 G>A maps to NM_007117.3 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:72863685 T>C maps to NM_013381.2 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:72667256 G>A maps to NM_013381.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr12:72956766 T>C maps to NM_013381.2 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr12:72969050 T>C maps to NM_013381.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:73014964 T>A maps to NM_013381.2 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr12:73046209 T>C maps to NM_013381.2 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr12:72863562 G>A maps to NM_013381.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr12:72666935 G>A maps to NM_013381.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:110100046 T>G maps to NM_003301.4 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:110099785 G>A maps to NM_003301.4 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr8:110100334 C>A maps to NM_003301.4 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:110100430 C>T maps to NM_003301.4 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:126448361 C>A maps to NM_025195.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:12863636 G>A maps to NM_021643.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr2:12880832 G>A maps to NM_021643.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:12863669 C>T maps to NM_021643.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr2:12880541 C>T maps to NM_021643.3 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr20:372100 C>A maps to ENST00000422053 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr20:372118 C>T maps to ENST00000422053 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:30122213 G>A maps to NM_006778.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:30121850 A>C maps to NM_006778.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:30121843 G>A maps to NM_006778.3 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:100854203 C>T maps to NM_033219.1 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:30139990 C>T maps to NM_033229.2 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr6:30131742 C>T maps to NM_033229.2 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr17:15539379 C>T maps to ENST00000455584 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:18630983 C>T maps to NM_001037330.1 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:18638406 C>T maps to NM_001037330.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr17:18631040 G>A maps to NM_001037330.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr17:18631019 G>A maps to NM_001037330.1 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr1:228598775 C>T maps to NM_016102.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:154216754 C>T maps to NM_015271.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr4:154191515 C>A maps to NM_015271.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:154191515 C>A maps to NM_015271.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr4:154191515 C>A maps to NM_015271.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr4:154197233 T>G maps to NM_015271.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr11:4406670 A>G maps to NM_003141.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr11:5730578 A>T maps to NM_006074.4 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:64887739 A>G maps to NM_001656.3 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:64909975 C>T maps to NM_001656.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:138210039 A>G maps to NM_015905.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:138189059 C>T maps to NM_015905.2 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:138239680 G>A maps to NM_015905.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr17:54981776 C>A maps to NM_005082.4 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr17:54981759 C>T maps to NM_005082.4 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:54969486 C>T maps to NM_005082.4 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr17:54981615 C>T maps to NM_005082.4 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:54969105 C>T maps to NM_005082.4 W616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:54990911 C>T maps to NM_005082.4 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:30166570 G>A maps to NM_003449.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:30154087 C>T maps to NM_003449.3 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr6:30166570 G>A maps to NM_003449.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:30166871 C>A maps to NM_003449.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:30153691 C>T maps to NM_003449.3 W527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr6:28887842 G>A maps to NM_006510.4 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:59057201 G>A maps to NM_005762.2 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:59060483 C>T maps to NM_005762.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:120008517 C>T maps to NM_012101.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:6472625 G>A maps to NM_033278.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:6477740 G>A maps to NM_033278.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:6471804 C>T maps to NM_033278.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr11:6478558 G>A maps to NM_033278.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr6:30079498 G>A maps to NM_007028.3 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:30080570 C>T maps to NM_007028.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr6:30073010 G>A maps to NM_007028.3 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:119460782 G>A maps to NM_012210.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr9:119461124 A>T maps to NM_012210.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:114967377 C>T did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:5656042 C>T maps to NM_001003819.3 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr11:5653908 C>A maps to NM_001003819.3 C470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:27145378 G>A maps to NM_171982.3 H390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:27145309 C>T maps to NM_171982.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:27146720 G>A maps to NM_171982.3 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:27145135 G>A maps to NM_171982.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:27145237 G>A maps to NM_171982.3 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:27145435 G>A maps to NM_171982.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr8:27145132 G>A maps to NM_171982.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:27146780 C>A maps to NM_171982.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:27168383 G>A maps to NM_171982.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:114462532 A>G maps to NM_018700.3 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:114472804 C>A maps to NM_018700.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:57126582 C>A maps to NM_015294.3 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:57158517 A>G maps to NM_015294.3 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:57134369 A>G maps to NM_015294.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:57126657 G>A maps to NM_015294.3 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr17:57109275 A>T maps to NM_015294.3 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr6:25969608 G>A maps to NM_006355.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:25966794 C>A maps to NM_006355.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:30297301 C>T maps to NM_021253.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr6:30309798 A>G maps to NM_021253.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:30308350 T>C maps to NM_021253.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr5:180661378 G>A maps to NM_033549.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:140401501 C>T maps to NM_152616.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr3:140407104 C>T maps to NM_152616.4 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr3:140401462 G>A maps to NM_152616.4 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:35684865 G>A maps to NM_017583.4 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:117659353 G>A maps to NM_025188.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:155147962 C>A maps to NM_025058.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:155156380 G>A maps to NM_025058.3 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:155154562 C>T maps to NM_025058.3 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:155152111 T>C maps to NM_025058.3 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:155156329 G>A maps to NM_025058.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr17:73871175 G>A maps to NM_033452.2 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:73871508 A>G maps to NM_033452.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:55033086 A>G maps to ENST00000357530 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr11:55032399 A>G maps to ENST00000357530 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr11:89531651 A>T maps to NM_020358.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:5699618 G>A maps to NM_033034.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr11:5686757 G>A maps to NM_033092.2 H341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:5686299 T>G maps to NM_033034.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:5701380 T>C maps to NM_033034.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:72738500 C>T maps to NM_178125.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr7:72734220 G>T maps to NM_178125.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:72733042 C>T maps to NM_178125.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:180687727 G>A maps to NM_032765.2 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr5:180687439 T>C maps to NM_032765.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:27505616 T>G maps to NM_032546.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:27528558 A>G maps to NM_032546.3 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:27529182 G>A maps to NM_032546.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:67039508 C>T maps to NM_184085.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr8:67049352 C>T maps to NM_184085.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:67047353 G>A maps to NM_184085.1 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:67039508 C>T maps to NM_184085.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr7:100732368 C>T maps to NM_030961.1 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr1:248020712 C>T maps to NM_015431.3 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:248039616 T>C maps to NM_015431.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:248020688 G>A maps to NM_015431.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr1:248028116 A>G maps to NM_015431.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:160156197 G>A maps to ENST00000483754 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr11:5629606 G>A maps to NM_001003819.3 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr11:5632277 T>G maps to ENST00000380109 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr4:165962339 T>A maps to NM_152620.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:165961349 A>G maps to NM_152620.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:165962585 T>C maps to NM_152620.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr4:165962193 C>T maps to NM_152620.2 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:33612783 G>A maps to NM_018207.2 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:33612804 C>T maps to NM_018207.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr1:33623902 G>A maps to NM_018207.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:33625512 G>A maps to NM_018207.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:33646802 G>A maps to NM_018207.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:26385069 G>A maps to NM_032588.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:26384892 G>T maps to NM_032588.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:26387825 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr1:26380446 C>A maps to NM_032588.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr17:73888349 G>A maps to NM_173547.2 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:231337126 C>T maps to NM_001004342.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:231344780 C>T maps to NM_001004342.3 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:4621604 G>T maps to NM_018073.5 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:45059667 C>A maps to NM_182985.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:180622450 G>A maps to NM_203293.1 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr5:180622402 C>T maps to NM_203293.1 W433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:180622612 G>A maps to NM_203293.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:32932495 T>C maps to NM_001039111.1 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:32915307 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:32859685 G>A maps to NM_001039111.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:32932738 G>A maps to NM_001039111.1 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:32859643 G>A maps to NM_001039111.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:32932816 G>A maps to NM_001039111.1 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr3:32932135 C>T maps to NM_001039111.1 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr3:32860360 G>A maps to NM_001039111.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:32932741 C>T maps to NM_001039111.1 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:31235535 G>A maps to NM_001008274.3 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:31232240 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:31236012 G>A maps to NM_001008274.3 W457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr10:104416987 C>T maps to NM_030912.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:104416969 G>A maps to NM_030912.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:51560868 G>A maps to ENST00000338969 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:51561102 G>A maps to ENST00000338969 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr14:51448528 C>T maps to ENST00000338969 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:51561492 G>A maps to ENST00000338969 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr14:51561330 C>T maps to ENST00000338969 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr14:51467487 C>T maps to ENST00000338969 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr14:51467556 A>C maps to NM_015163.5 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr14:51477194 G>A maps to ENST00000338969 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr14:51467457 C>T maps to ENST00000338969 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:51464798 G>A maps to ENST00000338969 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr4:189068024 G>A maps to NM_178556.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:189061098 C>T maps to NM_178556.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:189060813 C>T maps to NM_178556.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr4:189012856 C>T maps to ENST00000326754 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr4:189012826 T>C maps to ENST00000326754 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:189026086 C>A did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:14504648 C>T maps to NM_007118.2 V2853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr5:14363854 C>T maps to NM_007118.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr5:14504648 C>T maps to NM_007118.2 V2853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:14461389 G>A maps to NM_007118.2 A1822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:14462880 C>T maps to NM_007118.2 G1838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:14364894 G>A maps to NM_007118.2 Q908Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:14363929 C>T maps to NM_007118.2 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr5:14406051 C>G maps to NM_007118.2 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr5:14488284 C>T maps to NM_007118.2 H2516H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr5:14359555 G>A maps to NM_007118.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr5:14487618 C>G maps to NM_007118.2 G2294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:14504591 C>G maps to NM_007118.2 R2834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:14280524 C>A maps to NM_007118.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:14381307 C>T maps to NM_007118.2 Q1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:14366988 C>T maps to NM_007118.2 N925N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr22:38130974 G>A maps to NM_001039141.2 A1544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr22:38120423 C>T maps to NM_001039141.2 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr22:38130722 G>A maps to NM_001039141.2 W1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr22:38120198 C>T maps to NM_001039141.2 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:38165161 C>T maps to NM_001039141.2 Q2235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:38120704 C>A maps to NM_001039141.2 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr22:38121667 C>T maps to NM_001039141.2 H1035H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:38120783 C>T maps to NM_001039141.2 R741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr22:38122363 G>A maps to NM_001039141.2 R1267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:6743083 C>T maps to ENST00000313244 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr14:92488049 G>A maps to NM_004239.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:92472434 G>A maps to NM_004239.3 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:230633987 C>T maps to ENST00000389044 L1927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:230659896 G>A maps to ENST00000389044 G1295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:230655843 C>T maps to ENST00000389044 W1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:230633978 G>A maps to ENST00000389044 C1930C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:230664070 G>A maps to ENST00000389044 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:230678583 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:230668809 C>T maps to ENST00000389044 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:916036 C>T maps to NM_004237.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:64687595 G>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr15:64717781 C>T maps to NM_016213.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:100470350 C>T maps to NM_003302.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr1:40307583 C>T maps to ENST00000316891 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:13223782 G>A maps to NM_001136035.2 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:13226507 G>A maps to NM_001136035.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:13218413 C>T maps to NM_001136035.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:13223557 G>A maps to NM_001136035.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:126319757 T>G maps to NM_001031712.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr11:64084798 G>A maps to NM_016404.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:125463341 G>A maps to NM_017956.3 A58A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4257-01A-01D-1126-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-4280-01A-01D-1126-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr22:20100087 A>C maps to ENST00000439169 *644E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-7901-01A-11D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr22:20103937 T>C maps to ENST00000432879 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:20100979 G>A maps to ENST00000439169 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr22:20100531 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:100297066 C>A did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:100278520 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100292923 G>A did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:100274337 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:100292923 G>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:100292966 A>G did not map to a codon.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr23:100274307 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:100277015 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:100297269 G>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr14:61446284 G>A maps to NM_020810.2 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr14:61446377 G>A maps to NM_020810.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr14:61446528 C>T maps to NM_020810.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:5922652 C>T maps to NM_015939.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr20:5930952 C>T maps to NM_015939.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr14:103996626 C>A maps to ENST00000299201 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:29083986 G>A maps to NM_017910.3 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr22:46742424 G>A maps to NM_018006.4 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:54949722 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:54949811 G>A did not map to a codon.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr23:54956239 G>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:54957359 C>T did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:54956888 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:54955518 A>G did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:54955601 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:54955367 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:54955547 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:54955212 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:54949890 G>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:54955295 A>C did not map to a codon.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr23:54953053 C>A did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:54949398 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:54957417 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:54956699 T>C did not map to a codon.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr23:54956443 A>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:54951443 A>G did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr23:54950961 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:54949008 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:54949189 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:54953051 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr23:54950058 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:54952110 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr23:54949374 A>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:49719531 T>C maps to NM_005480.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:49722990 G>A maps to NM_005480.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr12:49719628 C>T maps to NM_005480.3 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:49719341 A>G maps to NM_005480.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:193045116 G>T maps to NM_004600.5 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:193051377 T>C maps to NM_004600.5 C422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:193051753 T>C maps to NM_004600.5 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr1:193045045 T>G maps to NM_004600.5 L226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr8:72973966 A>G maps to NM_007332.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:72968042 A>G maps to NM_007332.2 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:72946563 T>C maps to NM_007332.2 K868K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:72950277 A>G maps to NM_007332.2 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:72973945 C>T maps to NM_007332.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr8:72959381 C>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:72950231 G>A maps to NM_007332.2 Q791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:72969970 T>C maps to NM_007332.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr8:72975179 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:72964967 G>A maps to NM_007332.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr8:72950286 A>T maps to NM_007332.2 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr8:72971669 A>T maps to NM_007332.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr8:72966068 C>T maps to NM_007332.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr8:72984021 G>T maps to NM_007332.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:72967982 G>A maps to NM_007332.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:142467293 G>A maps to ENST00000476941 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr3:142467218 A>T maps to ENST00000476941 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:122853626 C>T maps to NM_001130698.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr4:122800955 C>A maps to NM_001130698.1 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr4:122853758 G>A maps to NM_001130698.1 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr4:122831495 C>T maps to NM_001130698.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:122831396 C>T maps to NM_001130698.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A663-01A-11D-A31L-08 chr4:122853758 G>A maps to NM_001130698.1 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:122833041 G>T maps to NM_001130698.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr13:38357090 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:38357395 T>C maps to NM_003306.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr13:38229239 A>T maps to NM_003306.1 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr13:38229233 T>C maps to NM_003306.1 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr13:38357278 A>G maps to NM_003306.1 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr20:33591320 C>T maps to NM_015638.2 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:33593525 G>A maps to NM_015638.2 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:33592317 C>T maps to NM_015638.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:111155718 C>G did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:111090439 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:111095588 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:111155754 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:111019869 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:111195482 C>T did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr23:111155769 T>G did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:111022218 A>C did not map to a codon.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr23:111155846 C>T did not map to a codon.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr23:111155644 T>G did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:111022244 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:111195318 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:111078167 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:111155847 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:111195334 C>T did not map to a codon.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr23:111195327 T>G did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:111020003 G>A did not map to a codon.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr23:111078193 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:111155846 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr23:111020034 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:111090506 C>T did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:111195327 T>G did not map to a codon.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr23:111019599 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:101374853 A>G maps to NM_004621.5 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:101375464 A>G maps to NM_004621.5 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:101375455 G>A maps to NM_004621.5 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:101359688 G>A maps to NM_004621.5 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr11:101362340 G>A maps to NM_004621.5 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:101374811 C>A maps to NM_004621.5 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr5:135692642 C>A maps to NM_020389.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:31358306 C>T maps to NM_002420.4 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:31332389 G>T maps to NM_002420.4 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr15:31355373 G>A maps to NM_002420.4 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr15:31334371 G>A maps to NM_002420.4 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:31352770 G>T maps to NM_002420.4 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr15:31332425 G>A maps to NM_002420.4 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr15:31295125 G>A maps to NM_002420.4 I1237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:31320617 G>A maps to NM_002420.4 G1048G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr15:31341634 G>A maps to NM_002420.4 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:31320575 G>A maps to NM_002420.4 V1062V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:31355442 G>A maps to NM_002420.4 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:31355361 C>T maps to NM_002420.4 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr15:31329940 C>T maps to NM_002420.4 A826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr15:31320629 G>C maps to NM_002420.4 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr21:45811267 C>T maps to ENST00000397932 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr21:45859041 C>T maps to ENST00000397932 C1470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr21:45833789 G>A maps to ENST00000397932 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr21:45820245 C>T maps to ENST00000397932 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr21:45811231 C>T maps to ENST00000397932 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr21:45833813 C>T maps to ENST00000397932 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr21:45833837 C>A maps to ENST00000397932 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr21:45811282 C>T maps to ENST00000397932 Y523Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr21:45789216 C>T maps to ENST00000397932 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr21:45815349 C>A maps to ENST00000397932 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr21:45855097 G>A maps to ENST00000397932 T1403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr21:45838402 G>A maps to ENST00000397932 Q1142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr21:45861582 C>T maps to ENST00000397932 H1515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr9:73167766 G>A maps to ENST00000419692 Y1143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:73213555 G>A maps to ENST00000419692 Q897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr9:73240172 A>C maps to ENST00000419692 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr9:73477847 T>A maps to ENST00000419692 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:73152134 C>T maps to ENST00000419692 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr9:73167807 G>A maps to ENST00000419692 R1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:73151633 T>C maps to ENST00000419692 R1419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:73213484 G>A maps to ENST00000419692 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:73151090 G>A maps to ENST00000419692 R1600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr9:73151246 G>A maps to ENST00000419692 C1548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr9:73442844 G>A maps to ENST00000419692 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:73152122 C>T maps to ENST00000419692 T1256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr9:73442844 G>A maps to ENST00000419692 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr9:73230948 C>A maps to ENST00000419692 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:49674944 T>C maps to NM_017636.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:49685881 G>T maps to NM_017636.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr19:49705383 C>T maps to NM_017636.3 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:49692269 G>A maps to NM_017636.3 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:49703690 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:49674845 C>T maps to NM_017636.3 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr19:49671853 C>T maps to NM_017636.3 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F5-01A-12D-A33T-08 chr19:49686348 G>A maps to NM_017636.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:49686363 G>A maps to NM_017636.3 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr19:49684718 G>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:2436250 C>T maps to ENST00000452833 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr11:2436671 G>A maps to ENST00000452833 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:77415328 C>T maps to NM_017662.4 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:77418751 C>T maps to NM_017662.4 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:77377202 C>A maps to NM_017662.4 E1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:77457093 G>T maps to NM_017662.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr9:77411800 T>A maps to NM_017662.4 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:50878622 A>G maps to NM_017672.4 C1484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr15:50899394 A>G did not map to a codon.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr15:50902159 T>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:50905918 C>T maps to NM_017672.4 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr15:50885863 A>G maps to NM_017672.4 D1186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:50884705 C>T maps to NM_017672.4 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:234851359 C>A maps to NM_024080.4 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr2:234869688 C>T maps to NM_024080.4 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:234835262 C>T maps to NM_024080.4 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:234854618 C>T maps to NM_024080.4 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:234846107 C>T maps to NM_024080.4 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:234873390 C>A maps to NM_024080.4 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:116426262 T>C maps to NM_014112.2 K1291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:116426652 A>G maps to NM_014112.2 N1161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:116427197 G>A maps to NM_014112.2 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:116599383 G>A maps to NM_014112.2 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:116617109 T>C maps to NM_014112.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:116631922 G>A maps to NM_014112.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr8:116599424 C>A maps to NM_014112.2 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:116631975 C>A maps to NM_014112.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr8:116427157 A>C maps to NM_014112.2 L993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:116599542 G>A maps to NM_014112.2 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:116599389 C>T maps to NM_014112.2 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr8:116599449 C>A maps to NM_014112.2 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:116599269 C>T maps to NM_014112.2 S886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr8:116599581 C>T maps to NM_014112.2 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:116599311 G>A maps to NM_014112.2 G872G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:116616338 C>T maps to NM_014112.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr8:116599812 G>A maps to NM_014112.2 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:3470150 G>A maps to ENST00000399756 D837D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:3494384 C>T maps to ENST00000399756 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:3458105 G>C maps to ENST00000381913 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr17:3422076 G>A maps to ENST00000381913 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr12:110226432 G>A maps to NM_021625.4 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:110246173 G>A maps to NM_021625.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr12:110230483 C>T maps to NM_021625.4 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr12:110221547 G>A maps to NM_021625.4 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:110226264 G>T maps to NM_021625.4 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:110226518 G>A maps to NM_021625.4 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr12:110222175 C>T maps to NM_021625.4 K801K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:110236478 G>A maps to NM_021625.4 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr7:142609645 A>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:142622640 G>A maps to NM_019841.4 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:142625287 C>T maps to NM_019841.4 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr7:142574256 G>A maps to NM_018646.2 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:142571314 G>T maps to NM_018646.2 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:142574267 A>G maps to NM_018646.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6521-01A-11D-1800-08 chr7:142569460 C>T maps to NM_018646.2 *726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:98530902 C>A maps to ENST00000359863 R1298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:98609071 G>T maps to ENST00000359863 E3737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:98547351 C>T maps to ENST00000359863 R1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr10:116702489 C>T maps to NM_139169.4 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:135772973 G>T maps to NM_000368.4 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:135786002 G>A maps to NM_000368.4 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr9:135771816 G>A maps to NM_000368.4 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr9:135786041 G>T maps to NM_000368.4 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:135771921 C>T maps to NM_000368.4 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr16:2114385 C>T maps to NM_000548.3 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:2126083 C>A maps to NM_000548.3 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:2106664 C>T maps to NM_000548.3 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:2131647 G>A maps to NM_000548.3 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:2131668 G>A maps to NM_000548.3 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:2121605 C>A maps to NM_000548.3 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr16:2120491 G>A maps to NM_000548.3 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:2106226 G>A maps to NM_000548.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:2124373 G>A maps to NM_000548.3 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:2110687 C>T maps to NM_000548.3 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr13:45149754 C>T maps to NM_183422.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr3:150127811 G>C maps to NM_014779.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:150128714 T>C maps to NM_014779.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:150127427 G>T maps to NM_014779.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:106957918 G>T did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:106957905 A>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:106957755 G>A did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:106960003 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:107018612 C>T did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:106957912 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:107018463 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:106959927 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:12570414 C>T maps to NM_025265.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:12545180 C>T maps to NM_025265.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:54696166 C>T maps to NM_001077446.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr12:58180065 T>C maps to NM_001172696.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:18531131 A>T maps to NM_006292.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr2:99725895 G>A maps to NM_025244.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr2:99636756 C>T maps to NM_025244.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:130356600 G>A maps to NM_052933.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:130356561 C>T maps to NM_052933.2 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:81422083 C>T maps to NM_000369.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:81610525 G>A maps to NM_000369.2 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:81609784 C>T maps to NM_000369.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr14:81609865 G>A maps to NM_000369.2 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:72999578 G>A maps to NM_005786.4 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:72999866 C>T maps to NM_005786.4 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:72998528 C>T maps to NM_005786.4 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr18:72999536 C>T maps to NM_005786.4 N680N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:72998126 C>T maps to NM_005786.4 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:72999305 C>T maps to NM_005786.4 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr18:72997562 G>A maps to NM_005786.4 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr18:72998525 G>A maps to NM_005786.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:72999833 G>T maps to NM_005786.4 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:72999245 G>A maps to NM_005786.4 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr18:72999596 G>A maps to NM_005786.4 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr18:72998003 T>C maps to NM_005786.4 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:72997589 G>A maps to NM_005786.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:51870149 C>T maps to NM_173485.5 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr20:51871043 C>T maps to NM_173485.5 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:51872036 C>T maps to NM_173485.5 C680C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr20:51872837 T>G maps to NM_173485.5 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr20:51871799 G>A maps to NM_173485.5 K601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr20:51871967 G>A maps to NM_173485.5 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr20:51872222 G>A maps to NM_173485.5 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr20:51872906 G>A maps to NM_173485.5 E970E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr20:51872930 G>A maps to NM_173485.5 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:51872627 G>T maps to NM_173485.5 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr20:51871289 G>A maps to NM_173485.5 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr20:51871053 C>T maps to NM_173485.5 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:31769888 G>A maps to NM_020856.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:31769549 C>T maps to NM_020856.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:31769836 G>A maps to NM_020856.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr19:31767521 G>A maps to NM_020856.2 H1059H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr19:31768178 G>A maps to NM_020856.2 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:31769081 G>A maps to NM_020856.2 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr19:31769897 C>T maps to NM_020856.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:31767826 G>T maps to NM_020856.2 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr19:31769495 G>A maps to NM_020856.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:31768424 C>T maps to NM_020856.2 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr19:31767752 C>T maps to NM_020856.2 A982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr19:31767989 G>T maps to NM_020856.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:31768676 C>T maps to NM_020856.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:31769222 G>A maps to NM_020856.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr19:31768381 T>A maps to NM_020856.2 K773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:31769315 G>A maps to NM_020856.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr19:31770542 G>A maps to NM_020856.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:50249872 G>A maps to NM_021733.1 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:50265281 G>A maps to NM_021733.1 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:50247621 G>A maps to NM_021733.1 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:50249944 C>T maps to NM_021733.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:76507475 T>G maps to NM_015516.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:110409324 A>G maps to NM_033035.4 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr5:110407620 A>T maps to NM_033035.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr8:143425713 G>T maps to ENST00000445818 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:143425534 G>A maps to ENST00000445818 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr8:143425588 G>A maps to ENST00000445818 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:143425615 C>T maps to ENST00000445818 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:143310909 G>A maps to ENST00000445818 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr1:231678313 A>T maps to NM_005999.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:67861893 T>C maps to ENST00000339830 *713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr17:79612271 C>T maps to NM_031945.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:31135579 G>A maps to NM_001080509.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:120455797 A>G maps to NM_012338.3 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:16815912 C>T maps to NM_014399.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:16817464 C>T maps to NM_014399.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:82269184 C>T maps to NM_030927.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:115604797 C>T maps to NM_005725.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr15:77348190 C>T maps to NM_005724.5 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr12:58140370 G>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:99399868 G>A maps to NM_005723.3 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:99891686 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:99891681 G>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:38535093 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:38540529 G>A did not map to a codon.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr23:38420807 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:38420802 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:3388232 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr22:43558870 G>A maps to NM_000714.4 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr24:6115676 T>C did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr6:116599804 T>A maps to NM_003309.3 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr6:116600396 A>G maps to NM_003309.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:116599991 C>T maps to NM_003309.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:53113996 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:53112244 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:53114009 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:116574208 G>A maps to ENST00000368611 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:116573985 G>A maps to ENST00000368611 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:98289166 C>T maps to NM_033512.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:98289907 A>G maps to NM_033512.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:98289973 C>T maps to NM_033512.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:98290066 G>A maps to NM_033512.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr8:98289372 G>A maps to NM_033512.2 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:54483006 G>A maps to NM_001003937.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr2:54482766 C>T maps to NM_001003937.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr17:2235605 C>T maps to NM_018128.4 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr17:2236863 C>T maps to NM_018128.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:2237831 G>A maps to NM_018128.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:54470967 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:54470536 A>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:54470915 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr23:54470969 G>T did not map to a codon.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr2:3341899 G>A maps to ENST00000398659 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr2:3261131 G>A maps to ENST00000398659 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:2424405 C>T maps to NM_005706.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:2424090 G>A maps to NM_005706.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr11:2424471 G>A maps to NM_005706.2 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr11:2424219 C>T maps to NM_005706.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:112769927 G>A maps to NM_032028.3 G203G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4256-01A-01D-1126-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BR-4361-01A-01D-1158-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CD-A4MI-01A-21D-A25D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HU-A4GU-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:19119299 C>T maps to NM_053006.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:24676541 C>T maps to NM_001184739.1 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:19626061 G>A maps to NM_032037.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:19626212 G>A maps to NM_032037.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr19:19625816 G>A maps to NM_032037.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:19625897 G>A maps to NM_032037.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:19625900 C>T maps to NM_032037.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:19625627 G>A maps to NM_032037.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:19626125 G>A maps to NM_032037.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:19625930 C>T maps to NM_032037.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr22:37407214 G>A maps to NM_003312.4 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr22:37414491 C>T maps to NM_003312.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:144695701 C>A maps to NM_003313.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:144698769 C>T maps to NM_003313.3 W38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:144696577 G>A maps to NM_003313.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr9:100367773 G>C maps to NM_139246.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr9:100380086 G>T maps to NM_139246.4 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:43225665 G>A maps to NM_032538.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:43252029 G>A maps to NM_032538.1 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:43223578 C>G maps to NM_032538.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:43251420 C>T maps to NM_032538.1 N981N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:43252035 A>G maps to NM_032538.1 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:43251222 C>T maps to NM_032538.1 G915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:43226883 C>T maps to NM_032538.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:43222807 C>T maps to NM_032538.1 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr6:43251384 C>T maps to NM_032538.1 G969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr6:43230988 G>A maps to NM_032538.1 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr6:43227000 C>T maps to NM_032538.1 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:43120160 G>A maps to ENST00000263802 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr15:43038031 G>A maps to ENST00000263802 P1637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:43067377 C>T maps to ENST00000263802 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr15:43067922 T>C did not map to a codon.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr15:43044334 C>A maps to ENST00000263802 E1442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:43067848 G>A maps to ENST00000263802 C899C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:113210044 C>T maps to NM_017868.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr11:113235629 T>G maps to NM_017868.3 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr11:113187018 A>T maps to NM_017868.3 K14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr11:113222929 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr11:113220806 G>A maps to NM_017868.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:231061266 G>A maps to NM_024525.4 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:231081167 G>A maps to NM_024525.4 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:180321107 C>T maps to NM_133462.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr3:180322067 C>G maps to NM_133462.3 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr3:180324311 G>T maps to NM_133462.3 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:3469365 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:3481519 C>T maps to NM_016030.5 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr11:43428961 A>G maps to NM_018259.5 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:75051760 A>G maps to NM_145170.3 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:75051440 A>G maps to NM_145170.3 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr17:15909802 T>C maps to NM_017775.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:15928376 C>T maps to NM_017775.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr17:15902816 G>A maps to NM_017775.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:39179774 T>C maps to ENST00000301819 Y1239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:39174571 G>A maps to ENST00000301819 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr3:39166986 C>T maps to ENST00000301819 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:39162528 C>T maps to ENST00000301819 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:39162564 C>G maps to ENST00000301819 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:166758246 G>A maps to NM_024753.3 C914C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:166767930 A>G maps to NM_024753.3 N789N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:166767939 T>C maps to NM_024753.3 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:166747427 T>C maps to NM_024753.3 R1007R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:99740198 T>C maps to NM_022905.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:34845771 A>G maps to NM_144725.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:40093139 C>T maps to ENST00000377543 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:40107250 C>T maps to ENST00000377543 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr17:40094981 T>C maps to ENST00000377543 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr17:40107316 G>A maps to ENST00000377543 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:138832997 T>C maps to NM_024926.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:33002974 T>C maps to NM_017735.4 C569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:32889535 T>C did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr2:33007731 C>T maps to NM_017735.4 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:33036125 G>A maps to NM_017735.4 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:32958959 C>A maps to NM_017735.4 C433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr2:33002968 C>G maps to NM_017735.4 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr4:147788680 A>C maps to ENST00000513335 L311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr4:147755034 G>A maps to ENST00000513335 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr4:147628704 T>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr21:38498384 G>A maps to NM_003316.3 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr21:38538592 T>C maps to NM_003316.3 Y1359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr21:38462539 C>A maps to NM_003316.3 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr21:38573746 A>T maps to NM_003316.3 K1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:178482853 G>A maps to NM_152275.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:178483201 C>T maps to NM_152275.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:178482763 A>G maps to NM_152275.3 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:178483075 C>T maps to NM_152275.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:178416243 A>G maps to NM_152517.2 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr2:178417161 G>A maps to NM_152517.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:178416798 A>G maps to NM_152517.2 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:40716357 T>G maps to NM_012382.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:118399498 C>T maps to NM_001080441.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr11:118398292 C>T maps to NM_001080441.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr5:94872519 C>T did not map to a codon.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr5:94850561 T>C maps to NM_014639.3 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:94859445 T>C maps to NM_014639.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:94838699 C>T maps to NM_014639.3 E1075E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr22:46681139 C>T maps to NM_017931.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:51767381 G>A maps to ENST00000447632 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:15192691 C>A maps to NM_152574.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr9:15185373 G>A maps to NM_152574.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:21703855 G>A maps to NM_001135993.1 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:21708913 C>T maps to NM_001135993.1 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr1:55188387 C>T maps to NM_004623.4 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:55199345 G>A maps to NM_004623.4 W314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:47251449 C>T maps to ENST00000394850 D531D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HU-A4GN-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr14:91211165 G>A maps to NM_001010854.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:91282552 G>A maps to NM_001010854.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr14:91247166 G>A maps to NM_001010854.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr14:91077133 G>A maps to NM_001010854.1 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:91211186 A>G maps to NM_001010854.1 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr14:71109098 C>T maps to NM_015351.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:40724060 A>G maps to NM_152479.5 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:62496490 G>C maps to NM_173810.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:62496514 C>T maps to NM_173810.3 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:135251409 G>A maps to NM_007344.2 D870D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:135278106 G>A maps to NM_007344.2 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:135251547 G>A maps to NM_007344.2 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:135277149 G>A maps to NM_007344.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr1:117618399 C>T maps to NM_003594.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:117618231 T>C maps to NM_003594.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:80721601 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:80749998 T>C did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr6:80751870 T>C maps to NM_003318.4 H842H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:80723017 C>T maps to NM_003318.4 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr6:80741242 A>T maps to NM_003318.4 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:113277873 C>T maps to NM_153712.4 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:113286287 C>T maps to NM_153712.4 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr22:43442564 C>T maps to NM_012263.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:43460218 C>T maps to NM_012263.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr22:43447890 C>T maps to NM_012263.4 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:43447857 G>A maps to NM_012263.4 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr22:43442432 G>A maps to NM_012263.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:1120410 A>G maps to NM_001130045.1 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:1115537 T>C maps to NM_001130045.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:1115546 C>T maps to NM_001130045.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:1119314 G>A maps to NM_001130045.1 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:124751995 T>C maps to NM_001139442.1 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:124801572 G>A maps to NM_001139442.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:124751770 G>A maps to NM_001139442.1 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:124752031 G>A maps to NM_001139442.1 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr22:43576903 G>A maps to NM_015140.3 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr22:43567875 G>A maps to NM_015140.3 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr22:43570380 G>A maps to NM_015140.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr22:43570377 G>A maps to NM_015140.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:167753657 C>T maps to NM_031949.4 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr3:9877136 G>A maps to NM_001025930.3 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:219614015 C>T maps to NM_014640.4 R881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:219617635 C>T maps to NM_014640.4 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:219603187 G>A maps to NM_014640.4 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr14:76368502 G>A maps to NM_015072.4 G1253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr14:76368496 G>A maps to NM_015072.4 A1251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4462-01A-01D-1158-08 chr14:76147916 C>T maps to NM_015072.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr14:76249811 C>A maps to NM_015072.4 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:76135818 T>C maps to NM_015072.4 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:46847393 C>T maps to NM_001130918.1 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:46862564 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:84394846 G>A maps to NM_024686.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:84394886 A>G maps to NM_024686.4 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr1:84412919 A>G maps to NM_024686.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:84386821 G>A maps to NM_024686.4 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr1:84412913 G>A maps to NM_024686.4 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:84399299 C>T maps to NM_024686.4 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:50470405 G>A maps to NM_001080447.1 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr22:50470378 C>T maps to NM_001080447.1 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:50471776 G>A maps to NM_001080447.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr22:50485623 G>A maps to NM_001080447.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr20:30521648 C>T maps to NM_001008409.2 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:30526968 C>T maps to NM_001008409.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:179429561 A>G maps to NM_133378.4 D24531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:179434796 G>A maps to NM_133378.4 C22786C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr2:179665320 A>G maps to NM_133378.4 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:179411327 G>A maps to NM_133378.4 Y29041Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr2:179414980 A>G maps to NM_133378.4 F27960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr2:179441340 G>A maps to NM_133378.4 Y20642Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:179393093 G>A maps to NM_133378.4 R33194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:179498194 G>A maps to NM_133378.4 G11729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:179665161 G>A maps to NM_133378.4 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:179474046 T>A maps to NM_133378.4 G14762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:179483421 G>A maps to NM_133378.4 Q13051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:179667000 G>A maps to NM_133378.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:179422585 G>A maps to NM_133378.4 D26597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:179444664 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:179472566 G>A maps to NM_133378.4 A15081A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179412968 G>T maps to NM_133378.4 S28560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179414848 A>G maps to NM_133378.4 N28004N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179414977 G>A maps to NM_133378.4 G27961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179418785 T>C maps to NM_133378.4 L27116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179429030 A>C maps to NM_133378.4 S24708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179437139 G>A maps to NM_133378.4 C22005C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179437288 G>A maps to NM_133378.4 Q21956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179456052 T>C maps to NM_133378.4 S17565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179456446 T>C maps to NM_133378.4 L17465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179463328 T>C maps to NM_133378.4 A16437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179495655 G>A maps to NM_133378.4 L12109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179517021 A>G maps to NM_133378.4 P10626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179542933 C>T maps to NM_133378.4 V10060V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179544993 T>C maps to NM_133378.4 A9891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179571292 G>A maps to NM_133378.4 R8526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179578861 A>T maps to NM_133378.4 V7597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179578873 T>C maps to NM_133378.4 E7593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179592342 G>A maps to NM_133378.4 S5410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179594595 T>C maps to NM_133378.4 Q4884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179616244 C>A maps to ENST00000375038 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:179621294 T>C maps to NM_133437.3 A3465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr2:179437106 T>C maps to NM_133378.4 Q22016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:179427506 C>T maps to NM_133378.4 T25216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr2:179458568 T>C maps to NM_133378.4 P16918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:179501127 C>A maps to NM_133378.4 E11208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:179416765 A>T maps to NM_133378.4 P27719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:179439491 G>A maps to NM_133378.4 T21221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr2:179611316 T>C maps to ENST00000375038 V5272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:179430620 G>A maps to NM_133378.4 N24178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:179598398 C>T maps to NM_133378.4 T3995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:179606043 G>A maps to NM_133437.3 F3801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr2:179398444 T>C maps to NM_133378.4 K31731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr2:179407392 A>T maps to NM_133378.4 I29828I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr2:179398048 C>A maps to NM_133378.4 T31863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:179440721 G>A maps to NM_133378.4 T20811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr2:179419222 G>C maps to NM_133378.4 G27049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:179590651 C>T maps to NM_133378.4 R5555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr2:179398822 G>A maps to NM_133378.4 G31605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr2:179604776 G>A maps to NM_133437.3 L4224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:179407140 G>A maps to NM_133378.4 L29880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr2:179498050 G>A maps to NM_133378.4 R11749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr2:179452434 G>A maps to NM_133378.4 R18633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr2:179419222 G>C maps to NM_133378.4 G27049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:179424437 A>G maps to NM_133378.4 R26239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:179500702 G>A maps to NM_133378.4 C11297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr2:179634997 G>A maps to NM_133378.4 A2810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:179455635 C>T maps to NM_133378.4 P17704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr2:179421665 C>T maps to NM_133378.4 Q26837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr2:179647716 C>T maps to NM_133378.4 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179393422 G>A maps to NM_133378.4 I33117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179398238 A>C maps to NM_133378.4 L31800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179418746 T>C maps to NM_133378.4 G27129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179438978 G>A maps to NM_133378.4 I21392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179446660 G>T maps to NM_133378.4 S19577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179547582 C>A maps to NM_133378.4 E9735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179567307 G>T maps to NM_133378.4 S8858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179579256 G>A maps to NM_133378.4 V7504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179589095 G>T maps to NM_133378.4 I5758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179596149 C>T maps to NM_133378.4 E4537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179638811 T>C maps to NM_133378.4 G2361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:179647544 G>A maps to NM_133378.4 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr2:179485110 T>C maps to NM_133378.4 K12811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr2:179584365 G>A maps to NM_133378.4 A6707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr2:179600640 G>A maps to NM_133378.4 S3600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr2:179586748 A>C maps to NM_133378.4 T6303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr2:179452393 A>G maps to NM_133378.4 D18646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr2:179472998 T>C maps to NM_133378.4 G14969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr2:179473037 C>G maps to NM_133378.4 L14956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr2:179419222 G>C maps to NM_133378.4 G27049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:179498021 G>A maps to NM_133378.4 Y11758Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:179578855 C>T maps to NM_133378.4 T7599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr2:179640749 A>G maps to NM_133378.4 P1947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:179398977 C>A maps to NM_133378.4 G31554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:179404475 A>C maps to NM_133378.4 T30204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:179596092 A>G maps to NM_133378.4 Y4556Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:179466063 G>A maps to NM_133378.4 R15986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:179585804 G>A maps to NM_133378.4 S6403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr2:179638309 T>C maps to NM_133378.4 V2491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:179414546 C>A maps to NM_133378.4 G28066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:179422677 G>A maps to NM_133378.4 L26567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:179463685 T>C maps to NM_133378.4 T16349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:179474815 C>T did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:179569606 T>A maps to NM_133378.4 T8653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:179471745 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:179485916 T>C maps to NM_133378.4 L12608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:179599674 T>C maps to NM_133378.4 L3748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr2:179419405 C>T maps to NM_133378.4 R26988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr2:179579037 G>A maps to NM_133378.4 F7577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:179436697 G>A maps to NM_133378.4 L22153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:179500909 C>T maps to NM_133378.4 Q11228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr2:179543552 A>G maps to NM_133378.4 P10005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr2:179395549 T>C maps to NM_133378.4 V32696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr2:179597038 G>A maps to NM_133378.4 Q4309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:179395405 T>C maps to NM_133378.4 L32744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:179425760 A>G maps to NM_133378.4 V25798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:179440976 G>A maps to NM_133378.4 T20726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:179497271 A>G maps to NM_133378.4 S11919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:179616446 A>G maps to ENST00000375038 H3562H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:179484757 G>A maps to NM_133378.4 C12894C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:179590717 T>C maps to NM_133378.4 E5533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:179621108 T>A maps to NM_133437.3 A3527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:179669351 C>T maps to NM_133378.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr2:179456551 C>T maps to NM_133378.4 W17430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5732-01A-11D-1600-08 chr2:179654209 G>A maps to NM_133378.4 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr2:179594856 A>G maps to NM_133378.4 V4846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr2:179404631 G>A maps to NM_133378.4 G30152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr2:179613043 C>A maps to ENST00000375038 E4697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr2:179400403 G>C maps to NM_133378.4 V31078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr2:179583902 G>A maps to NM_133378.4 L6828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr2:179604390 T>C maps to NM_133437.3 E4352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8574-01A-13D-2340-08 chr2:179612558 T>C maps to ENST00000375038 E4858E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr2:179398460 G>T maps to NM_133378.4 S31726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr2:179587839 C>A maps to NM_133378.4 G6054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr2:179613893 T>C maps to ENST00000375038 Q4413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr2:179542888 T>C maps to NM_133378.4 T10075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr2:179604150 C>T maps to NM_133437.3 E4432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:179393908 T>C maps to NM_133378.4 Q32955Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:179437709 C>T maps to NM_133378.4 S21815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:179647123 A>G maps to NM_133378.4 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:179428618 G>A maps to NM_133378.4 R24846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:179480515 C>A did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr2:179483530 G>A maps to NM_133378.4 G13014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr2:179424094 C>A maps to NM_133378.4 E26354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:179501175 A>G maps to NM_133378.4 L11192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:179413213 G>A maps to NM_133378.4 R28479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:179501200 G>A maps to NM_133378.4 S11183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr2:179464439 C>A maps to NM_133378.4 E16162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:179478830 A>G maps to NM_133378.4 Y13863Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:179544075 C>T maps to NM_133378.4 P10000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr2:179615030 T>C maps to ENST00000375038 K4034K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:179409150 G>A maps to NM_133378.4 Y29367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:179410268 A>C maps to NM_133378.4 R29288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:179433560 T>C maps to NM_133378.4 E23198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:179650793 G>T maps to NM_133378.4 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:179666973 G>A maps to NM_133378.4 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:179669303 G>A maps to NM_133378.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr2:179393869 G>C maps to NM_133378.4 V32968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:179433098 G>A maps to NM_133378.4 G23352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:179479339 G>A maps to NM_133378.4 Q13733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr2:179416513 C>T maps to NM_133378.4 W27803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr2:179444696 G>A maps to NM_133378.4 P19871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:179442422 T>C maps to NM_133378.4 G20342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr2:179586739 T>C maps to NM_133378.4 K6306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:179605032 A>G maps to NM_133437.3 N4138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:179640695 A>G maps to NM_133378.4 D1965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:179417884 T>G maps to NM_133378.4 I27346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:179474027 G>A maps to NM_133378.4 R14769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:179591895 A>G maps to NM_133378.4 T5488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:179421599 C>T maps to NM_133378.4 G26859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:179474579 A>C maps to NM_133378.4 G14622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:179546139 C>T maps to NM_133378.4 V9826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:179543551 C>A maps to NM_133378.4 E10006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:179584493 C>A maps to NM_133378.4 E6665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:179395822 G>A maps to NM_133378.4 A32605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:179414507 G>A maps to NM_133378.4 D28079D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr2:179669351 C>T maps to NM_133378.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:179583309 T>A maps to NM_133378.4 K6931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr2:179485077 C>T maps to NM_133378.4 P12822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr2:179406036 G>T maps to NM_133378.4 S30021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:179517033 C>T maps to NM_133378.4 V10622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:179650442 C>T maps to NM_133378.4 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr2:179654101 T>C maps to NM_133378.4 Q687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr2:179419186 G>A maps to NM_133378.4 N27061N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr2:179596486 G>A maps to NM_133378.4 G4461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr2:179595868 A>C maps to NM_133378.4 T4597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr2:179399662 C>T maps to NM_133378.4 E31325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr2:179465770 T>C maps to NM_133378.4 A16052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr2:179478614 G>A maps to NM_133378.4 D13897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr2:179647000 G>A maps to NM_133378.4 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr2:179566919 C>T maps to NM_133378.4 T8918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:179435897 G>A maps to NM_133378.4 N22419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:179440286 T>C maps to NM_133378.4 T20956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:179578657 G>A maps to NM_133378.4 G7665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:179602878 G>A maps to NM_133378.4 C3523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:179634404 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr2:179423164 C>T maps to NM_133378.4 E26439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr2:179495995 T>C maps to NM_133378.4 Q12025Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr2:179604701 T>G maps to NM_133437.3 R4249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr2:179456220 G>A maps to NM_133378.4 S17509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr8:63978605 G>A maps to NM_000370.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:43115283 C>T maps to NM_024331.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:43109031 C>T maps to NM_024331.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr20:43108869 C>T maps to NM_024331.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:72249892 G>A did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr17:72227068 C>T maps to NM_032646.5 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr17:72233437 C>T maps to NM_032646.5 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:2687617 C>T maps to NM_025250.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:2698072 C>T maps to NM_025250.2 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:2697961 G>A maps to NM_025250.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:2689575 C>T maps to NM_025250.2 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:2698051 C>T maps to NM_025250.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:8111722 A>G maps to NM_003320.4 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:49579011 G>A maps to NM_006009.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:49579152 A>G maps to NM_006009.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:49523057 G>T maps to NM_006082.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:49523373 T>G maps to NM_006082.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:49663408 A>G maps to NM_032704.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr13:19752451 G>A maps to NM_006001.1 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr13:19753646 G>A maps to NM_006001.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr2:132237022 C>T maps to NM_080386.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr2:132240408 C>T maps to NM_080386.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr2:130951687 G>A maps to NM_207312.2 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr2:130949654 G>A maps to NM_207312.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:130951631 C>T maps to NM_207312.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:130951526 G>A maps to NM_207312.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:18604277 G>A maps to NM_018943.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:18613869 G>A maps to NM_018943.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:18604385 C>A maps to NM_018943.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr10:5436180 C>A maps to NM_024803.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:5443014 G>A maps to NM_024803.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:30692146 C>T maps to NM_178014.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr6:30691660 C>T maps to NM_178014.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:57599036 G>A maps to NM_030773.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr20:57597952 C>T maps to NM_030773.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:57597916 T>C maps to NM_030773.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:57599543 C>T maps to NM_030773.3 C354C. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:3154870 C>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:3154816 G>C maps to NM_001069.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:3154141 G>A maps to NM_001069.2 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr6:3224987 C>T maps to NM_178012.4 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:3225035 C>T maps to NM_178012.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr6:3224999 G>A maps to NM_178012.4 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:90001974 G>A maps to ENST00000304984 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:89999010 C>T maps to ENST00000304984 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:90002142 C>T maps to ENST00000304984 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:90001914 C>T maps to ENST00000304984 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr16:90001515 G>A maps to ENST00000304984 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:6496188 C>T maps to NM_006087.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:6495654 C>T maps to NM_006087.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:6495957 G>A maps to NM_006087.2 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:6501364 G>A maps to NM_006087.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr19:6495528 G>A maps to NM_006087.2 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:6495702 G>A maps to NM_006087.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:6495672 C>T maps to NM_006087.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr18:12308305 G>A maps to NM_032525.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr18:12325615 C>T maps to NM_032525.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr18:12325603 G>A maps to NM_032525.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:12325999 T>C maps to NM_032525.1 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:94046 A>G maps to NM_177987.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:93797 G>A maps to NM_177987.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr10:93746 G>A maps to NM_177987.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr6:112393233 C>T maps to NM_016262.4 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr6:112400914 C>T maps to NM_016262.4 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:40765934 C>T maps to NM_001070.4 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:40764453 C>T maps to NM_001070.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:40766566 G>A maps to NM_001070.4 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:40814995 C>T maps to NM_016437.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:40814989 G>T did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr10:135099057 C>T maps to NM_006659.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr10:135096605 G>A maps to NM_006659.2 C755C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr10:135098973 C>T maps to NM_006659.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:135101641 G>A maps to NM_006659.2 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr13:113212595 G>A maps to NM_006322.4 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:43677987 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:22851103 C>T maps to NM_052903.4 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:22872544 A>G maps to NM_001102610.1 *1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:22855086 C>T maps to NM_052903.4 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:50656170 G>A maps to NM_020461.3 D1818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr22:50656673 G>A maps to NM_020461.3 G1704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr22:50682243 G>A maps to NM_020461.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr22:50659883 C>T maps to NM_020461.3 G968G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr22:50660486 C>T maps to NM_020461.3 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr22:50656170 G>A maps to NM_020461.3 D1818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr22:50658983 G>T maps to NM_020461.3 T1268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr22:50682330 T>C maps to NM_020461.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:50664612 A>G maps to NM_020461.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr22:50682249 C>T maps to NM_020461.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr22:50657577 C>T maps to NM_020461.3 A1515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr22:50682480 G>A maps to NM_020461.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr16:28855125 G>A maps to NM_003321.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:151552159 C>T maps to NM_020127.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr1:151536459 C>T maps to NM_020127.2 I106I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-4257-01A-01D-1126-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:35471338 T>C maps to NM_003322.3 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:35471368 C>T maps to NM_003322.3 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr6:35478784 C>A maps to NM_003322.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:35466127 G>A maps to NM_003322.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr6:35467756 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:35480430 C>T maps to NM_003322.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:49400604 C>T maps to NM_003323.2 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:49398378 C>T maps to NM_003323.2 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:49400622 C>T maps to NM_003323.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:49391479 A>G maps to NM_003323.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:49391389 G>A maps to NM_003323.2 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:49398260 G>A maps to NM_003323.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:49398399 G>A maps to NM_003323.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:3018722 C>T maps to NM_001160408.1 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:158923298 C>T maps to NM_020245.3 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:158834179 C>T maps to NM_020245.3 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:158923877 G>A maps to NM_020245.3 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:158923937 C>T maps to NM_020245.3 T1081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:158925038 G>A maps to NM_020245.3 R1448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr6:158922884 T>C maps to NM_020245.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:158914724 G>A maps to NM_020245.3 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:158924180 C>T maps to NM_020245.3 D1162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr6:158834149 G>A maps to NM_020245.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:158924492 C>T maps to NM_020245.3 Y1266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:158914603 G>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:158923692 C>T maps to NM_020245.3 Q1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr6:158873232 G>A maps to NM_020245.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:158914685 C>T maps to NM_020245.3 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr6:158923410 C>A maps to NM_020245.3 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:158870164 C>T maps to NM_020245.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:50363584 G>A maps to NM_007275.1 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr8:15601050 C>T maps to NM_006765.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr8:15519705 T>G maps to NM_006765.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:15588213 G>T maps to NM_006765.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr8:15480609 G>T maps to NM_006765.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:15605938 A>G maps to NM_006765.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:1183345 C>T maps to NM_172367.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:1183639 C>T maps to NM_172367.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr11:62348888 C>T maps to NM_022830.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:62349014 G>A maps to NM_022830.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:62343366 C>T maps to NM_022830.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr11:62346055 G>A maps to NM_022830.2 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr11:62343651 G>T maps to NM_022830.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:62348932 A>G maps to NM_022830.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:62342781 C>T maps to NM_022830.2 W841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr11:62358924 C>T maps to NM_022830.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr12:44191513 C>T maps to NM_002822.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:52265208 C>T maps to NM_007284.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:52263138 G>A maps to NM_007284.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:52263753 G>A maps to ENST00000494383 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:19744469 C>A maps to NM_001002926.1 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr4:48097179 G>A maps to NM_003328.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr4:48116414 G>A maps to NM_003328.2 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr4:48082119 G>A maps to NM_003328.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:32655735 C>T maps to NM_175852.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr6:139583901 C>T maps to ENST00000358430 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:139563929 T>A maps to ENST00000358430 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr6:139563884 G>A maps to ENST00000358430 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:139569027 T>G maps to ENST00000358430 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1V-01A-21D-A410-08 chr6:139609679 T>C maps to ENST00000358430 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:16859703 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:16846368 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:16857988 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:16838316 T>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:16847734 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:16850812 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:16859627 G>A did not map to a codon.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr23:16847764 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:16859879 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:16836811 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:11785785 C>T maps to ENST00000356957 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:11773599 G>A maps to ENST00000356957 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:11785752 C>T maps to ENST00000356957 Q458Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:11829887 A>G maps to ENST00000356957 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:11792004 G>A maps to ENST00000356957 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:11785524 T>C maps to ENST00000356957 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:11773182 C>T maps to ENST00000356957 A942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:52949651 A>G maps to NM_020784.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:52981595 A>G did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr14:52981656 C>T maps to NM_020784.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr14:52948966 A>G maps to NM_020784.2 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:9887066 C>A maps to NM_001098529.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr7:37890312 A>G maps to NM_016616.4 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr7:37924816 A>C maps to NM_016616.4 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr7:37890030 T>C maps to NM_016616.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:37907311 C>T maps to NM_016616.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:37896880 A>G maps to NM_016616.4 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:37889885 A>G maps to NM_016616.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:37890309 C>T maps to NM_016616.4 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr7:37927876 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr3:138023785 G>A maps to ENST00000333911 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:113088521 T>C did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr2:99944023 G>A maps to NM_005783.3 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr12:104733052 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:104681125 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:104705126 C>T maps to NM_001093771.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:104732930 C>A maps to NM_001093771.1 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr22:19868174 G>A maps to NM_006440.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:19898958 G>T maps to NM_006440.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr22:19898898 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:10463615 G>A maps to NM_003331.4 D1062D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:10489040 G>A maps to NM_003331.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:10465244 C>T maps to NM_003331.4 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:10463753 C>T maps to NM_003331.4 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:10463633 G>A maps to NM_003331.4 R1056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:50967982 C>T maps to ENST00000395681 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr22:50967594 G>A maps to ENST00000395681 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr22:50965662 C>T maps to ENST00000395681 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:88911702 C>T maps to NM_000372.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:89028413 C>A maps to NM_000372.4 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr11:88911582 G>A maps to NM_000372.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr11:88911804 T>C maps to NM_000372.4 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:41859580 G>A maps to NM_006293.3 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr15:41863316 G>C did not map to a codon.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr15:41865310 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr19:36398348 C>T maps to NM_003332.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:12695536 A>G maps to NM_000550.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr9:12694212 C>A maps to NM_000550.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr10:71902508 C>T maps to NM_173555.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:71899685 C>T maps to NM_173555.2 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:71902580 G>A maps to NM_173555.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:66648138 G>A maps to NM_018264.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:66582481 G>A maps to NM_018264.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:66482880 G>A maps to NM_018264.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr7:66463937 G>A maps to NM_018264.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr7:66582481 G>A maps to NM_018264.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:66660203 C>A maps to NM_018264.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:66582481 G>A maps to NM_018264.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:72281203 G>A maps to NM_001145440.1 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:72267522 G>A maps to NM_001145440.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:72267522 G>A maps to NM_001145440.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr21:44515559 G>A maps to NM_001025203.1 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr21:44514834 G>A maps to NM_001025203.1 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:56166520 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:56172556 T>C did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:56181033 C>T maps to NM_007279.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:70960241 C>T maps to NM_018003.2 E927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:70963406 G>A maps to NM_018003.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:70961644 G>A maps to NM_018003.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr15:70959700 G>A maps to NM_018003.2 Q1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:162551116 T>C maps to ENST00000367925 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:139973062 C>T maps to NM_207309.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr9:139973874 C>T maps to NM_207309.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:47061594 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47065664 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:47062549 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:47060959 G>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:47058615 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:34929584 G>A maps to NM_005499.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:34934769 T>C maps to NM_005499.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:34929588 C>T maps to NM_005499.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr19:34935938 A>C maps to NM_005499.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:34935920 C>T maps to NM_005499.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:69105034 G>A maps to NM_003968.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:68528930 T>C maps to NM_018227.5 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr4:68536190 C>T maps to NM_018227.5 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:68547903 T>C maps to NM_018227.5 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:68536259 G>A maps to NM_018227.5 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:68490786 G>A maps to NM_018227.5 D879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr4:68499961 G>A maps to NM_018227.5 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:68484759 C>T maps to NM_018227.5 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr3:49846864 A>G maps to NM_003335.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:49847795 C>G maps to NM_003335.2 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:138839709 C>T maps to NM_016172.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr9:138847165 G>A maps to NM_016172.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr9:138831532 G>A maps to NM_016172.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:138830128 A>G maps to NM_016172.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr9:138838154 C>T maps to NM_016172.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr9:138825265 G>A maps to NM_016172.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr9:138837032 C>T maps to NM_016172.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr13:99966474 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:34242048 C>A maps to NM_001171201.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:33927810 C>T maps to NM_018449.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:33996301 A>G maps to NM_018449.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:33927912 G>A maps to NM_018449.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr1:154233468 C>T maps to NM_014847.3 Q894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:154223781 C>A maps to NM_014847.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr21:43833293 C>T maps to NM_018961.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr21:43857604 G>A maps to NM_018961.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr21:43836626 G>A maps to NM_018961.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:122659944 C>T maps to NM_032873.4 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr11:122650308 G>A maps to NM_032873.4 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:122653920 T>A maps to NM_032873.4 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr17:16285490 C>T maps to NM_018955.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr17:16285496 A>G maps to NM_018955.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:125397324 C>T maps to NM_021009.5 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:118708929 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:118715481 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:118717106 C>A did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:44444241 G>A maps to NM_007019.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:83667138 G>A maps to NM_198920.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr6:83667135 G>C maps to NM_198920.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr7:43978041 T>C maps to NM_015983.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:238881817 G>A maps to NM_080678.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:238940867 C>T maps to NM_080678.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:46207999 C>T maps to NM_003343.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr21:46207832 A>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr21:46191375 C>T maps to NM_003343.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr16:1374748 C>T maps to NM_194259.1 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:1190729 C>A maps to NM_194315.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:1190609 G>A maps to NM_194315.1 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:1190786 G>A maps to NM_194315.1 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:1192458 C>T maps to NM_194315.1 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:21947246 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:142967328 T>A did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:142967518 T>C did not map to a codon.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr23:142967340 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:142967463 A>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:142967498 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:142967542 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:142967581 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:142967615 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:142967656 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:142967509 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr17:74396251 C>T maps to NM_022066.3 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr17:74395810 A>G maps to NM_022066.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:154523895 G>A maps to NM_017582.6 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:154525263 G>A maps to NM_017582.6 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr9:33900230 A>G maps to NM_017811.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:55918225 G>A maps to NM_014501.2 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr19:55915846 C>G did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr1:202304779 G>A maps to NM_014176.3 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:202301043 G>A maps to NM_014176.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr15:25616246 T>A maps to NM_000462.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr15:25605638 C>T maps to NM_000462.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr12:109921442 G>A maps to NM_183415.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr12:109940855 G>A maps to NM_183415.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:109961808 A>G maps to NM_183415.1 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:109959292 C>A maps to NM_183415.1 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr7:157046670 G>A maps to NM_014671.2 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:157046706 G>A maps to NM_014671.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:157046697 C>T maps to NM_014671.2 N915N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:157041135 C>T maps to NM_014671.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr11:118243290 C>T maps to NM_004788.2 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr11:118245729 C>T maps to NM_004788.2 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:10155570 G>A maps to NM_001105562.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:10166512 C>T maps to NM_001105562.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:10166464 G>A maps to NM_001105562.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:10207064 C>T maps to NM_001105562.2 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:10163013 C>A maps to NM_001105562.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr1:10228246 C>A maps to NM_001105562.2 R1084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:10155591 G>A maps to NM_001105562.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:11345716 C>T maps to NM_013319.2 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:30341396 G>A maps to NM_007106.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:153714221 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr23:153713952 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:4908570 T>C maps to NM_016936.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:4920856 G>A maps to NM_016936.3 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:4911012 G>A maps to NM_016936.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:4911084 C>T maps to NM_016936.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:4925233 C>T maps to NM_016936.3 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:4920578 G>A maps to NM_016936.3 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr7:138978727 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr7:138957169 C>T maps to NM_173569.3 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr7:138978662 A>C maps to NM_173569.3 G1310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:86276734 A>C maps to NM_013438.4 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:86292639 A>G did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:56591819 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:56592132 C>T did not map to a codon.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr23:56592014 C>T did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr23:56590795 T>G did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr11:5528835 C>T maps to NM_017481.2 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:5529609 G>A maps to NM_017481.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:5529132 C>T maps to NM_017481.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr11:5529219 G>C maps to NM_017481.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:5529849 T>C maps to NM_017481.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr11:5529714 A>C maps to NM_017481.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:156020123 A>G maps to NM_020131.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr11:5536465 A>T maps to NM_145053.4 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:5537635 G>T maps to NM_145053.4 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr11:5536501 C>T maps to NM_145053.4 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr11:5537611 C>A maps to NM_145053.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr11:5536963 T>C maps to NM_145053.4 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr11:5537479 T>C maps to NM_145053.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr11:5536702 G>T maps to NM_145053.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr11:5537521 G>A maps to NM_145053.4 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr15:43351981 T>C maps to NM_174916.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:43237586 C>T maps to NM_174916.2 E1730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:43351379 C>T maps to NM_174916.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr15:43378375 T>A maps to NM_174916.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:42562039 G>T maps to NM_015255.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:42603280 A>G maps to NM_015255.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:42647507 A>G maps to NM_015255.2 L1552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr6:42625807 G>A maps to NM_015255.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:170863658 A>T maps to ENST00000442603 K1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:170863621 G>A maps to ENST00000442603 W1384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:19524462 G>A maps to ENST00000375267 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr1:19449412 G>A maps to ENST00000375267 L3244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:19404514 G>A maps to ENST00000375267 S5093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:19439223 G>A maps to ENST00000375267 G3865G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:19488196 G>A maps to ENST00000375267 G1687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:19487482 A>C maps to ENST00000375267 A1778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:19404514 G>A maps to ENST00000375267 S5093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:19433461 T>C did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:19448466 G>A maps to ENST00000375267 R3286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr1:19499974 C>T maps to ENST00000375267 W1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr1:19489099 C>T maps to ENST00000375267 V1590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr1:19446104 C>T maps to ENST00000375267 Q3467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:19487641 C>A did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:19499674 C>T maps to ENST00000375267 Q1097Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr1:19467342 G>A maps to ENST00000375267 S2844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr1:19454158 G>A maps to ENST00000375267 F3062F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:19500109 G>T maps to ENST00000375267 A996A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:19488088 G>A maps to ENST00000375267 S1723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:19525085 T>C maps to ENST00000375267 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr1:19524516 T>A maps to ENST00000375267 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:103287983 T>C maps to NM_015902.4 E2194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr8:103289204 A>G maps to NM_015902.4 S2168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:103340001 G>T maps to NM_015902.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr8:103297905 G>A maps to NM_015902.4 N1773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr8:103297969 A>C maps to NM_015902.4 L1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr8:103358482 G>A maps to NM_015902.4 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:103297392 C>T maps to NM_015902.4 A1886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:103359304 A>G maps to NM_015902.4 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr8:103269925 A>G maps to NM_015902.4 L2707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:103274145 T>C maps to NM_015902.4 G2613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:103282386 G>A maps to NM_015902.4 I2370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr10:99329964 G>A maps to NM_024954.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:42286717 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:42285113 G>A maps to NM_014233.2 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr11:62446024 A>G maps to NM_015853.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:20517260 C>A maps to NM_152376.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:26612349 G>A maps to NM_183008.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:26608996 A>G maps to NM_183008.2 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr1:26608882 A>G maps to NM_183008.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:136513160 G>A maps to NM_014607.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:4446123 C>T maps to NM_025241.2 W374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr3:196098765 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:196098826 G>A maps to NM_015562.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:30620807 C>T maps to ENST00000265616 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:30623789 C>T maps to ENST00000265616 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr9:134404542 G>A maps to NM_031432.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:134401364 C>T did not map to a codon.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr9:134404551 G>A maps to NM_031432.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:165876940 C>T maps to NM_012474.4 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:165865546 G>A maps to NM_012474.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:62577178 C>T maps to NM_017859.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:62572015 G>A maps to NM_017859.3 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr20:62575949 G>A maps to NM_017859.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr20:62571560 G>A maps to NM_017859.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr20:62571772 C>A maps to NM_017859.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:62572045 G>A maps to NM_017859.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:62572554 C>T maps to NM_017859.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:13276240 G>A maps to NM_145314.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr10:13275753 C>T maps to NM_145314.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:141483360 C>T maps to NM_021833.4 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:73714924 G>A maps to NM_003356.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4183-01A-02D-1126-08 chr22:19445626 G>A maps to ENST00000399525 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr22:19444142 G>A maps to ENST00000399525 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:19438228 T>C maps to ENST00000399525 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr4:186336376 T>A maps to NM_018359.3 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr2:128903420 C>T maps to NM_020120.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:128865512 T>C maps to NM_020120.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:128886645 C>T maps to NM_020120.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:128927860 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:96665656 G>A maps to NM_020121.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr13:96589279 A>G maps to NM_020121.3 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr13:96592281 G>A maps to NM_020121.3 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr13:96529619 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:64114741 A>G maps to NM_006759.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:234668981 C>T maps to NM_000463.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:234669109 C>T maps to NM_000463.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:234681072 C>T maps to ENST00000373460 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr2:234676493 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:234676935 C>T maps to ENST00000373460 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:234676526 G>A maps to ENST00000373460 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:234545407 G>A maps to NM_019075.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:234638242 C>T maps to NM_019093.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:234637814 G>T maps to NM_019093.2 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:234627639 G>A maps to NM_007120.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:234621646 G>T maps to NM_019078.1 G4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr2:234622227 A>G maps to NM_019078.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:234621912 T>C maps to NM_019078.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:234622038 T>C maps to NM_019078.1 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:234602123 C>T maps to NM_001072.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:234601953 C>T maps to NM_001072.3 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr2:234526743 C>T maps to NM_019076.4 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr4:70513343 G>A maps to ENST00000514019 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr4:70460193 C>G did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr4:70505296 A>T maps to NM_001105677.1 L13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:69795766 G>A maps to NM_024743.3 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:69811056 T>G maps to NM_024743.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr4:69795653 G>A maps to NM_024743.3 Y487Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr4:69696563 T>C maps to NM_001075.4 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:69696452 C>T maps to NM_001075.4 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr4:69431298 G>A maps to NM_001076.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr4:69519912 G>A maps to NM_001076.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr4:69536156 A>G maps to NM_001076.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:70146645 C>G maps to NM_053039.1 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:70351059 G>A maps to NM_021139.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:69973971 A>G maps to NM_001074.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:69962816 C>T maps to NM_001074.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr5:35957326 C>T maps to NM_152404.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr5:35957517 A>G maps to NM_152404.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr5:35954432 A>G maps to NM_152404.3 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:35957482 C>T maps to NM_152404.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:35955928 C>T maps to NM_152404.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr5:36037996 G>A maps to NM_174914.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr5:36049479 C>T maps to NM_174914.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:36035841 A>G maps to NM_174914.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:36064363 A>G maps to NM_174914.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:36039717 G>A maps to NM_174914.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr4:115544173 C>T maps to NM_003360.3 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr4:115597176 T>C maps to NM_003360.3 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:162467855 G>A maps to NM_175866.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:162467888 C>A maps to NM_175866.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr19:4929358 C>T maps to ENST00000398240 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:4932941 G>A maps to ENST00000398240 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:4941596 G>A maps to ENST00000398240 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr19:4954688 G>A maps to ENST00000455180 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr19:4954799 G>A maps to ENST00000398240 A711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:4945883 G>A maps to ENST00000398240 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:34825968 G>A maps to NM_017754.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:34802026 G>A maps to NM_017754.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr6:34825516 C>T maps to NM_017754.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:34824083 C>T maps to NM_017754.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr6:34826292 C>A maps to NM_017754.3 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:100482807 T>C maps to NM_015054.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:100453798 G>A maps to NM_015054.1 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr12:100453650 G>A maps to NM_015054.1 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:6504627 C>T maps to NM_152896.1 C733C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr9:6475402 A>T maps to NM_152896.1 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:6482084 A>T maps to NM_152896.1 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:6486849 T>C maps to NM_152896.1 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:6434146 C>T maps to NM_152896.1 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr5:176333040 G>A maps to ENST00000377219 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr5:176395771 A>G maps to ENST00000377219 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr5:176397787 C>T maps to ENST00000377219 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:150290279 G>T maps to NM_025218.2 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr6:150290453 G>T maps to NM_025218.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr6:150290470 C>T maps to NM_025218.2 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:132399916 G>A maps to NM_003565.2 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:132404022 G>A maps to NM_003565.2 A897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:132398926 C>T maps to NM_003565.2 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr12:132403120 C>T maps to NM_003565.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:132399916 G>A maps to NM_003565.2 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr12:132394488 C>T maps to NM_003565.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr12:132405878 G>A maps to NM_003565.2 S1042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:132394351 C>T maps to NM_003565.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr12:132393745 C>T maps to NM_003565.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:19679709 A>G maps to NM_014683.3 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr17:19748625 C>T maps to NM_014683.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:19720161 T>C maps to NM_014683.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr17:19746442 T>C maps to NM_014683.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:75131044 G>A maps to NM_001099436.1 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr3:41938396 G>A maps to NM_017886.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr3:41288431 G>A maps to NM_017886.2 A1272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr3:41954326 C>A maps to NM_017886.2 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:41957544 C>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:41938396 G>A maps to NM_017886.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:20360286 G>A maps to ENST00000424589 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr16:20347988 A>G maps to ENST00000424589 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr21:43529774 C>T maps to NM_173568.3 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr21:43531395 C>T maps to NM_173568.3 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr21:43557705 C>T maps to NM_173568.3 F1439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr21:43496222 C>T maps to NM_173568.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr21:43533906 G>T maps to NM_173568.3 E905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr21:43546474 G>A maps to NM_173568.3 V1184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr21:43546525 G>A maps to NM_173568.3 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr21:43547787 T>C maps to NM_173568.3 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr21:43496204 G>A maps to NM_173568.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr3:124462819 C>T maps to NM_000373.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr17:26875114 C>G maps to NM_005148.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:17743649 G>T maps to ENST00000428389 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:17759366 C>T maps to ENST00000428389 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:17783304 C>A did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:17756597 G>A maps to ENST00000428389 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr19:17756597 G>A maps to ENST00000428389 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:17766789 G>T maps to ENST00000428389 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:17785509 G>A maps to ENST00000428389 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:35380472 C>T maps to ENST00000396787 C667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr9:35375188 C>T maps to ENST00000396787 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr9:35382431 C>T maps to ENST00000396787 N841N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:35403976 C>T maps to ENST00000396787 R1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:35295714 C>T maps to ENST00000396787 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:35382467 C>A maps to ENST00000396787 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:54793038 C>T maps to ENST00000260323 Q1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:54307697 T>C maps to ENST00000260323 D866D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:54307736 T>C maps to ENST00000260323 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr15:54307548 C>T maps to ENST00000260323 Q817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr15:54307853 A>G maps to ENST00000260323 Q918Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:54306968 A>G maps to ENST00000260323 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr15:54916050 A>G maps to ENST00000260323 E2086E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr15:54586258 T>C maps to ENST00000260323 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr15:54919040 A>G maps to ENST00000260323 E2125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:54793147 T>A maps to ENST00000260323 L1758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr15:54529878 T>C maps to ENST00000260323 N1073N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr15:54586248 C>G maps to ENST00000260323 V1325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr15:54586258 T>C maps to ENST00000260323 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr15:54306145 C>A maps to ENST00000260323 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:54306981 G>T maps to ENST00000260323 G628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr15:54630686 G>A maps to ENST00000260323 P1571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr17:73831087 G>T maps to ENST00000412096 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:73831531 G>A maps to ENST00000412096 N602N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr17:73836397 G>T maps to ENST00000412096 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:73840375 A>G maps to ENST00000412096 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr15:91491479 G>A maps to NM_018671.3 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91491945 T>A maps to NM_018671.3 Y600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:91496277 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:91493833 C>T maps to NM_018671.3 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:91478772 G>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr17:33497135 G>A maps to NM_173167.2 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr17:33504124 G>A maps to NM_173167.2 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr17:33495163 G>A maps to NM_173167.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:176301280 C>T maps to NM_133369.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:176295868 C>T maps to NM_133369.2 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:176301101 C>T maps to NM_133369.2 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:73059018 C>T maps to NM_170744.3 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:73050708 G>A maps to NM_170744.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:73056441 C>T maps to NM_170744.3 C811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:73050684 A>G maps to NM_170744.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr10:73050855 G>C maps to NM_170744.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr10:73053608 C>G maps to NM_170744.3 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr4:96091444 C>T maps to NM_003728.3 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:96166238 G>A maps to NM_003728.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr4:96163631 G>A maps to NM_003728.3 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr4:96123914 G>T maps to NM_003728.3 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr4:96163618 A>G maps to NM_003728.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:96469891 G>A maps to NM_003728.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr6:40998413 G>T maps to NM_173561.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr6:40996258 C>T maps to NM_173561.2 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:35544117 A>G maps to ENST00000416672 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:35406930 C>T maps to ENST00000416672 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:35624427 G>A maps to ENST00000416672 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr8:35631941 C>T maps to ENST00000416672 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr8:35425751 C>T maps to ENST00000416672 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:35544066 T>C maps to ENST00000416672 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr8:35606062 T>C maps to ENST00000416672 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr6:167721270 G>A maps to NM_018974.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr6:167721270 G>A maps to NM_018974.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:167717521 G>A maps to NM_018974.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:167728873 G>A maps to NM_018974.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:167728783 C>T maps to NM_018974.3 C406C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:167717456 C>T maps to NM_018974.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:1273255 C>T maps to NM_001080461.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr7:1275538 G>A maps to NM_001080461.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:1275517 A>G maps to NM_001080461.1 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr12:109536373 G>C maps to NM_080911.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:73805972 C>T maps to NM_001080419.1 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr17:73805996 C>T maps to NM_001080419.1 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:73806044 C>T maps to NM_001080419.1 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:24896162 C>T maps to NM_016327.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:18967768 C>T maps to ENST00000418384 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr19:18965494 G>A maps to ENST00000418384 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:18972940 C>T maps to ENST00000418384 N871N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr19:18966036 C>T maps to ENST00000418384 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:18976944 C>T maps to ENST00000418384 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:18956892 C>A maps to ENST00000418384 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:12001355 C>T did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr10:11994152 C>T maps to NM_015542.2 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr10:12071234 A>G maps to NM_015542.2 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr13:115048365 C>T maps to NM_023011.2 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:118972429 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:118968984 A>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:118971949 G>A did not map to a codon.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr23:118972013 T>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:118979165 T>C did not map to a codon.
Sequencing variant TCGA-IN-A7NR-01A-11D-A34U-08 chr23:118968952 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:118971998 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:36157788 C>T maps to NM_007000.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr19:36164135 C>A maps to NM_007000.2 Y96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:36166830 G>A maps to NM_007000.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:118906707 C>T maps to NM_006952.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:118917941 C>T maps to NM_006952.3 H229H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:118909884 T>G maps to NM_006952.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr11:118828882 C>T maps to NM_006760.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr22:45691479 C>T maps to NM_006953.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr7:76140157 G>A maps to NM_030570.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:48147887 C>T maps to NM_003364.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:48142892 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:158978110 T>C maps to NM_001135098.1 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:158971749 C>T maps to NM_001135098.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:158980285 G>A maps to NM_001135098.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:74523345 A>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:74494452 C>A did not map to a codon.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr23:74494177 G>T did not map to a codon.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr23:74519689 A>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:74520739 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:74513338 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:1599522 G>A maps to NM_006830.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr3:48638476 C>T maps to NM_003365.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:48636572 C>T maps to NM_003365.2 W477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr19:29698481 G>A maps to NM_006003.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:29698961 G>A maps to NM_006003.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr19:29698475 G>A maps to NM_006003.2 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:29698556 T>C maps to NM_006003.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr19:29698916 A>C maps to NM_006003.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:46775924 A>G maps to NM_006004.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:46769467 T>C maps to NM_006004.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr1:46782255 A>G maps to NM_006004.2 *92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:229772441 A>G maps to NM_014777.2 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr1:229772996 G>A maps to NM_014777.2 K879K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr1:229787055 G>A maps to NM_014777.2 R1408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:229783438 T>C maps to NM_014777.2 Y1363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr7:43917870 G>A maps to NM_001077663.1 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr7:43918101 G>A maps to NM_001077663.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:43921521 G>A maps to NM_001077663.1 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:43916922 A>G maps to NM_001077663.1 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:43916373 A>G maps to NM_001077663.1 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:43917819 A>G maps to NM_001077663.1 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:43917999 G>A maps to NM_001077663.1 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:43918149 G>T maps to NM_001077663.1 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr3:126216936 G>A maps to NM_001165974.1 D525D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:126226619 C>T maps to NM_001165974.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:126207084 G>A maps to NM_001165974.1 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:126222902 T>C maps to NM_001165974.1 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:45479615 C>T maps to NM_000374.4 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:17327090 G>A maps to NM_018467.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:161011633 C>T maps to NM_007122.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:161009745 G>A maps to NM_007122.3 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr11:17546042 G>A maps to NM_153676.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr11:17519711 G>A maps to NM_153676.3 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:17531358 C>T maps to NM_153676.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:17547981 G>A maps to NM_153676.3 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr11:17531367 C>T maps to NM_153676.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr17:72916294 G>A maps to NM_173477.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:72916756 C>T maps to NM_173477.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:215814032 A>C maps to ENST00000366943 S4945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:216262382 G>A maps to ENST00000366943 G1619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr1:215901419 G>A maps to ENST00000366943 P4006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr1:216052347 A>C maps to ENST00000366943 T2772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr1:215821985 C>T maps to ENST00000366943 L4822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:216258043 T>G maps to ENST00000366943 G1721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:216246577 C>T maps to ENST00000366943 V1879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:215844334 A>C maps to ENST00000366943 P4704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:216419953 C>A maps to ENST00000366943 G928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:216420287 G>T maps to ENST00000366943 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:216496916 C>T maps to ENST00000366943 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr1:216498889 T>C maps to ENST00000366943 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:215987140 G>A maps to ENST00000366943 R3226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:215812515 A>C maps to ENST00000366943 Y5011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:216420131 A>G maps to ENST00000366943 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr1:216262388 A>G maps to ENST00000366943 A1617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:215853643 G>A maps to ENST00000366943 N4047N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:216260157 G>A maps to ENST00000366943 S1630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr1:216373110 A>G maps to ENST00000366943 C1223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:215848808 C>T maps to ENST00000366943 L4148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:216073534 C>T maps to ENST00000366943 S2492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:216143999 T>C maps to ENST00000366943 A2308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr1:216258094 G>A maps to ENST00000366943 N1704N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr1:216052335 T>C maps to ENST00000366943 L2776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:215956109 A>G maps to ENST00000366943 L3519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:215824086 G>A maps to ENST00000366943 T4730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:215848448 T>C maps to ENST00000366943 P4268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr1:216172285 G>A maps to ENST00000366943 F2200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:215933090 T>C maps to ENST00000366943 Q3714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:215847676 G>A maps to ENST00000366943 R4526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:216497037 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:17362445 G>A maps to NM_031941.3 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr19:17361063 C>T maps to NM_031941.3 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:17373639 G>A maps to NM_031941.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr10:105151962 C>A maps to NM_032747.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr4:76725284 A>T did not map to a codon.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:62916396 T>C maps to NM_003368.4 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:62916033 G>A maps to NM_003368.4 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:84778356 T>C maps to NM_005153.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr16:84797842 C>T maps to NM_005153.2 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:47101687 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:47098874 C>T did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:47101539 C>T did not map to a codon.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr23:47092438 G>A did not map to a codon.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr23:47107236 C>T did not map to a codon.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr23:47104244 C>T did not map to a codon.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr23:47106470 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:47100774 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:47107039 G>A did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:47104477 A>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:47100029 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:47098544 C>A did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:27664253 G>A maps to NM_182488.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:179437788 G>A maps to NM_003940.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr3:179478996 C>T maps to NM_003940.2 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr3:179459995 C>T maps to NM_003940.2 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr18:180255 G>A maps to NM_005151.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr12:62786831 G>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr21:30414845 T>C maps to NM_006447.2 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:30409639 A>G maps to NM_006447.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr21:30408597 C>T maps to NM_006447.2 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:11994796 C>T maps to NM_201402.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:11995921 T>C maps to NM_201402.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr8:11996203 A>C maps to NM_201402.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr22:18644673 C>A maps to NM_017414.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:49153555 C>T maps to ENST00000434032 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:49148576 A>G maps to ENST00000434032 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:49148784 C>T maps to ENST00000434032 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:49147937 A>G maps to ENST00000434032 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:49152279 C>T maps to ENST00000434032 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:119243938 G>A maps to NM_004205.4 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr11:119230348 G>A maps to NM_004205.4 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr11:119244094 C>T maps to NM_004205.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr11:119228270 G>A maps to NM_004205.4 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:119230922 G>A maps to NM_004205.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:119243866 G>A maps to NM_004205.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr9:132630615 G>A maps to NM_001008563.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:132630543 G>A maps to NM_001008563.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:132637207 C>T maps to NM_001008563.3 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr9:132640636 C>T maps to NM_001008563.3 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:161132825 C>A maps to NM_012475.4 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr1:161133409 G>C did not map to a codon.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr17:20911278 G>A maps to ENST00000455117 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr17:20911257 A>G maps to ENST00000455117 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:20907519 G>A maps to ENST00000455117 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:20911278 G>A maps to ENST00000455117 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:55562760 G>A maps to NM_015306.2 R1934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:55624618 G>A maps to NM_015306.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr21:17191086 T>C maps to ENST00000285681 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr21:17205808 G>A maps to ENST00000285681 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:132160098 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:132161100 G>A did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr23:132161819 A>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:132160700 G>A did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:132160632 A>C did not map to a codon.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr23:132160681 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:132161216 C>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:132160802 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:132159804 C>A did not map to a codon.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr23:132161672 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J5-01A-21D-A25D-08 chr23:132161204 A>T did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:132162026 A>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:132161367 C>T did not map to a codon.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr23:132161317 G>C did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:132161101 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:132161680 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:132161703 C>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:113672346 T>C maps to NM_020886.2 V972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:113700068 T>C did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:113670120 G>A maps to NM_020886.2 C1025C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:113684654 A>G maps to NM_020886.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr11:113704990 C>A maps to NM_020886.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr11:113675421 T>C maps to NM_020886.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:113674533 G>T maps to NM_020886.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr19:57641824 C>T maps to NM_020903.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr19:57641626 A>G maps to NM_020903.2 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:63824852 G>A maps to NM_006537.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:63862712 C>T maps to NM_006537.2 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr15:63866243 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:23079918 G>A maps to NM_020718.3 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:23080572 G>A maps to NM_020718.3 D951D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:23091265 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:23080167 C>T maps to NM_020718.3 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:23091491 C>A maps to NM_020718.3 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:23079453 C>T maps to NM_020718.3 P1324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:23080764 C>T maps to NM_020718.3 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr16:23080713 A>G maps to NM_020718.3 D904D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr17:58259001 G>A maps to NM_032582.3 L1411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr17:58299832 G>A maps to NM_032582.3 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:58297061 C>T maps to NM_032582.3 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:58343334 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:58260598 C>T maps to NM_032582.3 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr17:58270287 G>A maps to NM_032582.3 D1146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:78205093 C>T maps to NM_015017.3 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:78195592 A>G maps to NM_015017.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:78163100 A>G maps to NM_015017.3 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:61575221 G>A maps to NM_014709.3 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:61597499 G>A maps to NM_014709.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:61475802 T>C maps to NM_014709.3 K2079K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:61575063 T>A maps to NM_014709.3 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:61607406 A>T maps to NM_014709.3 L304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr2:61430386 G>A maps to NM_014709.3 D3132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr2:61575983 G>A maps to NM_014709.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:61515895 G>A maps to NM_014709.3 S1555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:61522167 C>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:61575027 G>A maps to NM_014709.3 H754H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:61439036 G>A maps to NM_014709.3 Q2904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:77911745 G>A maps to NM_020798.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:77920553 G>A maps to NM_020798.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:77921180 C>T maps to NM_020798.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:77907362 C>T maps to NM_020798.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr11:77921696 G>A maps to NM_020798.2 E932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr11:77921618 C>G maps to NM_020798.2 V906V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr17:76803160 T>C maps to NM_025090.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:76803319 G>A maps to NM_025090.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr17:76799588 C>T maps to NM_025090.3 V896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:76803592 C>T maps to NM_025090.3 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:219350421 A>T maps to NM_020935.2 C545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr2:219341574 T>C maps to NM_020935.2 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr2:219324514 C>A maps to NM_020935.2 E881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:219339557 T>C maps to NM_020935.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr2:219319720 G>A maps to NM_020935.2 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr2:219328044 G>A maps to NM_020935.2 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr2:219410942 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:219414618 A>T maps to NM_020935.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr4:144106971 C>T maps to NM_032557.5 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr4:144134808 T>G maps to NM_032557.5 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:144135651 A>G maps to NM_032557.5 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr4:144141530 C>T maps to NM_032557.5 N1017N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr4:144141575 A>G maps to NM_032557.5 G1032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:85846391 G>A maps to NM_006590.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:85852702 C>T maps to NM_006590.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:85852762 T>C maps to NM_006590.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:85848664 T>C maps to NM_006590.2 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:49362428 C>T maps to NM_003363.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr3:49377391 G>T maps to NM_003363.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:234442368 A>T maps to NM_018218.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr2:234468455 C>A did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:6189800 C>T maps to ENST00000404835 N658N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:6180572 A>G maps to ENST00000404835 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr17:9570014 T>C maps to NM_153210.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:95926868 C>T maps to NM_032147.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr6:99958033 A>G maps to NM_001080481.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:53494162 G>A maps to NM_022832.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:53494204 C>T maps to NM_022832.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr11:11926989 C>T maps to ENST00000399455 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:11954636 C>T maps to ENST00000399455 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:11957977 C>T maps to ENST00000399455 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:11969621 C>T maps to ENST00000399455 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:22048162 C>T maps to NM_032236.5 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr1:22079021 A>C maps to NM_032236.5 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5720-01A-11D-1600-08 chr1:22073597 G>C maps to NM_032236.5 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:22016487 A>G maps to NM_032236.5 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:22079510 A>G maps to NM_032236.5 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr1:22048171 A>T maps to NM_032236.5 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:41767602 T>C maps to ENST00000373009 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr6:41766456 C>T maps to NM_018561.3 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr6:41774529 C>T maps to ENST00000373009 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:41773521 C>T maps to ENST00000373009 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr6:41774586 G>A maps to ENST00000373009 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:41774418 C>T maps to ENST00000373009 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr6:41773694 C>A maps to ENST00000373009 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr6:41774064 C>T maps to ENST00000373009 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:41773671 C>T maps to ENST00000373009 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:6972413 C>T maps to NM_001098536.1 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr12:6968672 G>A maps to NM_001098536.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:6973051 C>T maps to NM_001098536.1 D671D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:6975192 G>A maps to NM_001098536.1 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr12:6964599 G>A maps to NM_001098536.1 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:50838686 G>A maps to ENST00000456636 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr15:50836809 G>A maps to ENST00000456636 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:55514471 C>T did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:55514443 C>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:55514917 C>T did not map to a codon.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr23:55515194 G>A did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:55514660 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:55515231 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:55515174 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:55513676 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:55515143 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr23:55513295 A>G did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:55513610 A>C did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:55513437 A>G did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:55513607 G>A did not map to a codon.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr23:55513294 A>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:55514296 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr23:55513740 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr23:55514454 T>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:120192601 A>G maps to NM_019050.2 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr4:120193036 G>A maps to NM_019050.2 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:120181690 C>T maps to NM_019050.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:120213819 G>A maps to NM_019050.2 E892E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr4:120192808 T>C maps to NM_019050.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr4:120194822 T>C maps to NM_019050.2 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:120161048 C>T maps to NM_019050.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr10:75276307 C>T maps to NM_152586.3 T1292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr10:75258562 G>A maps to NM_152586.3 R1627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr10:75279628 C>T maps to NM_152586.3 Q868Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr17:5041041 C>T maps to NM_004505.2 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr17:5050418 C>T maps to NM_004505.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:5042568 C>A maps to NM_004505.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr17:5073912 A>G maps to NM_004505.2 S1219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr17:5040980 G>A maps to NM_004505.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr10:11505654 C>T maps to NM_001080491.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:11504532 A>G maps to NM_001080491.2 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr10:11505519 G>A maps to NM_001080491.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr10:11505273 G>A maps to NM_001080491.2 Y568Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr10:11505339 G>A maps to NM_001080491.2 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:11505018 G>A maps to NM_001080491.2 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:8988947 C>T maps to NM_003470.2 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr16:8988968 A>G maps to NM_003470.2 N986N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:9000407 C>A maps to NM_003470.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:8987860 A>G maps to NM_003470.2 H1101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr16:9017166 T>C maps to NM_003470.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:8996252 G>A maps to NM_003470.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:8999107 G>A maps to NM_003470.2 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:8988639 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:9014265 G>A maps to NM_003470.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr15:50782047 C>T maps to NM_005154.3 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:40996214 A>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:41000616 T>C did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:41012335 T>C did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr23:41043382 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:41089040 A>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:41027441 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:41075794 G>A did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:41027343 A>G did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr23:41069825 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:41000423 G>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:41025386 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:41075794 G>A did not map to a codon.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr23:41088542 G>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:40994030 A>C did not map to a codon.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr23:41075641 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:41060360 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G6-01A-11D-A24D-08 chr23:41000003 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:41045866 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:41082471 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:41069786 C>T did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:41088921 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr23:41025370 C>G did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr24:14951942 G>A did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr24:14848462 C>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr24:14898559 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr24:14898520 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr24:14837084 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr24:14968299 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:14898718 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:14952971 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr24:14954180 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr24:14924931 C>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:31205138 C>T maps to NM_005800.4 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:31233354 C>T maps to NM_005800.4 C1047C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:31233465 C>T maps to NM_005800.4 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:149342519 C>T maps to NM_005715.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr6:149395059 C>T maps to NM_005715.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr6:149394999 G>A maps to NM_005715.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:129055390 C>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:129041388 G>C did not map to a codon.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr23:129060229 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:129055421 G>C did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:129060264 C>T did not map to a codon.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr23:129042699 C>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:129053460 A>G did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:129054500 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:129055485 T>G did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:129055438 G>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr13:52605099 C>T maps to NM_021645.5 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:52603293 T>C maps to NM_021645.5 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:72868405 C>T maps to NM_032175.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr17:49350768 T>C maps to NM_016001.2 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:101763572 G>A maps to NM_014503.2 E2153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:101693534 T>A maps to NM_014503.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr12:101684665 A>G maps to NM_014503.2 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr12:101720871 C>T maps to NM_014503.2 R1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr12:101776958 G>A maps to NM_014503.2 A2599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr12:101759385 G>C maps to NM_014503.2 L2036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:101685881 A>G maps to NM_014503.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr12:101764870 C>T maps to NM_014503.2 I2241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr12:101736729 C>T maps to NM_014503.2 F1436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr12:101723148 C>T maps to NM_014503.2 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:101720871 C>T maps to NM_014503.2 R1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:101750390 C>T maps to NM_014503.2 V1818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:117783834 A>C maps to NM_032334.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr4:71554417 C>T maps to NM_020368.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:30213044 G>A maps to NM_018428.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:144612999 C>T maps to NM_007124.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr6:144724271 C>T maps to NM_007124.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr6:144878336 G>A maps to NM_007124.2 A2393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:144898276 G>A maps to NM_007124.2 T2444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:145156924 G>A maps to NM_007124.2 E3225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:144999591 C>T maps to NM_007124.2 D2510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:145161968 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:145095483 A>G maps to NM_007124.2 L2872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:144724271 C>T maps to NM_007124.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr6:144811232 T>C maps to NM_007124.2 H1387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr6:144758744 C>T maps to NM_007124.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:190995909 C>T maps to NM_198152.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:190993101 C>T maps to NM_198152.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr24:15522891 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:75826987 A>G maps to NM_003369.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr11:75852177 G>A maps to NM_003369.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr2:106729101 C>T maps to ENST00000283148 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:47516674 C>T did not map to a codon.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:70815823 G>A maps to NM_018052.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:70806019 A>G maps to NM_018052.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:70765530 C>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:70721925 G>A maps to NM_018052.3 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr16:70796864 G>A maps to NM_018052.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:6574080 A>G maps to ENST00000396308 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:155119135 A>G did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:155127785 G>A did not map to a codon.
Sequencing variant TCGA-BR-8371-01A-11D-2340-08 chr1:116226630 C>A maps to NM_001172412.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr1:160389261 G>A maps to NM_020335.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr1:160394939 T>C maps to NM_020335.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr1:160389027 G>A maps to NM_020335.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr6:31760166 A>G did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr6:31747486 G>T maps to NM_006295.2 P1062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr6:31747776 A>G maps to NM_006295.2 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:31752207 C>T maps to NM_006295.2 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:30892198 C>T maps to NM_001167734.1 C875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr6:30886683 C>T maps to NM_001167734.1 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr6:30890002 G>A maps to NM_001167734.1 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:30890884 C>T maps to NM_001167734.1 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:30890972 T>C maps to NM_001167734.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr6:30887542 C>T maps to NM_001167734.1 H391H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr6:30890691 C>T maps to NM_001167734.1 H738H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr6:30882768 A>G maps to NM_001167734.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:4431966 C>T maps to NM_138440.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:4432308 C>T maps to NM_138440.2 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:46027365 A>C maps to NM_003370.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr16:77913090 G>A maps to NM_020927.1 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:77859246 C>T maps to NM_020927.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr16:78005790 C>T maps to NM_020927.1 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:6821673 C>A maps to NM_005428.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:6853058 G>A maps to NM_005428.2 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:6821667 G>A maps to NM_005428.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr19:6833744 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:136677304 G>A maps to NM_001134398.1 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:136637092 G>A maps to NM_001134398.1 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:136640121 G>A maps to NM_001134398.1 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:136662842 G>A maps to NM_001134398.1 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:136726542 C>T maps to NM_001134398.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:136641199 C>T maps to NM_001134398.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr9:136677298 C>T maps to NM_001134398.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:136637092 G>A maps to NM_001134398.1 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:108116788 G>A maps to NM_006113.4 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr1:108145688 T>C maps to NM_006113.4 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:108315355 C>T did not map to a codon.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:118897522 G>A maps to NM_001112704.1 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr10:118897536 G>A maps to NM_001112704.1 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:71148369 C>T maps to NM_012476.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr2:71160186 G>A maps to NM_012476.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:154448585 T>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:154464612 A>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:101194750 C>A maps to NM_001078.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:101186086 T>C maps to NM_001078.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:101198115 G>A maps to NM_001078.3 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr5:82815519 C>T maps to NM_004385.4 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:82779372 T>A maps to NM_004385.4 C12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr5:82835532 G>A maps to NM_004385.4 P2237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr5:82816101 T>A maps to NM_004385.4 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:82815966 T>C maps to NM_004385.4 N614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr5:82836237 A>G maps to NM_004385.4 P2472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:82835590 G>T maps to NM_004385.4 G2257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:82834773 T>G maps to NM_004385.4 S1984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr5:82816416 A>G maps to NM_004385.4 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr5:82850853 A>G maps to NM_004385.4 T3244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:82834122 A>G maps to NM_004385.4 S1767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:82817019 T>G maps to NM_004385.4 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:82817100 A>C maps to NM_004385.4 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:82817460 C>T maps to NM_004385.4 H1112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:82832847 A>G maps to NM_004385.4 V1342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:82835439 C>T maps to NM_004385.4 F2206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr5:82850773 G>T did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr5:82815447 T>G maps to NM_004385.4 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr5:82836091 T>C maps to NM_004385.4 L2424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr5:82836789 T>G maps to NM_004385.4 T2656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr5:82836372 C>T maps to NM_004385.4 D2517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr5:82815288 A>G maps to NM_004385.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:82808006 A>G maps to NM_004385.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr5:82808054 C>T maps to NM_004385.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr5:82841380 G>A maps to NM_004385.4 P3097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:75877824 T>C maps to NM_014000.2 S1101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:75868742 T>C maps to NM_014000.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr10:75868772 T>C maps to NM_014000.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr10:75863687 T>C did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr10:75864998 C>T maps to NM_014000.2 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr10:75834639 T>C maps to NM_014000.2 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr10:75871827 G>A maps to NM_014000.2 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:75832549 C>T maps to NM_014000.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr10:75854082 C>A maps to NM_014000.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr9:35066768 C>T maps to NM_007126.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:35059576 A>G maps to NM_007126.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:35062111 G>A maps to NM_007126.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:67578875 A>G maps to NM_025054.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:67576861 G>A maps to NM_025054.4 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:67578032 C>T maps to NM_025054.4 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:7812011 A>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:7811948 G>T did not map to a codon.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr23:7812017 G>T did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:7811944 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr23:7811738 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr23:8138168 G>A did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:6451830 T>G did not map to a codon.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr23:6451794 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:6451811 C>T did not map to a codon.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr23:6451824 C>A did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:6452057 C>T did not map to a codon.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr23:6451863 C>T did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr23:8434348 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QI-01A-12D-A25D-08 chr23:8433818 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DL-01A-11D-A364-08 chr23:8433556 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr5:133328038 G>A maps to NM_003374.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:133311612 C>T maps to NM_003374.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr10:76980623 G>A maps to NM_001184783.1 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr12:48238573 C>T maps to NM_001017535.1 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:48251367 C>T maps to NM_001017535.1 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr12:48272748 A>G did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr12:48272868 G>A maps to NM_001017535.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:177713366 C>T maps to NM_005429.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr4:177649057 C>T maps to NM_005429.2 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr4:177632777 A>T maps to NM_005429.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr4:177648955 G>T maps to NM_005429.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr10:135053261 C>T maps to NM_014468.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:157031508 A>G maps to NM_001167912.1 H637H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr3:157188201 G>T maps to NM_001167912.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:157081320 C>A maps to NM_001167912.1 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:157188276 G>T maps to NM_001167912.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr12:95656839 G>A maps to NM_017599.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr12:95663938 C>T maps to NM_017599.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:135631111 C>T did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:135638645 T>G did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:135631136 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:135631046 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr23:135630852 C>T did not map to a codon.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr3:87027811 G>T maps to NM_016206.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr3:86996203 T>C maps to NM_016206.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr3:87027841 G>A maps to NM_016206.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr3:87017830 T>C maps to NM_016206.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr3:11600158 C>G maps to NM_014667.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:10191487 C>T maps to NM_000551.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr3:10191561 C>T maps to NM_000551.2 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7957-01A-11D-2201-08 chr2:219290513 C>G maps to NM_007127.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr2:219297562 C>T maps to NM_007127.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:219295596 C>T maps to NM_007127.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr3:38048185 A>C maps to NM_015873.3 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:38035837 C>T maps to NM_015873.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr3:38045883 G>A maps to NM_015873.3 W648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:38035201 C>T maps to NM_015873.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr3:38047334 G>A maps to NM_015873.3 W668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:38035423 C>T maps to NM_015873.3 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:38039622 G>A maps to NM_015873.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:38039782 C>T maps to NM_015873.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr3:38035801 C>T maps to NM_015873.3 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:38035888 C>T maps to NM_015873.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:38039622 G>A maps to NM_015873.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:17277250 C>T maps to NM_003380.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr10:17271609 G>A maps to NM_003380.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr10:17276729 C>T maps to NM_003380.3 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:17271879 G>A maps to NM_003380.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr10:17276789 C>A maps to NM_003380.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr10:17271774 C>T maps to NM_003380.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr6:153073407 T>G maps to NM_003381.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr6:153073353 T>C maps to NM_003381.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:77900220 T>C maps to ENST00000445370 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr14:77917638 G>A maps to ENST00000445370 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:77907408 C>T maps to ENST00000445370 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:42568961 C>T maps to NM_004624.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:42569497 G>A maps to NM_004624.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr3:42576491 C>T maps to NM_004624.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr7:158824742 G>T maps to ENST00000402066 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr2:37035949 C>T maps to NM_053276.3 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:37035709 C>T maps to NM_053276.3 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr16:31104639 T>A maps to ENST00000319788 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:65419073 C>T maps to NM_173517.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:65419288 G>A maps to ENST00000434382 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:2635504 T>C maps to NM_003383.3 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr9:2646468 T>C maps to NM_003383.3 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:2644969 C>T maps to NM_003383.3 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:2646514 C>T maps to NM_003383.3 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr9:2652950 T>C did not map to a codon.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr9:2639981 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:2643346 C>T maps to NM_003383.3 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:2651937 G>A maps to NM_003383.3 W800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:150573446 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:4688914 G>A maps to NM_182566.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:53762611 C>T maps to NM_173856.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:53762650 C>T maps to NM_173856.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:53770717 T>C maps to NM_173857.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:53770111 A>G maps to NM_173857.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:53770579 T>C maps to NM_173857.2 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:133005620 T>C maps to NM_004666.2 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:133079001 T>G maps to NM_004665.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr6:133072430 A>G maps to NM_004665.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:51457722 G>A maps to ENST00000273612 R901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr3:51458365 G>A maps to ENST00000273612 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr3:51455628 A>G maps to ENST00000273612 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr3:51458109 G>T maps to ENST00000273612 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr22:22599385 G>A maps to NM_007128.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr22:22599373 G>A maps to NM_007128.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr22:22599236 T>A maps to NM_007128.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:22599400 C>A maps to NM_007128.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:118949008 C>T maps to NM_021729.4 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr11:118947750 T>C maps to NM_021729.4 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44U-01A-11D-A24D-08 chr11:118938708 C>T maps to NM_021729.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:118951927 T>C maps to NM_021729.4 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr9:79954742 C>T maps to ENST00000376646 D2230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:79910751 C>T maps to ENST00000376646 R1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr9:79841515 T>C did not map to a codon.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr9:79933225 G>T maps to ENST00000376646 E1678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr9:79836273 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:79908402 G>A maps to ENST00000376646 T1162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr9:79890550 A>C maps to ENST00000376646 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr9:79933277 T>A maps to ENST00000376646 L1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:100568809 C>T maps to NM_017890.3 V1651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:100147901 C>T maps to NM_017890.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:100844799 A>G maps to NM_017890.3 P3203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr8:100520117 T>C maps to NM_017890.3 N1426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:100493894 T>C maps to NM_017890.3 N1245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:100568702 C>T maps to NM_017890.3 R1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:100108586 T>C maps to NM_017890.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:100133549 T>C maps to NM_017890.3 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr8:100673651 A>T maps to NM_017890.3 I2018I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:100833586 A>G maps to NM_017890.3 K3045K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:100871691 A>G maps to NM_017890.3 V3701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:100847854 G>A maps to NM_017890.3 P3302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:100883772 C>T maps to NM_017890.3 L3890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:100789119 C>T maps to NM_017890.3 C2480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:100443828 T>C maps to NM_017890.3 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:62147067 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:62155652 A>G maps to NM_020821.2 L3646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:62208152 A>G maps to NM_020821.2 G2708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:62243141 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:62325717 C>A maps to NM_020821.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr15:62209577 G>T maps to NM_020821.2 R2673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr15:62173133 G>A maps to NM_020821.2 Q3266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:62165446 G>A maps to NM_020821.2 R3526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr15:62204163 G>A maps to NM_020821.2 R2864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:62261495 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:62264931 A>G maps to NM_020821.2 D883D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZA-A8F6-01A-23D-A364-08 chr15:62212322 G>A maps to NM_020821.2 Q2474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:12405566 G>A did not map to a codon.
Sequencing variant TCGA-CD-A486-01A-11D-A24D-08 chr1:12336132 C>T maps to NM_015378.2 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:2844007 C>T maps to NM_022575.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:2841437 C>T maps to NM_022575.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr15:41192155 C>A maps to NM_020857.2 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8525-01A-11D-2340-08 chr15:41192977 C>T maps to NM_020857.2 N654N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr15:41191771 G>A maps to NM_020857.2 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:41192110 G>A maps to NM_020857.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr15:41192111 C>T maps to NM_020857.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr15:41192971 C>T maps to NM_020857.2 C652C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr2:86733007 C>T maps to ENST00000439940 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:86756341 G>T maps to ENST00000439940 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:86737478 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:70930974 C>T maps to NM_004896.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:134104899 C>T maps to NM_052875.3 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr8:145649443 G>A maps to NM_183057.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:110929812 A>T maps to NM_057180.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:122716927 G>A maps to NM_022916.4 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:122720407 C>T maps to NM_022916.4 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr12:122723198 G>A maps to NM_022916.4 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:91549002 G>A maps to NM_018668.3 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:91553067 C>T maps to NM_018668.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr15:91548975 G>A maps to NM_018668.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6520-01A-11D-1800-08 chr13:53016580 C>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:123351982 G>A maps to NM_024667.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr12:123351917 G>A maps to NM_024667.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr12:123380548 G>A maps to NM_024667.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:38816278 C>T maps to NM_014396.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:38765893 A>G maps to NM_014396.3 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:38798009 C>T maps to NM_014396.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:150049302 C>T maps to NM_007259.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:69352775 C>T maps to NM_013245.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:61067314 A>G maps to NM_004869.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:61067279 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr18:61058234 A>G maps to NM_004869.3 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:33236882 T>C maps to NM_022553.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr6:33231790 C>T maps to NM_022553.4 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr6:33236382 G>A maps to NM_022553.4 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:534800 G>A maps to NM_001128159.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:465885 G>A maps to NM_001128159.2 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr17:613825 G>A maps to NM_001128159.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr17:559154 G>A maps to NM_001128159.2 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr2:64189219 G>A maps to NM_016516.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr1:151156850 G>T maps to ENST00000354473 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:151158054 C>T maps to ENST00000354473 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr3:184675266 T>C maps to ENST00000437079 T1047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:184557511 T>C maps to ENST00000437079 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr3:184648265 C>A maps to ENST00000437079 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:184675213 G>T maps to ENST00000437079 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr3:184587292 C>T maps to ENST00000437079 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr2:58386560 C>T maps to NM_001130480.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:58386761 T>G maps to NM_001130480.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr2:58386566 T>C maps to NM_001130480.2 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:50512564 G>A maps to NM_016440.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:107310300 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:107310350 C>T did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:107319358 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:107310234 G>A did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:107320331 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr12:118519947 G>A maps to NM_019086.5 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:124618371 C>T maps to NM_014312.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr11:124618377 C>T maps to NM_014312.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr11:124621976 C>G maps to NM_014312.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr11:124618612 G>C maps to NM_014312.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:65242698 C>T did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:65259783 A>G did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:65252407 T>G did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:65242138 T>G did not map to a codon.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr23:65259788 A>T did not map to a codon.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr2:17773403 G>A maps to NM_003385.4 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:54545206 T>C maps to NM_198481.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:54561662 C>T maps to NM_198481.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr20:36572447 C>T maps to NM_080607.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:117699262 G>A maps to NM_024626.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr17:26697011 A>G maps to NM_000638.3 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr17:26695959 G>A maps to NM_000638.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:1372676 C>T maps to NM_022834.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:116038532 G>A maps to NM_198496.1 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:116046100 C>T maps to NM_198496.1 H467H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr10:116048904 G>A maps to NM_198496.1 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A748-01A-12D-A32N-08 chr10:116049195 T>G maps to NM_198496.1 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr16:22163921 C>T maps to NM_173615.3 H1124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:22149749 G>T maps to NM_173615.3 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr16:22130290 C>T maps to NM_173615.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:22166967 G>A maps to NM_173615.3 W1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:98737905 C>T maps to NM_144992.4 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:98797647 G>A maps to NM_144992.4 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr11:124007943 T>C maps to NM_014622.4 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr7:49842416 C>T maps to NM_198570.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr7:49951711 T>G maps to NM_198570.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr2:215278973 C>T maps to NM_001080500.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr2:215279273 C>T maps to NM_001080500.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr2:215301357 T>C maps to NM_001080500.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr11:61058811 G>A maps to NM_152718.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr11:61053784 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr11:61048267 G>A maps to NM_152718.2 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:6127783 C>T maps to NM_000552.3 A1600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr12:6122734 G>A maps to NM_000552.3 G1844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr12:6131130 G>A maps to NM_000552.3 G1203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr12:6120873 G>T maps to NM_000552.3 V1917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr12:6128083 C>T maps to NM_000552.3 A1500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:6135069 A>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:6058966 A>G maps to NM_000552.3 D2746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:6062706 C>T maps to NM_000552.3 T2647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:6101134 A>G maps to NM_000552.3 C2216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr12:6103070 C>A maps to NM_000552.3 R2185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr12:6204655 T>C maps to NM_000552.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr12:6125697 T>C maps to NM_000552.3 G1765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr12:6128812 C>T maps to NM_000552.3 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:6103259 C>T maps to NM_000552.3 T2122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:28878771 G>A maps to NM_016628.3 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:28903521 A>G maps to NM_016628.3 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:28900755 A>C maps to NM_016628.3 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr10:28905167 A>G maps to NM_016628.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr10:88230819 G>A maps to ENST00000342368 R776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr10:88260129 T>C maps to ENST00000342368 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:88227088 G>A maps to ENST00000342368 R858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:88213060 G>A maps to ENST00000342368 D1040D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr14:100835429 C>T maps to NM_173701.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:119575542 A>G maps to NM_015836.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:119575734 G>A maps to NM_015836.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr1:119575731 C>T maps to NM_015836.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:119575803 G>A maps to NM_015836.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr23:48545267 C>A did not map to a codon.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr23:48544340 G>A did not map to a codon.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr23:48544501 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:48547415 G>A did not map to a codon.
Sequencing variant TCGA-CG-4440-01A-01D-1158-08 chr23:48542700 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:110421799 C>T maps to NM_003931.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr6:110423043 C>T maps to NM_003931.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:110424717 A>C maps to NM_003931.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:110423399 C>A maps to NM_003931.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:27744872 G>A maps to NM_006990.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr1:27755292 G>A maps to NM_006990.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr1:27736342 G>A maps to NM_006990.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr13:27257104 C>T maps to NM_006646.5 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr13:27259975 C>T maps to NM_006646.5 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:27256953 G>A maps to NM_006646.5 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr13:27256944 G>A maps to NM_006646.5 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:27259823 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:123346870 G>A maps to NM_003941.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr12:14940007 C>A maps to NM_016312.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr13:41650291 G>A maps to NM_007187.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr13:41639424 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:41656920 A>G maps to NM_007187.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr13:41645699 C>T maps to NM_007187.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:102612765 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:102612759 A>G did not map to a codon.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr7:70853292 G>T maps to NM_022479.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:70886092 T>C did not map to a codon.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr7:70800596 G>A maps to NM_022479.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IU-01A-22D-A25D-08 chr7:71175810 T>C maps to NM_022479.1 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:70597961 C>A maps to NM_022479.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr7:70885959 C>T maps to NM_022479.1 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr7:71036344 C>A maps to NM_022479.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8209-01A-11D-2340-08 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr7:70886088 C>A maps to NM_022479.1 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:71036317 C>T maps to NM_022479.1 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:73108000 T>C did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr7:73279549 T>C maps to NM_182504.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:73275583 G>A maps to NM_182504.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:73279654 G>A maps to NM_182504.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:224758989 G>A maps to NM_020830.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:224758992 G>A maps to NM_020830.3 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:224782710 G>A maps to NM_020830.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:224746714 G>A maps to NM_020830.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr13:52277736 T>C maps to NM_052950.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:85658382 C>T maps to NM_014991.4 R2237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr4:85719167 A>G maps to NM_014991.4 S972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:85719239 A>G maps to NM_014991.4 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:85598425 T>C maps to NM_014991.4 S3461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J2-01A-21D-A25D-08 chr4:85715864 G>A maps to NM_014991.4 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr4:85661554 T>A maps to NM_014991.4 S2083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:85660160 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:85694042 C>T maps to NM_014991.4 A1598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:85609394 G>A maps to NM_014991.4 T3129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr4:85674912 A>G maps to NM_014991.4 P1892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr4:85701356 A>G maps to NM_014991.4 D1423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr4:85708633 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr4:85675008 C>T maps to NM_014991.4 E1860E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:85605245 G>A maps to NM_014991.4 I3192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:85654599 G>A maps to NM_014991.4 R2386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:55429710 C>T maps to NM_007086.3 E830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:55434066 G>A maps to NM_007086.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr14:55462348 G>A maps to NM_007086.3 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr4:10080544 G>A maps to NM_017491.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:122626115 C>T maps to NM_018117.11 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:122661811 C>T maps to NM_018117.11 Q911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:203772678 A>G maps to NM_018256.3 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:203772675 G>A maps to NM_018256.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:48458723 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48457142 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:48458824 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:48458952 A>G did not map to a codon.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr23:48457986 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:48460230 G>A did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:48457774 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:48458099 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:48457786 G>A did not map to a codon.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr17:9511500 G>A maps to NM_145054.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr17:9503481 G>A maps to NM_145054.4 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:177041099 G>A maps to NM_170710.4 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr4:177046414 T>A maps to NM_170710.4 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:39278678 A>G maps to NM_025132.3 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr4:39246133 C>T maps to NM_025132.3 Y869Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:39276563 C>T maps to NM_025132.3 I1234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr4:39188157 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr14:102675163 C>T maps to ENST00000454394 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr14:102676052 C>T maps to ENST00000454394 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr14:102661430 G>T maps to ENST00000454394 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr14:102676081 G>A maps to ENST00000454394 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:739556 G>A maps to ENST00000248142 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:735691 C>T maps to ENST00000248142 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:739372 G>A maps to ENST00000248142 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:737599 G>A maps to ENST00000248142 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr16:739544 G>T maps to ENST00000248142 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr14:100992377 G>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr14:100996335 C>T maps to NM_001161476.1 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:224599215 T>C maps to NM_025160.6 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6563-01A-13D-2053-08 chr6:170068233 G>A maps to NM_182552.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr6:170036600 C>G did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr6:170089044 A>T maps to NM_182552.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:116080895 G>A maps to NM_001012361.2 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:116094236 G>A maps to NM_001012361.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:116079150 A>G maps to NM_001012361.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr2:128466299 G>A maps to NM_018383.4 H1244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:128471326 C>T maps to NM_018383.4 R1046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr2:128476877 C>T maps to NM_018383.4 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:128467157 T>A did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:128520647 T>A maps to NM_018383.4 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr2:128466262 G>A maps to NM_018383.4 R1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr2:128467287 G>A maps to NM_018383.4 R1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:128525816 T>C maps to NM_018383.4 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:131396154 C>T maps to NM_052844.3 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:131403002 G>A maps to NM_052844.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr9:131399201 G>A maps to NM_052844.3 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:20136077 T>C maps to NM_001006657.1 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:20188932 C>T maps to NM_001006657.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:20130155 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:20145701 G>A maps to NM_001006657.1 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr2:20178575 A>G maps to NM_001006657.1 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:110445991 C>T maps to NM_139281.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:110456839 G>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:1149660 C>T maps to ENST00000416775 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr10:1151105 C>A maps to ENST00000416775 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:1126002 G>A maps to ENST00000416775 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:1118154 C>A maps to ENST00000416775 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:127616497 C>A maps to NM_001045476.1 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr21:44283597 G>A maps to NM_018669.4 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:44270182 C>T maps to NM_018669.4 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr21:44273681 C>T maps to NM_018669.4 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:76785280 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:29152515 G>A maps to NM_015131.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:29124899 T>C maps to NM_015131.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:29117731 G>A maps to NM_015131.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:117529235 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:117528053 C>T did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:117526602 A>G did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:117527126 C>G did not map to a codon.
Sequencing variant TCGA-D7-8579-01A-11D-2340-08 chr23:117577560 A>C did not map to a codon.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr23:117575478 T>C did not map to a codon.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr23:117582880 A>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:117512386 C>A did not map to a codon.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr23:48934154 A>G did not map to a codon.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr23:48934165 T>C did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:48933233 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:48934087 C>T did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr17:80606148 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr6:33255221 G>A maps to NM_005452.5 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr1:109553686 A>G maps to NM_001142550.1 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:39107348 C>T maps to NM_020839.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr3:167277850 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:167272580 C>T maps to NM_178824.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:137005058 G>A maps to NM_052821.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:137007768 C>T maps to NM_052821.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:113099763 A>G maps to NM_001164496.1 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr3:113118802 G>A maps to NM_001164496.1 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZE-01B-11D-A34U-08 chr3:113118803 G>A maps to NM_001164496.1 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:196281461 G>A maps to NM_182627.1 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:74649300 C>A maps to NM_032118.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr5:140044508 T>C maps to NM_017706.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:74985387 G>A maps to NM_030581.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr16:74990458 G>A maps to NM_030581.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:74990458 G>A maps to NM_030581.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:74927700 G>A maps to NM_030581.3 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:74943404 C>A maps to NM_030581.3 G546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:122133952 G>A maps to NM_019069.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr3:49050373 C>T maps to NM_018031.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8486-01A-31D-2394-08 chr3:49051914 G>A maps to NM_018031.3 E952E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:49050487 G>A maps to NM_018031.3 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:49052399 G>A maps to NM_018031.3 E1045E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr3:49052463 G>T maps to NM_018031.3 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:158734692 G>A maps to NM_018051.4 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:158726879 G>A maps to NM_018051.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:158711468 T>C maps to NM_018051.4 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:158711456 T>C maps to NM_018051.4 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:36583593 C>T maps to NM_001083961.1 C738C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:36575647 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:36593711 T>C maps to NM_001083961.1 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:36594726 G>T maps to NM_001083961.1 E1333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:36593954 C>T maps to NM_001083961.1 Y1147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:36557259 A>G maps to NM_001083961.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:36564417 C>T maps to NM_001083961.1 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:36592919 C>T maps to NM_001083961.1 C1029C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:36593977 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:85560139 C>T maps to NM_145172.3 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:85598647 C>G maps to NM_145172.3 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:85546975 C>T maps to NM_145172.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr1:85550329 C>T maps to NM_145172.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:85550269 T>C maps to NM_145172.3 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr1:241907813 T>C maps to NM_144625.4 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:241904845 G>A maps to NM_144625.4 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:43647223 C>T maps to NM_001195831.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:43647388 T>G maps to NM_001195831.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:122372181 C>T maps to NM_144668.4 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:122439463 C>T maps to NM_144668.4 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr12:122359525 G>A maps to NM_144668.4 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr12:122441651 C>T maps to NM_144668.4 S1144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr12:122404866 G>A maps to NM_144668.4 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:122361763 C>T maps to NM_144668.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr8:124140618 C>T maps to NM_145647.3 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:124153050 A>G maps to NM_145647.3 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr8:124096453 G>A maps to NM_145647.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr8:124121564 A>G maps to NM_145647.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:124162315 G>A maps to NM_145647.3 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:228769706 G>A maps to NM_178821.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr2:228769685 A>C maps to NM_178821.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr18:54448762 G>T did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr18:54363662 T>A maps to NM_015285.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:54398626 T>C maps to NM_015285.2 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr18:54483304 T>C maps to NM_015285.2 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:54358981 G>A maps to NM_015285.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:54591217 C>T maps to NM_015285.2 R1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr18:54385205 G>A maps to NM_015285.2 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:37721215 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:37703146 T>C maps to NM_018034.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:53992121 A>G maps to NM_182758.2 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr15:54003110 C>T maps to NM_182758.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr15:53908005 C>A maps to NM_182758.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr15:53815460 C>T maps to NM_182758.2 V1069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:53997239 G>T maps to NM_182758.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:54005034 G>A maps to NM_182758.2 C215C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr15:53815466 T>C maps to NM_182758.2 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr15:85197505 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:190328453 C>T maps to NM_032168.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr15:44131848 C>T maps to NM_024908.3 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr15:44120183 C>T maps to NM_024908.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr15:44127266 G>A maps to NM_024908.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr15:44127281 C>T maps to NM_024908.3 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:44143343 C>T maps to NM_024908.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:67356834 A>G did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:67313176 A>G maps to NM_024763.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr1:67306238 G>A maps to NM_024763.4 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr1:67301454 T>C maps to NM_024763.4 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr1:67292600 A>T maps to NM_024763.4 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr1:67299380 G>A maps to NM_024763.4 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr1:67299305 G>A maps to NM_024763.4 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:3552528 T>C maps to NM_017818.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr1:3564022 C>T maps to NM_017818.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:1636824 C>T maps to NM_001163809.1 D1498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr17:1640708 C>T maps to NM_001163809.1 T1852T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr17:1637457 G>A maps to NM_001163809.1 P1709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:52292563 C>T maps to NM_025222.3 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr9:140449885 G>A maps to NM_138778.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:33623131 G>A maps to NM_173479.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr19:33647372 C>T maps to NM_173479.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:33647410 T>C maps to NM_173479.3 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:33623224 G>A maps to NM_173479.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:33666453 G>A maps to NM_173479.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:33623131 G>A maps to NM_173479.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:33623248 C>T maps to NM_173479.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr19:33628608 C>T maps to NM_173479.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr14:64066594 C>T maps to NM_080666.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:716351 T>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:701680 G>T maps to NM_145294.4 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:711648 C>T maps to NM_145294.4 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:701656 G>A maps to NM_145294.4 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr16:705072 G>A maps to NM_145294.4 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr16:716274 C>T maps to NM_145294.4 C1555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:717483 C>T maps to NM_145294.4 A1714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:134878102 C>T maps to NM_014149.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:134878328 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr7:134878090 C>T maps to NM_014149.3 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr7:134889046 C>T maps to NM_014149.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:90276279 C>T maps to NM_020212.1 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:90255297 C>A maps to NM_020212.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr15:90258250 G>A maps to NM_020212.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr15:90280802 G>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr1:27620578 G>A maps to ENST00000319394 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:124453600 C>T maps to NM_018024.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr8:124449569 T>C maps to NM_018024.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr8:124453656 C>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:141424038 A>G maps to NM_001105558.1 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93J-01A-11D-A397-08 chr7:141423756 T>C maps to NM_001105558.1 C348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr7:141418930 T>G maps to NM_001105558.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:44313563 G>A maps to NM_172131.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:43739137 G>A maps to ENST00000307971 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:44166680 A>G maps to ENST00000396669 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:683372 G>A maps to NM_053284.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr16:683048 G>A maps to NM_053284.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:682784 C>T maps to NM_053284.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:683441 C>T maps to NM_053284.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:682652 C>G maps to NM_053284.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:48917875 C>T maps to NM_175575.5 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:48913366 G>A maps to NM_175575.5 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr17:48918373 G>A maps to NM_175575.5 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr17:48917803 G>A maps to NM_175575.5 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:6303750 C>T maps to NM_006005.3 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:6302886 G>A maps to NM_006005.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr15:83499799 A>G maps to NM_001080435.1 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr15:83478510 C>T maps to NM_001080435.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr15:83499703 C>A maps to NM_001080435.1 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr15:83499505 G>A maps to NM_001080435.1 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr4:1961358 C>T maps to NM_133335.3 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr4:1978260 G>A maps to NM_133335.3 R1227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr4:1957836 C>T maps to NM_133335.3 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr4:1962796 C>T maps to NM_133335.3 I1097I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr4:1906091 T>C maps to NM_133335.3 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr4:1957068 T>C did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr4:1920061 A>G maps to NM_133335.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr4:1940188 C>T maps to NM_133335.3 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr4:1940248 G>A maps to NM_133335.3 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr8:38133957 G>A maps to NM_023034.1 R1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr8:38156989 C>T maps to NM_023034.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr8:38139038 G>T maps to NM_023034.1 I1188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:38194919 G>A maps to NM_023034.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:38194919 G>A maps to NM_023034.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr12:65456300 A>G maps to NM_007191.4 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr2:175437097 A>G maps to NM_003387.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:175432802 T>C did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:38421183 T>G maps to NM_133264.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:29923496 C>A maps to NM_001080529.1 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:66446985 C>G maps to NM_017983.5 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:5270511 C>T maps to NM_015610.3 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4369-01A-01D-1158-08 chr7:5256763 G>A maps to NM_015610.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:5232778 T>A maps to NM_015610.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:5267770 C>T maps to NM_015610.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:5266846 C>T maps to NM_015610.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr7:5256763 G>A maps to NM_015610.3 A174A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VQ-A8P2-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:5254166 C>T maps to ENST00000315176 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:134232920 C>T maps to NM_003882.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:134237660 C>T maps to NM_003882.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr8:134225357 C>T maps to NM_003882.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:134232914 C>T maps to NM_003882.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:134225300 G>A maps to NM_003882.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr8:134232989 C>T maps to NM_003882.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:134233082 C>T maps to NM_003882.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:134225273 C>T maps to NM_003882.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:134232962 G>A maps to NM_003882.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:134232917 C>T maps to NM_003882.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr8:134239805 C>T maps to NM_003882.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:134232869 C>T maps to NM_003882.2 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr8:134203443 C>T maps to NM_003882.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:43355864 C>T maps to NM_003881.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:112385970 T>C maps to NM_198239.1 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:112390714 C>A maps to NM_198239.1 C337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6565-01A-11D-1800-08 chr19:15538060 G>A maps to ENST00000389282 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:68564377 A>T maps to NM_001002292.3 Y523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:68603589 G>A maps to NM_024911.6 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr12:992680 C>T maps to NM_001184985.1 Q1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr12:989016 G>T maps to NM_018979.3 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr12:994220 A>G maps to NM_001184985.1 T1677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:1003797 T>C maps to NM_001184985.1 F2120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:978005 C>T maps to NM_001184985.1 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:1009684 G>A maps to NM_001184985.1 Q2424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:992974 G>A maps to NM_001184985.1 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:977714 A>G maps to NM_001184985.1 K941K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:970262 C>T maps to NM_001184985.1 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:54224913 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:54263436 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:54319443 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:54263864 A>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:54275627 C>T did not map to a codon.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr23:54276023 C>A did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:54228488 T>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:54278031 T>C did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:54263783 G>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:54275764 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:54263763 A>G did not map to a codon.
Sequencing variant TCGA-BR-8679-01A-11D-2394-08 chr23:54328234 C>T did not map to a codon.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr23:54263945 T>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr23:54359574 G>C did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:54259312 C>A did not map to a codon.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr23:54324756 C>G did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr23:54263435 G>T did not map to a codon.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr23:54259258 T>G did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:40940730 C>T maps to NM_032387.4 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr17:40940149 T>C maps to NM_032387.4 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr17:40935984 G>A maps to NM_032387.4 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8576-01A-11D-2340-08 chr17:40936101 T>C maps to NM_032387.4 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr17:40936491 C>T maps to NM_032387.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:219745807 C>T maps to NM_025216.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:219754703 A>G did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr12:49361902 G>A maps to NM_003394.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr12:49364276 C>T maps to NM_003394.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr11:75898132 G>A maps to NM_004626.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr11:75902891 G>A maps to NM_004626.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:120978939 C>T maps to NM_057168.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:116960774 C>T maps to NM_003391.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:116955280 G>A maps to NM_003391.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:116955196 C>A maps to NM_003391.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:113033682 G>A maps to NM_004185.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr1:113058861 T>C maps to NM_024494.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr17:44846084 C>T maps to NM_030753.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr17:44845922 G>A maps to NM_030753.3 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:44847268 G>A maps to NM_030753.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:228210568 C>T maps to ENST00000366753 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr1:228210472 C>T maps to ENST00000366753 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:228238549 C>T maps to ENST00000366753 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:22447840 G>A maps to NM_030761.4 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr1:22447971 G>A maps to NM_030761.4 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:55513441 C>T maps to NM_003392.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:55508418 G>T maps to NM_003392.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:55513420 G>A maps to NM_003392.3 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:1748922 C>T maps to NM_032642.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:1754979 C>T maps to NM_032642.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr2:219736228 G>A maps to NM_006522.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr2:219736387 G>A maps to NM_006522.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:219736501 C>T maps to NM_006522.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:13860878 G>A maps to NM_004625.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr3:13916591 C>T maps to NM_004625.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr22:46318807 G>T maps to NM_058238.2 C326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr5:137426674 G>A maps to NM_058244.2 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr5:137426752 C>A maps to NM_058244.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:228109596 G>A maps to NM_003395.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr17:44950020 C>T maps to NM_003396.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:44949948 C>T maps to NM_003396.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr17:44954023 C>T maps to NM_003396.1 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:44950107 C>T maps to NM_003396.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:7604985 G>A maps to NM_018081.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:7606722 G>C maps to NM_018081.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:30999109 G>A maps to NM_000553.4 T1044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:30933737 T>C maps to NM_000553.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:31007892 T>G maps to NM_000553.4 G1203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr8:30958371 G>A maps to NM_000553.4 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:30969165 T>C maps to NM_000553.4 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:30977829 T>G maps to NM_000553.4 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:30924661 T>C maps to NM_000553.4 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr8:30924661 T>C maps to NM_000553.4 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:30948392 A>G maps to NM_000553.4 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:30949414 G>A did not map to a codon.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr8:30938647 C>T maps to NM_000553.4 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:2770509 C>T maps to NM_020135.2 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:25637144 C>T maps to NM_015626.8 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:25630635 T>A maps to NM_015626.8 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:25630428 C>T maps to NM_015626.8 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr12:118480754 G>A maps to ENST00000441406 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:6023722 C>T maps to NM_015253.1 Y490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr17:6023791 C>T maps to NM_015253.1 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr17:6023722 C>T maps to NM_015253.1 Y490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr12:108634184 C>T maps to ENST00000261400 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr12:108600078 C>A maps to ENST00000261400 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr12:108589683 C>G maps to ENST00000261400 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HB-01A-12D-A25D-08 chr12:108603930 C>T maps to ENST00000261400 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr12:108641942 G>T maps to ENST00000261400 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr12:108603924 C>T maps to ENST00000261400 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:108634199 C>T maps to ENST00000261400 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:32450130 G>A maps to NM_024426.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr19:34991048 C>T maps to ENST00000270288 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr5:167850694 C>T maps to NM_001161661.1 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:167855036 G>T did not map to a codon.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr5:167858360 G>A maps to NM_001161661.1 W731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:10077956 C>T did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:10085204 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:10092341 G>A did not map to a codon.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:10106970 C>T did not map to a codon.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr23:10046904 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:10058908 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:10077875 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:10096687 C>T did not map to a codon.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr23:10058912 C>T did not map to a codon.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr23:10094278 C>T did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:10077876 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:10078028 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr23:10058818 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:10094191 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:10090658 C>A did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:10046874 C>A did not map to a codon.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr23:10093129 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:10096129 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:10077878 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:10107540 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:10085332 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:10085201 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr23:10085314 G>A did not map to a codon.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr16:78466498 C>G maps to NM_016373.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:79245554 G>A maps to NM_016373.1 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:87447903 C>T maps to NM_007013.3 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:87443719 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:87410843 G>A maps to NM_007013.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr8:87464853 T>C maps to NM_007013.3 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:69969757 G>A maps to NM_007014.3 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr16:69964093 C>T maps to NM_007014.3 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:69905706 G>T maps to NM_007014.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:69963367 G>T maps to NM_007014.3 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:69875981 G>A maps to NM_007014.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:69905709 G>A maps to NM_007014.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:69973247 C>T maps to NM_007014.3 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:149238735 T>C maps to NM_001168278.1 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:7692151 G>A maps to NM_020196.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:7688073 G>A maps to NM_020196.2 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:7687231 G>A maps to NM_020196.2 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:7689247 G>A maps to NM_020196.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:7687493 G>A maps to NM_020196.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:7691039 G>T maps to NM_020196.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:7685555 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:7692179 G>A maps to NM_020196.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:7690849 C>A maps to NM_020196.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:6661422 C>T maps to NM_017523.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:52893813 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:52842214 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:29193151 T>C maps to ENST00000403532 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:168550313 A>G maps to NM_002995.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr1:168511328 G>C maps to NM_003175.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:46062692 C>T maps to NM_005283.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr3:46063376 C>T maps to NM_005283.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr3:46062452 G>A maps to NM_005283.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr3:46063061 G>A maps to NM_005283.2 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:31610721 C>T maps to NM_000379.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:31588900 A>G maps to NM_000379.3 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:31593289 G>A maps to NM_000379.3 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:31570414 G>A maps to NM_000379.3 S1083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr2:31595104 G>A maps to NM_000379.3 H615H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:31589789 G>A maps to NM_000379.3 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr2:31625915 G>A maps to NM_000379.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr2:31628781 T>G maps to NM_000379.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr23:2707734 G>A did not map to a codon.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr23:2712608 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:123020224 G>A did not map to a codon.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr23:123020261 C>T did not map to a codon.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr23:123020087 A>G did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:123026608 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr3:39230480 G>A maps to NM_194293.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:39228563 G>A maps to NM_194293.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:39226594 G>A maps to NM_194293.2 Q1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:39229877 C>T maps to NM_194293.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:39227495 G>A maps to NM_194293.2 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:39227572 T>G maps to NM_194293.2 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:39228161 G>A maps to NM_194293.2 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:39229745 G>A maps to NM_194293.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:168102521 T>C maps to NM_152381.5 T1540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4357-01A-01D-1158-08 chr2:168096363 G>T did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr2:168102548 C>A maps to NM_152381.5 G1549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:168114853 T>C maps to ENST00000420519 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:168105929 A>G maps to NM_152381.5 K2676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr2:168104633 T>G maps to NM_152381.5 T2244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:168098326 G>A maps to NM_152381.5 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:168100109 C>T maps to NM_152381.5 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr2:168103938 A>T maps to NM_152381.5 R2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr2:168115843 A>C maps to ENST00000420519 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr2:168104459 T>G maps to NM_152381.5 T2186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr2:168099122 G>A maps to NM_152381.5 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:168106520 A>G maps to NM_152381.5 Q2873Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr2:168101279 T>C maps to NM_152381.5 T1126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:168100397 A>G maps to NM_152381.5 K832K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr2:167760303 G>A maps to NM_152381.5 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr2:168102818 A>G maps to NM_152381.5 Q1639Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr2:168102104 A>G maps to NM_152381.5 E1401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:168101880 C>T maps to NM_152381.5 R1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr2:168102836 T>C maps to NM_152381.5 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:168099704 G>A maps to NM_152381.5 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:168099779 C>T maps to NM_152381.5 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:168115173 G>A maps to ENST00000420519 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr2:168101036 A>G maps to NM_152381.5 Q1045Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:37553708 C>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:37545410 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:37545385 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:37545369 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4J8-01A-11D-A25D-08 chr23:37586942 A>G did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:37587420 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr23:37586942 A>C did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:37586935 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr22:17265192 C>T maps to NM_175878.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr22:17280679 T>C maps to NM_175878.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr8:56015464 C>T maps to NM_052898.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr8:56436681 C>T maps to NM_052898.1 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr8:56270252 A>T maps to NM_052898.1 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:56436611 A>G maps to NM_052898.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:56015464 C>T maps to NM_052898.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:56435963 C>T maps to NM_052898.1 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr8:56015092 C>T maps to NM_052898.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr8:6679543 C>T maps to NM_207411.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:11058404 C>T maps to NM_173683.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr8:11058770 G>A maps to NM_173683.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:30556121 G>A maps to NM_001011718.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:30584554 A>G maps to NM_001011718.1 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr20:30584797 G>A maps to NM_001011718.1 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:30584329 C>T maps to NM_001011718.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr8:71646271 G>A maps to NM_001011720.1 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr8:71646320 T>C maps to NM_001011720.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr8:71646211 C>T maps to NM_001011720.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:100183184 T>C did not map to a codon.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr23:100183003 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:100169758 G>A did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:100169451 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100169341 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:100177864 A>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:100169732 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:100183283 C>G did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:100183087 T>C did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:100177863 G>A did not map to a codon.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr23:100178028 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:100169871 C>T did not map to a codon.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr23:100183205 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:100449521 C>T maps to NM_000380.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr9:100456039 G>A maps to NM_000380.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:14190162 C>T maps to NM_004628.4 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:111642210 A>G maps to NM_020383.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr10:111667487 C>T maps to NM_020383.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:128879209 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:128877955 T>C did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:128879239 C>T did not map to a codon.
Sequencing variant TCGA-CG-4474-01A-02D-1158-08 chr23:128878048 T>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:128880624 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr23:128901662 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:128881605 G>A did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr22:41310310 G>A maps to NM_022098.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:41305151 C>T maps to NM_022098.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:61706035 A>G maps to NM_003400.3 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:61719259 G>A maps to NM_003400.3 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:61709582 A>G maps to NM_003400.3 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EZ-01A-11D-A31L-08 chr2:61719472 G>A maps to NM_003400.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:21373448 C>T maps to NM_022459.4 W726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr13:21358037 G>A maps to NM_022459.4 V1093V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:21417070 G>A maps to NM_022459.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:21382667 G>A maps to NM_022459.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr13:21396421 G>A maps to NM_022459.4 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr13:21396278 A>G maps to NM_022459.4 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr13:21417956 G>A maps to NM_022459.4 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr13:21382647 C>T maps to NM_022459.4 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr6:43515413 C>T maps to NM_020750.2 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:28117777 A>G maps to NM_015171.2 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:28133083 C>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr8:21857141 C>T maps to ENST00000434536 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:21848323 C>T maps to ENST00000434536 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:21835278 A>G did not map to a codon.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:21846546 A>G maps to ENST00000434536 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr8:21856728 C>G maps to ENST00000434536 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr8:21847890 G>T maps to ENST00000434536 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:64827207 G>A maps to NM_007235.3 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:180849226 C>T maps to NM_004736.3 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:44056176 C>T maps to NM_006297.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:44048330 C>T maps to NM_006297.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:44057060 C>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:44056176 C>T maps to NM_006297.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:44050753 T>C maps to NM_006297.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:152345945 T>C maps to NM_005431.1 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr7:152345888 G>A maps to NM_005431.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J6-01A-11D-A25D-08 chr14:104165275 C>T maps to NM_005432.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:104174898 T>C maps to NM_005432.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr14:104165790 G>A maps to NM_005432.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr5:82406985 T>C maps to NM_022406.2 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:82400806 T>C maps to NM_022406.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:216981554 A>G maps to NM_021141.3 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr2:216997074 C>T maps to NM_021141.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:42032526 A>G maps to NM_001469.3 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr22:42033615 C>T maps to NM_001469.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr22:42052905 G>T did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr3:142048334 G>A maps to NM_019001.3 R1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:21314802 A>T maps to NM_012255.3 K405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr20:21312984 C>T maps to NM_012255.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:21314714 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:21307217 C>A maps to NM_012255.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr20:21328890 G>A maps to NM_012255.3 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr20:21306993 G>A maps to NM_012255.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:21338388 T>C maps to NM_012255.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:74570274 T>C maps to NM_182969.1 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr11:74638465 G>A maps to NM_182969.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:74556175 G>A maps to NM_182969.1 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:74618230 G>A maps to NM_182969.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr16:17451880 G>T maps to NM_022166.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:17211734 T>A maps to NM_022166.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:17202698 G>A maps to NM_022166.3 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:17292121 G>A maps to NM_022166.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:17353109 C>T maps to NM_022166.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:48433537 C>A maps to NM_022167.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr17:48434594 C>T maps to NM_022167.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:48434498 G>A maps to NM_022167.2 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8528-01A-11D-2340-08 chr17:48433957 T>C maps to NM_022167.2 Y523Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr17:48433885 C>T maps to NM_022167.2 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:33272091 G>A maps to NM_003680.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:33252033 G>A maps to NM_003680.3 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr12:32908613 G>A maps to NM_001040436.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr12:32908784 G>T maps to NM_001040436.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:183521068 A>G maps to NM_018023.4 A1176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:183435469 T>C maps to NM_018023.4 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr3:183521824 G>A maps to NM_018023.4 K1211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:183528313 T>C maps to NM_018023.4 I1404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr3:183493772 C>T maps to NM_018023.4 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr12:69756671 A>G maps to NM_006530.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr12:69753803 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:745762 A>T maps to NM_005433.3 Y223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr18:732848 G>T maps to NM_005433.3 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GD-01A-11D-A25D-08 chr18:736826 A>G maps to NM_005433.3 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr18:747954 A>G maps to NM_005433.3 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr11:66053173 T>C maps to ENST00000376904 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:66052411 G>A maps to ENST00000376904 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:66052849 A>G did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:38795993 A>G maps to NM_001039672.2 *315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:11034601 C>T maps to NM_024029.3 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:11038347 G>T maps to NM_024029.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:11034827 G>A maps to NM_024029.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:32515613 G>T maps to NM_032312.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr2:32517417 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:32515675 T>C maps to NM_032312.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:143540083 T>G maps to NM_030799.7 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:67751833 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr4:44624559 G>A maps to NM_182592.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr4:44626736 A>G maps to NM_182592.2 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:19640290 C>T maps to NM_198537.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:44251850 G>A maps to NM_006555.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr14:75265780 C>T maps to NM_019589.2 R1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr14:75264546 G>A maps to NM_019589.2 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr14:75248530 C>T maps to NM_019589.2 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr14:75283359 A>G maps to NM_019589.2 K1884K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr14:75296046 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:75295976 C>T maps to NM_019589.2 S2075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr14:75264708 C>T maps to NM_019589.2 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:27403476 G>A maps to NM_139312.1 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:27436424 A>G did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr10:27434471 T>C maps to NM_139312.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr10:27425267 T>C maps to NM_139312.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr10:27412509 C>G maps to NM_139312.1 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr10:27400932 A>G maps to NM_139312.1 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr1:207222943 T>G maps to NM_018566.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:207224174 G>T maps to NM_018566.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr22:22057703 G>A maps to NM_013313.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:22057673 C>T maps to NM_013313.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:30381636 C>T maps to NM_001127399.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:135756476 C>T maps to NM_025052.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr2:135738674 G>T maps to NM_025052.3 A1212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:135741298 C>A maps to NM_025052.3 E1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr2:135745628 C>T maps to NM_025052.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr2:135745058 G>A maps to NM_025052.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:69203418 A>G maps to NM_001031732.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:69203597 G>A maps to NM_001031732.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:69202828 G>A maps to NM_001031732.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr4:69202928 C>T maps to NM_001031732.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:112862460 T>C maps to NM_022828.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:112862483 T>C did not map to a codon.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr5:112884711 T>A maps to NM_022828.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8533-01A-11D-2340-08 chr5:112868581 C>T maps to NM_022828.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr5:112868661 C>T maps to NM_022828.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr5:112860770 A>G maps to NM_022828.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:61834967 A>G maps to NM_017798.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:61834232 G>A maps to NM_017798.3 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr20:61834048 C>A maps to NM_017798.3 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:61845260 A>C maps to NM_017798.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr20:61835024 G>A maps to NM_017798.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr20:61833842 A>G maps to NM_017798.3 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:29070188 C>T maps to NM_016258.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr1:29069897 A>C maps to NM_016258.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr1:29069768 G>A maps to NM_016258.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4188-01A-01D-1126-08 chr8:64098992 C>T maps to ENST00000339066 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr8:64098805 T>C maps to ENST00000339066 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr20:43535057 C>T maps to NM_139323.2 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:43530374 T>C maps to NM_139323.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr20:43530311 C>T maps to NM_139323.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr17:1248761 G>A maps to NM_006761.4 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr17:1264465 C>T maps to NM_006761.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:75959436 C>T maps to NM_012479.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr22:32352259 A>G maps to NM_003405.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:9728311 G>A maps to NM_006826.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:9731521 T>C maps to NM_006826.2 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr8:101961018 T>C maps to NM_003406.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:155629927 G>A maps to ENST00000368339 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:21875158 C>T did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:21874824 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:21874648 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:21875628 T>C did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:21875410 C>T did not map to a codon.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr23:21874727 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:74077482 G>A maps to NM_180990.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr17:74077645 G>A maps to NM_180990.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr17:74075791 C>T maps to NM_180990.3 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr2:174074512 G>A maps to NM_016653.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr2:174074512 G>A maps to NM_016653.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:174131420 C>T maps to NM_016653.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:100388640 A>G maps to ENST00000349350 T2478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:100350271 A>G maps to ENST00000349350 E848E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:100361491 G>A maps to ENST00000349350 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:100350793 A>G maps to ENST00000349350 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr7:100348416 G>A maps to ENST00000349350 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr7:100348326 C>T maps to ENST00000349350 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:100377176 G>A maps to ENST00000349350 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:100358105 C>T maps to ENST00000349350 F1263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:100385563 T>G maps to ENST00000349350 A2344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:100345206 A>G maps to ENST00000349350 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr7:100357452 G>A maps to ENST00000349350 K1227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr7:100373338 G>A maps to ENST00000349350 G2025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:98351850 C>T maps to NM_001079.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr2:98351886 C>T maps to NM_001079.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr2:98351811 C>T maps to NM_001079.3 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:98354254 C>T maps to NM_001079.3 Y506Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:98351850 C>T maps to NM_001079.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr2:98340771 C>T maps to NM_001079.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr2:98354510 G>A maps to NM_001079.3 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr2:98351886 C>T maps to NM_001079.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr2:98340735 A>G maps to NM_001079.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr2:98351711 G>T did not map to a codon.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr2:98340790 C>T maps to NM_001079.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr4:48492718 G>A maps to NM_175619.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:167035315 A>G maps to ENST00000307529 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:166958586 A>G maps to ENST00000307529 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:167045769 A>G maps to ENST00000307529 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr3:166960345 T>G maps to ENST00000307529 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:167023610 A>G maps to ENST00000307529 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr3:167023730 A>C maps to ENST00000307529 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr3:167016177 A>G maps to ENST00000307529 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:2408096 C>T did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr23:2407302 G>A did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:2406918 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:2408216 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:2408365 C>T did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:2408342 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:2407119 C>T did not map to a codon.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr23:2406721 C>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:2406790 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr23:2407992 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:2406721 C>G did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:2407149 C>T did not map to a codon.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr23:2407740 G>A did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:2408191 T>C did not map to a codon.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr23:2408701 C>T did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:2408489 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:2406989 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:2408296 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr23:2408015 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:2408418 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:2408505 C>A did not map to a codon.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr3:111312781 A>C maps to NM_024508.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr3:111312682 C>T maps to NM_024508.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:111312951 C>A maps to NM_024508.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:50277561 C>T maps to NM_014838.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:50277789 C>T maps to NM_014838.2 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr22:50280129 C>T maps to NM_014838.2 F940F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr22:50280282 C>T maps to NM_014838.2 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr22:50277798 C>T maps to NM_014838.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr22:50279691 G>A maps to NM_014838.2 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr22:50277970 C>T maps to NM_014838.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:50280309 G>A maps to NM_014838.2 P1000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr22:50277671 G>A maps to NM_014838.2 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:56191407 G>A maps to NM_030776.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:56190020 G>A maps to NM_030776.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:56188237 C>T maps to NM_030776.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr14:64988890 T>C maps to NM_001123329.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr14:64988533 A>G maps to NM_001123329.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr14:64988812 C>T maps to NM_001123329.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:81431714 C>A maps to NM_001105539.1 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:81411871 A>G maps to NM_001105539.1 G372G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8680-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:31868725 G>A maps to NM_181842.2 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr6:31868437 C>T maps to NM_181842.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:113934372 G>A maps to NM_001018011.1 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:114121132 C>T maps to NM_001018011.1 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:114121138 G>T maps to NM_001018011.1 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:114121252 G>A maps to NM_001018011.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:16270391 T>C did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:151687600 G>A maps to NM_020861.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr6:151694618 A>G maps to NM_020861.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr6:151687264 G>A maps to NM_020861.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr6:151686763 G>A maps to NM_020861.1 D479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr3:114058127 G>A maps to NM_001164342.1 N650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:114070564 G>A maps to NM_001164342.1 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr3:114070105 C>T maps to NM_001164342.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:114057857 G>A maps to NM_001164342.1 D740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr3:114070177 C>T maps to NM_001164342.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr3:114069712 A>C maps to NM_001164342.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr3:114069727 C>T maps to NM_001164342.1 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr3:114070237 C>A maps to NM_001164342.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:114069325 T>C maps to NM_001164342.1 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:114069919 G>A maps to NM_001164342.1 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr3:114069778 G>A maps to NM_001164342.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:33283796 G>A maps to NM_001145338.1 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr6:109787638 G>A maps to NM_014797.2 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:109787302 T>C maps to NM_014797.2 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr14:64953978 G>A maps to NM_006977.2 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:125681250 G>A maps to NM_020924.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr9:125681732 G>A maps to NM_020924.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr9:125681319 A>G maps to NM_020924.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:62520497 T>A maps to NM_024784.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:36207581 C>A maps to NM_014383.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:36206270 C>A maps to NM_014383.1 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:119388798 G>A did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:119388374 G>T did not map to a codon.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr23:119387550 G>C did not map to a codon.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr23:119389022 C>G did not map to a codon.
Sequencing variant TCGA-CG-5717-01A-11D-1600-08 chr23:119387472 T>C did not map to a codon.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr23:119389083 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:119387795 G>A did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:119387537 A>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr9:129642790 G>A maps to ENST00000319119 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:129642635 C>T maps to ENST00000319119 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr9:129642863 C>T maps to ENST00000319119 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4279-01A-01D-1126-08 chr3:141161550 C>T maps to NM_001080412.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8295-01A-11D-2340-08 chr3:141161649 A>G maps to NM_001080412.2 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr3:141164325 C>T maps to NM_001080412.2 H1032H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr3:141163524 T>C maps to NM_001080412.2 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:57397342 G>A maps to NM_014830.2 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4294-01A-01D-1126-08 chr12:57397687 C>T maps to NM_014830.2 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr12:57398125 G>A maps to NM_014830.2 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:57397713 A>G maps to NM_014830.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr12:57398419 T>C maps to NM_014830.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:7369844 C>T maps to NM_020899.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr17:7365270 G>A maps to NM_020899.3 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr17:7365564 A>G maps to NM_020899.3 A912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr17:7369454 G>A maps to NM_020899.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr17:7365531 C>T maps to NM_020899.3 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:7369877 G>A maps to NM_020899.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:22848915 G>A maps to NM_014870.3 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr1:22837715 G>C maps to NM_014870.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:22816533 T>C maps to NM_014870.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:22843934 C>T maps to NM_014870.3 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RJ-01A-21D-A33T-08 chr1:22817020 C>T maps to NM_014870.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr1:22843904 C>G maps to NM_014870.3 G927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr1:197147551 C>T maps to NM_194314.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:197168673 C>T maps to NM_194314.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:197144168 G>A maps to NM_194314.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:129595579 C>T maps to NM_014007.3 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:130108386 G>A maps to ENST00000397753 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:59028800 C>T maps to NM_032792.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:59028964 G>A maps to NM_032792.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:59025429 A>C maps to NM_032792.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:59028287 G>A maps to NM_032792.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:59027858 G>A maps to NM_032792.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:59028677 A>G maps to NM_032792.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr20:62421219 C>T maps to NM_025224.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr20:62421540 G>A maps to NM_025224.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:62421702 G>A maps to NM_025224.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr20:62378594 G>A maps to NM_025224.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:62407139 G>A maps to NM_025224.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:62421309 C>T maps to NM_025224.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr20:62421540 G>A maps to NM_025224.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr20:62421441 G>A maps to NM_025224.2 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr20:62422080 G>A maps to NM_025224.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr20:62421705 C>T maps to NM_025224.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr20:62407295 G>A maps to NM_025224.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:62378428 G>A maps to NM_025224.2 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:42701037 G>A maps to NM_145166.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:42705831 C>T maps to NM_145166.3 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5818-01A-11D-1600-08 chr1:6646026 T>C maps to NM_005341.2 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr1:6649094 G>A maps to NM_005341.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:6649172 C>T maps to NM_005341.2 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:6647650 G>A maps to NM_005341.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:6641352 T>C maps to NM_005341.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr1:6642125 G>A maps to NM_005341.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr4:4304087 G>A maps to NM_145291.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:4304087 G>A maps to NM_145291.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:4304081 G>A maps to NM_145291.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr4:4322607 G>A maps to NM_145291.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:37440559 G>A maps to NM_014872.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr9:37441516 G>A maps to NM_014872.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr9:37442080 T>C maps to NM_014872.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr9:125673697 A>G maps to NM_006626.4 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:125673937 T>C maps to NM_006626.4 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:125674192 A>G maps to NM_006626.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr9:125673880 A>G maps to NM_006626.4 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr9:125673315 G>A maps to NM_006626.4 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr1:154988857 C>T maps to ENST00000417934 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:154987333 C>T maps to ENST00000417934 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:154988173 G>A maps to ENST00000417934 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr1:154987333 C>T maps to ENST00000417934 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:154987420 G>A maps to ENST00000417934 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr1:154988857 C>T maps to ENST00000417934 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr18:45567232 A>G maps to NM_001039360.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:45567391 G>A maps to NM_001039360.2 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:45567052 A>G maps to NM_001039360.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:45566743 T>C maps to NM_001039360.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr18:45566725 G>A maps to NM_001039360.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr18:45555954 G>A maps to NM_001039360.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr18:45556140 G>A maps to NM_001039360.2 C450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:33423509 G>A maps to NM_152735.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:56515287 T>C maps to NM_032786.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:203798732 G>A maps to NM_014827.4 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:203820222 T>C maps to NM_014827.4 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr1:203798732 G>A maps to NM_014827.4 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:203802955 A>G maps to NM_014827.4 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr1:203821511 A>G maps to NM_014827.4 E806E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr1:203797470 A>G maps to NM_014827.4 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr1:203798643 C>T maps to NM_014827.4 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr1:37948941 A>G maps to NM_025079.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr1:37948725 G>T maps to NM_025079.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:37948725 G>A maps to NM_025079.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:37948614 A>G maps to NM_025079.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr1:37947262 C>T maps to NM_025079.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr1:37948665 A>G maps to NM_025079.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:64722377 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:64721988 G>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:64722732 C>T did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr23:64708738 G>A did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:64722912 A>G did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:64722867 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:64722332 C>T did not map to a codon.
Sequencing variant TCGA-HU-8238-01A-11D-2340-08 chr23:64722779 C>G did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:110035522 G>A maps to NM_033390.1 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:110035978 C>T maps to NM_033390.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr11:110030104 G>A maps to NM_033390.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:110035933 G>A maps to NM_033390.1 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:110007957 G>T maps to NM_033390.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6ET-01A-32D-A32N-08 chr6:149772562 C>T maps to NM_207360.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:149778019 C>T maps to NM_207360.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:46559476 G>A maps to ENST00000242848 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr13:46544500 A>G maps to ENST00000242848 D856D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:46542001 G>A maps to ENST00000242848 Q1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:46542049 G>A maps to ENST00000242848 R1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:46541686 G>A maps to ENST00000242848 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:46541740 G>A maps to ENST00000242848 R1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr13:46585642 T>C maps to ENST00000242848 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr13:46541932 G>A maps to ENST00000242848 R1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:46541687 C>G maps to ENST00000242848 V1424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr13:46544098 T>C maps to ENST00000242848 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr13:46616330 G>A maps to ENST00000242848 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr13:46541792 G>A maps to ENST00000242848 R1389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr13:46549463 G>A maps to ENST00000242848 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:187366109 C>T maps to NM_018471.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:88697553 G>A maps to ENST00000452588 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7723-01A-11D-2053-08 chr16:88691081 C>T maps to ENST00000452588 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:88643557 G>T maps to ENST00000452588 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr16:88643771 C>T maps to ENST00000452588 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr16:88643734 C>T maps to ENST00000452588 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr8:144557661 G>A maps to NM_015117.2 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:144620192 G>T maps to NM_015117.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr8:144620764 G>A maps to NM_015117.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr8:144618478 C>T maps to NM_015117.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr8:144522226 G>T maps to NM_015117.2 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:144590004 A>G maps to NM_015117.2 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:144620681 C>T maps to NM_015117.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr8:144522355 T>C maps to NM_015117.2 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr2:113088705 C>G maps to NM_198581.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:113090014 C>T maps to NM_198581.2 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr2:113088966 T>C maps to NM_198581.2 D824D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr2:113081978 C>T maps to NM_198581.2 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:11868229 C>T maps to NM_014153.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:11868833 A>G did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:11846592 G>A maps to NM_014153.3 F886F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:11846688 C>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:11857355 G>A maps to NM_014153.3 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr22:41752692 G>A maps to ENST00000351589 K870K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr22:41753256 C>T maps to ENST00000351589 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr22:41735149 C>T maps to ENST00000351589 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr22:41753225 C>T maps to ENST00000351589 C925C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:41751492 G>A maps to ENST00000351589 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr22:41753408 T>C maps to ENST00000351589 A986A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr22:41721567 G>A maps to ENST00000351589 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr2:112994206 G>A maps to NM_032494.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:138764924 A>G maps to ENST00000464606 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:138764822 C>T maps to ENST00000464606 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr7:138713580 C>T maps to NM_080660.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr7:138711298 G>A maps to NM_080660.3 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:64140007 C>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:64140024 G>A did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:64140120 T>C did not map to a codon.
Sequencing variant TCGA-EQ-5647-01A-01D-1600-08 chr23:64137661 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:52940629 G>A maps to NM_001009881.2 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:52981600 C>A maps to NM_001009881.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:52961104 A>G maps to NM_001009881.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr1:52962852 T>C maps to NM_001009881.2 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:52940506 G>A maps to NM_001009881.2 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:117960019 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:117959501 C>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:117959763 G>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:117959710 A>C did not map to a codon.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:73524362 C>T did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:73524179 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:73524220 C>T did not map to a codon.
Sequencing variant TCGA-D7-6519-01A-11D-1800-08 chr23:73524417 G>A did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr16:87525316 G>A maps to NM_015144.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:111698833 G>A did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:111698081 A>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:111698263 T>C did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:111698540 A>C did not map to a codon.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr23:111698711 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:103359828 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:103359144 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:103359096 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr18:60243810 G>T maps to NM_017742.4 *1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr20:279292 A>C maps to NM_033089.6 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr4:25334862 C>T maps to NM_024936.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:25315705 G>T maps to NM_024936.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7958-01A-21D-2340-08 chr23:77913792 T>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:77913150 A>C did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:77913451 A>C did not map to a codon.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr23:77912677 T>A did not map to a codon.
Sequencing variant TCGA-D7-6522-01A-11D-1800-08 chr23:77912592 C>T did not map to a codon.
Sequencing variant TCGA-D7-A6F2-01A-12D-A31L-08 chr23:77912604 C>T did not map to a codon.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr23:77913638 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:77913464 T>C did not map to a codon.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr23:77913458 G>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr23:77913433 G>A did not map to a codon.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr23:77913701 T>C did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr23:77913464 T>C did not map to a codon.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr23:77913660 T>C did not map to a codon.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:88967931 A>T maps to NM_024617.3 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:88937943 G>A maps to NM_024617.3 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:88925683 T>G maps to NM_024617.3 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr9:37349415 C>T maps to NM_032226.2 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:37356832 A>G maps to NM_032226.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:37349449 G>A did not map to a codon.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr9:37126556 C>A maps to NM_032226.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr12:122958718 G>A maps to NM_017612.2 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr12:122958508 G>A maps to NM_017612.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr12:122958811 T>C maps to NM_017612.2 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:80600734 A>G maps to NM_032280.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr5:80607036 T>A maps to NM_032280.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr5:80604768 A>G maps to NM_032280.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr12:42707746 G>A maps to NM_033114.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:99998687 C>T maps to NM_017984.3 Q632Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr7:99999536 T>C maps to NM_017984.3 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:207171006 T>C maps to NM_020923.1 C585C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr2:207171141 C>A maps to NM_020923.1 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:207173625 T>G maps to NM_020923.1 S1458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6455-01A-11D-1800-08 chr2:207172944 G>A maps to NM_020923.1 T1231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:207172263 T>C maps to NM_020923.1 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr2:207171519 G>A maps to NM_020923.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8080-01A-11D-2340-08 chr2:207172842 T>C maps to NM_020923.1 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr2:207174183 T>C maps to NM_020923.1 D1644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr2:207172798 G>T maps to NM_020923.1 E1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr2:207170955 C>T maps to NM_020923.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr2:207174387 T>C maps to NM_020923.1 F1712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr5:837554 G>A maps to NM_024786.2 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:850498 G>A maps to NM_024786.2 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr5:843739 C>T maps to NM_024786.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr5:840652 G>A maps to NM_024786.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr9:131483603 G>A maps to ENST00000372667 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:74649027 T>C did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:74651313 G>A did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:74641701 G>T did not map to a codon.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr23:74698781 A>C did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr23:74644603 C>T did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr23:74742852 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr12:77244671 C>T maps to NM_015336.2 C602C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr12:77244666 C>T maps to NM_015336.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:27175192 C>T maps to NM_032283.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr1:27159096 C>T maps to NM_032283.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr3:195938171 C>T maps to NM_001039617.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr3:195937535 G>A maps to NM_001039617.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr8:17055133 C>A maps to NM_016353.4 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr13:21976958 C>T maps to ENST00000400590 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5578-01A-01D-1600-08 chr13:22033232 G>A maps to ENST00000400590 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:14618999 T>C maps to NM_178566.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:113673203 G>A maps to NM_173570.3 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr3:113675183 A>G did not map to a codon.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr3:44968198 C>T maps to NM_016598.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr7:6621868 T>A maps to NM_018106.3 C119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:6624662 T>C maps to NM_018106.3 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr11:57466722 C>T maps to NM_015457.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8MW-01A-11D-A364-08 chr11:57460087 G>A maps to NM_015457.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr10:114194117 C>A maps to NM_022494.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:85009966 G>A maps to NM_001145548.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:85024122 G>A maps to NM_001145548.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr22:20128441 G>A maps to NM_013373.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr22:20130874 C>T maps to NM_013373.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr22:20131180 G>A maps to NM_013373.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr22:20131088 C>T maps to NM_013373.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr22:20130310 C>T maps to NM_013373.3 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr22:20131090 G>A maps to NM_013373.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr22:20131021 C>A maps to NM_013373.3 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr22:20126834 C>T maps to NM_013373.3 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:128944951 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:128963036 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:128975837 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr10:31791273 A>G did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr10:31810824 A>G maps to NM_001174096.1 Q855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:31815876 C>T maps to NM_001174096.1 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:31815670 C>T maps to NM_001174096.1 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:31809765 C>T maps to NM_001174096.1 N502N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:31815921 C>T maps to NM_001174096.1 D1036D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr10:31809057 G>A maps to NM_001174096.1 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr10:31815807 G>A maps to NM_001174096.1 E998E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr2:145187335 C>A maps to NM_014795.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:145156755 G>A maps to NM_014795.3 N666N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr2:145157310 T>C maps to NM_014795.3 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:145153985 T>C maps to NM_014795.3 E1020E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr2:145156169 A>G maps to NM_014795.3 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:145147101 A>G maps to NM_014795.3 D1187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr2:145156047 G>A maps to NM_014795.3 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr2:145156635 T>C maps to NM_014795.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr9:131503843 G>A maps to NM_006336.2 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr9:131495727 C>T maps to NM_006336.2 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr9:131502298 G>A maps to NM_006336.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:131515483 G>A maps to NM_006336.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:131515849 G>A maps to NM_006336.2 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:82615251 G>A maps to NM_024699.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr2:220073043 C>A maps to NM_138802.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:38120050 C>T maps to NM_021943.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr15:80423564 C>T maps to NM_019006.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr15:80414052 G>A did not map to a codon.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr15:80412778 A>G maps to NM_019006.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:80429858 A>G maps to NM_019006.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr8:135614833 C>T maps to NM_020863.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8384-01A-21D-2394-08 chr8:135669924 C>T maps to NM_020863.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:135649908 C>T maps to NM_020863.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:135614221 G>A maps to NM_020863.3 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr8:135614314 C>T maps to NM_020863.3 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr12:72024377 A>C did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr12:72027124 A>G maps to NM_144982.4 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr12:72026033 A>C maps to NM_144982.4 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr12:72013180 G>A maps to NM_144982.4 G1686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr12:72025966 C>A maps to NM_144982.4 E1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr12:72026029 C>A maps to NM_144982.4 E1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr12:72008421 T>A maps to NM_144982.4 K1807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr16:72993576 G>T maps to NM_006885.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:72993843 C>T maps to NM_006885.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr16:72984508 G>A maps to NM_006885.3 N1025N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:72829353 A>G maps to NM_006885.3 L2409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:72831786 A>G maps to NM_006885.3 C1598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:72993165 G>T maps to NM_006885.3 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:72993335 G>A maps to NM_006885.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr16:72845890 G>A maps to NM_006885.3 T1192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:72821575 C>T maps to NM_006885.3 A3533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:72831384 T>C maps to NM_006885.3 Q1732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr16:72831390 T>C maps to NM_006885.3 Q1730Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:72991710 A>C maps to NM_006885.3 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:72829503 C>T maps to NM_006885.3 G2359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:72831384 T>C maps to NM_006885.3 Q1732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:72822268 C>T maps to NM_006885.3 L3302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:72992655 C>T maps to NM_006885.3 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:72845838 G>A maps to NM_006885.3 R1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:72993279 G>A maps to NM_006885.3 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:72993369 G>A maps to NM_006885.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr16:72992628 C>T maps to NM_006885.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:72845606 G>A maps to NM_006885.3 Q1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr16:72993114 G>A maps to NM_006885.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:72821566 G>A maps to NM_006885.3 S3536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:72821599 G>A maps to NM_006885.3 G3525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:72821629 G>A maps to NM_006885.3 G3515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:72992700 G>A maps to NM_006885.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr16:72984715 G>A maps to NM_006885.3 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:72821413 C>T maps to NM_006885.3 S3587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:72829760 G>A maps to NM_006885.3 Q2274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr8:77776431 C>T maps to NM_024721.4 V3494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr8:77776773 C>T maps to NM_024721.4 S3608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:77763548 C>T maps to NM_024721.4 P1464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr8:77776233 C>T maps to NM_024721.4 F3428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:77618449 T>C maps to NM_024721.4 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr8:77618401 G>A maps to NM_024721.4 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr8:77690511 C>A maps to NM_024721.4 Y1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:77766905 C>T maps to NM_024721.4 D2583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:77768042 A>G maps to NM_024721.4 L2962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:77767658 A>G maps to NM_024721.4 K2834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:77617894 C>A maps to NM_024721.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr8:77764976 C>T maps to NM_024721.4 G1940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:77618297 C>T maps to NM_024721.4 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:77767532 G>T maps to NM_024721.4 G2792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr8:77768495 C>T maps to NM_024721.4 N3113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr8:77775679 C>T maps to NM_024721.4 Q3244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:77767832 G>A maps to NM_024721.4 P2892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr8:77765162 G>A maps to NM_024721.4 T2002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:77616634 C>T maps to NM_024721.4 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:77763269 C>A maps to NM_024721.4 P1371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:77766791 G>A maps to NM_024721.4 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:77767736 C>T maps to NM_024721.4 C2860C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:77616880 G>A maps to NM_024721.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr8:77618344 T>A maps to NM_024721.4 C674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr8:77762598 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:77766596 G>A maps to NM_024721.4 T2480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr8:77763746 G>A maps to NM_024721.4 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RS-01A-12D-A34U-08 chr8:77767841 C>T maps to NM_024721.4 N2895N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr8:77618656 C>T maps to NM_024721.4 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr8:77767092 A>T maps to NM_024721.4 K2646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BW-01A-11D-A32N-08 chr8:77765709 C>T maps to NM_024721.4 R2185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:77768372 C>T maps to NM_024721.4 D3072D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr8:77619910 T>C maps to NM_024721.4 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr8:77776509 C>A maps to NM_024721.4 C3520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr8:77768376 C>T maps to NM_024721.4 L3074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:75203277 T>C maps to NM_153688.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr16:75203883 A>G maps to NM_153688.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr15:42743353 C>T maps to NM_022473.1 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr15:42734561 G>A maps to NM_022473.1 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr15:42743851 A>G maps to NM_022473.1 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr15:42743713 T>C maps to NM_022473.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N2-01A-12D-A364-08 chr15:42713330 C>T did not map to a codon.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr15:42743572 G>A maps to NM_022473.1 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:36853089 C>T maps to NM_020917.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr19:36831554 A>G maps to NM_020917.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:36831890 A>C maps to NM_020917.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr18:5291264 G>A maps to NM_003409.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:5291939 G>A maps to NM_003409.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr5:178359696 G>A maps to NM_030613.2 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr5:178359696 G>A maps to NM_030613.2 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr5:178359582 A>G maps to NM_030613.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr5:178359642 C>T maps to NM_030613.2 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr5:178359222 C>T maps to NM_030613.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:57065620 A>T maps to NM_020828.1 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:57059233 G>A maps to NM_020828.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr19:57065059 A>T maps to NM_020828.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr19:57065905 T>C maps to NM_020828.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr17:4995827 G>A maps to NM_153018.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr17:4996146 G>T maps to NM_153018.2 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:38127189 A>G maps to NM_014898.2 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:38127030 A>G maps to NM_014898.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:38134163 A>G did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr19:38126844 G>A maps to NM_014898.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:38126853 T>C maps to NM_014898.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr19:38135592 T>C maps to NM_014898.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr14:69256405 G>A maps to NM_004926.2 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr2:43452231 G>C maps to NM_006887.4 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:115805376 A>G maps to NM_003408.1 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr9:115806462 A>G maps to NM_003408.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr9:115818896 C>T maps to NM_003408.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:144332456 C>T maps to NM_173832.3 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8676-01A-11D-2394-08 chr8:144332285 G>A maps to NM_173832.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr8:144332291 G>A maps to NM_173832.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5802-01A-11D-1600-08 chr6:29643827 G>A maps to NM_001109809.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr6:29643776 T>A maps to NM_001109809.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:50701278 G>A maps to NM_199427.2 C585C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr20:50769725 G>A maps to NM_018197.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr20:50701173 G>A maps to NM_199427.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:50701512 C>T maps to NM_199427.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:50769440 G>A maps to NM_018197.2 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr20:50769644 C>T maps to NM_018197.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:50769088 G>A maps to NM_018197.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:50769392 C>T maps to NM_018197.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:36896523 C>A maps to NM_133466.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr19:36884059 G>A maps to NM_133466.2 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr19:36884062 A>C maps to NM_133466.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:68597620 C>T maps to NM_133458.2 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:68597622 G>A maps to NM_133458.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:68598357 T>C maps to NM_133458.2 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr16:68597364 G>T maps to NM_133458.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:88599109 G>A maps to NM_153813.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:88598419 C>T maps to NM_153813.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:88599305 G>A maps to NM_153813.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:88599103 G>T maps to NM_153813.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr8:106813749 C>A maps to NM_012082.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr8:106815516 C>T maps to NM_012082.3 H1069H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr8:106813815 T>G maps to NM_012082.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr8:106815453 G>A maps to NM_012082.3 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:106814403 G>A maps to NM_012082.3 R698R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-A4J4-01A-12D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-A4J4-01A-12D-A25D-08 chr8:106800946 G>A maps to ENST00000378472 G1G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr8:106456568 G>A maps to NM_012082.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr8:106813707 T>C maps to NM_012082.3 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:106431519 T>C maps to NM_012082.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr8:106815405 G>A maps to NM_012082.3 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr8:106815063 A>G maps to NM_012082.3 K918K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr8:106431375 G>T maps to NM_012082.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr8:106573609 G>A maps to NM_012082.3 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr8:106815237 A>G maps to NM_012082.3 K976K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr8:106815457 C>T maps to NM_012082.3 Q1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr8:106811057 G>A maps to NM_012082.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7O7-01A-11D-A33T-08 chr8:106814328 C>A maps to NM_012082.3 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr5:32380246 C>T maps to NM_016107.3 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr19:3831838 G>T maps to NM_015174.1 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:3831667 G>A maps to NM_015174.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:3823258 C>T maps to NM_015174.1 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:3823258 C>T maps to NM_015174.1 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:3819149 C>A maps to NM_015174.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:3834968 C>T maps to NM_015174.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:3821381 C>T maps to NM_015174.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr19:3834821 G>T maps to NM_015174.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr19:3819221 C>T maps to NM_015174.1 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:24228589 T>C did not map to a codon.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr23:24228400 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:24226348 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:24228817 C>T did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr23:24226359 T>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:24229410 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:24228544 C>T did not map to a codon.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr23:24197706 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr24:2847735 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr24:2848016 G>T did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:73437630 G>A maps to NM_021260.2 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:73491078 C>T maps to NM_021260.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr14:73441485 C>G did not map to a codon.
Sequencing variant TCGA-VQ-A92D-01A-11D-A410-08 chr14:73491098 G>A maps to NM_021260.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr5:79735831 C>A maps to NM_014733.3 C800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:79746388 T>C maps to NM_014733.3 Y1122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr5:79746296 T>C maps to NM_014733.3 L1092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:79733733 A>G maps to NM_014733.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:79734456 A>G maps to NM_014733.3 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr3:15123963 G>A maps to NM_022340.2 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr14:104194222 C>T maps to ENST00000216602 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr14:104199059 C>T maps to ENST00000216602 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr14:68249833 C>T maps to NM_015346.3 V1345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr14:68251917 C>T maps to NM_015346.3 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr14:68222802 C>T maps to NM_015346.3 K2216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr14:68217771 G>A maps to NM_015346.3 N2471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr14:68241784 G>A maps to NM_015346.3 P1756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr14:68249736 G>A maps to NM_015346.3 R1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr10:99511149 C>T maps to NM_001002261.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr10:99509311 G>A maps to NM_001002261.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr4:2306440 G>A maps to NM_020972.2 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr1:52703679 T>C maps to NM_004799.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:52703745 G>A maps to NM_004799.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr1:52803537 G>A maps to NM_004799.2 A1255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr1:52811787 T>C maps to NM_004799.2 D1391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:62366006 G>A maps to NM_032527.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:62366009 C>T maps to NM_032527.4 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:62367193 C>T maps to NM_032527.4 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:62366009 C>T maps to NM_032527.4 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:62366608 C>T maps to NM_032527.4 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr20:62365997 G>C maps to NM_032527.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:124267571 G>A maps to NM_007222.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:124265716 T>G maps to NM_007222.3 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr8:123964439 C>T maps to NM_014943.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr8:123965483 G>A maps to NM_014943.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:123964289 G>T maps to NM_014943.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:123964439 C>T maps to NM_014943.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr8:123966230 C>T maps to NM_014943.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr8:123964841 G>A maps to NM_014943.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr8:123966245 A>G maps to NM_014943.3 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:123964151 C>T maps to NM_014943.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr20:39831062 G>A maps to NM_015035.3 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr20:39833082 G>A maps to NM_015035.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr3:147128282 C>T maps to NM_003412.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:147128882 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:147128744 C>A maps to NM_003412.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PE-01A-31D-A25D-08 chr3:147128474 G>A maps to NM_003412.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr3:147127955 G>A maps to NM_003412.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr3:147128363 G>A maps to NM_003412.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:147128762 A>G maps to NM_003412.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr3:147128033 C>T maps to NM_003412.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr3:147127955 G>A maps to NM_003412.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr13:100637713 A>T maps to NM_007129.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:136649749 G>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:136651094 T>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:136651097 C>T did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:136649718 C>T did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:136649261 G>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:136649418 G>T did not map to a codon.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr23:136652213 C>A did not map to a codon.
Sequencing variant TCGA-CG-5719-01A-11D-1600-08 chr23:136651178 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:136649821 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:136649855 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:136649465 C>T did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr3:147108881 C>T maps to NM_001168379.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr3:147113918 G>A maps to NM_001168379.1 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr3:147108941 G>A maps to NM_001168379.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:147108998 G>A maps to NM_001168379.1 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:100617834 G>A maps to NM_033132.3 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr13:100622672 C>T maps to NM_033132.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr13:100622657 C>T maps to NM_033132.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr13:100617885 C>T maps to NM_033132.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A7NT-01A-21D-A34U-08 chr13:100617630 C>T maps to NM_033132.3 *664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:58102492 C>T maps to NM_001010879.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr19:57286429 T>G maps to NM_001146326.1 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr19:57286490 A>C maps to NM_001146326.1 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:57286616 T>C maps to NM_001146326.1 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:57286561 G>A maps to NM_001146326.1 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:57286337 A>G maps to NM_001146326.1 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:57286259 G>A maps to NM_001146326.1 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:57647392 G>A maps to NM_052882.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RI-01A-11D-A32N-08 chr19:57646366 A>C maps to NM_052882.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr7:99627870 G>A did not map to a codon.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr16:25255184 G>A maps to NM_001012981.4 C634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr16:25268436 G>A maps to NM_001012981.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr6:28327510 C>T maps to NM_024493.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:28327576 C>T maps to NM_024493.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr6:28213205 C>T maps to NM_019110.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr6:28219398 G>A maps to NM_019110.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr6:28214866 A>G maps to NM_019110.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4455-01A-01D-1158-08 chr7:99117465 A>G maps to NM_014569.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:99129067 T>C maps to NM_014569.3 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr23:101138865 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:101152908 G>A did not map to a codon.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr23:101138751 T>C did not map to a codon.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr23:101139162 A>C did not map to a codon.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr23:101139538 G>A did not map to a codon.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr23:101138597 T>A did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:101139415 T>C did not map to a codon.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr23:101141678 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:101138595 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:101138489 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr23:101138837 G>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr5:140085280 C>T maps to NM_144723.1 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr3:178785522 G>A maps to NM_022470.3 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:178745552 A>G maps to NM_022470.3 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr8:40554920 C>T did not map to a codon.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr8:40532367 G>A maps to NM_024645.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr22:30134377 G>A maps to NM_019103.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:81050714 G>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr10:81060695 C>T maps to NM_020338.3 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr10:81052025 A>G maps to NM_020338.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:81056310 G>A maps to NM_020338.3 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GY-01A-21D-A24D-08 chr10:81064967 C>A maps to NM_020338.3 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr10:81052013 G>A maps to NM_020338.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A805-01A-11D-A364-08 chr10:81060644 C>T maps to NM_020338.3 H655H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:81049540 G>A maps to NM_020338.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:81065310 C>T maps to NM_020338.3 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:44806204 C>T maps to NM_031449.3 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:44802876 C>T maps to NM_031449.3 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:44806228 T>C maps to NM_031449.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr7:44801437 C>G maps to NM_031449.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:44804019 C>T maps to NM_031449.3 C621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:44805865 C>A maps to NM_031449.3 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:44805814 G>A maps to NM_031449.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:40735798 G>A maps to NM_005857.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:35579863 C>T maps to NM_024772.3 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr13:20638642 C>T maps to NM_001190965.1 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr13:20579331 G>T maps to NM_001190965.1 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr13:20567632 C>T maps to NM_001190965.1 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7806-01A-11D-2053-08 chr13:20641134 C>T maps to NM_001190965.1 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:70462270 G>A did not map to a codon.
Sequencing variant TCGA-BR-6709-01A-11D-1882-08 chr23:70465870 G>C did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:70468577 T>G did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:70469891 C>T did not map to a codon.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr23:70465280 C>A did not map to a codon.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr23:70466473 T>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:70460932 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:70471055 T>C did not map to a codon.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr23:70462829 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:70467210 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:70462271 T>C did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr13:20399054 C>T maps to NM_001142684.1 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr13:20411870 G>T maps to NM_001142684.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5579-01A-01D-1600-08 chr1:35457895 G>A maps to NM_007167.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr1:35474520 G>T maps to NM_007167.3 C499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:35478107 A>G maps to NM_007167.3 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr3:50379245 C>T maps to NM_015896.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:50379572 T>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr10:255849 T>C maps to NM_006624.4 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:294868 G>A maps to NM_006624.4 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr10:294977 C>T maps to NM_006624.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:42915621 C>A maps to NM_032257.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr17:4647918 G>T did not map to a codon.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:4647737 C>T maps to NM_001136046.1 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr17:4646745 C>T maps to NM_001136046.1 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:140481456 G>A maps to NM_138462.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:140476995 C>T maps to NM_138462.2 *228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr9:140477599 A>C maps to NM_138462.2 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-5577-01A-01D-1600-08 chr20:45852979 G>T maps to ENST00000471951 C1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr12:133733400 C>T maps to NM_015394.4 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr12:133732656 C>T maps to NM_015394.4 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:21909814 T>C maps to NM_173531.3 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr7:64168652 T>A maps to NM_016220.3 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr7:64168628 A>G maps to NM_016220.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr7:64167491 A>G maps to NM_016220.3 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr7:64168520 T>C maps to NM_016220.3 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:64168536 C>T maps to NM_016220.3 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:48790080 G>A maps to NM_153608.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:64438700 G>A maps to NM_015852.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr7:64439915 T>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:6730757 G>A maps to ENST00000330442 Y662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr7:6731975 A>G maps to ENST00000330442 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:6731627 A>G maps to ENST00000330442 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr1:247319981 T>C maps to NM_003431.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr5:43174880 C>T maps to ENST00000509156 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:58944989 G>A maps to NM_003433.3 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5803-01A-11D-1600-08 chr19:58946279 G>A maps to NM_003433.3 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr19:58944794 C>T maps to NM_003433.3 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr19:58944764 A>G maps to NM_003433.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4475-01A-01D-1158-08 chr20:18297429 G>A maps to ENST00000401790 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:18296187 T>C maps to ENST00000401790 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:18295924 G>T maps to ENST00000401790 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr19:58132515 G>A maps to NM_003435.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8483-01A-31D-2394-08 chr19:58132647 T>C maps to NM_003435.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:58132191 C>T maps to NM_003435.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:58578556 G>A maps to NM_007134.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr19:58578733 T>C maps to NM_007134.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:58574898 C>T maps to NM_007134.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:58573063 G>T maps to NM_007134.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:58574814 A>G maps to NM_007134.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:12298590 T>C maps to NM_003437.3 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr7:64275418 T>C maps to ENST00000307355 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr7:64292081 A>G maps to ENST00000307355 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8380-01A-11D-2340-08 chr19:19824903 G>A maps to NM_021030.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:19822954 G>A maps to NM_021030.2 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:19822870 G>A maps to NM_021030.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr2:219511045 C>T maps to NM_001105537.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr2:219508076 G>A maps to NM_001105537.1 G1054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:219509336 T>G maps to NM_001105537.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr2:219509369 G>C maps to NM_001105537.1 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:219507068 C>T maps to NM_001105537.1 R1390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5734-01A-11D-1600-08 chr2:219508124 G>C maps to NM_001105537.1 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr2:219508171 G>A maps to NM_001105537.1 Q1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr2:219507530 C>T maps to NM_001105537.1 T1236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr2:219509669 C>A maps to NM_001105537.1 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr2:219503412 G>A maps to NM_001105537.1 G1571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr11:9522758 A>C maps to NM_003442.5 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr11:9522662 C>T maps to NM_003442.5 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr11:9492968 T>C did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:36727779 T>C maps to NM_007145.2 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr3:125007066 G>A maps to NM_021964.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5813-01A-11D-1600-08 chr19:58213859 T>A maps to NM_001085384.1 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr19:58213437 T>C maps to NM_001085384.1 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:44495768 C>T maps to NM_003445.2 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr23:47272406 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:47269705 A>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:47271937 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:47272742 G>A did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:47269694 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:47271824 A>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47272102 A>G did not map to a codon.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr23:47272402 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:47272095 T>C did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr8:146156789 G>A maps to NM_006958.2 H461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:53571350 G>A maps to NM_001102603.1 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:53577420 C>T maps to NM_001102603.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:28056986 C>A maps to NM_003447.3 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr6:28053570 T>C maps to NM_003447.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr3:44607106 T>A maps to NM_018651.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr9:97062922 C>T maps to NM_194320.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:97062107 G>T maps to NM_194320.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr9:97062748 C>A maps to NM_194320.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:57931168 C>T maps to NM_006959.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:57932497 A>G maps to NM_006959.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:3452238 C>T maps to NM_003450.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:52091617 G>A maps to NM_007147.2 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:9489756 C>A maps to NM_001172651.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr19:9492005 T>C maps to NM_001172651.1 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr19:9491771 T>C maps to NM_001172651.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:11881836 C>A maps to NM_144680.2 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:44982337 T>C maps to NM_013256.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr19:44980911 G>A maps to NM_013256.3 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr19:44980956 G>A maps to NM_013256.3 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:35232233 T>G maps to ENST00000392232 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8286-01A-12D-2340-08 chr19:35232158 A>G maps to ENST00000392232 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:47836702 A>G did not map to a codon.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr23:47837004 C>T did not map to a codon.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr23:47836189 A>G did not map to a codon.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr23:47836328 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:47842801 T>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:47836479 G>A did not map to a codon.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr23:47835937 A>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr6:27420688 T>A maps to NM_007149.2 K217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr6:27420699 G>T maps to NM_007149.2 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr6:27425140 T>C maps to NM_007149.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr23:152128369 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:152128249 A>T did not map to a codon.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr23:152085674 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:152083706 G>A did not map to a codon.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr23:152113916 G>A did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr23:152137957 G>A did not map to a codon.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr23:152135748 A>C did not map to a codon.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr23:152134006 G>A did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:152083287 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr9:104170263 G>T maps to NM_003452.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:104171447 T>C maps to NM_003452.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr16:71512173 T>A maps to NM_006961.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:71509153 C>T maps to NM_006961.3 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr6:28121104 C>T maps to NM_006298.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr6:28121578 A>G maps to NM_006298.2 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr6:28200860 C>T maps to ENST00000425468 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:28200919 C>T maps to ENST00000425468 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr11:3392214 G>A maps to NM_001130520.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr11:3380734 G>A maps to NM_001130520.1 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr11:3381027 C>A maps to NM_001130520.1 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr3:44672627 A>T maps to NM_006991.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr3:44670855 G>A maps to NM_006991.3 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr3:44684844 G>A maps to NM_006991.3 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr3:44683854 G>A maps to NM_006991.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:44683452 A>G maps to NM_006991.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr2:95847340 A>G maps to ENST00000453539 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr2:95847607 C>T maps to ENST00000453539 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:12243482 A>C maps to NM_021143.2 Y506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:12246373 T>C maps to NM_021143.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:12243601 G>A maps to NM_021143.2 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr11:123596941 G>A maps to NM_003455.2 C570C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr11:123596770 T>C maps to NM_003455.2 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr11:123597619 T>C maps to NM_003455.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:3168972 C>T maps to NM_001042428.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr16:3170172 C>T maps to NM_001042428.1 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:3165483 G>A maps to NM_001042428.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr16:3170055 G>A maps to NM_001042428.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr16:3166476 G>A maps to NM_001042428.1 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:30687714 C>T maps to ENST00000394679 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:22154679 A>C maps to NM_007153.3 A1052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:22156329 A>G maps to NM_007153.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:22156959 T>C maps to NM_007153.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:22171702 C>T maps to NM_007153.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr19:22156134 G>T maps to NM_007153.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:22155033 T>C maps to NM_007153.3 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr19:22157208 A>C maps to NM_007153.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:22156464 T>C maps to NM_007153.3 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr19:22154591 C>A maps to NM_007153.3 E1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:148947335 C>T maps to NM_012256.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr16:3190765 C>T maps to NM_001134655.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr16:3191065 G>A maps to NM_001134655.1 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BF-01A-12D-A24D-08 chr16:3190924 C>T maps to NM_001134655.1 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr11:7021533 A>G maps to NM_013249.2 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr11:7023985 G>T maps to NM_013249.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr11:6977488 A>G maps to NM_013250.2 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:52198528 C>T maps to NM_006526.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:52199044 C>T maps to NM_006526.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr20:52193273 T>G maps to NM_006526.2 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr20:52193562 A>C maps to NM_006526.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:52199170 C>T maps to NM_006526.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr20:52192755 A>C maps to NM_006526.2 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5727-01A-11D-1600-08 chr20:52192731 G>A maps to NM_006526.2 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:52198489 C>T maps to NM_006526.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:52199146 G>T maps to NM_006526.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:52198417 C>T maps to NM_006526.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr14:21560051 C>G maps to NM_001102454.1 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr14:21558907 C>T maps to NM_001102454.1 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr14:21561362 G>A maps to NM_001102454.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:45499106 T>C maps to NM_006963.4 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:45498977 C>T maps to NM_006963.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:44469185 C>T maps to NM_013359.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7196-01A-11D-2053-08 chr19:44470469 T>C maps to NM_013359.2 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:44470845 G>T maps to NM_013359.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:44470959 C>T maps to NM_013359.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:44570343 C>T maps to NM_013361.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:44570670 A>G maps to NM_013361.4 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:44610780 C>A maps to NM_013398.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr19:44635940 C>T maps to NM_013362.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:44636029 G>A maps to NM_013362.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:44635768 T>C maps to NM_013362.2 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:44635700 C>T maps to NM_013362.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:44635660 T>C maps to NM_013362.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:44676239 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:44681080 G>T maps to NM_001032372.1 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:44680401 C>T maps to NM_001032372.1 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:44679756 T>C maps to NM_001032372.1 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr19:44740982 G>T maps to NM_182490.1 *800Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:44740601 G>A maps to NM_182490.1 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr19:44933033 G>C maps to NM_014518.2 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr19:44933773 G>C maps to NM_014518.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:44933611 C>T maps to NM_014518.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:44947007 A>G maps to NM_014518.2 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:44946744 A>G did not map to a codon.
Sequencing variant TCGA-R5-A7ZR-01A-11D-A34U-08 chr16:71483579 G>A maps to NM_145911.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:44513051 G>A maps to NM_006300.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:44778795 G>A maps to NM_181756.1 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:44778459 G>A maps to NM_181756.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:44661003 C>T maps to NM_006630.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:44661758 T>C maps to NM_006630.2 H530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:44660597 A>T maps to NM_006630.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:44660799 A>T maps to NM_006630.2 K211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6707-01A-11D-1882-08 chr19:44791903 G>A maps to NM_004234.4 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:44792075 G>A maps to NM_004234.4 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:44792900 C>T maps to NM_004234.4 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:44803828 C>T maps to NM_004234.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:44792699 A>G maps to NM_004234.4 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr18:74563867 G>A maps to NM_007345.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:74592190 G>A maps to NM_007345.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:74631810 G>A maps to NM_007345.3 T1116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr18:74649232 G>A maps to NM_007345.3 T1570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr18:74635025 G>T did not map to a codon.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr18:74607071 C>A maps to NM_007345.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:74593457 G>A maps to NM_007345.3 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr18:74620359 C>A maps to NM_007345.3 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr18:74639294 G>T maps to NM_007345.3 T1410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr18:74625804 C>T maps to NM_007345.3 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:74583713 G>A maps to NM_007345.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:74632002 C>T maps to NM_007345.3 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr1:244218293 C>T maps to NM_205768.2 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr18:32917732 A>G maps to NM_006965.2 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr10:38121106 C>T maps to NM_021045.1 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr10:38121916 A>C maps to NM_021045.1 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:38241570 G>T maps to NM_145011.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr10:38241393 A>G maps to NM_145011.2 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:38241876 A>G maps to NM_145011.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:38241906 G>T maps to NM_145011.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:146107412 G>A maps to NM_021061.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:145947421 C>T maps to NM_138367.1 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr8:145948630 G>A maps to NM_138367.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:145947730 G>A maps to NM_138367.1 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CR-01A-11D-A24D-08 chr19:20003001 G>T maps to NM_021047.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:20003045 T>C maps to ENST00000427401 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IV-01A-31D-A25D-08 chr19:24309935 C>A maps to NM_203282.2 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr19:24310226 A>G maps to NM_203282.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr19:24309870 A>T maps to NM_203282.2 K357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6G-01A-11D-A410-08 chr19:24309324 A>C maps to NM_203282.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:58453319 G>A maps to NM_005773.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:58453788 A>G maps to NM_005773.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4366-01A-01D-1158-08 chr19:22272024 A>G maps to NM_033468.2 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:22271241 A>G maps to NM_033468.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:22270959 T>C maps to NM_033468.2 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr19:22271541 C>T maps to NM_033468.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr11:116658316 C>A maps to NM_003904.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:37006131 G>A maps to NM_001166038.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8485-01A-11D-2394-08 chr19:57723985 A>G maps to NM_003417.4 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:57723709 G>A maps to NM_003417.4 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:9524025 G>A maps to NM_006631.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31927165 C>T maps to NM_003414.4 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31927342 T>C maps to NM_003414.4 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr16:31925887 T>C maps to NM_003414.4 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:31927585 G>A maps to NM_003414.4 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:64377978 T>C maps to NM_021148.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr7:64378003 G>T maps to NM_021148.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr7:64388277 C>G maps to NM_021148.2 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7134-01A-11D-2053-08 chr7:64388200 A>G maps to NM_021148.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr7:64378632 C>T maps to NM_021148.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:64389199 C>T maps to NM_021148.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:58724307 C>T maps to NM_133502.1 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:58723002 C>T maps to NM_133502.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:152613217 C>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:152612685 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:152612853 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:152612322 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:152612854 G>A did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:89804287 C>T maps to NM_001113525.1 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7C1-01A-11D-A32N-08 chr16:89804287 C>T maps to NM_001113525.1 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr7:111958266 C>T maps to NM_021994.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:111958289 C>T maps to NM_021994.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:53304071 T>C maps to NM_006969.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr22:22869531 G>A maps to NM_080740.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr22:22868373 A>G maps to NM_080740.3 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6K-01A-11D-A410-08 chr22:22868667 G>C maps to NM_080740.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr22:22843015 T>C maps to NM_080764.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:129380905 T>G did not map to a codon.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr23:129370482 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:129339306 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:129362956 A>G did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:129380884 G>A did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr23:129380890 C>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:129364677 A>G did not map to a codon.
Sequencing variant TCGA-BR-8381-01A-11D-2394-08 chr23:129339385 G>T did not map to a codon.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr15:56974619 G>C maps to NM_017661.2 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr15:56959097 G>T maps to NM_017661.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr15:56924163 G>T maps to NM_017661.2 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:56970886 A>G maps to NM_017661.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr15:56996376 G>A maps to NM_017661.2 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr1:200377111 A>C maps to NM_012482.3 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr1:200377573 G>A maps to NM_012482.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:200376619 C>T maps to NM_012482.3 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr7:148921306 C>T maps to NM_003575.2 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr7:148895531 G>A maps to NM_003575.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:148921351 G>A maps to NM_003575.2 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:44352262 C>T maps to NM_181845.1 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:44339698 C>A maps to NM_181845.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:44341287 C>T maps to NM_181845.1 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:44351313 T>G maps to NM_181845.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:44890965 C>A maps to NM_152354.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:44892259 G>A maps to NM_152354.3 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A747-01A-22D-A33T-08 chr19:44891923 G>A maps to NM_152354.3 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:15620582 T>G maps to NM_020652.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr17:18566377 A>G maps to NM_001145045.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr17:18565270 A>C maps to NM_001145045.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr17:16466544 T>C maps to NM_020653.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr17:16455517 T>C maps to NM_020653.2 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr6:87965770 T>G maps to NM_015021.1 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr6:87970081 A>G maps to NM_015021.1 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:87967379 A>T maps to NM_015021.1 K1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:87970367 T>C maps to NM_015021.1 L2341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:87970810 T>C maps to NM_015021.1 F2488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:87967535 C>T maps to NM_015021.1 R1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:87969689 C>T maps to NM_015021.1 R2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr6:87966656 G>T maps to NM_015021.1 G1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:87964572 T>A maps to NM_015021.1 L409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:87969202 T>A maps to NM_015021.1 P1952P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8243-01A-11D-2340-08 chr6:87971419 C>T maps to NM_015021.1 T2691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:87966823 A>G maps to NM_015021.1 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr6:87969689 C>T maps to NM_015021.1 R2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr21:43411999 T>C maps to NM_020727.4 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr21:43411231 T>C maps to NM_020727.4 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr21:43411984 G>A maps to NM_020727.4 H740H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:45575761 G>A maps to NM_145288.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:45574969 C>T maps to NM_145288.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:35434571 C>T maps to NM_001099438.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr5:150276527 C>T maps to NM_001172831.1 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr5:150278008 G>A maps to NM_001172831.1 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr5:150275534 G>A maps to NM_001172831.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr5:150275501 A>G maps to NM_001172831.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:35174066 C>T maps to ENST00000221282 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr19:35174130 A>T maps to ENST00000221282 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:35175799 A>G maps to ENST00000221282 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:57868910 T>G maps to ENST00000391705 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:28962825 T>C maps to NM_001010877.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr6:28963559 T>G maps to NM_001010877.2 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:9271916 C>T maps to NM_020933.4 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr19:9272048 C>T maps to NM_020933.4 H576H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:9271916 C>T maps to NM_020933.4 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:9271301 G>A maps to NM_020933.4 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr19:9271727 G>A maps to NM_020933.4 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:9270836 C>T maps to NM_020933.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:9267981 C>T maps to NM_020933.4 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:9271916 C>T maps to NM_020933.4 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4191-01A-02D-1126-08 chr6:43323883 C>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr6:43323193 T>C maps to NM_014345.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr6:43325441 G>A maps to NM_014345.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr6:43323651 G>A maps to NM_014345.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:43306478 C>A maps to NM_014345.2 E1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:43323493 A>G maps to NM_014345.2 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr6:43305045 G>A maps to NM_014345.2 G2230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr6:43325430 G>A maps to NM_014345.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr6:43325105 G>A maps to NM_014345.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr6:43307448 T>C maps to NM_014345.2 E1429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7133-01A-11D-2053-08 chr6:43305126 C>T maps to NM_014345.2 L2203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr6:43323103 G>A maps to NM_014345.2 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr6:43310599 A>G maps to NM_014345.2 N1030N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:58031050 G>A maps to NM_020807.1 C373C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:58031251 C>T maps to NM_020807.1 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:58031416 C>T maps to NM_020807.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:58030906 G>A maps to NM_020807.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:58031067 C>A maps to NM_020807.1 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr16:58030555 G>A maps to NM_020807.1 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:58031707 G>A maps to NM_020807.1 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr10:44139886 G>A maps to NM_006973.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:44139886 G>A maps to NM_006973.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:53385078 C>T maps to NM_207333.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr19:53384220 T>A maps to NM_207333.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr6:28294499 G>A maps to NM_030899.4 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr6:28294404 T>C maps to NM_030899.4 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:58967762 G>A maps to NM_207395.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:58967033 G>A maps to NM_207395.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:58966985 C>T maps to NM_207395.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:58967705 C>T maps to NM_207395.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr19:58967600 C>T maps to NM_207395.2 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6F-01A-31D-A410-08 chr19:58967576 G>A maps to NM_207395.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:90473077 C>T maps to NM_182976.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:90478718 G>A maps to NM_182976.2 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:58640600 A>C maps to NM_024620.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr19:58639802 C>T maps to NM_024620.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:54081130 C>T maps to NM_001079907.1 Y439Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:14830031 C>A maps to NM_032433.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:14815915 G>A maps to NM_032433.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:45130648 A>G maps to NM_018102.3 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:45131023 C>T maps to NM_018102.3 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4444-01A-01D-1158-08 chr20:45130816 G>A maps to NM_018102.3 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:45140719 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr20:45131158 A>C maps to NM_018102.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:44592273 C>T maps to NM_022095.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr20:44596987 C>T maps to NM_022095.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr20:44587965 C>T maps to NM_022095.3 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr20:44596235 A>T maps to NM_022095.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:44592441 C>T maps to NM_022095.3 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr20:25657196 G>A maps to NM_015655.2 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr20:25656020 G>A maps to NM_015655.2 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr20:25657028 G>A maps to NM_015655.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:25656356 G>A maps to NM_015655.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr20:25656873 G>A maps to NM_015655.2 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:38345454 A>T maps to NM_006954.1 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr10:38344179 A>G maps to NM_006954.1 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:38345256 A>G maps to NM_006954.1 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr10:43089407 T>C maps to NM_006955.1 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr10:43089479 A>G maps to NM_006955.1 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:145999195 G>A maps to NM_030580.3 R380*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BR-6452-01A-12D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:145999511 A>G maps to NM_030580.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:145999667 T>C maps to NM_030580.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr20:32344952 G>T did not map to a codon.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:32345063 C>T maps to ENST00000375200 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr20:32332957 G>A maps to ENST00000375200 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr20:32346585 C>T maps to ENST00000375200 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr20:32379190 G>A maps to ENST00000375200 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr20:32369094 A>G did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr20:2464826 C>T maps to NM_024325.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7959-01A-11D-2340-08 chr20:2464883 G>A maps to NM_024325.4 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:2465246 A>G maps to NM_024325.4 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr20:2463856 G>A maps to NM_024325.4 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:2464232 C>T maps to NM_024325.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr20:2463940 G>A maps to NM_024325.4 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:37369177 C>T maps to NM_003419.3 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr19:37367986 T>A maps to NM_003419.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr19:37368218 C>A maps to NM_003419.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr5:176468801 G>A maps to ENST00000503039 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:53644778 G>A maps to NM_001172674.1 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7901-01A-11D-2201-08 chr19:53643982 G>A maps to NM_001172674.1 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:53645114 A>T maps to NM_001172674.1 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:53645326 G>A maps to NM_001172674.1 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:53644889 T>C maps to NM_001172674.1 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr19:53643590 G>A maps to NM_001172674.1 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:44692630 A>G maps to NM_003420.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:44701409 C>T maps to NM_003420.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr3:44692630 A>G maps to NM_003420.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:44700934 G>A maps to NM_003420.3 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr3:44694074 G>A maps to NM_003420.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:52471831 T>C maps to NM_021632.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:52469194 G>A maps to NM_021632.3 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:52469107 G>A maps to NM_021632.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DT-01A-11D-A364-08 chr19:52468849 C>A maps to NM_021632.3 G286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:178152395 A>G maps to NM_005649.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr5:178152389 G>A maps to NM_005649.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr5:178139552 T>C maps to NM_005649.2 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr5:178152389 G>A maps to NM_005649.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr5:178139579 A>G maps to NM_005649.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:178311126 T>G maps to NM_058230.2 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr5:178506880 T>G maps to NM_014594.1 L483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr5:178505937 T>C maps to NM_014594.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:7585780 C>T maps to NM_018083.4 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:7584409 C>T maps to NM_018083.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:7585042 G>A maps to NM_018083.4 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr19:7584565 C>T maps to NM_018083.4 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr19:7584475 C>T maps to NM_018083.4 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr1:33741706 C>T maps to NM_152493.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr10:64414647 G>A maps to NM_199452.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4363-01A-01D-1158-08 chr10:64136620 C>T maps to NM_199451.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr10:64415332 G>A maps to NM_199452.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr10:64415332 G>A maps to NM_199452.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr10:64136335 C>A maps to NM_199451.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr10:64159484 C>T maps to NM_014951.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr5:71756780 G>A maps to NM_152625.1 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr5:71756246 G>A maps to NM_152625.1 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr5:71740011 C>A maps to NM_152625.1 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr5:71757206 G>T maps to NM_152625.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr5:71756600 G>A maps to NM_152625.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:71740080 G>A maps to NM_152625.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:71756465 G>A maps to NM_152625.1 C286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr9:99150629 G>A maps to NM_153695.3 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:99150563 C>T maps to NM_153695.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr10:38406456 C>T maps to NM_003421.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:37100893 T>G maps to NM_032825.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:37117656 T>G maps to NM_032825.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:37726530 A>G maps to NM_152604.1 L30L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4370-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr12:54764722 G>C maps to NM_001130967.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr2:180634425 C>T maps to NM_152520.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:180348095 C>T maps to NM_152520.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:180348059 G>A maps to NM_152520.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4304-01A-01D-1158-08 chr2:180309653 C>T maps to NM_152520.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr3:21606140 T>C maps to NM_024697.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr3:21606134 C>T maps to NM_024697.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:21552413 G>A maps to NM_024697.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:99092050 C>A maps to NM_032164.2 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr8:28206253 G>A maps to NM_018660.2 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr8:28217188 A>G maps to NM_018660.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr18:32837895 T>C maps to NM_032347.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:148876130 C>A maps to NM_170686.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:148876829 C>T maps to NM_170686.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr7:148876197 A>C maps to NM_170686.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:44377219 T>C maps to ENST00000324394 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr18:72343484 G>A maps to NM_017757.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr18:72344624 C>A maps to NM_017757.2 C550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr18:72345056 T>C maps to NM_017757.2 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr18:72344919 T>C maps to NM_017757.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr18:72353006 T>C maps to NM_017757.2 A1577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:72775952 C>T maps to NM_017757.2 A2092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:72776105 G>A maps to NM_017757.2 S2143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:72776237 C>T maps to NM_017757.2 S2187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr11:46727163 C>A maps to NM_024741.2 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr11:46726218 A>G maps to NM_024741.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr11:46727106 G>A maps to NM_024741.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr11:46726911 G>A maps to NM_024741.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr23:47308160 A>G did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:47307609 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47308809 C>A did not map to a codon.
Sequencing variant TCGA-BR-8682-01A-11D-2394-08 chr23:47308223 A>C did not map to a codon.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr23:47306847 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr23:47307845 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:53612487 T>C maps to NM_001164309.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr19:53612517 C>T maps to NM_001164309.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:53612859 A>G maps to NM_001164309.1 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:58083690 G>A maps to NM_017879.1 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr19:58084146 A>C maps to NM_017879.1 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr19:58420783 G>A maps to NM_152475.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:58421255 A>G maps to NM_152475.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr19:58420922 C>G maps to NM_152475.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:58420031 G>A maps to NM_152475.2 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:58437733 C>T maps to NM_133460.1 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:58439287 A>G maps to NM_133460.1 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:58439170 C>T maps to NM_133460.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EV-01A-11D-A31L-08 chr19:58439373 T>A maps to NM_133460.1 K59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr19:58439317 A>T maps to NM_133460.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:58437526 A>G maps to NM_133460.1 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:37619795 A>T maps to NM_144689.3 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:37619815 A>G maps to NM_144689.3 K641K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:37619821 T>C maps to NM_144689.3 Y643Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:37619899 A>G maps to NM_144689.3 K669K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:37618264 T>G maps to NM_144689.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:49672417 G>T maps to NM_015069.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:49670323 C>T maps to NM_015069.2 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:49764856 G>A maps to NM_015069.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr16:49669864 G>A maps to NM_015069.2 C1066C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:49671571 C>T maps to NM_015069.2 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:49764856 G>A maps to NM_015069.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr16:49671763 G>A maps to NM_015069.2 H433H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:49671547 G>T maps to NM_015069.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:49823440 G>T maps to NM_015069.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr16:49669948 A>G maps to NM_015069.2 H1038H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr16:49669966 C>T maps to NM_015069.2 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr16:49672705 G>A maps to NM_015069.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr16:49669759 G>A maps to NM_015069.2 N1101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:49764835 C>T maps to NM_015069.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr16:49670152 C>T maps to NM_015069.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr16:49669726 G>A maps to NM_015069.2 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:49669879 C>T maps to NM_015069.2 Q1061Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:49670224 C>T maps to NM_015069.2 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr7:148801228 G>A maps to NM_001001661.2 D578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr7:148802269 G>T maps to NM_001001661.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:148800886 C>T maps to NM_001001661.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:148815332 G>A maps to NM_001001661.2 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A804-01A-11D-A364-08 chr7:148801756 G>A maps to NM_001001661.2 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:148802125 G>A maps to NM_001001661.2 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:9639178 C>T maps to NM_024106.1 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr19:9639570 T>G maps to NM_024106.1 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr19:9639880 G>A maps to NM_024106.1 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:9639673 C>T maps to NM_024106.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:9639397 C>T maps to NM_024106.1 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A6F7-01A-12D-A32N-08 chr19:44112041 G>A maps to NM_182498.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:21720711 A>G maps to NM_001001415.2 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8683-01A-11D-2394-08 chr19:21720042 C>T maps to NM_001001415.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:21719280 C>T maps to NM_001001415.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PQ-01A-11D-A410-08 chr19:21720537 A>G maps to NM_001001415.2 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:21991812 G>A maps to NM_003423.2 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:21991362 G>A maps to NM_003423.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H6-01A-11D-A25D-08 chr19:21991524 G>A maps to NM_003423.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr19:21992232 G>T maps to NM_003423.2 C202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N5-01A-12D-A364-08 chr19:21991215 T>C maps to NM_003423.2 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:21991272 G>T maps to NM_003423.2 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:21203610 T>C did not map to a codon.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:21240478 A>G maps to NM_025189.3 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr19:21240535 A>T maps to NM_025189.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:21365876 G>A maps to NM_133473.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:21365864 T>A maps to NM_133473.2 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr19:21324989 G>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:52537130 C>A maps to NM_014650.2 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:52537082 G>A maps to NM_014650.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:52537842 A>G maps to NM_014650.2 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:12127029 G>A maps to NM_001080411.1 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:12126793 G>T maps to NM_001080411.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:3434840 G>A maps to ENST00000396852 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:31137484 G>A maps to NM_182755.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr10:31139182 G>A maps to NM_182755.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr10:31137595 G>A maps to NM_182755.2 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr10:31134323 C>A maps to NM_182755.2 G685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:31137668 T>C maps to NM_182755.2 K555K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:31134201 T>C maps to NM_182755.2 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr10:31139180 C>T maps to NM_182755.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:11978738 T>C maps to NM_152262.2 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:11979191 A>G maps to NM_152262.2 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:11978699 T>C maps to NM_152262.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:11979026 G>A maps to NM_152262.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:11979350 A>T maps to NM_152262.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr19:12384412 G>A maps to NM_001164276.1 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:11942181 G>A did not map to a codon.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:11943256 A>G maps to NM_152357.2 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:11943259 G>C maps to NM_152357.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:11891709 G>A maps to NM_152355.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:11891985 T>C maps to NM_152355.2 C449C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:12461252 A>G maps to NM_030824.2 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:12461819 C>T maps to NM_030824.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:12461258 C>T maps to NM_030824.2 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:12461305 G>A maps to NM_030824.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:12541998 G>T maps to NM_005815.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:12541722 A>G maps to NM_005815.4 H421H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:56671149 C>A maps to NM_018337.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr3:44497023 C>T maps to NM_181489.5 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:44490136 C>T maps to NM_181489.5 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr3:44489668 G>A maps to NM_181489.5 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr3:44497032 T>C maps to NM_181489.5 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:58988884 A>G maps to NM_017908.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr19:58991585 G>A maps to NM_017908.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr19:58989170 C>T maps to NM_017908.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr19:58992029 C>T maps to NM_017908.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:58988662 C>A maps to NM_017908.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:58988597 C>T maps to NM_017908.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr19:58991756 C>T maps to NM_017908.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:58988845 C>T maps to NM_017908.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:134494770 A>C did not map to a codon.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr23:134494826 A>G did not map to a codon.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr23:134494413 C>T did not map to a codon.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr23:134494365 C>T did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:134494811 G>A did not map to a codon.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr6:57013171 G>A maps to NM_001031623.2 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr6:56963932 T>C maps to NM_001031623.2 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr6:57013492 T>C did not map to a codon.
Sequencing variant TCGA-VQ-A8E2-01A-11D-A364-08 chr6:57012445 C>T maps to NM_001031623.2 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr5:178392184 G>A maps to NM_182594.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A487-01A-21D-A24D-08 chr5:178392721 T>G maps to NM_182594.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr5:178392713 G>T maps to NM_182594.2 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr5:178392166 A>G maps to NM_182594.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr5:178392091 G>A maps to NM_182594.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr5:178392206 G>T maps to NM_182594.2 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr5:178392251 C>T maps to NM_182594.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:57802979 T>C maps to NM_006635.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:57803351 C>T maps to NM_006635.3 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:57803240 A>G maps to NM_006635.3 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:57803525 G>A maps to NM_006635.3 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr19:37130885 C>A maps to NM_153257.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:37130847 G>A maps to NM_153257.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:37130484 G>T maps to NM_153257.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:109691643 G>A maps to NM_021224.4 K1817K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr9:109689882 G>A maps to NM_021224.4 T1230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr9:109690809 G>A maps to NM_021224.4 P1539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr9:109690809 G>A maps to NM_021224.4 P1539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:109687845 A>G maps to NM_021224.4 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:109689201 G>A maps to NM_021224.4 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr9:109746635 C>T maps to NM_021224.4 Y2334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr9:109690842 C>T maps to NM_021224.4 H1550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr9:109694806 G>A maps to NM_021224.4 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr9:109690561 C>T maps to NM_021224.4 Q1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr9:109687804 C>T maps to NM_021224.4 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:149463206 C>T maps to NM_207336.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A453-01A-11D-A24D-08 chr7:149461946 G>A maps to NM_207336.1 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:149462933 G>A maps to NM_207336.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr7:149462849 C>T maps to NM_207336.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:149461868 G>A maps to NM_207336.1 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:53344667 A>G maps to NM_001008801.1 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:57089758 T>C maps to NM_001001668.3 C654C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr19:57088126 T>C maps to NM_001001668.3 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr19:57088194 C>A maps to NM_001001668.3 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8677-01A-11D-2394-08 chr19:57088330 G>T maps to NM_001001668.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:57088136 G>T maps to NM_001001668.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6525-01A-11D-1800-08 chr19:57088867 T>C maps to NM_001001668.3 H357H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PM-01A-21D-A410-08 chr19:57089068 T>C maps to NM_001001668.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8297-01A-12D-2340-08 chr19:57036545 T>C maps to NM_020813.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:57036398 A>G maps to NM_020813.2 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:57036725 T>C maps to NM_020813.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr19:57036977 T>G maps to NM_020813.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-8663-01A-11D-2394-08 chr19:57037313 T>G maps to NM_020813.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr19:57036447 A>T maps to NM_020813.2 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:57037082 G>A maps to NM_020813.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:50550018 T>C maps to NM_015428.1 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:50545071 C>T maps to NM_015428.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:50542497 G>A maps to NM_015428.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:50548644 A>G maps to NM_015428.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr19:50548395 T>G maps to NM_015428.1 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:50549259 C>T maps to NM_015428.1 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:50548668 C>T maps to NM_015428.1 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:50548542 G>A maps to NM_015428.1 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr5:121488778 A>G maps to NM_207317.1 *365W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr5:121488305 C>T maps to NM_207317.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr7:57188752 T>C maps to NM_033273.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CQ-01A-12D-A25D-08 chr7:57188695 A>T maps to NM_033273.1 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N1-01A-12D-A364-08 chr7:57188320 T>C maps to NM_033273.1 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:57188092 A>G maps to NM_033273.1 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr16:30409176 G>A maps to ENST00000495929 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr16:30410361 G>A maps to ENST00000495929 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr16:30409954 C>T maps to ENST00000495929 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr16:30410094 A>G maps to ENST00000495929 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:52826014 T>C maps to NM_144684.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:52825646 C>T maps to NM_144684.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:52825330 A>G maps to NM_144684.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4J7-01A-31D-A25D-08 chr19:52817461 C>T maps to NM_144684.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:52825456 T>C maps to NM_144684.2 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:114305074 G>A maps to NM_133464.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr9:114305050 C>T maps to NM_133464.2 C612C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:95610225 G>A maps to NM_031486.1 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr9:95609709 T>C maps to NM_031486.1 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr9:95609460 C>T maps to NM_031486.1 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr9:95610072 G>A maps to NM_031486.1 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr9:95610081 T>C maps to NM_031486.1 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr10:44112702 T>C maps to NM_145312.3 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr10:44112042 G>A maps to NM_145312.3 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:20308760 G>A maps to ENST00000428290 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:20308529 T>C maps to ENST00000428290 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr10:48371036 C>T maps to NM_153034.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr10:48370747 G>A maps to NM_153034.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:12721452 G>T maps to NM_020714.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:11916971 G>A maps to NM_152356.3 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:11917521 T>C maps to NM_152356.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:22847067 C>T maps to NM_020855.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8099-01A-11D-2340-08 chr19:22847937 C>T maps to NM_020855.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:22847986 A>T maps to NM_020855.2 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr19:22847577 A>G maps to NM_020855.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:21605805 T>C maps to NM_001076678.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:21606363 T>G maps to NM_001076678.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:21606087 T>G maps to NM_001076678.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:21606417 A>G maps to NM_001076678.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:21606888 T>C maps to NM_001076678.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr1:247492679 G>A maps to NM_032752.1 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr1:247464039 G>A maps to NM_032752.1 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:247473055 G>A maps to NM_032752.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:247464564 C>T maps to NM_032752.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr1:247464039 G>A maps to NM_032752.1 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:58868128 C>T maps to NM_198458.1 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:58867744 G>A maps to NM_198458.1 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:58867594 G>A maps to NM_198458.1 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:58868866 C>T maps to NM_198458.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:58868275 G>A maps to NM_198458.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:58868089 G>A maps to NM_198458.1 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:99219141 C>T maps to NM_145115.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr7:99226970 G>A maps to NM_145115.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:99227096 C>T maps to NM_145115.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8631-01A-11D-2394-08 chr7:99227573 C>T maps to NM_145115.2 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr16:4803009 C>T maps to NM_021646.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr16:4810568 G>A maps to NM_021646.1 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr16:4810505 C>T maps to NM_021646.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA69-01A-11D-A410-08 chr16:4812304 C>T maps to NM_021646.1 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr10:77158836 G>A maps to NM_032772.4 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr10:77158593 C>T maps to NM_032772.4 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr10:77159094 G>A maps to NM_032772.4 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr10:77158989 C>T maps to NM_032772.4 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr10:77159253 C>T maps to NM_032772.4 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:19905492 T>C maps to NM_001099269.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:32844938 A>G maps to NM_014910.4 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:32873489 G>A maps to NM_014910.4 A826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:32845352 G>A maps to NM_014910.4 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr19:32873806 G>T maps to NM_014910.4 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr19:32873896 G>T maps to NM_014910.4 E924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:32844563 C>A maps to NM_014910.4 C276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:99522502 G>A maps to NM_014930.1 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr9:99521448 G>A maps to NM_014930.1 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr9:99521473 A>G maps to NM_014930.1 C546C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8610-01A-22D-2394-08 chr10:135123306 C>G maps to NM_145806.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:27821011 G>A maps to NM_032434.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr2:27844168 C>T maps to NM_032434.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr2:27838090 G>A maps to NM_032434.2 W396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PK-01A-12D-A410-08 chr2:27821116 C>T maps to NM_032434.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:62595543 G>A maps to NM_020713.1 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr20:62598744 G>A maps to NM_020713.1 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr20:62595508 G>A maps to NM_020713.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr20:62598852 G>A maps to NM_020713.1 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr20:62591324 G>A maps to NM_020713.1 D865D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr20:62595879 C>T maps to NM_020713.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HB-01A-12D-A25D-08 chr20:62592660 C>T did not map to a codon.
Sequencing variant TCGA-BR-A4J1-01A-11D-A25D-08 chr2:95815683 A>G maps to NM_032788.1 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8608-01A-11D-2394-08 chr2:95815287 C>T maps to NM_032788.1 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr18:74091753 G>A maps to ENST00000443185 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr18:74091363 C>T maps to ENST00000443185 Q902Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr18:74091690 C>T maps to ENST00000443185 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr18:74083440 G>T maps to ENST00000443185 A1115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:74091003 G>A maps to ENST00000443185 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:74091003 G>A maps to ENST00000443185 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr18:74091972 C>T maps to ENST00000443185 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr8:146033177 G>T maps to NM_213605.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr10:97916955 G>T maps to NM_014803.3 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr10:97916642 T>A maps to NM_014803.3 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr10:97917461 G>A maps to NM_014803.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:10446425 A>C maps to NM_053042.2 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr4:10445915 C>T maps to NM_053042.2 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr4:10447358 A>G maps to NM_053042.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr4:10447910 G>A maps to NM_053042.2 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:10445840 A>G maps to NM_053042.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr4:10446887 A>G maps to NM_053042.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6527-01A-11D-1800-08 chr4:10445603 G>A maps to NM_053042.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DZ-01A-11D-A364-08 chr4:10447809 G>T maps to NM_053042.2 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr18:14105974 T>C maps to NM_145287.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr18:14106214 A>G maps to NM_145287.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr18:22805223 G>A maps to NM_015461.2 Y886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr18:22805349 T>G maps to NM_015461.2 T844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8284-01A-11D-2340-08 chr18:22806393 G>T maps to NM_015461.2 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr18:22807023 G>A maps to NM_015461.2 C286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr18:22806756 C>T maps to NM_015461.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6820-01A-11D-1882-08 chr18:22805130 G>T maps to NM_015461.2 A917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr18:22807107 C>T maps to NM_015461.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr18:22671938 G>T maps to NM_015461.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr18:22806414 G>C maps to NM_015461.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:56114035 G>A maps to NM_153219.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:42729379 C>T maps to NM_133444.1 C275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:42729655 C>T maps to NM_133444.1 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:37879512 C>T maps to NM_032453.1 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr19:37879379 G>A maps to NM_032453.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:37879313 T>C maps to NM_032453.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:37037872 A>G maps to NM_001145649.1 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:58117150 C>A maps to NM_020880.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr18:56587201 G>A maps to NM_018181.4 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr18:56651463 C>T maps to NM_018181.4 I1224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr18:56587462 T>C maps to NM_018181.4 H648H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr18:56587297 A>G maps to NM_018181.4 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr18:56651280 G>A maps to NM_018181.4 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr18:56586415 G>A maps to NM_018181.4 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr18:56586742 G>A maps to NM_018181.4 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6B-01A-11D-A410-08 chr18:56585988 C>G maps to NM_018181.4 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8060-01A-11D-2340-08 chr19:52937308 G>A maps to NM_001143939.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:52942411 C>T maps to NM_001143939.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr19:31025844 G>A maps to NM_014717.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TK-01A-12D-A31L-08 chr19:31025808 C>T maps to NM_014717.1 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:30935716 C>T maps to NM_014717.1 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:31039375 C>T maps to NM_014717.1 H950H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:31039609 G>T maps to NM_014717.1 A1028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8077-01A-11D-2340-08 chr19:30935863 G>C maps to NM_014717.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:30936376 C>T maps to NM_014717.1 C636C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:30936401 C>T maps to NM_014717.1 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A44T-01A-32D-A24D-08 chr19:31039732 C>A maps to NM_014717.1 I1069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:30934861 G>A maps to NM_014717.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr19:30934927 G>A maps to NM_014717.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:30935839 G>A maps to NM_014717.1 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:31040041 C>A maps to NM_014717.1 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6875-01A-11D-2053-08 chr19:31040278 G>A maps to NM_014717.1 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:30934951 G>A maps to NM_014717.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:31040128 C>T maps to NM_014717.1 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8244-01A-11D-2340-08 chr19:30934804 C>A maps to NM_014717.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr19:31039369 A>G maps to NM_014717.1 K948K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:30935278 G>A maps to NM_014717.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:30934930 C>T maps to NM_014717.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:31040212 G>A maps to NM_014717.1 P1229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr19:31040059 C>T maps to NM_014717.1 N1178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DU-01A-11D-A364-08 chr19:30935239 G>A maps to NM_014717.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:30934690 C>T maps to NM_014717.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:30935398 G>A maps to NM_014717.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:31039225 C>T maps to NM_014717.1 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:38103200 A>G maps to NM_152606.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:38103014 G>A maps to NM_152606.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:57839232 T>C maps to NM_213598.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:57839291 T>C maps to NM_213598.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6705-01A-12D-1882-08 chr19:57839486 G>C maps to NM_213598.3 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:57840272 C>T maps to NM_213598.3 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:57838088 C>A maps to NM_213598.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4438-01A-01D-1158-08 chr19:57840314 G>A maps to NM_213598.3 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:57839138 A>G maps to NM_213598.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:57839960 C>T maps to NM_213598.3 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:57839441 C>T maps to NM_213598.3 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:57840063 C>T maps to NM_213598.3 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:58773027 G>A maps to NM_014480.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:58773441 A>G maps to NM_014480.2 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:58773474 C>T maps to NM_014480.2 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:40521504 C>A maps to NM_178544.3 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:40520373 C>T maps to NM_178544.3 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40519986 G>A maps to NM_178544.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:57909913 G>T maps to NM_001172773.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6526-01A-11D-1800-08 chr19:58048764 T>G maps to ENST00000376233 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4Z0-01A-22D-A25D-08 chr19:58048992 A>G maps to ENST00000376233 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr19:58049739 C>T maps to ENST00000376233 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:58199014 C>T maps to ENST00000356715 Q458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8573-01A-11D-2340-08 chr19:58199304 T>A maps to ENST00000356715 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:58320007 T>C maps to NM_024762.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:58320274 G>A maps to NM_024762.3 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:2834252 C>T maps to NM_001102651.1 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:2827740 G>T maps to NM_001102651.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:2834222 G>T maps to NM_001102651.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4477-01A-01D-1158-08 chr19:2834816 G>A maps to NM_001102651.1 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:2833973 C>T maps to NM_001102651.1 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr19:2852503 G>A maps to NM_152791.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:2852713 G>A maps to NM_152791.4 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:2877813 G>A maps to NM_024967.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:2877954 C>T maps to NM_024967.1 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:7076448 C>T maps to NM_024341.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:7075714 C>T maps to NM_024341.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6518-01A-11D-1800-08 chr19:7081984 G>A maps to NM_024341.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:8932717 G>A maps to NM_144693.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:8932735 T>C maps to NM_144693.1 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9452435 C>T maps to NM_032497.1 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr19:9452552 C>T maps to NM_032497.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr19:9578203 T>C maps to NM_152476.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:9578488 A>G maps to NM_152476.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:9577405 G>A maps to NM_152476.2 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:9578884 C>T maps to NM_152476.2 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr19:9583909 G>A maps to NM_152476.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr19:9721706 T>G maps to NM_152289.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:9764017 G>T maps to NM_001130032.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4441-01A-01D-1800-08 chr19:9764239 G>A maps to NM_001130032.1 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:9764461 A>G maps to NM_001130032.1 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:9763879 T>C maps to NM_001130032.1 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:9764326 C>T maps to NM_001130032.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:12430622 A>G maps to NM_145276.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:12429442 T>G maps to NM_145276.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:12638104 T>G maps to NM_144976.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:36673868 T>C maps to ENST00000355114 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:36673883 G>A maps to ENST00000355114 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:36674585 G>A maps to ENST00000355114 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:37210720 T>A maps to ENST00000423498 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YU-01A-21D-A25D-08 chr19:37211521 C>G maps to ENST00000423498 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:37210792 T>C maps to ENST00000423498 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr19:37210999 C>T maps to ENST00000423498 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr19:37440969 T>G maps to NM_198539.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr19:37440969 T>G maps to NM_198539.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8529-01A-11D-2340-08 chr19:37441300 A>T maps to NM_198539.2 K416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:37440778 C>T maps to NM_198539.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr19:37441188 G>A maps to NM_198539.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:37441104 T>C maps to NM_198539.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:37441801 G>T maps to NM_198539.2 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:37917232 C>T maps to NM_152484.2 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr19:37903984 A>G maps to NM_152484.2 N525N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr19:37903786 A>C maps to NM_152484.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr19:37905138 A>G maps to NM_152484.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr19:37904952 T>A maps to NM_152484.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:2917761 A>G maps to NM_173480.2 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:2917974 C>T maps to NM_173480.2 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:2917857 G>A maps to NM_173480.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:37966811 A>C maps to NM_144694.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RO-01A-12D-A33T-08 chr19:37966831 G>A maps to NM_144694.1 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:37975156 C>A maps to NM_144694.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr19:38057128 T>C maps to NM_016536.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8058-01A-31D-2340-08 chr8:125989940 C>T maps to NM_152412.2 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:38230301 A>G maps to NM_001172690.1 C363C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr19:38229530 A>G maps to NM_001172690.1 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:38230163 A>T maps to NM_001172690.1 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:42584302 C>T maps to ENST00000222339 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:42584905 C>A maps to ENST00000222339 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:42584248 C>T maps to ENST00000222339 C587C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:42583294 G>A maps to ENST00000222339 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:42583216 C>T maps to ENST00000222339 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:42583759 C>T maps to ENST00000222339 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:44039616 C>T maps to ENST00000458714 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:44039442 C>T maps to ENST00000458714 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:52376894 T>C maps to NM_032679.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:52376329 T>G maps to NM_032679.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:52376177 T>C maps to NM_032679.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr19:52380604 C>A maps to NM_032679.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:53014344 C>T maps to NM_001099694.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr19:53014773 T>C maps to NM_001099694.1 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:53014932 T>C maps to NM_001099694.1 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P3-01A-11D-A364-08 chr19:53014995 T>C maps to NM_001099694.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:56090213 C>T maps to NM_152600.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:56153894 G>A maps to NM_001163423.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr19:56156206 C>T maps to NM_016535.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr19:56895713 G>A maps to NM_144690.1 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:56895606 T>C maps to NM_144690.1 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6802-01A-11D-1882-08 chr19:56935313 T>G maps to NM_001159861.1 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr19:56925783 G>A maps to NM_001159861.1 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:56935007 T>C maps to NM_001159861.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:56935079 T>C maps to NM_001159861.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr19:58929138 C>T maps to NM_173548.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PF-01A-11D-A25D-08 chr19:58928788 G>T maps to NM_173548.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr19:58928241 C>T maps to NM_173548.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:37643372 G>A maps to ENST00000356958 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:37644344 A>G maps to ENST00000356958 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:37642493 A>C maps to ENST00000356958 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:37642736 T>C maps to ENST00000356958 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:37642790 G>T maps to ENST00000356958 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:37677526 G>A maps to NM_152279.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:58288014 C>T maps to NM_017652.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:58290578 C>T maps to NM_017652.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:58371387 T>C maps to NM_032828.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:58369950 G>A maps to NM_032828.2 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:58370823 A>G maps to NM_032828.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr15:85326907 C>T maps to NM_014630.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5800-01A-11D-1600-08 chr15:85326088 C>T maps to NM_014630.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:85342438 C>T maps to NM_014630.2 C1045C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr15:85341638 C>T maps to NM_014630.2 G890G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N9-01A-12D-A397-08 chr15:85326611 C>T maps to NM_014630.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:5085733 A>G maps to NM_032530.1 N606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr17:5085394 C>T maps to NM_032530.1 W719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr17:5085406 T>C maps to NM_032530.1 K715K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:87141 A>C maps to NM_182524.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr4:60008 C>A maps to NM_182524.2 C63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:192900 C>T maps to NM_001042416.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr8:196025 C>T maps to NM_001042416.1 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr8:195480 C>T maps to NM_001042416.1 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr8:195869 A>G maps to NM_001042416.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IP-7968-01A-11D-2201-08 chr8:195984 C>T maps to NM_001042416.1 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr16:3487175 G>A maps to NM_152457.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr16:3486470 A>G maps to NM_152457.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:3493135 C>T maps to NM_152457.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr16:3486536 G>A maps to NM_152457.1 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:2051134 C>T maps to ENST00000431526 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr16:2052541 G>A maps to ENST00000431526 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr16:2052541 G>A maps to ENST00000431526 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:35250658 C>T maps to NM_001007248.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr19:35251099 C>T maps to NM_001007248.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4449-01A-01D-1158-08 chr19:35250429 T>A maps to NM_001007248.2 K426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:35250007 A>G maps to NM_001007248.2 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:53269379 G>A maps to NM_198457.2 C543C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr19:53270699 G>A maps to NM_198457.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:53269925 A>G maps to NM_198457.2 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:53269289 A>G maps to NM_198457.2 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:58500077 G>T maps to NM_025027.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:58490718 A>G maps to NM_025027.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:58490394 G>A maps to NM_025027.3 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr19:58490438 C>A maps to NM_025027.3 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr19:38189171 T>C maps to NM_032689.4 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7722-01A-31D-2201-08 chr19:38190611 T>C maps to NM_032689.4 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:123983850 T>A maps to NM_020747.2 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr5:123984641 G>A maps to NM_020747.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr5:123984435 G>A maps to NM_020747.2 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr5:124080610 A>G maps to NM_020747.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr5:124036755 A>C maps to NM_020747.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr5:124080349 A>C maps to NM_020747.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr15:64966837 G>A maps to NM_015042.1 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr15:64792133 C>T maps to NM_015042.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr15:64973050 C>A maps to NM_015042.1 P1384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr15:64791863 A>G maps to NM_015042.1 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:52869923 T>C maps to NM_001161425.1 N431N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr19:52869269 T>C maps to NM_001161425.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TJ-01A-11D-A31L-08 chr19:53208739 G>C maps to NM_001161500.1 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:53209716 G>T maps to NM_001161500.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:52448839 T>C maps to NM_001031721.3 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr19:52448839 T>G maps to NM_001031721.3 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:52521297 C>T maps to NM_025040.3 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:52520478 C>T maps to NM_025040.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr19:52519595 G>A maps to NM_025040.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:52519356 G>A maps to NM_025040.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:52497290 A>G maps to ENST00000354939 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8PE-01A-11D-A410-08 chr19:52496986 G>A maps to ENST00000354939 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:52619371 C>A maps to NM_178523.3 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:52618937 G>A maps to NM_178523.3 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:52619000 T>C maps to NM_178523.3 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:52619215 G>A maps to NM_178523.3 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr19:52619684 A>G maps to NM_178523.3 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EA-01A-12D-A34U-08 chr19:52619204 A>G maps to NM_178523.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr9:116812206 C>T maps to ENST00000374126 Y875Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr9:116811192 G>A maps to ENST00000374126 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr9:116812113 C>T maps to ENST00000374126 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr9:116750618 C>T maps to ENST00000374126 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr9:116811441 G>T maps to ENST00000374126 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr9:116770826 C>T maps to ENST00000374126 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr9:116812047 C>T maps to ENST00000374126 H822H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:40523361 C>T maps to NM_001145082.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr3:40529419 G>A maps to NM_001145082.2 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:40557939 C>T maps to NM_175888.2 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr3:40557735 T>A maps to NM_175888.2 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr8:144732140 G>A maps to NM_014789.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr8:144733544 C>T maps to NM_014789.3 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr17:16538058 T>C maps to NM_020787.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr17:16526576 T>C maps to NM_020787.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr17:16526348 G>A maps to NM_020787.3 C617C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:12256531 G>A maps to ENST00000439556 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:12256588 A>G maps to ENST00000439556 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:20807893 G>A maps to NM_001076675.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:20808103 T>C maps to NM_001076675.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A9TM-01A-11D-A397-08 chr19:20829211 C>A did not map to a codon.
Sequencing variant TCGA-HU-A4H5-01A-21D-A25D-08 chr19:20808344 A>T maps to NM_001076675.2 L113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:11728368 C>T maps to NM_145295.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:11728452 C>T maps to NM_145295.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:55993234 G>A maps to NM_033113.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr19:55994461 C>T maps to NM_033113.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:55993936 C>T maps to NM_033113.2 C455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:55995121 C>A maps to NM_033113.2 V850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:55995310 T>C maps to NM_033113.2 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:30794712 G>A maps to NM_001080417.1 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr16:30795015 G>A maps to NM_001080417.1 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:30794412 G>A maps to NM_001080417.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:30795219 C>T maps to NM_001080417.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:30795243 C>T maps to NM_001080417.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr16:30794490 G>A maps to NM_001080417.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:47926264 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:47917968 T>C did not map to a codon.
Sequencing variant TCGA-BR-6706-01A-11D-1882-08 chr23:47918754 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:47919042 T>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:47919907 T>G did not map to a codon.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr23:47919006 T>G did not map to a codon.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr23:47919289 A>G did not map to a codon.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr2:71635328 T>C maps to NM_014497.3 G1071G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:71625867 A>G maps to NM_014497.3 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr2:71629218 T>C did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:71653941 T>G maps to NM_014497.3 L1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr2:71658541 G>A maps to NM_014497.3 A1912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:179051264 G>A maps to NM_016331.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:179046092 T>A maps to NM_016331.1 Y4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr3:179052208 G>C maps to NM_016331.1 *486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr12:48737165 G>A maps to NM_152320.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr12:48737326 G>C maps to NM_152320.2 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:40961583 T>C maps to NM_198494.2 H478H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:40960995 A>G maps to NM_198494.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr1:40947450 T>C maps to NM_198494.2 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr1:40947492 A>G maps to NM_198494.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:91406586 A>G maps to NM_201269.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:91382480 T>A maps to NM_201269.1 R1286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:91404465 A>G maps to NM_201269.1 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:22291372 G>A did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:22291584 G>A did not map to a codon.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr23:22292313 G>A did not map to a codon.
Sequencing variant TCGA-BR-8289-01A-11D-2340-08 chr23:22292331 A>C did not map to a codon.
Sequencing variant TCGA-BR-8678-01A-11D-2394-08 chr23:22291238 A>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:22291517 G>A did not map to a codon.
Sequencing variant TCGA-CG-5725-01A-11D-1600-08 chr23:22291217 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:22291396 C>T did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:31088571 G>A maps to NM_014699.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr16:31091410 C>T maps to NM_014699.3 R1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr16:31088709 G>A maps to NM_014699.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:31091607 C>T maps to NM_014699.3 H1321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G3-01A-11D-A24D-08 chr16:31091208 T>C maps to NM_014699.3 T1188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr16:31089801 T>C maps to NM_014699.3 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr1:182026635 A>G maps to NM_001009992.1 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr1:182026464 C>T maps to NM_001009992.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8690-01A-11D-2394-08 chr1:182026305 C>T maps to NM_001009992.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:182026560 C>T maps to NM_001009992.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4437-01A-01D-1800-08 chr1:182026101 C>T maps to NM_001009992.1 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YX-01A-11D-A25D-08 chr1:182025648 G>A maps to NM_001009992.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:182026137 C>T maps to NM_001009992.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:182026329 G>A maps to NM_001009992.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:182026338 C>T maps to NM_001009992.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:182026818 C>T maps to NM_001009992.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:52394602 G>A maps to NM_023074.3 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:52399818 C>T maps to NM_023074.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr17:47394292 G>A maps to NM_014897.2 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr17:47389291 G>A maps to NM_014897.2 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:11598443 G>A maps to NM_138783.3 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr3:88189153 C>T maps to NM_018293.2 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr7:99170984 T>C maps to NM_001083956.1 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:99161657 G>A maps to NM_024061.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr9:40772342 T>A maps to NM_033160.5 K978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr3:42950327 G>A maps to NM_001134656.1 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr3:42956104 T>C maps to NM_001134656.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7717-01A-11D-2053-08 chr3:42956440 G>A maps to NM_001134656.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6822-01A-11D-1882-08 chr19:53669150 T>A maps to NM_024733.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr19:56952724 T>G maps to ENST00000342634 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:56952901 G>A maps to ENST00000342634 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr19:56953231 T>G maps to ENST00000342634 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G2-01A-11D-A25D-08 chr19:56953316 C>T maps to ENST00000342634 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:31075336 G>T maps to NM_001172669.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr16:31072721 A>G maps to NM_001172669.1 A532A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-4368-01A-01D-1158-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31072649 C>T maps to NM_001172669.1 R556R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-6452-01A-12D-1800-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31072970 C>T maps to ENST00000417110 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:31075474 G>A maps to NM_001172669.1 H125H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BR-8588-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BR-8588-01A-11D-2394-08 chr16:31073216 C>T maps to ENST00000417110 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr16:31075372 G>A maps to NM_001172669.1 G159G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-4460-01A-01D-1158-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CG-5721-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:31073348 G>A maps to ENST00000417110 A179A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CG-5728-01A-11D-1600-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr16:31073393 G>A maps to ENST00000417110 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:247264101 C>T maps to NM_024804.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:247263915 G>A maps to NM_024804.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr1:247263837 A>G maps to NM_024804.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RN-01A-12D-A33T-08 chr1:247201662 C>T maps to NM_033213.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:58232448 G>A maps to ENST00000335820 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:58238779 C>T maps to ENST00000335820 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6I-01A-11D-A410-08 chr19:58232421 G>A maps to ENST00000335820 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:249142780 C>T maps to NM_024836.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6453-01A-11D-1800-08 chr23:46359573 G>A did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr23:46387796 G>A did not map to a codon.
Sequencing variant TCGA-BR-8687-01A-11D-2394-08 chr23:46360232 T>G did not map to a codon.
Sequencing variant TCGA-CG-4469-01A-01D-1158-08 chr23:46360071 T>G did not map to a codon.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:23836084 G>A maps to NM_138330.2 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:23836864 G>A maps to NM_138330.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:23844985 C>T maps to NM_138330.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QM-01A-12D-A25D-08 chr19:22364349 G>A maps to NM_001001411.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:22363693 A>G maps to NM_001001411.2 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:22363168 T>C maps to NM_001001411.2 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:22363510 G>A maps to NM_001001411.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:53741577 T>C maps to NM_182609.2 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8570-01A-11D-2340-08 chr19:53741802 A>G maps to NM_182609.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TI-01A-11D-A31L-08 chr1:227842445 G>A maps to NM_178549.3 W220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:227843126 T>C maps to NM_178549.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr1:227842352 C>T maps to NM_178549.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EX-01A-11D-A31L-08 chr1:227842406 C>A maps to NM_178549.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr7:63726407 G>T maps to NM_153363.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr7:63726382 A>G maps to NM_153363.2 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr7:63982036 A>G maps to NM_178558.4 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr7:63981712 C>T maps to NM_178558.4 W473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:23927901 G>T maps to NM_138286.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A489-01A-11D-A24D-08 chr19:23937634 G>A maps to NM_138286.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:23927061 A>C maps to NM_138286.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6J-01A-11D-A410-08 chr19:23927439 A>G maps to NM_138286.2 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:20117227 T>C maps to NM_033196.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:20117539 G>A maps to NM_033196.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr19:20117897 G>C maps to NM_033196.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:20117671 G>A maps to NM_033196.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:20116963 G>A maps to NM_033196.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr1:26691259 G>A maps to ENST00000436292 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr1:26688422 G>T maps to ENST00000436292 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BT-01A-11D-A33T-08 chr1:26691178 C>A maps to ENST00000436292 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:41007383 T>C did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr1:41007368 C>T maps to NM_152373.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:151259207 C>T maps to NM_020832.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr1:151259492 C>T maps to NM_020832.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr1:151263645 G>A maps to NM_020832.1 A1225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr16:30581664 G>A maps to NM_145271.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr16:30616696 G>A maps to NM_138447.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:43317174 G>A maps to ENST00000442768 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr1:43317330 C>T maps to ENST00000442768 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:247162689 C>T maps to NM_020394.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr1:247150277 A>G maps to NM_020394.3 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:247150913 A>G maps to NM_020394.3 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:144375209 C>T maps to NM_030895.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr8:144378516 C>T maps to NM_030895.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr8:144378510 G>A maps to NM_030895.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr8:144378555 C>T maps to NM_030895.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-8211-01A-11D-2340-08 chr8:144378435 C>T maps to NM_030895.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr8:144378684 C>T maps to NM_030895.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr1:120165558 C>T maps to NM_001080470.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr1:120165708 G>A maps to NM_001080470.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A666-01A-11D-A31L-08 chr1:120165813 G>A maps to NM_001080470.1 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:120166593 A>G maps to NM_001080470.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:9407100 T>G maps to NM_198535.1 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:9413054 T>G maps to NM_198535.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr8:146067085 C>T maps to ENST00000446747 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr8:146054476 T>C did not map to a codon.
Sequencing variant TCGA-IN-A7NU-01A-22D-A34U-08 chr8:146067829 T>C maps to ENST00000446747 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr22:24086655 G>A maps to NM_021916.2 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:12060660 C>T maps to NM_144566.1 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:12060492 C>T maps to NM_144566.1 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6524-01A-11D-1800-08 chr19:12059219 C>T maps to NM_144566.1 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-A4SO-01A-11D-A25D-08 chr19:12060326 A>G maps to NM_144566.1 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:12060509 T>C maps to NM_144566.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr19:12060746 G>A maps to NM_144566.1 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4255-01A-01D-1126-08 chr8:81553642 G>A maps to NM_001033723.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr8:81555313 C>T maps to NM_001033723.2 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr8:81553606 G>A maps to NM_001033723.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr8:81577211 C>T maps to NM_001033723.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr8:81553606 G>A maps to NM_001033723.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr8:81605278 C>T maps to NM_001033723.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr8:144776045 G>A maps to NM_173831.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr8:144776210 C>T maps to NM_173831.3 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:21493360 T>C maps to NM_021269.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:21476765 T>C maps to NM_021269.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:12576150 A>G maps to ENST00000428311 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:12576396 A>G maps to ENST00000428311 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:57133473 C>T maps to NM_021216.4 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:57133347 G>A maps to NM_021216.4 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:57133350 C>T maps to NM_021216.4 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr19:57133641 C>T maps to NM_021216.4 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:57133692 C>T maps to NM_021216.4 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr19:57134037 G>A maps to NM_021216.4 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:57133764 G>A maps to NM_021216.4 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:57133302 C>T maps to NM_021216.4 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:57133125 G>A maps to NM_021216.4 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:57133563 C>T maps to NM_021216.4 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:57133305 C>T maps to NM_021216.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A7BS-01A-11D-A32N-08 chr19:57133785 C>A maps to NM_021216.4 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr15:90617398 C>T maps to NM_198526.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr15:90611247 G>A maps to NM_198526.2 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr15:90611199 C>T maps to NM_198526.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:84523320 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:84510754 T>A did not map to a codon.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr23:84510393 T>G did not map to a codon.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr23:84526508 T>C did not map to a codon.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr23:84510641 G>A did not map to a codon.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr23:84526497 G>C did not map to a codon.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr23:84526108 A>G did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:84510603 A>C did not map to a codon.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr23:84510293 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:84519312 G>A did not map to a codon.
Sequencing variant TCGA-VQ-A91Q-01A-12D-A410-08 chr23:84525767 A>G did not map to a codon.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr7:56007542 T>C maps to NM_182633.1 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:55990858 C>A maps to NM_182633.1 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:55990943 C>T maps to NM_182633.1 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA68-01A-11D-A410-08 chr7:55990901 G>A maps to NM_182633.1 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:21299730 A>G maps to NM_182515.3 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:21300336 T>C maps to NM_182515.3 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:21300087 C>T maps to NM_182515.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:57529465 G>A maps to NM_001159279.1 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr7:57522221 C>A maps to NM_001159279.1 C32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr7:57528733 C>T maps to NM_001159279.1 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8575-01A-11D-2340-08 chr7:57522200 T>C maps to NM_001159279.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:57529540 T>C maps to NM_001159279.1 H458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-7808-01A-11D-2201-08 chr7:57529051 C>A maps to NM_001159279.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr4:436260 T>C maps to NM_133474.2 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr4:437304 G>A maps to NM_133474.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:436695 C>T maps to NM_133474.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr4:438177 C>T maps to NM_133474.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr4:265142 A>C maps to ENST00000419098 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GP-01A-11D-A25D-08 chr7:63809446 T>A maps to NM_001170905.1 C402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:20728102 C>T maps to NM_001159293.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr19:20727781 G>T maps to NM_001159293.1 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr19:20728761 G>A maps to NM_001159293.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:20728084 G>A maps to NM_001159293.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:20728474 A>G maps to NM_001159293.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr22:20760747 C>T maps to NM_003426.2 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr22:20761009 G>T maps to NM_003426.2 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:20760267 C>T maps to NM_003426.2 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7715-01A-11D-2053-08 chr22:20760723 C>T maps to NM_003426.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr22:20754926 G>A maps to NM_003426.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:20749677 G>A maps to NM_003426.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr22:20761149 A>G maps to NM_003426.2 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr12:53580193 C>T maps to NM_001004304.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr7:149171849 C>T maps to NM_001163474.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:149172248 C>T maps to NM_001163474.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr7:149174757 G>A maps to NM_001163474.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EQ-8122-01A-11D-2340-08 chr16:30545793 G>A maps to NM_023931.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:57956642 G>A maps to NM_001023561.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr19:57955691 T>C maps to NM_001023561.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr19:57956099 G>A maps to NM_001023561.2 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RL-01A-11D-A32N-08 chr19:57954665 G>A maps to NM_001023561.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:80788992 G>A maps to NM_024702.2 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:80788059 C>T maps to NM_024702.2 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr17:80789901 C>T maps to NM_024702.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8524-01A-11D-2340-08 chr17:80789022 C>T maps to NM_024702.2 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr17:80789297 G>A maps to NM_024702.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:80789205 G>A maps to NM_024702.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:80790228 G>A maps to NM_024702.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr16:3367640 G>A maps to NM_153028.2 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr16:3363137 T>C maps to NM_153028.2 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr23:134421740 A>C did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:134426265 A>G did not map to a codon.
Sequencing variant TCGA-BR-7704-01A-11D-2053-08 chr23:134426355 C>T did not map to a codon.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr23:134426207 T>A did not map to a codon.
Sequencing variant TCGA-IN-8462-01A-11D-2340-08 chr23:134426307 G>T did not map to a codon.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr6:35259392 C>T maps to NM_003427.3 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8578-01A-21D-2340-08 chr6:35260364 C>T maps to NM_003427.3 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr6:35262952 C>A maps to NM_003427.3 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:53958606 G>A maps to NM_001008401.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:53958093 A>G maps to NM_001008401.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4300-01A-01D-1158-08 chr19:53958796 C>T maps to NM_001008401.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:53958523 C>T maps to NM_001008401.3 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:12089890 A>G maps to NM_001012753.1 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-A5TN-01A-21D-A31L-08 chr16:30569371 C>T maps to NM_033410.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr16:30569344 G>A maps to NM_033410.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr16:30567396 C>T maps to NM_033410.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:30569371 C>T maps to NM_033410.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr16:30566703 C>T maps to NM_033410.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:53911305 G>A maps to NM_001040185.1 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr19:53911569 G>A maps to NM_001040185.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:52785393 G>T maps to NM_001010851.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:52793712 C>T maps to NM_001010851.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:52794057 G>A maps to NM_001010851.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr16:30536053 G>T maps to NM_024671.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr16:30536467 G>A maps to NM_024671.3 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5724-01A-11D-1600-08 chr16:30536080 G>A maps to NM_024671.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:2933648 G>A maps to NM_021217.2 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:2934022 G>A maps to NM_021217.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr15:35274312 T>C maps to NM_014106.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr15:35273958 T>C maps to NM_014106.3 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:57984674 G>A maps to NM_001024596.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:57984641 C>A maps to NM_001024596.2 *490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr19:57988659 C>T maps to NM_001024596.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:57985253 T>C maps to NM_001024596.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr19:57984944 G>A maps to NM_001024596.2 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:58018752 T>C maps to NM_198542.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr15:90902115 G>A maps to NM_001004309.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr15:90903581 C>T maps to NM_001004309.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr15:90904334 C>T maps to NM_001004309.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:90903713 C>T maps to NM_001004309.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:150094891 C>T maps to NM_173680.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:150094402 G>A maps to NM_173680.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8530-01A-11D-2340-08 chr19:58265397 T>G maps to NM_173632.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:149129100 C>T maps to ENST00000440594 E755E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr7:149129361 G>A maps to ENST00000440594 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr7:149129034 C>T maps to ENST00000440594 R777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4476-01A-01D-1158-08 chr7:149148159 G>A maps to ENST00000440594 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:149148195 T>C maps to ENST00000440594 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr7:149129439 G>A maps to ENST00000440594 C642C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr7:149129955 C>T maps to ENST00000440594 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:149129301 C>T maps to ENST00000440594 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr16:89294579 A>G maps to NM_182531.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr16:89294006 T>C maps to NM_182531.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr16:89293427 G>T maps to NM_182531.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:89293703 C>A maps to NM_182531.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr16:89293322 T>C maps to NM_182531.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5730-01A-11D-1600-08 chr16:89294279 C>T maps to NM_182531.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8686-01A-11D-2394-08 chr19:40589024 G>T maps to NM_001142577.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:40580565 G>A maps to NM_001142577.1 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:40541184 C>T maps to NM_001005851.2 K527K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:40541039 G>A maps to NM_001005851.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:40542306 A>G maps to NM_001005851.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr19:40542131 G>A maps to NM_001005851.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:38160614 C>T maps to NM_152605.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr9:99581155 C>T maps to NM_001001662.1 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:56133446 G>A maps to NM_203374.1 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:56133454 G>A maps to NM_203374.1 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:30594405 G>A maps to NM_152458.6 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7998-01A-11D-2201-08 chr16:30594147 G>A maps to NM_152458.6 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4CS-01A-11D-A24D-08 chr7:148768957 G>T maps to NM_152411.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:148768432 G>A maps to NM_152411.3 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr7:148767796 C>T maps to NM_152411.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr7:148768461 G>A maps to NM_152411.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8DV-01A-12D-A364-08 chr7:148769031 G>A maps to NM_152411.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:148768060 G>A maps to NM_152411.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:56600294 C>T maps to NM_001002836.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr19:56599514 G>A maps to NM_001002836.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7851-01A-11D-2201-08 chr19:56600435 G>A maps to NM_001002836.2 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8285-01A-11D-2340-08 chr19:56599505 C>T maps to NM_001002836.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:56600378 G>A maps to NM_001002836.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:99084465 G>A maps to NM_213603.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr7:99084555 G>A maps to NM_213603.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr9:130206659 G>A maps to NM_007135.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr9:130197366 A>G did not map to a codon.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr19:37310519 A>G maps to NM_206894.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr19:37310582 A>G maps to NM_206894.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4466-01A-01D-1158-08 chr19:12738762 C>G maps to NM_153358.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr19:12739380 C>T maps to NM_153358.2 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:12739128 C>T maps to NM_153358.2 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:35448880 G>T maps to NM_175872.4 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:38028432 C>T maps to NM_001013659.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:38027859 C>T maps to NM_001013659.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:12501738 A>G maps to NM_001080821.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:12502149 A>G maps to NM_001080821.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8369-01A-11D-2340-08 chr19:12502755 G>A maps to NM_001080821.2 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:12502374 T>C maps to NM_001080821.2 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:12501534 G>T maps to NM_001080821.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:58805953 T>C maps to NM_021089.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:58806851 G>T maps to NM_021089.2 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:58806665 C>T maps to NM_021089.2 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:58805557 G>A maps to NM_021089.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr3:113955753 G>A maps to NM_007136.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr7:127014060 T>C maps to NM_176814.3 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr7:127013400 A>G maps to NM_176814.3 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr2:185800758 C>T maps to NM_194250.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr2:185801191 G>T maps to NM_194250.1 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8059-01A-11D-2340-08 chr2:185800570 G>T maps to NM_194250.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr2:185802456 T>A maps to NM_194250.1 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A74A-01A-11D-A32N-08 chr2:185801427 A>C maps to NM_194250.1 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7131-01A-11D-2053-08 chr2:185800767 T>G maps to NM_194250.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8604-01A-11D-2394-08 chr2:185802546 T>G maps to NM_194250.1 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91U-01A-11D-A410-08 chr2:185803332 T>C maps to NM_194250.1 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr7:88964956 G>A maps to NM_181646.2 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6454-01A-11D-1800-08 chr7:88963319 G>T maps to NM_181646.2 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:88965793 G>A maps to NM_181646.2 Q1166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:88962740 G>T maps to NM_181646.2 G149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr7:88966012 A>G maps to NM_181646.2 S1239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr7:88964675 G>T maps to NM_181646.2 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:88963237 A>G maps to NM_181646.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H2-01A-11D-A25D-08 chr7:88965058 C>A maps to NM_181646.2 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr19:57765983 T>C maps to NM_001023563.3 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8370-01A-11D-2340-08 chr19:57765431 A>G maps to NM_001023563.3 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7703-01A-11D-2053-08 chr19:53058466 C>T maps to NM_001039886.3 N766N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:53058466 C>T maps to NM_001039886.3 N766N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr23:47774786 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:47774713 T>C did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:47774349 A>G did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr23:47774499 G>A did not map to a codon.
Sequencing variant TCGA-BR-4371-01A-01D-1158-08 chr23:47775486 C>A did not map to a codon.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr23:47775787 T>C did not map to a codon.
Sequencing variant TCGA-D7-6528-01A-11D-1800-08 chr23:47775718 T>A did not map to a codon.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr23:47775018 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr23:47775651 C>T did not map to a codon.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:53994943 G>A maps to NM_001004301.3 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:53994118 A>G maps to NM_001004301.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8589-01A-11D-2394-08 chr19:53454175 A>C maps to NM_001031665.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:53453914 A>G maps to NM_001031665.1 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4QL-01A-31D-A25D-08 chr19:53453155 A>G maps to NM_001031665.1 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:53453869 G>A maps to NM_001031665.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr16:71894460 T>C maps to ENST00000425432 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr16:71898145 C>A did not map to a codon.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:11832956 A>G maps to NM_001080493.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MX-A5UJ-01A-11D-A31L-08 chr19:11833451 C>T maps to NM_001080493.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:11833811 G>A maps to NM_001080493.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr4:146807028 G>A maps to ENST00000508784 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6457-01A-21D-1800-08 chr4:146806887 T>C maps to ENST00000508784 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr4:146807208 C>T maps to ENST00000508784 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4460-01A-01D-1158-08 chr4:146823704 G>A maps to ENST00000508784 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8382-01A-11D-2394-08 chr13:115090018 G>A maps to NM_032436.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8590-01A-11D-2394-08 chr19:37383032 A>G maps to NM_001171979.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H4-01A-21D-A25D-08 chr19:37398891 T>C maps to NM_001171979.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4HD-01A-11D-A25D-08 chr19:37399304 G>A maps to NM_001171979.1 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:53117121 A>C maps to NM_018300.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8081-01A-11D-2340-08 chr19:53117808 C>A maps to NM_018300.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4IY-01A-11D-A25D-08 chr19:53116896 G>A maps to NM_018300.3 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:53116557 C>T maps to NM_018300.3 W420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr17:33289082 A>G maps to NM_052857.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr17:33289325 G>A maps to NM_052857.3 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr20:57766919 T>A maps to NM_178457.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr20:57766658 G>A maps to NM_178457.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6801-01A-11D-1882-08 chr20:57767258 C>T maps to NM_178457.1 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7197-01A-11D-2201-08 chr20:57766526 C>T maps to NM_178457.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr20:57766301 G>A maps to NM_178457.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr20:57769283 T>C maps to NM_178457.1 G1070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8366-01A-11D-2340-08 chr20:57829764 C>T maps to NM_178457.1 S1667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr20:57766848 C>T maps to NM_178457.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr20:57766658 G>A maps to NM_178457.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8531-01A-11D-2340-08 chr20:57766976 G>A maps to NM_178457.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:57768026 C>T maps to NM_178457.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr20:57829278 C>A maps to NM_178457.1 A1505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr20:57829476 T>G maps to NM_178457.1 A1571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7916-01A-11D-2201-08 chr20:57766244 C>T maps to NM_178457.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GC-01A-12D-A25D-08 chr20:57766604 C>T maps to NM_178457.1 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr20:57766652 G>A maps to NM_178457.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:57766430 C>T maps to NM_178457.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:57767405 G>A maps to NM_178457.1 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZI-01A-11D-A34U-08 chr20:57766586 C>A maps to NM_178457.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8E7-01B-11D-A410-08 chr20:57767831 C>T maps to NM_178457.1 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr19:57175801 G>A maps to NM_001005850.1 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:57176389 T>C maps to NM_001005850.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr19:57175420 G>A maps to NM_001005850.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4368-01A-01D-1158-08 chr19:57176020 C>T maps to NM_001005850.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:57175249 C>T maps to NM_001005850.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:57176404 G>A maps to NM_001005850.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:57176221 G>A maps to NM_001005850.1 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr19:57175885 G>A maps to NM_001005850.1 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:57176404 G>A maps to NM_001005850.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:57175912 G>A maps to NM_001005850.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr19:57175954 C>T maps to NM_001005850.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr19:57175987 C>T maps to NM_001005850.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:57176317 G>A maps to NM_001005850.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GF-01A-11D-A24D-08 chr19:57175483 A>G maps to NM_001005850.1 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GT-01A-21D-A25D-08 chr19:57175363 G>A maps to NM_001005850.1 H423H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R5-A7ZF-01A-11D-A34U-08 chr19:57176296 C>A maps to NM_001005850.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA6A-01A-11D-A410-08 chr19:57184233 G>A maps to NM_001005850.1 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:52659093 C>T maps to NM_001102657.1 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:52659267 A>G maps to NM_001102657.1 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr19:52660032 C>T maps to NM_001102657.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr19:52660325 A>G maps to NM_001102657.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr19:52658931 A>G maps to NM_001102657.1 C668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7716-01A-21D-2053-08 chr19:52569232 G>A maps to NM_001136499.1 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:52569670 A>G maps to NM_001136499.1 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:52569289 A>G maps to NM_001136499.1 H615H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr19:12187209 A>G maps to NM_001136501.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:12187524 C>T maps to NM_001136501.1 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H0-01A-11D-A25D-08 chr19:53855523 T>C maps to NM_138374.1 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:9868339 C>T maps to NM_001077624.1 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:9868329 C>A maps to NM_001077624.1 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5801-01A-11D-1600-08 chr19:9868801 T>C maps to NM_001077624.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr19:9868447 C>T maps to NM_001077624.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:9868888 C>T maps to NM_001077624.1 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr19:21117753 G>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr19:21132747 T>C maps to NM_003429.4 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RD-A8N6-01A-11D-A364-08 chr19:21132108 T>C maps to NM_003429.4 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr3:32031023 C>T maps to NM_001137674.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MH-01A-11D-A25D-08 chr3:32030984 C>T maps to NM_001137674.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr7:149557748 A>G maps to NM_001099220.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:149547314 C>T maps to NM_001099220.1 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr7:149557772 G>A maps to NM_001099220.1 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr7:149558561 G>T maps to NM_001099220.1 A771A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr7:149559476 G>A maps to NM_001099220.1 T1076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr7:149559048 C>T maps to NM_001099220.1 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:52887919 C>T maps to NM_001145434.1 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A94T-01A-11D-A410-08 chr19:52887912 C>T maps to NM_001145434.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:20229334 C>A maps to NM_007138.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B7-5816-01A-21D-1600-08 chr19:23545333 G>T maps to NM_003430.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:23545150 A>G maps to NM_003430.2 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:23544352 G>T maps to NM_003430.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr19:23544025 A>G maps to NM_003430.2 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6874-01A-11D-1882-08 chr19:23544325 A>G maps to NM_003430.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr19:23557560 C>T maps to NM_003430.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr19:23543335 C>T maps to NM_003430.2 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr19:23543218 G>C maps to NM_003430.2 Y854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:64852844 G>T maps to NM_152626.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr7:64864784 C>T maps to NM_152626.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RR-01A-12D-A32N-08 chr7:64863275 A>G maps to NM_152626.2 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:20044417 A>G maps to NM_031218.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6818-01A-11D-1882-08 chr19:22574431 T>C maps to NM_001098626.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:22574530 G>A maps to NM_001098626.1 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6458-01A-11D-1800-08 chr19:22951152 T>C maps to ENST00000397104 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8535-01A-11D-2340-08 chr19:22941159 A>G maps to ENST00000397104 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:22940244 A>G maps to ENST00000397104 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:22940056 G>T maps to ENST00000397104 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SW-A7EB-01A-11D-A34U-08 chr19:22940991 A>G maps to ENST00000397104 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr20:47879933 T>C maps to NM_021035.2 E746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8527-01A-11D-2340-08 chr20:47866104 G>A maps to NM_021035.2 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4443-01A-01D-1158-08 chr20:47864682 G>A maps to NM_021035.2 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr20:47865237 G>A maps to NM_021035.2 C1441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7132-01A-11D-2053-08 chr20:47887639 G>A maps to NM_021035.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr20:47866122 G>T maps to NM_021035.2 C1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:47865966 C>T maps to NM_021035.2 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr20:47868061 A>C did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr7:100866976 T>C maps to NM_006349.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:100866014 C>T maps to NM_006349.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:64884012 T>C maps to NM_014205.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4267-01A-01D-1126-08 chr1:86123655 T>G did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr1:86173880 G>A maps to NM_017953.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr1:86173930 C>A maps to NM_017953.3 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4280-01A-01D-1126-08 chr7:30395356 T>C maps to NM_147128.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5726-01A-11D-1600-08 chr7:30363270 T>G maps to NM_147128.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr22:29440866 C>T maps to NM_032173.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8372-01A-11D-2340-08 chr22:29444420 C>T maps to NM_032173.2 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr22:29446743 C>T maps to NM_032173.2 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr22:29446743 C>T maps to NM_032173.2 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr22:29446259 C>T maps to NM_032173.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6564-01A-12D-1882-08 chr19:5456632 G>A maps to NM_181710.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8487-01A-11D-2394-08 chr19:5455561 G>A maps to NM_181710.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4436-01A-01D-1158-08 chr19:5456566 G>A maps to NM_181710.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5722-01A-21D-1600-08 chr19:5456203 G>A maps to NM_181710.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr11:60637913 C>T maps to NM_207341.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr11:60642609 C>T maps to NM_207341.2 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8592-01A-11D-2394-08 chr11:60640734 C>T maps to NM_207341.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr16:21213111 T>C maps to NM_003460.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr16:21222832 G>T maps to NM_003460.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8291-01A-11D-2340-08 chr16:21215497 G>T maps to NM_003460.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-7136-01A-11D-2053-08 chr16:21208826 C>A maps to NM_003460.1 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8484-01A-11D-2394-08 chr1:238053764 A>T maps to NM_021186.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr1:238048754 G>A maps to NM_021186.3 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-A4BE-01A-12D-A24D-08 chr1:238050694 A>C maps to NM_021186.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G8-01A-11D-A25D-08 chr1:238048809 G>A maps to NM_021186.3 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr7:50022935 A>G did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr17:38024800 G>A did not map to a codon.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:126631373 T>C maps to NM_017580.2 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4184-01A-01D-1126-08 chr10:126671766 G>A maps to NM_017580.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HJ-7597-01A-21D-2201-08 chr10:126670301 G>A maps to NM_017580.2 W484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GU-01A-11D-A25D-08 chr10:126671766 G>A maps to NM_017580.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr1:71536661 G>A maps to NM_203350.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr2:136029370 G>A maps to NM_032143.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr2:136261983 G>A maps to NM_032143.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr2:135988449 T>C maps to NM_032143.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr2:136107604 G>A maps to NM_032143.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr23:15822296 C>T did not map to a codon.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr23:15841246 G>A did not map to a codon.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr23:15841309 G>A did not map to a codon.
Sequencing variant TCGA-BR-4201-01A-01D-1126-08 chr19:58564965 C>T maps to NM_182572.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5733-01A-11D-1600-08 chr19:58565271 C>T maps to NM_182572.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YV-01A-11D-A25D-08 chr19:58565160 C>T maps to NM_182572.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6F0-01A-11D-A31L-08 chr19:58549416 G>A maps to NM_182572.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GH-01A-11D-A24D-08 chr19:58549308 A>G maps to NM_182572.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GQ-01A-11D-A25D-08 chr19:58549498 C>T maps to NM_182572.3 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:58563961 G>A maps to NM_182572.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A91V-01A-11D-A410-08 chr19:58565271 C>T maps to NM_182572.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4370-01A-01D-1158-08 chr16:3139112 G>A maps to NM_032805.1 H719H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8591-01A-11D-2394-08 chr16:3139544 G>A maps to NM_032805.1 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5723-01A-11D-1600-08 chr16:3140021 C>T maps to NM_032805.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-6815-01A-11D-1882-08 chr16:3139285 G>A maps to NM_032805.1 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5798-01A-11D-1600-08 chr19:58596468 C>T maps to NM_001145542.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8534-01A-11D-2340-08 chr19:58601553 G>A maps to NM_001145542.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8536-01A-11D-2340-08 chr19:58596462 G>A maps to NM_001145542.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FP-7829-01A-11D-2053-08 chr19:58596723 G>A maps to NM_001145542.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4256-01A-01D-1126-08 chr15:85163908 G>A maps to NM_181877.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr15:85164067 C>T maps to NM_181877.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr15:85165030 C>T maps to NM_181877.3 C535C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr15:85163986 C>G maps to NM_181877.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8363-01A-11D-2340-08 chr1:33957048 T>C maps to NM_145238.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5721-01A-11D-1600-08 chr1:33960490 T>C maps to NM_145238.3 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-A6RP-01A-21D-A33T-08 chr1:33956749 C>T maps to NM_145238.3 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr7:99654892 G>A maps to NM_145914.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr7:99655394 G>A maps to NM_145914.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MI-01A-21D-A25D-08 chr19:58846407 C>T maps to NM_181846.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr19:58850592 G>T maps to NM_181846.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-6177-01A-11D-1800-08 chr19:58850458 C>T maps to NM_181846.2 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr15:43662096 T>C maps to NM_152455.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A6EY-01A-21D-A31L-08 chr15:43658905 G>A maps to NM_152455.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4306-01A-01D-1158-08 chr19:58189781 G>T maps to NM_152677.2 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5728-01A-11D-1600-08 chr19:58189819 T>C maps to NM_152677.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YT-01A-11D-A25D-08 chr19:58189624 C>T maps to NM_152677.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A72C-01A-21D-A33T-08 chr19:58187554 C>T maps to NM_152677.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4H3-01A-21D-A25D-08 chr19:58189948 C>T maps to NM_152677.2 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr19:56736057 G>A maps to NM_024303.1 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A4PD-01A-11D-A25D-08 chr19:56733564 G>A maps to NM_024303.1 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr19:56736256 C>T maps to NM_024303.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr19:56702323 G>A maps to NM_001080456.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr19:56703251 G>T maps to NM_001080456.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-8532-01A-11D-2340-08 chr19:56704313 G>A maps to NM_001080456.2 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A48A-01A-12D-A24D-08 chr19:56702323 G>A maps to NM_001080456.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr20:44512181 A>G maps to NM_080603.4 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-AA64-01A-11D-A410-08 chr20:44511671 G>T maps to NM_080603.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4292-01A-01D-1126-08 chr2:187698687 C>T maps to NM_182521.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr2:187693277 A>G maps to NM_182521.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:187693319 T>C maps to NM_182521.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8361-01A-11D-2340-08 chr2:187713710 C>T maps to NM_182521.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr2:187693421 A>G maps to NM_182521.2 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-5718-01A-11D-1600-08 chr20:44506534 G>A maps to NM_080752.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr20:44505587 C>T maps to NM_080752.3 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr20:44507167 G>A maps to NM_080752.3 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-A4YY-01A-11D-A25D-08 chr19:13941296 C>G maps to NM_023072.2 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F1-A448-01A-11D-A24D-08 chr19:13930228 C>T maps to NM_023072.2 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4257-01A-01D-1126-08 chr1:45553697 G>T maps to NM_020883.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:45484248 A>G maps to NM_020883.1 A1145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8360-01A-11D-2340-08 chr1:45501385 G>T maps to NM_020883.1 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4442-01A-01D-1158-08 chr1:45504668 G>A maps to NM_020883.1 C611C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr17:15890644 A>G maps to NM_001042698.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr6:116987884 T>C maps to NM_145062.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-A4MJ-01A-11D-A25D-08 chr6:116966909 T>C maps to NM_145062.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-8602-01A-11D-2394-08 chr11:113610031 C>T maps to NM_004724.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr15:66811285 T>G maps to NM_017975.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr15:66819665 G>A maps to NM_017975.3 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IN-AB1X-01A-11D-A397-08 chr15:66838998 C>T maps to NM_017975.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4253-01A-01D-1126-08 chr10:58118564 C>T did not map to a codon.
Sequencing variant TCGA-BR-8373-01A-11D-2340-08 chr10:58119260 G>C maps to NM_032997.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-A452-01A-91D-A25D-08 chr10:58120972 C>A maps to NM_032997.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr23:57935776 A>T did not map to a codon.
Sequencing variant TCGA-BR-6852-01A-11D-1882-08 chr23:57936032 G>A did not map to a codon.
Sequencing variant TCGA-BR-8078-01A-11D-2340-08 chr23:57935670 C>T did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:57935216 C>T did not map to a codon.
Sequencing variant TCGA-CD-A48C-01A-11D-A24D-08 chr23:57936569 C>T did not map to a codon.
Sequencing variant TCGA-CD-A4MG-01A-11D-A25D-08 chr23:57935807 C>T did not map to a codon.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr23:57935574 C>T did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr23:57934627 T>G did not map to a codon.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr23:57935040 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4G9-01A-11D-A24D-08 chr23:57936382 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GX-01A-12D-A25D-08 chr23:57936147 G>A did not map to a codon.
Sequencing variant TCGA-HU-A4H8-01A-11D-A25D-08 chr23:57936600 C>T did not map to a codon.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr23:57935737 C>T did not map to a codon.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr23:57619667 C>T did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:57618746 G>A did not map to a codon.
Sequencing variant TCGA-BR-8368-01A-11D-2340-08 chr23:57620178 G>A did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr23:57619028 G>A did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr23:57619558 C>T did not map to a codon.
Sequencing variant TCGA-HU-A4GN-01A-11D-A25D-08 chr23:57620220 T>G did not map to a codon.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr3:126189736 C>T did not map to a codon.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:53236725 G>A maps to NM_024646.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:53279575 A>G maps to NM_024646.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-7707-01A-11D-2053-08 chr1:53237430 C>T maps to NM_024646.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CD-5804-01A-12D-2053-08 chr1:53262457 T>C did not map to a codon.
Sequencing variant TCGA-KB-A93G-01A-11D-A397-08 chr1:53282279 C>T maps to NM_024646.2 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr7:143085618 G>A maps to NM_001010972.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6566-01A-11D-1800-08 chr17:3980227 C>T maps to NM_015113.3 Q1015Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:3936193 G>T maps to NM_015113.3 C2229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CG-4305-01A-01D-1158-08 chr17:3974038 G>A maps to NM_015113.3 N1338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D7-8572-01A-11D-2340-08 chr17:3920946 G>A maps to NM_015113.3 S2573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HF-A5NB-01A-11D-A31L-08 chr17:3974200 G>A maps to NM_015113.3 D1284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:3924455 C>T maps to NM_015113.3 E2457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VQ-A8P2-01A-11D-A364-08 chr17:3981219 C>T maps to NM_015113.3 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4361-01A-01D-1158-08 chr1:78097959 A>G maps to NM_015534.4 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-4362-01A-01D-1158-08 chr1:78097899 G>T maps to NM_015534.4 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-6452-01A-12D-1800-08 chr1:78047778 A>G maps to NM_015534.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BR-8680-01A-11D-2394-08 chr1:78041750 A>G did not map to a codon.
Sequencing variant TCGA-CG-4465-01A-01D-1158-08 chr1:78098937 C>T maps to NM_015534.4 A34A. Only missense variants will be evaluated by CHASM.
